US3115441A - Timed release pharmaceutical preparations and method of making the same - Google Patents
Timed release pharmaceutical preparations and method of making the same Download PDFInfo
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- US3115441A US3115441A US200554A US20055462A US3115441A US 3115441 A US3115441 A US 3115441A US 200554 A US200554 A US 200554A US 20055462 A US20055462 A US 20055462A US 3115441 A US3115441 A US 3115441A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5084—Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
- A61K9/2081—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets with microcapsules or coated microparticles according to A61K9/50
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
Definitions
- an analgesic tablet which is capable of releasing the analgesic medication in a relatively constant stream over a rather long period of time.
- aspirin which is one of the best and most universal analgesic drugs
- the maxi-. mum time of effectiveness is only a few hours and the patient using such medication must take repeated dosages at frequent intervals. This, of course, is inconvenient during waking hours and is extremely undesirable during periods when the patient should be sleeping.
- analgesic compounds are usually dissolved very readily within the gastric juices of the stomach, and thus the total amount of the dosage is immediately fed into the blood stream. During the interval between dosages, therefore, the analgesic level in the blood stream will constantly decrease due to the biochemical decomposition of the analgesic in the body. Toward the end of the period, the level of the analgesic compound is so low, so that it is practically ineffective. As a result, the degree of pain-relief will fluctuate between dosages.
- the primary object of the present invention to provide a pharmaceutical preparation which is capable of quickly producing an analgesic level within the blood stream of a patient and maintaining such level over a long period of time.
- FIG. 1 is a perspective view of a prolonged release pharmaceutical preparation constructed in accordance with and embodying the present invention
- FIG. 2 is a sectional view taken along line 2-2 of FIG. 1;
- FIG. 3 is a graphical representation of the quantity of analgesic material in the blood stream over a period of time, when taken in conventional form by a series of successive tablets as compared with the prolonged release dosage form of the present invention.
- A designates a pharmaceutical tablet which comprises a plurality of analgesic particles 1 such as acetyl salicylic acid, acetominophen, salicyl salicylic acid, salicylamide, acetophenetidin, dipyrone, and similar drugs which must be administered in bulky dosages, which are surrounded by a timed-disintegration coating 2.
- the coated particles are carried in tableted form by a matrix 3 of aspirin and starch.
- the analgesic material such as aspirin
- any conventional comminuting device not shown
- the tablets are crushed or otherwise broken up to produce particles or granules which are sieved and the par- 'cles which are retained between 16 and 20 mesh screens are utilized for coating as hereinafter described.
- the material which is too large to pass through a 16 mesh screen is crushed and sieved again.
- the material which passes through a 20 mesh screen is regarded as fines or sittings and is used later as will be presently more fully explained.
- the granules or particles resulting from the aforementioned screening are placed in a coating pan. While being tumbled therein, the particles are coated with a thin coating of shellac, cellulose acetate phthalate, ethyl cellulose zein, or similar film-forming resin-like materials which are soluble in organic solvents such as alcohol but are insoluble in water.
- the wetted particles are quickly dusted with stearic acid, kaolin, terra alba, dicalcium phosphate, palmitic acid, linoleic acid, calcium stearate, or any other fatty acids, fatty acid salts, fatty acid esters, or similar non-toxic hydrophobic materials.
- aspirin for instance, is deleteriously affected by alcohol and water which are the common solvents usually employed in coating materials, but nevertheless, aspirin can tolerate alcohol in limited quantity, for a short period of time.
- the particles are given a first quick thin coating, preferably of shellac and stearic acid. This initial coating is thoroughly dried and compacted by tumbling the coated particles for approximately an hour while subjecting them to a gentle stream of cold air.
- the coated particles are additionally coated with an aqueous solution of sugar syrup, polyethylene glycols such as carbowaxes, gum such as gum acacia, or
- This second coating is dried by continuous tumbling for a period of 1530 minutes; Then a third coating just like the second coating is applied and dried.
- the second and third coatings may, if desired, include an inert non-toxic coloring material.
- the granules are removed from the coating pan and placed in thin layers on drying trays which are then placed in a heated drying room and dried overnight. It is essential to dry the particles thoroughly, whereupon the particles are again placed in a coating pan and two successive coatings of shellac and stearic acid are aplied as before. At this point in the procedure, a sample is tested in vitro and if the granules have the desired time-delay factor, no further coating is necessary. If, on the other hand, long periods of time-delay are desired, then further shellac-stearic acid coatings are applied.
- the coating of the particles When the coating of the particles has been completed, they are mixed with a quantity of powdered aspirin and starch and this mixture tableted in a conventional tablet compressing machine. Preferably, the fines or sittings can be used for this purpose.
- the mixture of aspirin and starch does two things. First; it supplies a readily available initial dosage which enters the patients blood stream very promptly and gives quick initial relief from pain. Second; it serves, uniquely and unexpectedly, as a cushioning matrix for the coated particles so that the latter are not mechanically disrupted or otherwise broken down during compression.
- a tablet made in accordance with the present invention reaches the patients stomach, the tablet A disintegrates almost immediately and the initial dosage comprising the matrix is absorbed.
- a substantially constant level of medication will then be maintained within the blood stream for a period of ten to twelve hours.
- the length of time during which the patient will be under the influence of the analgesic drug will depend upon the amount of material which has been incorporated into the tablet A, and the size thereof.
- the tablets of the present invention constitute the only way thus far known by which a time-delay dosage of aspirin or similar analgesic drug can be prepared and still keep the tablet within reasonable limits as to size and also produce a stable product.
- the next peak of the solid-line curve occurs when another aspirin tablet is ingested. It can also be seen by reference to FIG. 3 that when aspirin is administered in the prolonged release tablet of the present invention, the analgesic level in the blood stream rises as rapidly as when ingested in the conventional dosage form. However, it is to be noted that the amount of analgesic material in the blood stream is then maintained at a fairly constant level for a prolonged interval.
- Example I 360 lbs. of powdered aspirin are mixed with 40 lbs. starch and then tableted into hard slugs. The slugs are crushed through a Stokes oscillator having a mesh screen. The material which passes is sifted through a Sweco separator. Any oversized particles are recrushed through a Stokes oscillator having a 16 mesh screen and again sifted. This series of crushing and sifting steps yields 220 lbs. of granules (16-20 mesh screen) and 180 lbs. of siftings. The 220 lbs. of granules are placed in a coating pan and coated with 450 oz. of 4 lbs. cut shellac and then dusted with 19 /2 lbs.
- the coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz. of Sunset yellow certified color are applied in two 42 oz. applications with -20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with three coatings each comprising 150 oz. of 4 lbs. cut shellac and dusted with 11% lbs. stearic acid with one hour drying after each ap- 4 plication. The coated granules are then heat dried overnight at 110 F. This procedure results in 288% lbs. coated granules. These are mixed with the 180 lbs. of siftings and compressed into tablets, each weighing 13 grains and containing 10 grains of aspirin.
- Example II 400 lbs. of powdered aspirin are tableted into hard slugs.
- the slugs are crushed and initially screened (#10 mesh).
- the material which passes is sifted through a Sweco separator. Any oversized particles are recrushed through a Stokes oscillator having a 16 mesh screen and again sifted.
- This series of crushing and sifting steps yields 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings.
- the 220 lbs. of granules are placed in a coating pan and coated with oz. of 10% cellulose acetate phthalate in acetone dusted with 2 /2 lbs. talcum.
- the coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 24 oz. of 25% Carbowax 6000 (aqueous solution) without color are applied in two 42 oz. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at F. The granules are next placed back in a coating pan and coated with five coatings each comprising 50 oz. of 10% cellulose acetate phthalate dusted with 1% oz. of talcum with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 270 lbs. coated granules. These are mixed with the 180 lbs.
- Example III 400 lbs. powdered acetaminophen (4-hydroxy acetanilide) is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I again yielding 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 450 oz. of 4 lbs. cut shellac and dusted with 10 lbs. of calcium stearate.
- the coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing Sunset yellow certified color are applied in two 42 02. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with three coatings each comprising oz. of 4 lb. cut shellac and dusted with 6 lbs. of calcium stearate with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 288% lb. coated granules. These are mixed with the lb. of siftings to which 20 lbs. of starch are added. The resulting total mixture is then compressed into tablets each weighing 12.2 grains and containing 10 grains of acetaminophen.
- Example IV 400 lbs. powdered salicylamide are tableted into hard slugs. The slugs are crushed and initially screened (#10 mesh). The material which passes is sifted through a Sweco separator to yield 220* lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are coated with the several coatings as described in Example 11 and results in 288% lb. coated granules. These are mixed with the 180 lbs. of siftings and compressed into tablets each weighing 11.53 grains and con taming 10 grains of salicylamide.
- Example V 400 lbs. powdered salicyl salicylic acid is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (1620 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 200 oz. solution of zein in 90% isopropyl alcohol and dusted with 10 lbs. of a mixture of 2 parts kaolin and 1 part calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz.
- Example VI 400 lbs. powdered acetophenetidin is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 200 oz. 10% solution of zein in 90% isopropyl alcohol and dusted with 10 lb. of a mixture of 2 parts kaolin and 1 part calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz.
- Example VII 400 lbs. powdered dipyrone is tableted into hard slugs.
- the slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (16-20 mesh screen) and 180 lbs. sittings.
- the 220 lbs. of granules are placed in a coating pan and coated with 200 oz. 10% solution of zein in 90% isopropyl alcohol and dusted with 10 lbs. of a mixture of 2 parts kaolin and 1 part calcium stearate.
- the coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, and particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drum intermixed with a small amount of an inert material.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug intermixed with a small amount of starch.
- a prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug.
- a prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug intermixed with a small amount of an inert material.
- a prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug intermixed with a small amount of starch.
- a prolonged release analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said coating being a member of the class consisting of shellac and stearic acid, shellac and palmitic acid, shellac and linoleic acid, shellac and calcium stearate, shellac and a dry non-toxic hydrophobic powder, cellulose acetate phthalate and stearic acid, cellulose acetate phthalate and palmitic acid, cellulose acetate phthalate and linoleic acid, cellulose acetate phthalate and calcium stearate, cellulose acetate phthalate and a dry non-toxic hydrophobic powder, ethyl cellulose and stearic acid, ethyl cellulose and palmitic acid, ethyl cellulose and linoleic acid, ethyl cellulose and calcium stearate, eth
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resitsant coating consisting of zein and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of zein and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of zein and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resitsant coating consisting of zein and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- a prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated With a permeable solution-resistant coating consisting of zein and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
- Dragstedt Oral Medication With Preparations for Prolonged Action, I.A.M.A., vol. 168, No. 12, pages 1652-1655, November 22, 1958.
Description
Dec. 24, 1963 v. M. HERMELIN TIMED RELEASE PHARMACEUTICAL. PREPARATIONS AND METHOD OF MAKING THE SAME Flled June 6, 1962 CONTENT IN BLOOD STREAM TiME INVENTOR. VICTOR M. HERMELIN BY W ATTORNEY FIG.
United States Patent 3,135,441 Tilt HEB RELEASE PHARMACEUTIQAL PREPARA- TIGNS AND METHQD OF MAKING THE SAME Victor M. Hermeiin, 84% Girl Eenhomme Road, University fity, M0. Filed Kane 6, 1962, Ser. No. 209,554 3% Claims. (Cl. 167-82) This invention relates in general to certain new and useful improvements in pharmaceutical preparations and, more particularly, to a pharmaceutical preparation having timed release characteristics.
There has long been a need in the medical arts for an analgesic tablet which is capable of releasing the analgesic medication in a relatively constant stream over a rather long period of time. In the case of aspirin, which is one of the best and most universal analgesic drugs, the maxi-. mum time of effectiveness is only a few hours and the patient using such medication must take repeated dosages at frequent intervals. This, of course, is inconvenient during waking hours and is extremely undesirable during periods when the patient should be sleeping.
Moreover, analgesic compounds are usually dissolved very readily within the gastric juices of the stomach, and thus the total amount of the dosage is immediately fed into the blood stream. During the interval between dosages, therefore, the analgesic level in the blood stream will constantly decrease due to the biochemical decomposition of the analgesic in the body. Toward the end of the period, the level of the analgesic compound is so low, so that it is practically ineffective. As a result, the degree of pain-relief will fluctuate between dosages.
It is, therefore, the primary object of the present invention to provide a pharmaceutical preparation which is capable of quickly producing an analgesic level within the blood stream of a patient and maintaining such level over a long period of time.
It is another obejct of the present invention to provide a pharmaceutical preparation of the type stated which contains both immediate action and prolonged release dosage.
It is a further object of the present invention to provide a pharmaceutical preparation of the type stated which is stable and of swallowable size taking into account the quantity required for administration over the prolonged period for which the preparation is designed.
With the above and other objects in view, my invention resides in the novel features of form, construction, arrangement, and combination of parts presently described and pointed out in the claims.
In the acompanying drawing (one sheet) FIG. 1 is a perspective view of a prolonged release pharmaceutical preparation constructed in accordance with and embodying the present invention;
FIG. 2 is a sectional view taken along line 2-2 of FIG. 1; and
FIG. 3 is a graphical representation of the quantity of analgesic material in the blood stream over a period of time, when taken in conventional form by a series of successive tablets as compared with the prolonged release dosage form of the present invention.
Referring now in more detail and by reference characters to the drawing, which illustrates a preferred embodiment of the present invention, A designates a pharmaceutical tablet which comprises a plurality of analgesic particles 1 such as acetyl salicylic acid, acetominophen, salicyl salicylic acid, salicylamide, acetophenetidin, dipyrone, and similar drugs which must be administered in bulky dosages, which are surrounded by a timed-disintegration coating 2. The coated particles are carried in tableted form by a matrix 3 of aspirin and starch.
The analgesic material, such as aspirin, is very finely ground by any conventional comminuting device (not shown) and is then tableted in a conventional manner. The tablets are crushed or otherwise broken up to produce particles or granules which are sieved and the par- 'cles which are retained between 16 and 20 mesh screens are utilized for coating as hereinafter described. The material which is too large to pass through a 16 mesh screen is crushed and sieved again. The material which passes through a 20 mesh screen is regarded as fines or sittings and is used later as will be presently more fully explained. It has been discovered, in connection with the present invention, that when a drug such as aspirin is compressed into a tablet, a substantially thick case hardened shell is formed around the outside of the tablet and the interior or central portion thereof, although hard and solid, is nevertheless considerably less dense and more porous. Consequently, the mass of particles or granules retained on the 20 mesh screen and utilized for coating purposes will include solid particles of several different degrees of consolidation or, in other words, different degrees of permeability with respect to digestive fluids in the human body.
The granules or particles resulting from the aforementioned screening are placed in a coating pan. While being tumbled therein, the particles are coated with a thin coating of shellac, cellulose acetate phthalate, ethyl cellulose zein, or similar film-forming resin-like materials which are soluble in organic solvents such as alcohol but are insoluble in water. The wetted particles are quickly dusted with stearic acid, kaolin, terra alba, dicalcium phosphate, palmitic acid, linoleic acid, calcium stearate, or any other fatty acids, fatty acid salts, fatty acid esters, or similar non-toxic hydrophobic materials. In this connection, it may be noted that aspirin, for instance, is deleteriously affected by alcohol and water which are the common solvents usually employed in coating materials, but nevertheless, aspirin can tolerate alcohol in limited quantity, for a short period of time. Hence, the particles are given a first quick thin coating, preferably of shellac and stearic acid. This initial coating is thoroughly dried and compacted by tumbling the coated particles for approximately an hour while subjecting them to a gentle stream of cold air.
Thereupon, the coated particles are additionally coated with an aqueous solution of sugar syrup, polyethylene glycols such as carbowaxes, gum such as gum acacia, or
other non-toxic materials capable of forming an envelope or integument which resists the penetration of alcohol or similar organic solvents. This second coating is dried by continuous tumbling for a period of 1530 minutes; Then a third coating just like the second coating is applied and dried. The second and third coatings may, if desired, include an inert non-toxic coloring material.
When the third coating has dried, the granules are removed from the coating pan and placed in thin layers on drying trays which are then placed in a heated drying room and dried overnight. It is essential to dry the particles thoroughly, whereupon the particles are again placed in a coating pan and two successive coatings of shellac and stearic acid are aplied as before. At this point in the procedure, a sample is tested in vitro and if the granules have the desired time-delay factor, no further coating is necessary. If, on the other hand, long periods of time-delay are desired, then further shellac-stearic acid coatings are applied.
When the coating of the particles has been completed, they are mixed with a quantity of powdered aspirin and starch and this mixture tableted in a conventional tablet compressing machine. Preferably, the fines or sittings can be used for this purpose. The mixture of aspirin and starch does two things. First; it supplies a readily available initial dosage which enters the patients blood stream very promptly and gives quick initial relief from pain. Second; it serves, uniquely and unexpectedly, as a cushioning matrix for the coated particles so that the latter are not mechanically disrupted or otherwise broken down during compression.
Thus, when a tablet made in accordance with the present invention reaches the patients stomach, the tablet A disintegrates almost immediately and the initial dosage comprising the matrix is absorbed. The particles 1, however, resist disintegration for about three hours and then the drug begins to leach out in a steady attenuated trickle at a rate which almost identically offsets the rate at which the drug disappears from the blood stream. As a result, a substantially constant level of medication will then be maintained within the blood stream for a period of ten to twelve hours. It will, of course, be understood in this connection, that the length of time during which the patient will be under the influence of the analgesic drug will depend upon the amount of material which has been incorporated into the tablet A, and the size thereof. The tablets of the present invention constitute the only way thus far known by which a time-delay dosage of aspirin or similar analgesic drug can be prepared and still keep the tablet within reasonable limits as to size and also produce a stable product.
It has been found by various in vitro and in vivo tests that when aspirin is taken in the conventional manner, that is to say, one five grain tablet every four hours, the level of drug in the patients blood stream follows the solid-line curve as shown in FIG. 3. Similar in vitro and in vivo tests show that when aspirin is administered in the prolonged release tablet of the present invention, the analgesic level in the blood stream over a comparable period of time is represented by the dotted-line curve in FIG. 3. It can be seen by further reference to FIG. 3 that in the conventional dosage form, the level of the aspirin within the blood stream is materially increased almost immediately after ingestion thereof. Thereafter, the level of the aspirin in the blood stream begins to decrease rather rapidly over a period of time. The next peak of the solid-line curve occurs when another aspirin tablet is ingested. It can also be seen by reference to FIG. 3 that when aspirin is administered in the prolonged release tablet of the present invention, the analgesic level in the blood stream rises as rapidly as when ingested in the conventional dosage form. However, it is to be noted that the amount of analgesic material in the blood stream is then maintained at a fairly constant level for a prolonged interval.
By way of illustration and not for purposes of limitation, the following are examples of various types of medicinal tablets made in accordance with the present invention:
Example I 360 lbs. of powdered aspirin are mixed with 40 lbs. starch and then tableted into hard slugs. The slugs are crushed through a Stokes oscillator having a mesh screen. The material which passes is sifted through a Sweco separator. Any oversized particles are recrushed through a Stokes oscillator having a 16 mesh screen and again sifted. This series of crushing and sifting steps yields 220 lbs. of granules (16-20 mesh screen) and 180 lbs. of siftings. The 220 lbs. of granules are placed in a coating pan and coated with 450 oz. of 4 lbs. cut shellac and then dusted with 19 /2 lbs. stearic acid. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz. of Sunset yellow certified color are applied in two 42 oz. applications with -20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with three coatings each comprising 150 oz. of 4 lbs. cut shellac and dusted with 11% lbs. stearic acid with one hour drying after each ap- 4 plication. The coated granules are then heat dried overnight at 110 F. This procedure results in 288% lbs. coated granules. These are mixed with the 180 lbs. of siftings and compressed into tablets, each weighing 13 grains and containing 10 grains of aspirin.
Example II 400 lbs. of powdered aspirin are tableted into hard slugs. The slugs are crushed and initially screened (#10 mesh). The material which passes is sifted through a Sweco separator. Any oversized particles are recrushed through a Stokes oscillator having a 16 mesh screen and again sifted. This series of crushing and sifting steps yields 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with oz. of 10% cellulose acetate phthalate in acetone dusted with 2 /2 lbs. talcum. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 24 oz. of 25% Carbowax 6000 (aqueous solution) without color are applied in two 42 oz. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at F. The granules are next placed back in a coating pan and coated with five coatings each comprising 50 oz. of 10% cellulose acetate phthalate dusted with 1% oz. of talcum with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 270 lbs. coated granules. These are mixed with the 180 lbs. of siftings to which 11 lbs. of starch are added. The mixture is then compressed into tablets, each weighing 11.5 3 grains and containing 10 grains of aspirin. Example III 400 lbs. powdered acetaminophen (4-hydroxy acetanilide) is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I again yielding 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 450 oz. of 4 lbs. cut shellac and dusted with 10 lbs. of calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing Sunset yellow certified color are applied in two 42 02. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with three coatings each comprising oz. of 4 lb. cut shellac and dusted with 6 lbs. of calcium stearate with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 288% lb. coated granules. These are mixed with the lb. of siftings to which 20 lbs. of starch are added. The resulting total mixture is then compressed into tablets each weighing 12.2 grains and containing 10 grains of acetaminophen.
Example IV 400 lbs. powdered salicylamide are tableted into hard slugs. The slugs are crushed and initially screened (#10 mesh). The material which passes is sifted through a Sweco separator to yield 220* lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are coated with the several coatings as described in Example 11 and results in 288% lb. coated granules. These are mixed with the 180 lbs. of siftings and compressed into tablets each weighing 11.53 grains and con taming 10 grains of salicylamide.
Example V 400 lbs. powdered salicyl salicylic acid is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (1620 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 200 oz. solution of zein in 90% isopropyl alcohol and dusted with 10 lbs. of a mixture of 2 parts kaolin and 1 part calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz. of Sunset yellow certified color are applied in two 42 oz. applications with 20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with six coatings each comprising 75 oz. of the above zein solution and dusted with 6 lbs. of the above powder mixture with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 277 lbs. coated granules. These are mixed with the 180 lbs. of sittings to which lbs. of starch are added. The total mixture is then compressed into tablets, each weighing 11.9 grains and containing 10 grains of salicyl salicylic acid.
Example VI 400 lbs. powdered acetophenetidin is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (16-20 mesh screen) and 180 lbs. siftings. The 220 lbs. of granules are placed in a coating pan and coated with 200 oz. 10% solution of zein in 90% isopropyl alcohol and dusted with 10 lb. of a mixture of 2 parts kaolin and 1 part calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz. of Sunset yellow certified color are applied in two 42 02. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with six coatings each comprising 75 oz. of the above zein solution and dusted with 6 lbs. of the above powder mixture with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 277 lbs. coated granules. These are mixed with the 180 lbs. of sittings to which 20 lbs. of starch are added. The total mixture is then compressed into tablets, each weighing 11.9 grains and containing 10 grains of acetophenetidin.
Example VII 400 lbs. powdered dipyrone is tableted into hard slugs. The slugs are crushed and sifted as set forth in Example I to yield 220 lbs. of granules (16-20 mesh screen) and 180 lbs. sittings. The 220 lbs. of granules are placed in a coating pan and coated with 200 oz. 10% solution of zein in 90% isopropyl alcohol and dusted with 10 lbs. of a mixture of 2 parts kaolin and 1 part calcium stearate. The coated granules are dried by continued tumbling for approximately one hour while being subjected to a stream of cold air. Then 84 oz. of simple syrup containing 2 oz. of Sunset yellow certified color are applied in two 42 oz. applications with 15-20 minutes drying after each application. The granules are removed and heat dried on trays overnight at 110 F. The granules are next placed back in a coating pan and coated with six coatings each comprising 75 oz. the above zein solution and dusted with 6 lbs. of the above powder mixture with one hour drying after each application. The coated granules are then heat dried overnight at 110 F. This procedure results in 277 lbs. coated granules. These are mixed with the 180 lbs. of sittings to which 2 0 lbs. of starch are added. The total mixture is then compressed into tablets, each weighing 11.9 grains and containing 10 grains of dipyrone.
It should be understood that changes and modifications in the form, construction, arrangement, and combination of the several parts of the timed release pharmaceutical preparations and method of making the same, may
be made and substituted for those herein shown and described without departing from the nature and principle of my invention.
Having thus described my invention, what I claim and desire to secure by Letters Patent is:
1. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
2. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, and particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drum intermixed with a small amount of an inert material.
3. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug intermixed with a small amount of starch.
4. A prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug.
5. A prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug intermixed with a small amount of an inert material.
6. A prolonged analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each of said particles being individually coated with a permeable solution-resistant coating, said coated particles being carried by and being randomly dispersed throughout a matrix consisting predominantly of an analgesic drug intermixed with a small amount of starch.
7. A prolonged release analgesic tablet comprising a plurality of finely divided discrete particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating, said coating being a member of the class consisting of shellac and stearic acid, shellac and palmitic acid, shellac and linoleic acid, shellac and calcium stearate, shellac and a dry non-toxic hydrophobic powder, cellulose acetate phthalate and stearic acid, cellulose acetate phthalate and palmitic acid, cellulose acetate phthalate and linoleic acid, cellulose acetate phthalate and calcium stearate, cellulose acetate phthalate and a dry non-toxic hydrophobic powder, ethyl cellulose and stearic acid, ethyl cellulose and palmitic acid, ethyl cellulose and linoleic acid, ethyl cellulose and calcium stearate, ethyl cellulose and a dry non-toxic hydrophobic powder, zein and stearic acid, zein and palmtiic acid, zein and linoleic acid, zein and calcium stearate, and zein and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
8. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
9-. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
10. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
11. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
12. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of shellac and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
13. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
14. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
15. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
16. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
17. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of cellulose acetate phthalate and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
18. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
19. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
20. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
21. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
22. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of ethyl cellulose and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
23. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resitsant coating consisting of zein and stearic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
24. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of zein and palmitic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
25. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resistant coating consisting of zein and linoleic acid, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
26. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated with a permeable solution-resitsant coating consisting of zein and calcium stearate, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
27. A prolonged release analgesic tablet comprising a plurality of finely divided hard particles of an analgesic drug, each particle being individually coated With a permeable solution-resistant coating consisting of zein and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
28. The method of releasing an analgesic drug in the blood stream of a person over a prolonged period of time, said method comprising ingestion of a plurality of finely divided particles of the analgesic drug in tablet form, each particle being individually coated with a permeable solution-resistant coating, said coating being a member of the class consisting of shellac and stearic acid, shellac and palmitic acid, shellac and linoleic acid, shellac and calcium stearate, shellac and a dry non-toxic hydrophobic powder, cellulose acetate phthalate and stearic acid, cellulose acetate phthalate and palmitic acid, cellulose acetate phthalate and linoleic acid, cellulose acetate phthalate and calcium stearate, cellulose acetate phthalate and a dry non-toxic hydrophobic powder, ethyl cellulose and stearic acid, ethyl cellulose and palmitic acid, ethyl cellulose and lincleic acid, ethyl cellulose and calcium stearate, cth l cellulose and a dry nontoxic hydrophobic 9 powder, Zein and stearic acid, zein and palmitic acid, zein and linoleic acid, zein and calcium stearate, and Zein and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
29. The method of releasing an analgesic drug in the blood stream of a person over a prolonged period of time, said method comprising ingestion of a plurality of finely divided particles of the analgesic drug in tablet form, each particle being individually coated with a permeable solution-resistant coating, said coating being a member of the class consisting of shellac and stearic acid, shellac and palmitic acid, shellac and linoleic acid, shellac and calcium stearate, shellac and a dry non-toxic hydrophobic powder, cellulose acetate phthalate and stearic acid, cellulose acetate phthalate and palmitic acid, cellulose acetate phthalate and linoleic acid, cellulose acetate phthalate and calcium stearate, cellulose acetate phthalate and a dry nontoxic hydrophobic powder, ethyl cellulose and stearic acid, ethyl cellulose and palmitic acid, ethyl cellulose and linoleic acid, ethyl cellulose and calcium stearate, ethyl cellulose and a dry non-toxic hydrophobic powder, zein and stearic acid, zein and palmitic acid, zein and linoleic acid, zein and calcium stearate, and zein and a dry nontoxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug intermixed with a small amount of inert material.
30. The method of releasing an analgesic drug in the blood stream of a person over a prolonged period of time, said method comprising ingestion of a plurality of finely divided particles of the analgesic drug in tablet form, each particle being individually coated with a permeable solution-resistant coating, said coating being a member of the class consisting of shellac and stearic acid, shellac and palmitic acid, shellac and linoleic acid, shellac and calcium stearate, shellac and a dry non-toxic hydrophobic powder, cellulose acetate phthalate and stearic acid, cellulose acetate phthalate and palmitic acid, cellulose acetate phthalate and linoleic acid, cellulose acetate phthalate and calcium stearate, cellulose acetate phthalate and a dry nontoxic hydrophobic powder, ethyl cellulose and stearic acid, ethyl cellulose and palmitic acid, ethyl cellulose and linoleic acid, ethyl cellulose and calcium stearate, ethyl cellulose and a dry non-toxic hydrophobic powder, Zein and stearic acid, zein and palmitic acid, zein and linoleic acid, zein and calcium stearate, and Zein and a dry non-toxic hydrophobic powder, said particles being dispersed throughout a compressed matrix consisting predominantly of the same analgesic drug.
References (Cited in the file of this patent UNITED STATES FATENTS Shuyler Oct. 25, 1960 OTHER REFERENCES Chapmen et al.: Physiological Availability of Drugs in Tablets, Canad. Med. Assn 1., vol. 76, pages l02106, January 15, 1957.
Dragstedt: Oral Medication With Preparations for Prolonged Action, I.A.M.A., vol. 168, No. 12, pages 1652-1655, November 22, 1958.
Lazarus et al.: Oral Prolonged Action Medicaments: Their Pharmaceutical Control and Therapeutic Aspects, J. Pharm. and Pharmacol., vol. 11, No. 5, pages 257-290 (pages 266271, 277279, and 285-288 are especially pertinent to In Vivo Tablet Availability of Drugs), May 1959.
Campbell et al.: Oral Prolonged Action Medication, Practitioner, vol. 183, pages 758-765, December 1959.
Claims (1)
1. A PROLONGED RELEASE ANALGESIC TABLET COMPRISING A PLURALITY OF FINELY DIVIDED HARD PARTICLES OF AN ANALGESIC DRUG, EACH PARTICLE BEING INDIVIDUALLY COATED WITH A PERMEABLE SOLUTION-RESISTANT COATING, SAID PARTICLES BEING DISPERSED THROUGHOUT A COMPRESSED MATRIX CONSISTING PREDOMINANTLY OF THE SAME ANALGESIC DRUG.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US200554A US3115441A (en) | 1962-06-06 | 1962-06-06 | Timed release pharmaceutical preparations and method of making the same |
GB39356/62A GB1019146A (en) | 1962-06-06 | 1962-10-17 | Timed release pharmaceutical preparations and method of making the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US200554A US3115441A (en) | 1962-06-06 | 1962-06-06 | Timed release pharmaceutical preparations and method of making the same |
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Cited By (33)
Publication number | Priority date | Publication date | Assignee | Title |
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US3341416A (en) * | 1963-12-11 | 1967-09-12 | Ncr Co | Encapsulation of aspirin in ethylcellulose and its product |
US3344029A (en) * | 1963-06-03 | 1967-09-26 | U S Ethicals Inc | Sustained release composition |
US3350270A (en) * | 1964-09-18 | 1967-10-31 | Leeds Dixon Lab Inc | Aluminum aspirin film-enveloped therapeutic agents in sustained release dosage form |
US3362880A (en) * | 1963-09-20 | 1968-01-09 | Dow Chemical Co | Compressed drug tablets of ethyl cellulose, glyceryl monostearate, karaya gum, tragacanth, talc, and magnesium stearate |
US3371015A (en) * | 1962-06-28 | 1968-02-27 | Haessle Ab | Pharmaceutical core compositions with thin rapidly disintegrating coatings |
US3388041A (en) * | 1964-01-27 | 1968-06-11 | Richardson Merrell Inc | High dosage sustained release tablet |
US3476588A (en) * | 1964-10-20 | 1969-11-04 | Ile De France | Process for coating tablets |
US3488418A (en) * | 1965-11-18 | 1970-01-06 | Sterling Drug Inc | Sustained relief analgesic composition |
US3524910A (en) * | 1965-11-18 | 1970-08-18 | Sterling Drug Inc | Sustained relief analgesic compositions |
US3922339A (en) * | 1974-06-20 | 1975-11-25 | Kv Pharm Co | Sustained release medicant |
US3939259A (en) * | 1974-05-24 | 1976-02-17 | Anthony Pescetti | Coating composition and therapeutic preparation incorporating same |
US4025613A (en) * | 1971-07-19 | 1977-05-24 | Richard G. Powers | Timed-release aspirin |
US4261970A (en) * | 1979-05-18 | 1981-04-14 | Nikken Chemicals Co., Ltd. | Theophylline sustained release granule |
US4353887A (en) * | 1979-08-16 | 1982-10-12 | Ciba-Geigy Corporation | Divisible tablet having controlled and delayed release of the active substance |
WO1984004674A1 (en) * | 1983-05-31 | 1984-12-06 | Jang Choong Gook | Dry direct compression compositions for controlled release dosage forms |
US4499066A (en) * | 1981-08-05 | 1985-02-12 | Farmitalia Carlo Erba S.P.A. | Pharmaceutical sustained-release compositions |
US4503031A (en) * | 1982-12-17 | 1985-03-05 | Glassman Jacob A | Super-fast-starting-sustained release tablet |
US4590062A (en) * | 1984-04-16 | 1986-05-20 | Tech Trade Corp. | Dry direct compression compositions for controlled release dosage forms |
US4609542A (en) * | 1978-12-22 | 1986-09-02 | Elan Corporation, P.L.C. | New pharmaceutical forms for administration of medicaments by oral route, with programmed release |
EP0222411A2 (en) * | 1985-11-15 | 1987-05-20 | Taisho Pharmaceutical Co. Ltd | Method of preparing sustained-release pharmaceutical preparation |
US4704284A (en) * | 1982-08-12 | 1987-11-03 | Pfizer Inc. | Long-acting matrix tablet formulations |
US4720387A (en) * | 1983-06-22 | 1988-01-19 | Shionogi & Co., Ltd. | Sustained-release preparation of pinacidil |
US4863741A (en) * | 1985-03-25 | 1989-09-05 | Abbott Laboratories | Tablet composition for drug combinations |
US4874614A (en) * | 1985-03-25 | 1989-10-17 | Abbott Laboratories | Pharmaceutical tableting method |
US4940588A (en) * | 1984-10-30 | 1990-07-10 | Elan Corporation | Controlled release powder and process for its preparation |
EP0411590A2 (en) * | 1989-08-02 | 1991-02-06 | ARNOLD, John David | Method and preparation for reducing risk of myocardial infarction |
US5026559A (en) * | 1989-04-03 | 1991-06-25 | Kinaform Technology, Inc. | Sustained-release pharmaceutical preparation |
US5283065A (en) * | 1989-09-21 | 1994-02-01 | American Cyanamid Company | Controlled release pharmaceutical compositions from spherical granules in tabletted oral dosage unit form |
US6613353B1 (en) | 1993-12-13 | 2003-09-02 | Pii Drug Delivery, Llc | Pharmaceutical formulations |
US20050202085A1 (en) * | 2000-07-08 | 2005-09-15 | Lovercheck Dale R. | Unit dose of material in system and method |
WO2013175500A1 (en) * | 2012-04-23 | 2013-11-28 | Cadila Healthcare Limited | Delazed release pharmaceutical compositions of salsalate |
US20180338929A1 (en) * | 2017-05-23 | 2018-11-29 | Soon Kap Hahn | Method and Compounds for Treating Peripheral Neuropathy |
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FR2287216A1 (en) * | 1974-10-09 | 1976-05-07 | Narcisse Guy | Capsules contg. free and micro encapsulated ingredients - giving immediate and sustained release of drugs esp. aspirin |
FR2575040B1 (en) * | 1984-12-20 | 1990-02-09 | Rhone Poulenc Sante | NOVEL COMPOSITIONS FOR COATING FOOD ADDITIVES FOR RUMINANTS AND FOOD ADDITIVES THUS COATED |
CA1266235A (en) * | 1985-03-25 | 1990-02-27 | Wallace E. Becker | Tablet composition for drug combinations |
FR2584604B1 (en) * | 1985-07-15 | 1988-11-04 | Veyron Froment Laboratoire | THERAPEUTIC COMPOSITION CONSTITUTING A NEW ORAL GALENIC FORM FOR IMPROVING THE KINETICS OF BIOAVAILABILITY |
JPH10108630A (en) * | 1996-10-04 | 1998-04-28 | Showa Sangyo Co Ltd | Lustering coating agent for food having good workability at the time of coating |
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Cited By (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3371015A (en) * | 1962-06-28 | 1968-02-27 | Haessle Ab | Pharmaceutical core compositions with thin rapidly disintegrating coatings |
US3344029A (en) * | 1963-06-03 | 1967-09-26 | U S Ethicals Inc | Sustained release composition |
US3362880A (en) * | 1963-09-20 | 1968-01-09 | Dow Chemical Co | Compressed drug tablets of ethyl cellulose, glyceryl monostearate, karaya gum, tragacanth, talc, and magnesium stearate |
US3341416A (en) * | 1963-12-11 | 1967-09-12 | Ncr Co | Encapsulation of aspirin in ethylcellulose and its product |
US3388041A (en) * | 1964-01-27 | 1968-06-11 | Richardson Merrell Inc | High dosage sustained release tablet |
US3350270A (en) * | 1964-09-18 | 1967-10-31 | Leeds Dixon Lab Inc | Aluminum aspirin film-enveloped therapeutic agents in sustained release dosage form |
US3476588A (en) * | 1964-10-20 | 1969-11-04 | Ile De France | Process for coating tablets |
US3488418A (en) * | 1965-11-18 | 1970-01-06 | Sterling Drug Inc | Sustained relief analgesic composition |
US3524910A (en) * | 1965-11-18 | 1970-08-18 | Sterling Drug Inc | Sustained relief analgesic compositions |
DE1617374A1 (en) * | 1965-11-18 | 1971-04-01 | Sterling Drug Inc | Process for the production of a pharmaceutical preparation with delayed action |
US4025613A (en) * | 1971-07-19 | 1977-05-24 | Richard G. Powers | Timed-release aspirin |
US3939259A (en) * | 1974-05-24 | 1976-02-17 | Anthony Pescetti | Coating composition and therapeutic preparation incorporating same |
US3922339A (en) * | 1974-06-20 | 1975-11-25 | Kv Pharm Co | Sustained release medicant |
US4726951A (en) * | 1978-12-22 | 1988-02-23 | Elan Corporation P.L.C. | New pharmaceutical forms for administration of medicaments by oral route, with programmed release |
US4609542A (en) * | 1978-12-22 | 1986-09-02 | Elan Corporation, P.L.C. | New pharmaceutical forms for administration of medicaments by oral route, with programmed release |
US4261970A (en) * | 1979-05-18 | 1981-04-14 | Nikken Chemicals Co., Ltd. | Theophylline sustained release granule |
US4353887A (en) * | 1979-08-16 | 1982-10-12 | Ciba-Geigy Corporation | Divisible tablet having controlled and delayed release of the active substance |
US4499066A (en) * | 1981-08-05 | 1985-02-12 | Farmitalia Carlo Erba S.P.A. | Pharmaceutical sustained-release compositions |
US4704284A (en) * | 1982-08-12 | 1987-11-03 | Pfizer Inc. | Long-acting matrix tablet formulations |
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