CA2540333C - Sterilization wraps and methods for sterilizing articles - Google Patents
Sterilization wraps and methods for sterilizing articles Download PDFInfo
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- CA2540333C CA2540333C CA2540333A CA2540333A CA2540333C CA 2540333 C CA2540333 C CA 2540333C CA 2540333 A CA2540333 A CA 2540333A CA 2540333 A CA2540333 A CA 2540333A CA 2540333 C CA2540333 C CA 2540333C
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/26—Accessories or devices or components used for biocidal treatment
- A61L2/28—Devices for testing the effectiveness or completeness of sterilisation, e.g. indicators which change colour
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/26—Accessories or devices or components used for biocidal treatment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
- A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
- A61B50/3001—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments for sharps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
- A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
- A61B50/31—Carrying cases or bags, e.g. doctors' bags
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/05—Interconnection of layers the layers not being connected over the whole surface, e.g. discontinuous connection or patterned connection
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/04—Articles or materials wholly enclosed in single sheets or wrapper blanks
- B65D75/06—Articles or materials wholly enclosed in single sheets or wrapper blanks in sheets or blanks initially folded to form tubes
- B65D75/08—Articles or materials wholly enclosed in single sheets or wrapper blanks in sheets or blanks initially folded to form tubes with the ends of the tube closed by folding
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
- A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
- A61B2050/314—Flexible bags or pouches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
- A61L2/04—Heat
- A61L2/06—Hot gas
- A61L2/07—Steam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/20—Gaseous substances, e.g. vapours
- A61L2/206—Ethylene oxide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/10—Apparatus features
- A61L2202/18—Aseptic storing means
- A61L2202/181—Flexible packaging means, e.g. permeable membranes, paper
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/24—Medical instruments, e.g. endoscopes, catheters, sharps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/03—3 layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
- B32B2250/242—All polymers belonging to those covered by group B32B27/32
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2439/00—Containers; Receptacles
- B32B2439/02—Open containers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/19—Sheets or webs edge spliced or joined
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31913—Monoolefin polymer
Abstract
Improved sterilization wraps (30, 44) and methods for using the improved sterilization wraps (30, 44) to sterilize articles (36). The wraps (30, 44) are made of at least one panel (32, 46, 60) of sterilization material and an additional panel (34. 52, 76) which in some embodiments is made of an absorbent material (34, 52). The additional panel (76) of material may be bonded to the first panel (60) at approximately at a forty-five degree angle to the first panel (60). The article to be sterilized (36) is placed on the sterilization wrap (30, 44), is wrapped, and sterilant is applied to the wrapped article (36). The absorbent material (34, 52) provides sterility protection for the article (36) in addition to the panel (32, 46, 60) of sterilization material and also wicks moisture away from the article (36) after sterilization has taken place. A chemical visual indicator (42, 56, 88) is provided to indicate whether or not the article (36) has been exposed to adequate sterilization conditions.
Description
Sterilization Wraps And Methods For Sterilizing Articles Description Technical Field The invention relates to sterilisation wrap. More particularly, the invention relates to sterilization wrap utilizing at least two layers or panels of material.
Backgiround Art Reusable medical instruments must be sterilized prior to each use. Normally, these instruments are exposed to a sterilant to achieve sterilization. As used herein, the term steriliant refers to the sterilization effectors that are conventionally utilized with sterilization wrap, sterilization techniques, including but not limited to steam, ethylene-oxide, plasma, or the like. In order for the instruments to remain sterile after the sterilization procedure, the instruments must be wrapped in a material called sterilization wrap prior to the sterilization procedure.
The most common type of sterilization wrap is a three-ply laminate consisting of a layer of melt blown polypropylene sandwiched between two layers of spun bond polypropylene. The wrap includes bond points all across the face of the material so that the material is held together, i.e., laminated. This three-ply material is commonly referred to as "SMS," which is short for spun bond - melt blown - spun bond. Most hospitals specify SMS as the sterilization wrap to be used because SMS is sufficiently porous to permit steam, ethylene-oxide and other sterilization materials to penetrate through the material to the surgical instruments, but has filtration properties sufficient to prevent the passage of most pathogens therethrough so as to maintain sterility after the sterilization process. The wrap also protects articles during sterilization and acts as a filtration medium for the sterilant.
In most hospitals, there is a protocol which requires surgical instruments to be wrapped with two separate panels of material so that if one panel becomes torn but not discovered, there is a redundancy which will maintain the sterility of the surgical instruments. The wrapping of surgical instruments with two separate panels of sterilization wrap obviously is labor intensive in that the clinician must first place the instruments on one panel of sterilization material and wrap the instruments, and then place the wrapped package on another panel of sterilization material and again wrap the package containing the instruments.
In an attempt to reduce the labor required to provide dual wrapping of surgical instruments, Kimberly-Clark Corporation has developed a product called "One Step~ Sterilization Wrap." One Step~ Sterilization Wrap is made by bonding two separate panels of sterilization wrap together near two of the edges of the adjacent panels. The Kimberly-Clark One Step~ product is described in U.S. Patents 5,635,134 and 5,688,476.
Figure 1 herein shows one of the Kimberly-Clark One Steps products described in these Kimberly-Clark patents. Sterilization wrap 10 includes a top panel 12 made of SMS and a bottom panel 14 also made of SMS. The lengths and widths of top panel 12 and bottom panel 14 are identical and the outside edges of each panel align with one another. The two panels of SMS are bonded together near two opposing edges 16 and 18, as illustrated by bond lines 20 and 22. The method of bonding the two panels together may be ultrasonic bonding. The other two opposing edges 24 and 26 are not bonded together so there is a visible gap 28 between panels 12 and 14 so that the user of the sterilization wrap visually distinguishes the fact that there are, indeed, two panels. Apparently the purpose for ensuring that the two panels are visually distinguishable as separate panels is so that the user knows with certainty that the item to be sterilized has two panel protection.
However, because of this gap 28, debris could enter the region between the two panels.
With two of the edges being unbonded, it is possible that the panels become misaligned so that if a sharp object penetrates both panels, the resulting holes in each panel could also become misaligned, thus reducing ones ability to determine whether or not there is a hole through both panels. In addition, since edges 24 and 26 are not bonded and bond lines 20 and 22 are somewhat removed from edges 16 and 18, fibers from those edges cold become released from the wrap. Also, since the edges 24 and 26 are not bonded, the two panels might be pulled apart by mistake during use. Furthermore, since the wrap shown in Figure 1 is not sealed right to the edges 16 and 18, the user might perceive that there could be contamination between the panels.
Recently Cardinal Health has introduced a new two panel sterilization wrap called Simul-Wrap~ which overcomes the problems of the Kimberly-Clark One Step~ product described above. The Simul-Wraps product is made of two identical panels of SMS sterilization material which are bonded together along all four edges. The Cardinal Health Simul-Wrap~
product is shown in U.S. Patent No. 6,517,916. However, both the One Step~
product and the Simul-Wrap~ product could be improved.
Disclosure of Invention In one aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least a first panel of sterilization material and a panel of absorbent material bonded to the first panel of sterilization material. The panel of absorbent material is adapted to receive the article to be sterilized thereon; and (a) provides sterility protection for the article in addition to the first panel of sterilization material, and (b) wicks moisture away from the article after sterilization has taken place.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least a first panel of sterilization material; the first panel having an outer periphery and a central portion, and an additional panel of material bonded to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material and a panel of absorbent material attached to the panel of sterilization material.
The panel of absorbent material adapted to contact the article to be sterilized and is enabled to wick moisture away from the article after sterilization has taken place.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material having a central portion, and a panel attached to the central portion of the panel of sterilization material. The basis weight of the panel is higher than the basis weight of the panel of sterilization material.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material, and a chemical visual indicator responsive to the presence of sterilant so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material. The first panel of sterilization material has an outer periphery and a central portion.
An additional panel of material is bonded to the first panel. A substantial portion of the additional panel is adjacent to the central portion of the first panel. The perimeter of the additional panel is smaller than the perimeter of the first panel.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material. The first panel is rectangular and has an outer periphery and a central portion, the outer periphery including first, second, third and fourth edges. An additional panel of material is bonded to the first panel; a substantial portion of the additional panel being adjacent to the central portion of the first panel. The perimeter of the additional panel is smaller than the perimeter of the first panel.
A portion of the additional panel is bonded to the first panel along the first edge.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material, and an additional panel attached to the first panel. The first panel is multi-layered and includes at least one pathogen filtration layer, and the additional panel does not include a pathogen filtration layer.
Backgiround Art Reusable medical instruments must be sterilized prior to each use. Normally, these instruments are exposed to a sterilant to achieve sterilization. As used herein, the term steriliant refers to the sterilization effectors that are conventionally utilized with sterilization wrap, sterilization techniques, including but not limited to steam, ethylene-oxide, plasma, or the like. In order for the instruments to remain sterile after the sterilization procedure, the instruments must be wrapped in a material called sterilization wrap prior to the sterilization procedure.
The most common type of sterilization wrap is a three-ply laminate consisting of a layer of melt blown polypropylene sandwiched between two layers of spun bond polypropylene. The wrap includes bond points all across the face of the material so that the material is held together, i.e., laminated. This three-ply material is commonly referred to as "SMS," which is short for spun bond - melt blown - spun bond. Most hospitals specify SMS as the sterilization wrap to be used because SMS is sufficiently porous to permit steam, ethylene-oxide and other sterilization materials to penetrate through the material to the surgical instruments, but has filtration properties sufficient to prevent the passage of most pathogens therethrough so as to maintain sterility after the sterilization process. The wrap also protects articles during sterilization and acts as a filtration medium for the sterilant.
In most hospitals, there is a protocol which requires surgical instruments to be wrapped with two separate panels of material so that if one panel becomes torn but not discovered, there is a redundancy which will maintain the sterility of the surgical instruments. The wrapping of surgical instruments with two separate panels of sterilization wrap obviously is labor intensive in that the clinician must first place the instruments on one panel of sterilization material and wrap the instruments, and then place the wrapped package on another panel of sterilization material and again wrap the package containing the instruments.
In an attempt to reduce the labor required to provide dual wrapping of surgical instruments, Kimberly-Clark Corporation has developed a product called "One Step~ Sterilization Wrap." One Step~ Sterilization Wrap is made by bonding two separate panels of sterilization wrap together near two of the edges of the adjacent panels. The Kimberly-Clark One Step~ product is described in U.S. Patents 5,635,134 and 5,688,476.
Figure 1 herein shows one of the Kimberly-Clark One Steps products described in these Kimberly-Clark patents. Sterilization wrap 10 includes a top panel 12 made of SMS and a bottom panel 14 also made of SMS. The lengths and widths of top panel 12 and bottom panel 14 are identical and the outside edges of each panel align with one another. The two panels of SMS are bonded together near two opposing edges 16 and 18, as illustrated by bond lines 20 and 22. The method of bonding the two panels together may be ultrasonic bonding. The other two opposing edges 24 and 26 are not bonded together so there is a visible gap 28 between panels 12 and 14 so that the user of the sterilization wrap visually distinguishes the fact that there are, indeed, two panels. Apparently the purpose for ensuring that the two panels are visually distinguishable as separate panels is so that the user knows with certainty that the item to be sterilized has two panel protection.
However, because of this gap 28, debris could enter the region between the two panels.
With two of the edges being unbonded, it is possible that the panels become misaligned so that if a sharp object penetrates both panels, the resulting holes in each panel could also become misaligned, thus reducing ones ability to determine whether or not there is a hole through both panels. In addition, since edges 24 and 26 are not bonded and bond lines 20 and 22 are somewhat removed from edges 16 and 18, fibers from those edges cold become released from the wrap. Also, since the edges 24 and 26 are not bonded, the two panels might be pulled apart by mistake during use. Furthermore, since the wrap shown in Figure 1 is not sealed right to the edges 16 and 18, the user might perceive that there could be contamination between the panels.
Recently Cardinal Health has introduced a new two panel sterilization wrap called Simul-Wrap~ which overcomes the problems of the Kimberly-Clark One Step~ product described above. The Simul-Wraps product is made of two identical panels of SMS sterilization material which are bonded together along all four edges. The Cardinal Health Simul-Wrap~
product is shown in U.S. Patent No. 6,517,916. However, both the One Step~
product and the Simul-Wrap~ product could be improved.
Disclosure of Invention In one aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least a first panel of sterilization material and a panel of absorbent material bonded to the first panel of sterilization material. The panel of absorbent material is adapted to receive the article to be sterilized thereon; and (a) provides sterility protection for the article in addition to the first panel of sterilization material, and (b) wicks moisture away from the article after sterilization has taken place.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least a first panel of sterilization material; the first panel having an outer periphery and a central portion, and an additional panel of material bonded to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material and a panel of absorbent material attached to the panel of sterilization material.
The panel of absorbent material adapted to contact the article to be sterilized and is enabled to wick moisture away from the article after sterilization has taken place.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material having a central portion, and a panel attached to the central portion of the panel of sterilization material. The basis weight of the panel is higher than the basis weight of the panel of sterilization material.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises at least one panel of sterilization material, and a chemical visual indicator responsive to the presence of sterilant so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material. The first panel of sterilization material has an outer periphery and a central portion.
An additional panel of material is bonded to the first panel. A substantial portion of the additional panel is adjacent to the central portion of the first panel. The perimeter of the additional panel is smaller than the perimeter of the first panel.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material. The first panel is rectangular and has an outer periphery and a central portion, the outer periphery including first, second, third and fourth edges. An additional panel of material is bonded to the first panel; a substantial portion of the additional panel being adjacent to the central portion of the first panel. The perimeter of the additional panel is smaller than the perimeter of the first panel.
A portion of the additional panel is bonded to the first panel along the first edge.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material, and an additional panel attached to the first panel. The first panel is multi-layered and includes at least one pathogen filtration layer, and the additional panel does not include a pathogen filtration layer.
In another aspect a sterilization wrap for wrapping an article to be sterilized is provided which comprises a first panel of sterilization material, the first panel being rectangular. A rectangular an additional panel is bonded to the first panel, and oriented on the first panel so as to form a diamond shape with respect to the first panel.
In yet another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with a sterilization wrap which comprises at least a first panel of sterilization material; and a panel of absorbent material bonded to the first panel of sterilization material; the panel of absorbent material adapted to receive the article to be sterilized thereon; the panel of absorbent material (a) providing sterility protection for the article in addition to the panel of sterilization material, and (b) wicking moisture away from the article after sterilization has taken place. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized; wrapping the article to be sterilized with a sterilization wrap which comprises at least a first panel of sterilization material, the first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with sterilization wrap which comprises at least one panel of sterilization material; and a panel of absorbent material attached to the panel of sterilization materia,; the panel of absorbent material adapted to contact the article to be sterilized; the panel of absorbent material enabled to wick moisture away from the article after sterilization has taken place.
Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with sterilization wrap which comprises at least one panel of sterilization material having a central portion; and a panel attached to the central portion of the panel of sterilization material; the basis weight of the panel being higher than the basis weight of the panel of sterilization material.
Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized in sterilization wrap which comprises at least one panel of sterilization material; and a chemical visual indicator responsive to the presence of sterilant so as to indicate whether or not the article has been exposed to adequate sterilization conditions. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with a sterilization wrap which comprises a first panel of sterilization material, the first panel of sterilization material having an outer periphery and a central portion; and an additional panel of material, the additional panel being bonded to the first panel, a substantial portion of the additional panel being adjacent to the central portion of the first panel, and the perimeter of the additional panel being smaller than the perimeter of the first panel. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and providing sterilization wrap which comprises a first panel of sterilization material, the first panel being rectangular and having an outer periphery and a central portion;
the outer periphery including first, second, third and fourth edges; and an additional panel of material, the additional panel being bonded to the first panel, a substantial portion of the additional panel being adjacent to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel, and a portion of the additional panel being bonded to the first panel along the first edge. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
In yet another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with a sterilization wrap which comprises at least a first panel of sterilization material; and a panel of absorbent material bonded to the first panel of sterilization material; the panel of absorbent material adapted to receive the article to be sterilized thereon; the panel of absorbent material (a) providing sterility protection for the article in addition to the panel of sterilization material, and (b) wicking moisture away from the article after sterilization has taken place. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized; wrapping the article to be sterilized with a sterilization wrap which comprises at least a first panel of sterilization material, the first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with sterilization wrap which comprises at least one panel of sterilization material; and a panel of absorbent material attached to the panel of sterilization materia,; the panel of absorbent material adapted to contact the article to be sterilized; the panel of absorbent material enabled to wick moisture away from the article after sterilization has taken place.
Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with sterilization wrap which comprises at least one panel of sterilization material having a central portion; and a panel attached to the central portion of the panel of sterilization material; the basis weight of the panel being higher than the basis weight of the panel of sterilization material.
Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized in sterilization wrap which comprises at least one panel of sterilization material; and a chemical visual indicator responsive to the presence of sterilant so as to indicate whether or not the article has been exposed to adequate sterilization conditions. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and wrapping the article to be sterilized with a sterilization wrap which comprises a first panel of sterilization material, the first panel of sterilization material having an outer periphery and a central portion; and an additional panel of material, the additional panel being bonded to the first panel, a substantial portion of the additional panel being adjacent to the central portion of the first panel, and the perimeter of the additional panel being smaller than the perimeter of the first panel. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and providing sterilization wrap which comprises a first panel of sterilization material, the first panel being rectangular and having an outer periphery and a central portion;
the outer periphery including first, second, third and fourth edges; and an additional panel of material, the additional panel being bonded to the first panel, a substantial portion of the additional panel being adjacent to the central portion of the first panel, the perimeter of the additional panel being smaller than the perimeter of the first panel, and a portion of the additional panel being bonded to the first panel along the first edge. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized providing sterilization wrap which comprises a first panel of sterilization material;
and an additional panel material, the additional panel attached to the first panel, the first panel being multi-layered and including at least one pathogen filtration layer; and the additional panel not including a pathogen filtration layer. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and providing sterilization wrap which comprises a first panel of sterilization material, the first panel being rectangular; and an additional panel; the additional panel being rectangular, the additional panel being bonded to the first panel, and the additional panel being oriented on the first panel so as to form a diamond shape with respect to the first panel. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
Brief Description Of The Drawings Figure 1 is a perspective view of a prior art sterilization wrap;
Figure 2 is a perspective view of one embodiment of sterilization wrap;
Figure 3 is a plan view of the sterilization wrap of Figure 2 with an article to be sterilized received thereon;
Figure 4 is a sectional view of the sterilization wrap of Figure 2 taken through section line 4-4.
Figure 5 is a plan view of another embodiment of sterilization wrap.
Figure 6 is a sectional view of the sterilization wrap of Figure 5 taken through section lines 6-6.
Figure 7 is a plan view of yet another embodiment of sterilization wrap.
and an additional panel material, the additional panel attached to the first panel, the first panel being multi-layered and including at least one pathogen filtration layer; and the additional panel not including a pathogen filtration layer. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
In another aspect a method for sterilizing an article is provided which comprises the steps of providing an article to be sterilized and providing sterilization wrap which comprises a first panel of sterilization material, the first panel being rectangular; and an additional panel; the additional panel being rectangular, the additional panel being bonded to the first panel, and the additional panel being oriented on the first panel so as to form a diamond shape with respect to the first panel. The article to be sterilized is placed on the additional panel and wrapped with the sterilization wrap. Sterilant is applied to the wrapped article.
Brief Description Of The Drawings Figure 1 is a perspective view of a prior art sterilization wrap;
Figure 2 is a perspective view of one embodiment of sterilization wrap;
Figure 3 is a plan view of the sterilization wrap of Figure 2 with an article to be sterilized received thereon;
Figure 4 is a sectional view of the sterilization wrap of Figure 2 taken through section line 4-4.
Figure 5 is a plan view of another embodiment of sterilization wrap.
Figure 6 is a sectional view of the sterilization wrap of Figure 5 taken through section lines 6-6.
Figure 7 is a plan view of yet another embodiment of sterilization wrap.
Figure 8 is a sectional view of the sterilization wrap of Figure 7 taken through section lines 8-8.
Figure 9 is a plan view of yet another embodiment of sterilization wrap.
Figure 10 is a sectional view of the sterilization wrap of Figure 9 taken through section lines 10-10.
Figure 11 is a plan view of yet another embodiment of sterilization wrap.
Figure 12 is a sectional view of the sterilization wrap of Figure 11 taken through section lines 12-12.
Figure 13 is a plan view of the preferred embodiment of the invention.
Figure 14 is a perspective view of the embodiment of Figure 13.
Figure 15 shows the embodiment of Figure 13, including the article to be sterilized.
Figure 16 is a sectional view of the sterilization wrap of Figure 13 taken through section lines 16-16.
Figure 17 is a sectional view of the sterilization wrap of Figure 14 taken through section lines 17-17.
Figure 18 is a pictorial view of another embodiment of the invention.
Figure 19 is a sectional view of the sterilization wrap of Figure 18 taken through section lines 19-19.
Figure 20 is a pictorial view of yet another embodiment of the invention.
Figure 21 is a sectional view of the sterilization wrap of Figure 20 taken through sections lines 21-21.
The thicknesses of the materials shown in the drawings have been exaggerated for illustrative purposes and for ease of understanding. In addition, the thicknesses of the bond sites are exaggerated.
_g_ Best Mode for Carrying Out the Invention Referring now more particularly to Figure 2, in an exemplary embodiment sterilization wrap 30 has a first panel or layer 32 and a second or additional panel or layer 34. The first panel or layer 32 may be made of any fibrous or non-fibrous material so long as it can perform the function of sterilization wrap so as to inhibit pathogens from passing therethrough but will permit sterilant such as steam and ethylene to pass therethrough (hereinafter sometimes referred to as "sterilization material"). Preferably, the first panel 32, which is the outside panel, is made of SMS. The material from which the first panel 32 is made is sometimes referred to herein as a panel of sterilization material. The second panel 34, which is the inside panel and which, in the embodiment of Figure 2 is absorbent, may be made of cellulose or some other absorbent material, which absorbs liquids and aids in drying and which also permits a sterilant, such as steam or ethylene-oxide, to pass therethrough, but inhibits pathogens from passing therethrough. Other absorbent materials could include, but are not limited to, absorbent synthetics such as hydrophillic spunmelt polyolefins, polyester, nylon, as well as polyrayons and bicomponent fibers. The second panel 34 is sometimes referred to herein as a panel of absorbent material. In order to reduce the cost of the sterilization wrap 30 while not reducing its effectiveness, the second or inside panel 34 has a smaller perimeter than the first or outside panel 32. It is preferred that the perimeter of the inside panel 34 be at least 25% less than the outside panel 32.
As can be seen from Figure 3, the inside panel 34 receives the article to be sterilized 36 thereon. Often the article to be sterilized 36 is a tray containing surgical instruments. Wrapping protocol calls for article to be sterilized 36 to be oriented forty-five degrees with respect to SMS panel 32.
While inside panel 34 has a smaller perimeter than outside panel 32, it should be large enough so that when the article to be sterilized 36 is wrapped by sterilization wrap 30, both the bottom and sides of the article to be sterilized 36 is covered by inside panel 34.
Outside panel 32 includes a central portion 38. Inside panel 34 is adjacent to the central portion 38 and is attached to the first panel 32 by means _g_ of gluing, ultrasonic bonding or some other form of adherence. Glue spots 40 are illustrated in Figure 4. Alternatively, inside panel 34 may be made of any fibrous or non-fibrous material, preferably but not limited to SMS or spun bond polypropylene which adds strength but does not have the liquid absorbent properties of cellulose. The structure of inside panel 34 when it is made of SMS is discussed below in reference to Figure 9. The structure of inside panel 34 when it is made of spun bond polypropylene is discussed below in reference to Figures 13-19. In any event, this inside panel provides abuse resistance and containment properties over the prior art sterilization wrap described above.
By reinforcing the area of direct contact under the article to be sterilized 36, the primary point of potential damage to the wrap has been addressed. The method by which trays are wrapped yield several panels of material folds on the top of the article to be sterilized 36. In the event that wrapped articles get stacked on top of one another, thicker and/or heavier inside panel 34 protects the underside of the article 36 while the multiple folds are responsive to contact on the top side of article 36.
As noted, also the inner panel 34 may be made of a moisture absorbent material, such as cellulose, which provides an enhanced moisture absorption function. After the article to be sterilized 36 has been sterilized, in particularly through a steam sterilization process, moisture often remains on the article to be sterilized 36. This moisture enhances the growth of pathogens which may not have been killed during the sterilization process. By using an absorbent material, i.e., absorption material, as the material for panel 34, this moisture tends to be wicked away from the article to be sterilized 36 and more effectively dried. Thus the chances of pathogen growth on or around the article to be sterilized is greatly reduced.
It is preferred that outer panel 32 be of a different color from inner panel 34. Since inner panel 34 is always within the sterile field, this color differential will inform the sterile clinician that it is okay to touch any portion of the sterile field formed by the inside surface of outer panel 32 and inside panel 34.
It is also preferred that a sterilization chemical visual indicator 42, which may also be an integrator or emulator, be adhered to inside panel 34 or to the inside surface 41 of outside panel 32 in the vicinity of inside panel 34.
The sterilization indicator could be of a chemistry which meets or exceeds the requirements of Class 1 - Class 6 chemical indicators as defined by ISO 11140-1. The sterilization indicator turns color in the presence of steam or ethylene-oxide or other sterilant and will remain at that color after sterilization has taken place. This informs the clinician that the article to be sterilized has, indeed, been exposed to adequate sterilization conditions at the time that the clinician opens the wrapped article.
Sterilization indicators are known and two such indicators are described in U.S. Patent 4,514,361 issued to Hirsch and U.S. Patent 2,889,799 issued to Korpman. Sterilization integrators are known and one such integrator is described in U.S. Patent No. 4,448,548.
The sterilization wrap described above can be manufactured using conventional equipment and techniques readily available to those skilled in the medical fabric field.
The sterilization wrap described above may be used as set forth below. The article to be sterilized 36, as shown in Figure 3, is placed on the outside surface of inner panel 34. The article to be sterilized 36 is then wrapped utilizing standard sterilization wrapping techniques so that a portion of the inside panel 34 covers the bottom and sides of the article to be J
sterilized 36, and a portion of the outside panel 32 also covers the top of the article to be sterilized 36. The wrapped package is then exposed to a sterilization process. The wrapped package is subjected to sterilants, such as steam, ethylene-oxide or plasma, for a predetermined period of time so that substantially all of the pathogens which may be present on the article to be sterilized 36 are killed. The package is then stored for usage. When it is time to use the article to be sterilized 36, the package is unwrapped by the clinician.
The sterile clinician will know it is all right to touch the sterile field formed by the inner panel 34 because the inner panel 34 and the outside panel 32 are different colors. The clinician will then observe the status of sterilization indicator, integrator, or emulator 42 to determine whether or not the article has been exposed to adequate sterilization conditions. The article to be sterilized 36 may then be used.
The above-described improved sterilization wrap provides the two panels of protection and ease of use associated with Kimberly-Clark's One Step~ and Cardinal Health's Simul-Wrap, while having the added features of increased protection in the central area adjacent to the article to be sterilized and further providing an ability to wick moisture away from the article to be sterilized, particularly in the case of steam sterilization, and in addition, visually informs the clinician that the inside of the wrap is the sterile field and visually informs the clinician that the article has, indeed, been exposed to adequate sterilization conditions.
While Figures 2 through 4 show absorbent panel 34 attached to a single panel of sterilization material, it is preferred that two (2) panels of sterilization material are utilized.
Referring now more particularly to Figures 5 and 6, two-panel sterilization wrap 44 is provided and includes outside panel 46 and inside panel 48, each made of sterilization material such as SMS. The two panels 46 and 48 each have four edges 49, 51, 53 and 55 and are bonded together at the four edges about their outer peripheries 50, preferably by heat and pressure. The bonded two-panel sterilization material 44 may be the Simul-Wrap~ product which is commercially available from Cardinal Health (1500 Waukegan Road, McGaw Park, Illinois 60085) and which is described in U.S. Patent No.
6,517,916. Additional panel 52, which may be made of cellulose or another moisture absorbing substance, is bonded to the outside of inner panel 48 by gluing or another bonding technique, as illustrated by bond sites 54.
Alternatively, additional panel 52 may be made of any fibrous or non-fibrous material, preferably but not limited to SMS or spun bond polypropylene as discussed in reference to Figures 2, 9 and 13-19.
Referring now more particularly to Figures 7 and 8, a sterilization indicator device 56 is attached to absorbent panel 52.
Referring now more particularly to Figures 9 and 10, the absorbent panel 52 has been replaced with a reinforcement panel 58 made of either a fibrous or non-fibrous material, preferably but not limited to SMS.
Panel 58 has an equal to or higher basis weight than either panel 46 or 48.
The basis weight of panel 58 may range from 1.0 ounces per square yard (osy) to 3.0 osy (34 grams per square meter to 102 grams per square meter). The basis weight for each of panels 46 and 48 may range from 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter). While reinforcement panel 58 does not provide the moisture wicking function of absorption panel 52, it provides additional protection for the article to be sterilized 36 as shown in Figure 5, which is to be placed on reinforcement panel 58. The embodiment shown in Figures 9 and 10 results in a more cost effective product than the use of two full panels of SMS, but is equal functionally, since less material is used. Figure 9 also shows a sterilization indicator 56 having been placed on the outside surface of inner panel 48.
The embodiment of Figures 11 and 12 represents a combination of the embodiments of Figures 7 and 9. That is, reinforcement panel 58 is attached to inside SMS panel 48. Absorbent panel 52 is, in turn, attached to reinforcement panel 58. Chemical visual indicator 56 is attached to absorbent panel 52. Alternatively, indicator 56 may be attached to reinforcement panel or to inside panel 48. In addition, in the embodiment of Figures 11 and 12, outside SMS panel could be eliminated.
With reference to Figures 13-17, in another embodiment a first panel 60 of sterilization wrap is made of sterilization material and preferably includes a layer of pathogen filtration material, such as melt blown polypropylene. Preferably, first panel 60 is made of SMS. First panel 60 includes a central portion generally indicated within the bounds of dashed-lines 62 as shown in Figure 14. First panel 60 also includes an outer periphery 64.
Outer periphery 64 includes four edges 66, 68, 70 and 72. Preferably, a second panel 74 of .sterilization wrap is adjacent to and in register with first panel 60. Preferably, the first and second panels are rectangular. In the embodiment of Figures 13-17, the first panel 60 of sterilization material is bonded to the second panel 74 of sterilization material along all four edges 66, 68, 70 and 72. The preferred bonding method is ultrasonic bonding. An additional panel 76 is bonded to first panel 60. The additional panel 76 could be made from any fibrous or non-fibrous material. Preferably, the additional panel 76 does not include a pathogen filtration layer and is not made from sterilization material. More preferably, additional panel 76 is made of spun bond polypropylene. Additional panel 76 is oriented so that additional panel forms a diamond pattern with respect to first panel 60. As used herein, "diamond" includes both rhombus and square shapes. Preferably, additional panel 76 is oriented forty-five degrees with respect to first panel 60. A
substantial portion of additional panel 76 is adjacent to the central portion 62 of first panel 60. Additional panel 76 is preferably rectangular and includes four corners, namely, corners 78, 80, 82 and 84. In the preferred embodiment all four corners are bonded to first panel 60 as shown in Figure 15, i.e., corner of additional panel 76 is bonded to edge 66 of first panel 60; corner 80 is bonded to edge 68; corner 82 is bonded to edge 70; and corner 84 is bonded to edge 72. However, as shown in Figure 20, only three of the edges are bonded to the panel. Preferably, this corner to edge bonding is also accomplished by ultrasonic bonding. As used herein, the term corner includes a region of the additional panel 76 where two of its edges approach one another. The perimeter of additional panel 76 is less than the perimeter of first panel 60.
As shown in Figure 15, chemical visual indicator 88, which has previously been described, may be attached to additional layer 76. Figure 15 also illustrates the preferred orientation of the article to be sterilized 90 with respect to additional panel 76 and first panel 60. The protocol for wrapping articles to be sterilized with sterilization wrap is to orient the article at a forty-five degree angle with respect to the first sterilization panel 60.
Since, the preferred embodiment calls for the additional panel 76 to be oriented at a forty-five degree angle with respect to the first panel 60, the clinician may place the article to be sterilized with respect to additional panel 76 in alignment with the edges of that panel so that the article will automatically be positioned at a forty-five degree angle with respect to first panel 60.
It is preferred that additional panel 76 has a lower basis weight than first sterilization panel 60 or second sterilization panel 74.
Preferably, the basis weight of the additional panel 76 is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter). Preferably, the basis weight of each of the first panel 60 and the second panel 74 is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter). In addition, it is preferred that the grab tensile to basis weight ratio of additional panel 74 is equal to or greater than the grab tensile to basis weight ratio of the first panel 60.
Preferably, each corner of the additional panel 76 is bonded to the first panel 60 at or about the mid-point of each edge of the first panel 60.
The embodiment of Figures 18 and 19 is similar to the embodiment of Figures 14-17 except that a single sheet 92 of sterilization material is utilized which is folded in half, as illustrated by fold line 94, to provide two panels of sterilization material 96 and 98. Preferably, only three edges 100, 102 and 104 of the two panels 96 and 98 are bonded together, although these two panels 96 and 98 could also be bonded along fold 94. The corners 78, 80 and 82 of additional panel 76 are bonded to panel 96 along edges 100, 102 and 104. Corner 84 is bonded to panel 96 adjacent to fold 94.
The embodiment of Figures 20 and 21 is identical to the embodiment of Figures 18 and 19 except that corner 84 of additional panel 76 is not bonded to panel 96 adjacent to fold 94.
The method for sterilizing article 90 using the sterilization wrap described in reference to Figures 13-19 is the same method as described above in reference to the sterilization wrap shown in Figure 3.
The construction of the sterilization wrap shown in Figures 13-19 provides numerous advantages over the prior art. The additional panel 76 made of spun bond polypropylene which is adjacent to the central portion of one of the two SMS panels provides substantial physical protection for the article to be sterilized 90 compared to the prior art two panel SMS product.
The additional protection is provided precisely where it is needed, that is, in the central portion 62 where the article to be sterilized is placed. In addition, the forty-five degree orientation of the additional panel 76 with respect to first SMS
panel allows the clinician to more readily orient the article to be sterilized 90 in the correct position with respect to the SMS panels.
From the foregoing description of the preferred embodiments of the invention, it is apparent that many modifications may be made therein. It should be understood, however, that these embodiments of the invention are exemplifications of the invention only and that the invention is not limited thereto. It is to be understood, therefore, that it is intended in the appended claims to cover all modifications as fall within the true spirit and scope of the invention.
Industrial Applicability The way in which the invention is capable of being exploited and the way in which it can be made and used will be apparent from the foregoing.
Figure 9 is a plan view of yet another embodiment of sterilization wrap.
Figure 10 is a sectional view of the sterilization wrap of Figure 9 taken through section lines 10-10.
Figure 11 is a plan view of yet another embodiment of sterilization wrap.
Figure 12 is a sectional view of the sterilization wrap of Figure 11 taken through section lines 12-12.
Figure 13 is a plan view of the preferred embodiment of the invention.
Figure 14 is a perspective view of the embodiment of Figure 13.
Figure 15 shows the embodiment of Figure 13, including the article to be sterilized.
Figure 16 is a sectional view of the sterilization wrap of Figure 13 taken through section lines 16-16.
Figure 17 is a sectional view of the sterilization wrap of Figure 14 taken through section lines 17-17.
Figure 18 is a pictorial view of another embodiment of the invention.
Figure 19 is a sectional view of the sterilization wrap of Figure 18 taken through section lines 19-19.
Figure 20 is a pictorial view of yet another embodiment of the invention.
Figure 21 is a sectional view of the sterilization wrap of Figure 20 taken through sections lines 21-21.
The thicknesses of the materials shown in the drawings have been exaggerated for illustrative purposes and for ease of understanding. In addition, the thicknesses of the bond sites are exaggerated.
_g_ Best Mode for Carrying Out the Invention Referring now more particularly to Figure 2, in an exemplary embodiment sterilization wrap 30 has a first panel or layer 32 and a second or additional panel or layer 34. The first panel or layer 32 may be made of any fibrous or non-fibrous material so long as it can perform the function of sterilization wrap so as to inhibit pathogens from passing therethrough but will permit sterilant such as steam and ethylene to pass therethrough (hereinafter sometimes referred to as "sterilization material"). Preferably, the first panel 32, which is the outside panel, is made of SMS. The material from which the first panel 32 is made is sometimes referred to herein as a panel of sterilization material. The second panel 34, which is the inside panel and which, in the embodiment of Figure 2 is absorbent, may be made of cellulose or some other absorbent material, which absorbs liquids and aids in drying and which also permits a sterilant, such as steam or ethylene-oxide, to pass therethrough, but inhibits pathogens from passing therethrough. Other absorbent materials could include, but are not limited to, absorbent synthetics such as hydrophillic spunmelt polyolefins, polyester, nylon, as well as polyrayons and bicomponent fibers. The second panel 34 is sometimes referred to herein as a panel of absorbent material. In order to reduce the cost of the sterilization wrap 30 while not reducing its effectiveness, the second or inside panel 34 has a smaller perimeter than the first or outside panel 32. It is preferred that the perimeter of the inside panel 34 be at least 25% less than the outside panel 32.
As can be seen from Figure 3, the inside panel 34 receives the article to be sterilized 36 thereon. Often the article to be sterilized 36 is a tray containing surgical instruments. Wrapping protocol calls for article to be sterilized 36 to be oriented forty-five degrees with respect to SMS panel 32.
While inside panel 34 has a smaller perimeter than outside panel 32, it should be large enough so that when the article to be sterilized 36 is wrapped by sterilization wrap 30, both the bottom and sides of the article to be sterilized 36 is covered by inside panel 34.
Outside panel 32 includes a central portion 38. Inside panel 34 is adjacent to the central portion 38 and is attached to the first panel 32 by means _g_ of gluing, ultrasonic bonding or some other form of adherence. Glue spots 40 are illustrated in Figure 4. Alternatively, inside panel 34 may be made of any fibrous or non-fibrous material, preferably but not limited to SMS or spun bond polypropylene which adds strength but does not have the liquid absorbent properties of cellulose. The structure of inside panel 34 when it is made of SMS is discussed below in reference to Figure 9. The structure of inside panel 34 when it is made of spun bond polypropylene is discussed below in reference to Figures 13-19. In any event, this inside panel provides abuse resistance and containment properties over the prior art sterilization wrap described above.
By reinforcing the area of direct contact under the article to be sterilized 36, the primary point of potential damage to the wrap has been addressed. The method by which trays are wrapped yield several panels of material folds on the top of the article to be sterilized 36. In the event that wrapped articles get stacked on top of one another, thicker and/or heavier inside panel 34 protects the underside of the article 36 while the multiple folds are responsive to contact on the top side of article 36.
As noted, also the inner panel 34 may be made of a moisture absorbent material, such as cellulose, which provides an enhanced moisture absorption function. After the article to be sterilized 36 has been sterilized, in particularly through a steam sterilization process, moisture often remains on the article to be sterilized 36. This moisture enhances the growth of pathogens which may not have been killed during the sterilization process. By using an absorbent material, i.e., absorption material, as the material for panel 34, this moisture tends to be wicked away from the article to be sterilized 36 and more effectively dried. Thus the chances of pathogen growth on or around the article to be sterilized is greatly reduced.
It is preferred that outer panel 32 be of a different color from inner panel 34. Since inner panel 34 is always within the sterile field, this color differential will inform the sterile clinician that it is okay to touch any portion of the sterile field formed by the inside surface of outer panel 32 and inside panel 34.
It is also preferred that a sterilization chemical visual indicator 42, which may also be an integrator or emulator, be adhered to inside panel 34 or to the inside surface 41 of outside panel 32 in the vicinity of inside panel 34.
The sterilization indicator could be of a chemistry which meets or exceeds the requirements of Class 1 - Class 6 chemical indicators as defined by ISO 11140-1. The sterilization indicator turns color in the presence of steam or ethylene-oxide or other sterilant and will remain at that color after sterilization has taken place. This informs the clinician that the article to be sterilized has, indeed, been exposed to adequate sterilization conditions at the time that the clinician opens the wrapped article.
Sterilization indicators are known and two such indicators are described in U.S. Patent 4,514,361 issued to Hirsch and U.S. Patent 2,889,799 issued to Korpman. Sterilization integrators are known and one such integrator is described in U.S. Patent No. 4,448,548.
The sterilization wrap described above can be manufactured using conventional equipment and techniques readily available to those skilled in the medical fabric field.
The sterilization wrap described above may be used as set forth below. The article to be sterilized 36, as shown in Figure 3, is placed on the outside surface of inner panel 34. The article to be sterilized 36 is then wrapped utilizing standard sterilization wrapping techniques so that a portion of the inside panel 34 covers the bottom and sides of the article to be J
sterilized 36, and a portion of the outside panel 32 also covers the top of the article to be sterilized 36. The wrapped package is then exposed to a sterilization process. The wrapped package is subjected to sterilants, such as steam, ethylene-oxide or plasma, for a predetermined period of time so that substantially all of the pathogens which may be present on the article to be sterilized 36 are killed. The package is then stored for usage. When it is time to use the article to be sterilized 36, the package is unwrapped by the clinician.
The sterile clinician will know it is all right to touch the sterile field formed by the inner panel 34 because the inner panel 34 and the outside panel 32 are different colors. The clinician will then observe the status of sterilization indicator, integrator, or emulator 42 to determine whether or not the article has been exposed to adequate sterilization conditions. The article to be sterilized 36 may then be used.
The above-described improved sterilization wrap provides the two panels of protection and ease of use associated with Kimberly-Clark's One Step~ and Cardinal Health's Simul-Wrap, while having the added features of increased protection in the central area adjacent to the article to be sterilized and further providing an ability to wick moisture away from the article to be sterilized, particularly in the case of steam sterilization, and in addition, visually informs the clinician that the inside of the wrap is the sterile field and visually informs the clinician that the article has, indeed, been exposed to adequate sterilization conditions.
While Figures 2 through 4 show absorbent panel 34 attached to a single panel of sterilization material, it is preferred that two (2) panels of sterilization material are utilized.
Referring now more particularly to Figures 5 and 6, two-panel sterilization wrap 44 is provided and includes outside panel 46 and inside panel 48, each made of sterilization material such as SMS. The two panels 46 and 48 each have four edges 49, 51, 53 and 55 and are bonded together at the four edges about their outer peripheries 50, preferably by heat and pressure. The bonded two-panel sterilization material 44 may be the Simul-Wrap~ product which is commercially available from Cardinal Health (1500 Waukegan Road, McGaw Park, Illinois 60085) and which is described in U.S. Patent No.
6,517,916. Additional panel 52, which may be made of cellulose or another moisture absorbing substance, is bonded to the outside of inner panel 48 by gluing or another bonding technique, as illustrated by bond sites 54.
Alternatively, additional panel 52 may be made of any fibrous or non-fibrous material, preferably but not limited to SMS or spun bond polypropylene as discussed in reference to Figures 2, 9 and 13-19.
Referring now more particularly to Figures 7 and 8, a sterilization indicator device 56 is attached to absorbent panel 52.
Referring now more particularly to Figures 9 and 10, the absorbent panel 52 has been replaced with a reinforcement panel 58 made of either a fibrous or non-fibrous material, preferably but not limited to SMS.
Panel 58 has an equal to or higher basis weight than either panel 46 or 48.
The basis weight of panel 58 may range from 1.0 ounces per square yard (osy) to 3.0 osy (34 grams per square meter to 102 grams per square meter). The basis weight for each of panels 46 and 48 may range from 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter). While reinforcement panel 58 does not provide the moisture wicking function of absorption panel 52, it provides additional protection for the article to be sterilized 36 as shown in Figure 5, which is to be placed on reinforcement panel 58. The embodiment shown in Figures 9 and 10 results in a more cost effective product than the use of two full panels of SMS, but is equal functionally, since less material is used. Figure 9 also shows a sterilization indicator 56 having been placed on the outside surface of inner panel 48.
The embodiment of Figures 11 and 12 represents a combination of the embodiments of Figures 7 and 9. That is, reinforcement panel 58 is attached to inside SMS panel 48. Absorbent panel 52 is, in turn, attached to reinforcement panel 58. Chemical visual indicator 56 is attached to absorbent panel 52. Alternatively, indicator 56 may be attached to reinforcement panel or to inside panel 48. In addition, in the embodiment of Figures 11 and 12, outside SMS panel could be eliminated.
With reference to Figures 13-17, in another embodiment a first panel 60 of sterilization wrap is made of sterilization material and preferably includes a layer of pathogen filtration material, such as melt blown polypropylene. Preferably, first panel 60 is made of SMS. First panel 60 includes a central portion generally indicated within the bounds of dashed-lines 62 as shown in Figure 14. First panel 60 also includes an outer periphery 64.
Outer periphery 64 includes four edges 66, 68, 70 and 72. Preferably, a second panel 74 of .sterilization wrap is adjacent to and in register with first panel 60. Preferably, the first and second panels are rectangular. In the embodiment of Figures 13-17, the first panel 60 of sterilization material is bonded to the second panel 74 of sterilization material along all four edges 66, 68, 70 and 72. The preferred bonding method is ultrasonic bonding. An additional panel 76 is bonded to first panel 60. The additional panel 76 could be made from any fibrous or non-fibrous material. Preferably, the additional panel 76 does not include a pathogen filtration layer and is not made from sterilization material. More preferably, additional panel 76 is made of spun bond polypropylene. Additional panel 76 is oriented so that additional panel forms a diamond pattern with respect to first panel 60. As used herein, "diamond" includes both rhombus and square shapes. Preferably, additional panel 76 is oriented forty-five degrees with respect to first panel 60. A
substantial portion of additional panel 76 is adjacent to the central portion 62 of first panel 60. Additional panel 76 is preferably rectangular and includes four corners, namely, corners 78, 80, 82 and 84. In the preferred embodiment all four corners are bonded to first panel 60 as shown in Figure 15, i.e., corner of additional panel 76 is bonded to edge 66 of first panel 60; corner 80 is bonded to edge 68; corner 82 is bonded to edge 70; and corner 84 is bonded to edge 72. However, as shown in Figure 20, only three of the edges are bonded to the panel. Preferably, this corner to edge bonding is also accomplished by ultrasonic bonding. As used herein, the term corner includes a region of the additional panel 76 where two of its edges approach one another. The perimeter of additional panel 76 is less than the perimeter of first panel 60.
As shown in Figure 15, chemical visual indicator 88, which has previously been described, may be attached to additional layer 76. Figure 15 also illustrates the preferred orientation of the article to be sterilized 90 with respect to additional panel 76 and first panel 60. The protocol for wrapping articles to be sterilized with sterilization wrap is to orient the article at a forty-five degree angle with respect to the first sterilization panel 60.
Since, the preferred embodiment calls for the additional panel 76 to be oriented at a forty-five degree angle with respect to the first panel 60, the clinician may place the article to be sterilized with respect to additional panel 76 in alignment with the edges of that panel so that the article will automatically be positioned at a forty-five degree angle with respect to first panel 60.
It is preferred that additional panel 76 has a lower basis weight than first sterilization panel 60 or second sterilization panel 74.
Preferably, the basis weight of the additional panel 76 is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter). Preferably, the basis weight of each of the first panel 60 and the second panel 74 is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter). In addition, it is preferred that the grab tensile to basis weight ratio of additional panel 74 is equal to or greater than the grab tensile to basis weight ratio of the first panel 60.
Preferably, each corner of the additional panel 76 is bonded to the first panel 60 at or about the mid-point of each edge of the first panel 60.
The embodiment of Figures 18 and 19 is similar to the embodiment of Figures 14-17 except that a single sheet 92 of sterilization material is utilized which is folded in half, as illustrated by fold line 94, to provide two panels of sterilization material 96 and 98. Preferably, only three edges 100, 102 and 104 of the two panels 96 and 98 are bonded together, although these two panels 96 and 98 could also be bonded along fold 94. The corners 78, 80 and 82 of additional panel 76 are bonded to panel 96 along edges 100, 102 and 104. Corner 84 is bonded to panel 96 adjacent to fold 94.
The embodiment of Figures 20 and 21 is identical to the embodiment of Figures 18 and 19 except that corner 84 of additional panel 76 is not bonded to panel 96 adjacent to fold 94.
The method for sterilizing article 90 using the sterilization wrap described in reference to Figures 13-19 is the same method as described above in reference to the sterilization wrap shown in Figure 3.
The construction of the sterilization wrap shown in Figures 13-19 provides numerous advantages over the prior art. The additional panel 76 made of spun bond polypropylene which is adjacent to the central portion of one of the two SMS panels provides substantial physical protection for the article to be sterilized 90 compared to the prior art two panel SMS product.
The additional protection is provided precisely where it is needed, that is, in the central portion 62 where the article to be sterilized is placed. In addition, the forty-five degree orientation of the additional panel 76 with respect to first SMS
panel allows the clinician to more readily orient the article to be sterilized 90 in the correct position with respect to the SMS panels.
From the foregoing description of the preferred embodiments of the invention, it is apparent that many modifications may be made therein. It should be understood, however, that these embodiments of the invention are exemplifications of the invention only and that the invention is not limited thereto. It is to be understood, therefore, that it is intended in the appended claims to cover all modifications as fall within the true spirit and scope of the invention.
Industrial Applicability The way in which the invention is capable of being exploited and the way in which it can be made and used will be apparent from the foregoing.
Claims (115)
1. A sterilization wrap for wrapping an article to be sterilized, comprising:
at least a first panel of sterilization material; said first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel.
at least a first panel of sterilization material; said first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel.
2. A sterilization wrap as set forth in Claim 1 further including a second panel of sterilization material; said second panel of sterilization material bonded to said first panel of sterilization material.
3. A sterilization wrap as set forth in Claim 2, wherein the second panel of sterilization material includes an outer periphery; said outer periphery of said first panel of sterilization material being bonded to the outer periphery of said second panel of sterilization material.
4. A sterilization wrap as set forth in Claim 3 further including a chemical visual indicator, said chemical visual indicator being in one visual state prior to exposure to sterilant and being in another visual state after exposure to sterilant; said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
5. A sterilization wrap as set forth in Claim 1 further including a chemical visual indicator; said chemical visual indicator being in one visual state prior to exposure to sterilant and being in another visual state after exposure to sterilant; said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
6. A sterilization wrap as set forth in Claim 5 further including an absorbent panel attached to said additional panel.
7. A sterilization wrap as set forth in Claim 4, wherein said chemical visual indicator is a color change indicator.
8. A sterilization wrap as set forth in Claim 4, wherein said chemical visual indicator meets the requirements of ISO 11140-1.
9. A sterilization wrap as set forth in Claim 4, wherein said chemical visual indicator is attached to said additional panel.
10. A sterilization wrap as set forth in Claim 3, wherein said first and second panels of sterilization material and said additional panel are made of SMS.
11. A sterilization wrap as set forth in Claim 10, wherein the basis weight of said additional panel is equal to or greater than the basis weight of said first panel of sterilization material.
12. A sterilization wrap as set forth in Claim 10, wherein the basis weight of said first panel is in the range from 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter) and the basis weight of said additional panel is in the range from 1.0 osy to 3.0 osy (34 grams per square meter to 102 grams per square meter).
13. A sterilization wrap as set forth in Claim 3, wherein said additional panel is SMS.
14. A sterilization wrap as set forth in Claim 13 further including an absorbent panel attached to said additional panel.
15. A sterilization wrap as set forth in Claim 14 further including a chemical visual indicator; said chemical visual indicator being in one visual state prior to exposure to sterilant and being in another visual state after exposure to sterilant; said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
16. A sterilization wrap as set forth in Claim 1 further including an absorbent panel attached to said additional panel.
17. A sterilization wrap as set forth in Claim 14, wherein the perimeter of said absorbent panel is smaller than the perimeter of said additional panel.
18. A sterilization wrap as set forth in Claim 1, further comprising:
a second panel of sterilization material adjacent to and in register with said first panel;
wherein said first panel and said additional panel are rectangular;
wherein said additional panel is adapted to receive the article to be sterilized, is oriented on said first panel to form a diamond shape with respect to said first panel, and is foldable so that said additional panel contacts at least the bottom and sides of the article to be sterilized after wrapping;
wherein said first and second panels are formed by a single folded sheet of sterilization material;
wherein said first panel has first, second, third and fourth edges;
wherein said additional panel has first, second, third and fourth corners; and wherein exactly three corners of said additional panel are bonded to exactly three respective edges of said first panel approximately at the mid-point of said edges.
a second panel of sterilization material adjacent to and in register with said first panel;
wherein said first panel and said additional panel are rectangular;
wherein said additional panel is adapted to receive the article to be sterilized, is oriented on said first panel to form a diamond shape with respect to said first panel, and is foldable so that said additional panel contacts at least the bottom and sides of the article to be sterilized after wrapping;
wherein said first and second panels are formed by a single folded sheet of sterilization material;
wherein said first panel has first, second, third and fourth edges;
wherein said additional panel has first, second, third and fourth corners; and wherein exactly three corners of said additional panel are bonded to exactly three respective edges of said first panel approximately at the mid-point of said edges.
19. A sterilization wrap as set forth in Claim 1 wherein a substantial portion of said additional panel is adjacent to the central portion of said first panel.
20. A sterilization wrap as set forth in Claim 19 wherein said additional panel of material includes spun-bond polypropelene.
21. A sterilization wrap as set forth in Claim 19 further including a second panel of sterilization material; said second panel of sterilization material being bonded to said first panel of sterilization material.
22. A sterilization wrap as set forth in Claim 21 wherein the second panel of sterilization material includes an outer periphery; said outer periphery of said first panel of sterilization material being bonded to said outer periphery of said second panel of sterilization material.
23. A sterilization wrap as set forth in Claim 22 wherein said first and second panels of sterilization material are made of SMS.
24. A sterilization wrap for wrapping an article to be sterilized comprising:
a first panel of sterilization material; said first panel being rectangular and having an outer periphery and a central portion; said outer periphery including first, second, third and fourth edges; and an additional panel of material; said additional panel being bonded to said first panel; a substantial portion of said additional panel being adjacent to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel; a portion of said additional panel is bonded to said first panel along said first edge.
a first panel of sterilization material; said first panel being rectangular and having an outer periphery and a central portion; said outer periphery including first, second, third and fourth edges; and an additional panel of material; said additional panel being bonded to said first panel; a substantial portion of said additional panel being adjacent to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel; a portion of said additional panel is bonded to said first panel along said first edge.
25. A sterilization wrap as set forth in Claim 24 wherein said additional panel is rectangular; said additional panel having first, second, third and fourth corners; said first corner of said additional panel bonded to said first edge of said first panel; said second corner of said additional panel bonded to said second edge of said first panel; said third corner of said additional panel bonded to said third edge of said first panel.
26. A sterilization wrap as set forth in Claim 24, further including a second panel of sterilization material; said second panel adjacent to and in register with said first panel.
27. A sterilization wrap as set forth in Claim 26 wherein said second panel is bonded to said first panel.
28. A sterilization wrap as set forth in Claim 27 wherein said second panel has an outer periphery, including first, second, third and fourth edges; said first, second, third and fourth edges of said second panel bonded respectively to said first, second, third and fourth edges of said first panel.
29. A sterilization wrap as set forth in Claim 26 wherein said first and second panels are formed by a single folded sheet of sterilization material.
30. A sterilization wrap as set forth in Claim 24 wherein said additional panel is rectangular; said additional panel being oriented approximately forty-five degrees with respect to said first panel.
31. A sterilization wrap as set forth in Claim 24 wherein said additional panel is made of spun bond polypropylene.
32. A sterilization wrap as set forth in Claim 24 wherein said first panel is made of SMS.
33. A sterilization wrap as set forth in Claim 26 wherein said second panel is made of SMS.
34. A sterilization wrap as set forth in Claim 24 wherein said additional panel has a lower basis weight than said first panel.
35. A sterilization wrap as set forth in Claim 24 wherein the basis weight of said additional panel is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter) and the basis weight of said first panel is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter).
36. A sterilization wrap as set forth in Claim 24 wherein the grab tensile to basis weight ratio of said additional panel is equal to or greater than the grab tensile to basis weight ratio of said first panel.
37. A sterilization wrap as set forth in Claim 25 wherein at least three corners of said additional panel are bonded to respective edges of said first panel approximately at the mid-point of said edges.
38. A sterilization wrap as set forth in Claim 24, further including a chemical visual indicator; said chemical visual indicator being in one state prior to exposure to sterilant and being in another state after exposure to sterilant;
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
39. A sterilization wrap as set forth in Claim 38 wherein said chemical visual indicator is a color change indicator.
40. A sterilization wrap as set forth in Claim 38 wherein said chemical visual indicator meets the requirements of ISO 11140-1.
41. A sterilization wrap as set forth in Claim 38 wherein said chemical visual indicator is attached to said additional panel.
42. A sterilization wrap for wrapping an article to be sterilized comprising:
a first panel of sterilization material; said first panel being rectangular;
an additional panel; said additional panel being rectangular;
said additional panel being bonded to said first panel; said additional panel being oriented on said first panel so as to form a diamond shape with respect to said first panel; said additional panel being made of a material that permits a sterilant to pass through it.
a first panel of sterilization material; said first panel being rectangular;
an additional panel; said additional panel being rectangular;
said additional panel being bonded to said first panel; said additional panel being oriented on said first panel so as to form a diamond shape with respect to said first panel; said additional panel being made of a material that permits a sterilant to pass through it.
43. A sterilization wrap as set forth in Claim 42 wherein said first panel includes first, second, third and fourth edges; said additional panel having first, second, third and fourth corners; said first corner of said additional panel bonded to said first edge of said first panel; said second corner of said additional panel bonded to said second edge of said first panel; said third corner of said additional panel bonded to said third edge of said first panel.
44. A sterilization wrap as set forth in Claim 42, further including a second panel of sterilization material; said second panel adjacent to and in register with said first panel.
45. A sterilization wrap as set forth in Claim 44 wherein said second panel of sterilization material is bonded to said first panel of sterilization material.
46. A sterilization wrap as set forth in Claim 44 wherein said first and second panels are formed by a single folded sheet of sterilization material.
47. A sterilization wrap as set forth in Claim 42 wherein said additional panel is oriented approximately forty-five degrees with respect to said first panel.
48. A sterilization wrap as set forth in Claim 42 wherein said additional panel is made of spun bond polypropylene.
49. A sterilization wrap as set forth in Claim 42 wherein said first panel is made of SMS.
50. A sterilization wrap as set forth in Claim 44 wherein said second panel is made of SMS.
51. A sterilization wrap as set forth in Claim 42 wherein said additional panel has a lower basis weight than said first panel.
52. A sterilization wrap as set forth in Claim 42 wherein the basis weight of said additional panel is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter) and the basis weight of said first panel is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter).
53. A sterilization wrap as set forth in Claim 42 wherein the grab tensile to basis weight ratio of said additional panel is equal to or greater than the grab tensile to basis weight ratio of said first panel.
54. A sterilization wrap as set forth in Claim 43 wherein at least three corners of said additional panel are bonded to respective edges of said first panel approximately at the mid-point of said edges.
55. A sterilization wrap as set forth in Claim 42, further including a chemical visual indicator; said chemical visual indicator being in one state prior to exposure to sterilant and being in another state after exposure to sterilant;
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
56. A sterilization wrap as set forth in Claim 55 wherein said chemical visual indicator is a color change indicator.
57. A sterilization wrap as set forth in Claim 55 wherein said chemical visual indicator meets the requirements of ISO 11140-1.
58. A sterilization wrap as set forth in Claim 55 wherein said chemical visual indicator is attached to said additional panel.
59. A method for sterilizing an article comprising the steps of:
providing an article to be sterilized;
wrapping the article to be sterilized with a sterilization wrap which comprises:
at least a first panel of sterilization material; said first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel; and applying sterilant to the wrapped article.
providing an article to be sterilized;
wrapping the article to be sterilized with a sterilization wrap which comprises:
at least a first panel of sterilization material; said first panel having an outer periphery and a central portion; and an additional panel of material being bonded to the central portion of said first panel; said additional panel being made of a material that permits a sterilant to pass through it; the perimeter of said additional panel being smaller than the perimeter of said first panel; and applying sterilant to the wrapped article.
60. A method for sterilizing an article as set forth in Claim 59 further including a second panel of sterilization material; said second panel of sterilization material bonded to said first panel of sterilization material.
61. A method for sterilizing an article as set forth in Claim 60, wherein the second panel of sterilization material includes an outer periphery;
said outer periphery of said first panel of sterilization material being bonded to the outer periphery of said second panel of sterilization material.
said outer periphery of said first panel of sterilization material being bonded to the outer periphery of said second panel of sterilization material.
62. A method for sterilizing an article as set forth in Claim 61 further including a chemical visual indicator, said chemical visual indicator being in one visual state prior to exposure to sterilant and being in another visual state after exposure to sterilant; said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
63. A method for sterilizing an article as set forth in Claim 59 further including a chemical visual indicator; said chemical visual indicator being in one visual state prior to exposure to sterilant and being in another visual state after exposure to sterilant; said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
64. A method for sterilizing an article as set forth in Claim 62, wherein said chemical visual indicator meets the requirements of ISO 11140-1.
65. A method for sterilizing an article as set forth in Claim 62, wherein said chemical visual indicator is attached to said first panel of sterilization material.
66. A method for sterilizing an article as set forth in Claim 62, wherein said chemical visual indicator is attached to said additional panel.
67. A method for sterilizing an article as set forth in Claim 61, wherein said first and second panels of sterilization material and said additional panel are made of SMS.
68. A method for sterilizing an article as set forth in Claim 67, wherein the basis weight of said additional panel is equal to or greater than the basis weight of said first panel of sterilization material.
69. A method for sterilizing an article as set forth in Claim 68, wherein the basis weight of said first panel is in the range from 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter) and the basis weight of said additional panel is in the range from 1.0 osy to 3.0 osy (34 grams per square meter to 102 grams per square meter).
70. A method for sterilizing an article as set forth in Claim 61, wherein said additional panel is SMS.
71. A method for sterilizing an article as set forth in Claim 70 further including an absorbent panel attached to said additional panel.
72. A method for sterilizing an article as set forth in Claim 59 further including an absorbent panel attached to said additional panel.
73. A method for sterilizing an article as set forth in Claim 72 further including a chemical visual indicator responsive to the presence of sterilant so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
74. A method for sterilizing an article as set forth in Claim 72, wherein the perimeter of said absorbent panel is smaller than the perimeter of said additional panel.
75. A method for sterilizing an article comprising the steps of:
providing an article to be sterilized;
wrapping said article to be sterilized with a sterilization wrap which comprises:
a first panel of sterilization material; said first panel of sterilization material having an outer periphery and a central portion;
an additional panel of material; said additional panel being bonded to said first panel; said additional panel being made of a material that permits a sterilant to pass through it; a substantial portion of said additional panel being adjacent to the central portion of said first panel; the perimeter of said additional panel being smaller than the perimeter of said first panel;
applying sterilant to the wrapped article.
providing an article to be sterilized;
wrapping said article to be sterilized with a sterilization wrap which comprises:
a first panel of sterilization material; said first panel of sterilization material having an outer periphery and a central portion;
an additional panel of material; said additional panel being bonded to said first panel; said additional panel being made of a material that permits a sterilant to pass through it; a substantial portion of said additional panel being adjacent to the central portion of said first panel; the perimeter of said additional panel being smaller than the perimeter of said first panel;
applying sterilant to the wrapped article.
76. A method as set forth in Claim 75 wherein said additional panel of material includes spun-bond polypropylene.
77. A method as set forth in Claim 75 further including a second panel of sterilization material; said second panel of sterilization material being bonded to said first panel of sterilization material.
78. A method as set forth in Claim 77 wherein the second panel of sterilization material includes an outer periphery; said outer periphery of said first panel of sterilization material being bonded to the outer periphery of said second panel of sterilization material.
79. A method as set forth in Claim 78 wherein said first and second panels of sterilization material are made of SMS.
80. A method as set forth in Claim 75 further including the step of placing said article to be sterilized on said additional panel.
81. A method for sterilizing an article comprising the steps of:
providing an article to be sterilized;
providing sterilization wrap which comprises:
a first panel of sterilization material; said first panel being rectangular and having an outer periphery and a central portion; said outer periphery including first, second, third and fourth edges; and an additional panel of material; said additional panel being bonded to said first panel; said additional panel being made of a material that permits a sterilant to pass through it; a substantial portion of said additional panel being adjacent to the central portion of said first panel; the perimeter of said additional panel being smaller than the perimeter of said first panel; a portion of said additional panel is bonded to said first panel along said first edge;
placing said article to be sterilized on said additional panel;
wrapping said article to be sterilized with said sterilization wrap; and applying sterilant to the wrapped article.
providing an article to be sterilized;
providing sterilization wrap which comprises:
a first panel of sterilization material; said first panel being rectangular and having an outer periphery and a central portion; said outer periphery including first, second, third and fourth edges; and an additional panel of material; said additional panel being bonded to said first panel; said additional panel being made of a material that permits a sterilant to pass through it; a substantial portion of said additional panel being adjacent to the central portion of said first panel; the perimeter of said additional panel being smaller than the perimeter of said first panel; a portion of said additional panel is bonded to said first panel along said first edge;
placing said article to be sterilized on said additional panel;
wrapping said article to be sterilized with said sterilization wrap; and applying sterilant to the wrapped article.
82. A method as set forth in Claim 81 wherein said additional panel is rectangular; said additional panel having first, second, third and fourth corners; said first corner of said additional panel bonded to said first edge of said first panel; said second corner of said additional panel bonded to said second edge of said first panel; said third corner of said additional panel bonded to said third edge of said first panel.
83. A method as set forth in Claim 81, further including a second panel of sterilization material; said second panel adjacent to and in register with said first panel.
84. A method as set forth in Claim 83 wherein said second panel is bonded to said first panel.
85. A method as set forth in Claim 84 wherein said second panel has an outer periphery, including first, second, third and fourth edges; said first, second, third and fourth edges of said second panel bonded respectively to said first, second, third and fourth edges of said first panel.
86. A method as set forth in Claim 83 wherein said first and second panels are formed from a single folded sheet of sterilization material.
87. A method as set forth in Claim 81 wherein said additional panel is rectangular; said additional panel being oriented approximately forty-five degrees with respect to said first panel.
88. A method as set forth in Claim 87, further including the step of orienting said article to be sterilized approximately at a forty-five degree angle with respect to said first panel.
89. A method as set forth in Claim 81 wherein said additional panel is made of spun bond polypropylene.
90. A method as set forth in Claim 81 wherein said first panel is made of SMS.
91. A method as set forth in Claim 81 wherein said additional panel has a lower basis weight than said first panel.
92. A method as set forth in Claim 81 wherein the basis weight of said additional panel is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter) and the basis weight of said first panel is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter).
93. A method as set forth in Claim 81 wherein the grab tensile to basis weight ratio of said additional panel is equal to or greater than the grab tensile to basis weight ratio of said first panel.
94. A method as set forth in Claim 82 wherein at least three corners of said additional panel are bonded to respective edges of said first panel approximately at the mid-point of said edges.
95. A method as set forth in Claim 81, further including a chemical visual indicator; said chemical visual indicator being in one state prior to exposure to sterilant and being in another state after exposure to sterilant;
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
96. A method as set forth in Claim 95 wherein said chemical visual indicator is a color change indicator.
97. A method as set forth in Claim 95 wherein said chemical visual indicator meets the requirements of ISO 11140-1.
98. A method as set forth in Claim 95 wherein said chemical visual indicator is attached to said additional panel.
99. A method for sterilizing an article comprising the steps of:
providing an article to be sterilized;
providing sterilization wrap which comprises:
a first panel of sterilization material; said first panel being rectangular; and an additional panel; said additional panel being rectangular; said additional panel being bonded to said first panel; said additional panel being oriented on said first panel so as to form a diamond shape with respect to said first panel; said additional panel being made of a material that permits a sterility to pass through it;
placing said article to be sterilized on said additional panel;
wrapping said article to be sterilized with said sterilization wrap; and applying sterilant to the wrapped article.
providing an article to be sterilized;
providing sterilization wrap which comprises:
a first panel of sterilization material; said first panel being rectangular; and an additional panel; said additional panel being rectangular; said additional panel being bonded to said first panel; said additional panel being oriented on said first panel so as to form a diamond shape with respect to said first panel; said additional panel being made of a material that permits a sterility to pass through it;
placing said article to be sterilized on said additional panel;
wrapping said article to be sterilized with said sterilization wrap; and applying sterilant to the wrapped article.
100. A method as set forth in Claim 99 wherein said first panel includes first, second, third and fourth edges; said additional panel having first, second, third and fourth corners; said first corner of said additional panel bonded to said first edge of said first panel; said second corner of said additional panel bonded to said second edge of said first panel; said third corner of said additional panel bonded to said third edge of said first panel.
101. A method as set forth in Claim 99, further including a second panel of sterilization material adjacent to and in register with said first panel.
102. A method as set forth in Claim 100 wherein said second panel of sterilization material is bonded to said first panel of sterilization material.
103. A method as set forth in Claim 100 wherein said first and second panels are formed from a single sheet of sterilization material.
104. A method as set forth in Claim 99 wherein said additional panel is oriented forty-five degrees with respect to said first panel.
105. A method as set forth in Claim 104, further including the step of orienting said article to be sterilized approximately at a forty-five degree angle with respect to said first panel.
106. A method as set forth in Claim 99 wherein said additional panel is made of spun bond polypropylene.
107. A method as set forth in Claim 99 wherein said first panel is made of SMS.
108. A method as set forth in Claim 99 wherein said additional panel has a lower basis weight than said first panel.
109. A method as set forth in Claim 99 wherein the basis weight of said additional panel is in the range of 0.5 osy to 3.0 osy (17 grams per square meter to 102 grams per square meter) and the basis weight of said first panel is in the range of 0.75 osy to 2.9 osy (25 grams per square meter to 98 grams per square meter).
110. A method as set forth in Claim 99 wherein the grab tensile to basis weight ratio of said additional panel is equal to or greater than the grab tensile to basis weight ratio of said first panel.
111. A method as set forth in Claim 100 wherein at least three corners of said additional panel are bonded to respective edges of said first panel approximately at the mid-point of said edges.
112. A method as set forth in Claim 99, further including a chemical visual indicator; said chemical visual indicator being in one state prior to exposure to sterilant and being in another state after exposure to sterilant;
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
said chemical visual indicator being attached to said wrap so as to indicate whether or not the article has been exposed to adequate sterilization conditions.
113. A method as set forth in Claim 112 wherein said chemical visual indicator is a color change indicator.
114. A method as set forth in Claim 112 wherein said chemical visual indicator meets the requirements of ISO 11140-1.
115. A method as set forth in Claim 112 wherein said chemical visual indicator is attached to said additional panel
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US10/685,545 US20050079093A1 (en) | 2003-10-14 | 2003-10-14 | Sterilization wraps and methods for sterilizing articles |
US10/685,545 | 2003-10-14 | ||
PCT/US2004/033829 WO2005037333A1 (en) | 2003-10-14 | 2004-10-13 | Sterilization wraps and methods for sterilizing articles |
US10/966,354 | 2004-10-13 | ||
US10/966,354 US7560082B2 (en) | 2003-10-14 | 2004-10-13 | Sterilization wraps and methods for sterilizing articles |
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CA2540333A1 CA2540333A1 (en) | 2005-04-28 |
CA2540333C true CA2540333C (en) | 2011-12-06 |
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CA2540333A Active CA2540333C (en) | 2003-10-14 | 2004-10-13 | Sterilization wraps and methods for sterilizing articles |
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US (6) | US20050079093A1 (en) |
EP (2) | EP1682189B1 (en) |
JP (2) | JP4738341B2 (en) |
AU (1) | AU2004281759B2 (en) |
CA (1) | CA2540333C (en) |
ES (1) | ES2675351T3 (en) |
MX (1) | MXPA06003980A (en) |
NZ (5) | NZ582009A (en) |
WO (1) | WO2005037333A1 (en) |
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2003
- 2003-10-14 US US10/685,545 patent/US20050079093A1/en not_active Abandoned
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2004
- 2004-10-13 MX MXPA06003980A patent/MXPA06003980A/en active IP Right Grant
- 2004-10-13 NZ NZ582009A patent/NZ582009A/en unknown
- 2004-10-13 EP EP04795047.2A patent/EP1682189B1/en active Active
- 2004-10-13 EP EP14179915.5A patent/EP2845611B1/en active Active
- 2004-10-13 NZ NZ588688A patent/NZ588688A/en unknown
- 2004-10-13 JP JP2006535637A patent/JP4738341B2/en not_active Expired - Fee Related
- 2004-10-13 US US10/966,354 patent/US7560082B2/en active Active
- 2004-10-13 WO PCT/US2004/033829 patent/WO2005037333A1/en active Application Filing
- 2004-10-13 NZ NZ588766A patent/NZ588766A/en unknown
- 2004-10-13 ES ES04795047.2T patent/ES2675351T3/en active Active
- 2004-10-13 NZ NZ547116A patent/NZ547116A/en unknown
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- 2004-10-13 AU AU2004281759A patent/AU2004281759B2/en active Active
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2009
- 2009-06-11 US US12/482,897 patent/US7906070B2/en not_active Expired - Lifetime
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2010
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2013
- 2013-06-05 US US13/910,929 patent/US8821808B2/en not_active Expired - Lifetime
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2014
- 2014-08-28 US US14/472,004 patent/US20150147512A1/en not_active Abandoned
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JP2007508120A (en) | 2007-04-05 |
NZ588688A (en) | 2012-04-27 |
US20090246079A1 (en) | 2009-10-01 |
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AU2004281759A1 (en) | 2005-04-28 |
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NZ547116A (en) | 2010-07-30 |
MXPA06003980A (en) | 2006-06-27 |
NZ582009A (en) | 2011-07-29 |
US7560082B2 (en) | 2009-07-14 |
EP1682189B1 (en) | 2018-05-09 |
NZ588719A (en) | 2012-04-27 |
EP1682189A1 (en) | 2006-07-26 |
US7906070B2 (en) | 2011-03-15 |
ES2675351T3 (en) | 2018-07-10 |
CA2540333A1 (en) | 2005-04-28 |
US20050079093A1 (en) | 2005-04-14 |
EP2845611A1 (en) | 2015-03-11 |
WO2005037333A1 (en) | 2005-04-28 |
EP2845611B1 (en) | 2020-03-11 |
US8821808B2 (en) | 2014-09-02 |
US20150147512A1 (en) | 2015-05-28 |
JP2011078795A (en) | 2011-04-21 |
US20130340394A1 (en) | 2013-12-26 |
AU2004281759B2 (en) | 2010-12-09 |
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