|Publication number||US3922339 A|
|Publication date||Nov 25, 1975|
|Filing date||Jun 20, 1974|
|Priority date||Jun 20, 1974|
|Publication number||US 3922339 A, US 3922339A, US-A-3922339, US3922339 A, US3922339A|
|Inventors||Shear Jeff L|
|Original Assignee||Kv Pharm Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (11), Referenced by (35), Classifications (11)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1191 Shear 1 Nov. 25, 1975 1 SUSTAINED RELEASE MEDICANT  Inventor: Jeff L. Shear, Creve Coeur, Mo.
 Assignee: KV Pharmaceutical Company, St.
 Filed: June 20, 1974  Appl. No.: 481,056
 U.S. Cl. 424/22; 117/47; 117/100; 117/104; 264/118; 264/129; 264/131; 264/148; 424/19; 424/20; 424/34; 424/35 3,480,468 11/1969 Carletti et a1 117/84 3,524,756 8/1971) Signorino et al.. 117/72 3,555,144 1/1971 Pazar et a1 424/2 3,646,192 2/1972 Magid .424/35 3,728,445 4/1973 Bardani 424/22 3,758,679 9/1973 Seidler 424/19 Primary Examiner-Shep K. Rose Attorney, Agent, or Firm-Sidney B. Ring; Hyman F. Glass  ABSTRACT This invention relates to a sustained release pharmaceutical preparation of a medicant prepared by 1. Compacting a wet pharmaceutical preparation; 2. Drying and granulating the compacted preparations of 1); 3. Sealing the granules of (2); 4. Coating (3) with an enteric-soluble coating.
The medicant employed in the pharmaceutical preparation is preferably blended with an inert material.
16*Claims, N0 Drawings SUSTAINED RELEASE MEDICANT This invention relates in general to certain new and useful improvements in pharmaceutical preparations and,'rnore particularly, to medicated granules which release the medication into the human system gradually over a sustained period of time and methods of making the same. i
It has been accepted practice in the compounding of pharmaceutical tablets to provide certain types of tablets with what has been commonly referred to as an enteric coating. The enteric coating is one which will resist the action of the gastric juices in the stomach and will not dissolve therein or be otherwise affected thereby so that the drug which is incorporated in the tablet will pass through the stomach and into the intestine. The so-called enteric coating is of such a nature that it will be dissolved very readily in the intestinal fluids so that the drug which has been enclosed in the enteric coating will become effective in the intestinal tract rather than in the stomach. Such tablets, however, are merely delayed action tablets. In other words, by selecting an enteric coating of the proper type and by using an appropriate amount, it is possible to delay the effective entry of the drug into the patients system for a number of hours. The so-called enteric coated tablet is also used when it is desirable to introduce the medicant into the patients intestinal tract without discharging any of the medicant into the stomach These procedures are useful in certain applications, but the patient sooner or later receives the entire dosage in a single shot, so to speak.
However, pharmacological investigations have shown that with many drugs the patient responds far better to sustained minute-incremental dosage, that is to say, very minute quantities administered at very short intervals continuously over sustained periods of time. This can be referred to, for want of a better term, as the trickle system. As a result, there have been devised various methods of preparing sustained release pharmaceutical preparations which allow the medication to effect a sustained trickle by releasing minuteincremental dosages, which are continuously released over sustained periods of time.
One of these methods is described in US. Pat. No. 2,809,916 which describes a process for making sustained period minute-incremental dosage pharmaceutical preparations which comprise intimately mixing a powdered drug and an enteric water insoluble excipient to produce a pasty mass, drying the mass slowly without agitation in such a manner as to produce a rough granular material, breaking up the rough granular material by light crushing, whereby to reduce it to granular particles, said mixing, drying and crushing operations constituting one cycle, and remixing the granular particles with an additional quantity of the excipient to produce a pasty mass, redrying such pasty mass slowly and without agitation in such a manner as to produce'a granulated material, again breaking up the rough granular material by light crushing, whereby to reduce it again to granular particles, as second mixing, drying and crushing operations constituting a second cycle, said process consisting of not less than three nor more than mixing, crushing and drying cycles repeated in successive order, whereby to produce a pharmaceutical material consisting of gran ules having slow but continuous and attenuated solubility in the gastro-intestinal tract.
l have now discovered an improved method of preparing sustainedrelease pharmaceutical preparations which are prepared by a process comprising:
1. compacting a wet pharmaceutical preparation;
2. drying and granulating the compacted preparation of l 3. sealing the granules of (2);
4. coating (3) with an enteric-soluble coating,
The preferred method comprises:
1. blending the medicant with desired inert materials to form a uniform blend of active medicant and inert materials;
2. wetting (l) with sufficient-liquid material so as to act as a binder on compacting;
3. compacting (2) such as by extrusion to form a spaghetti-like material which is dried, broken and screened to the desired particle size;
4. spraying the particles of (3) with a liquid such as a solution, for example aqueous sugar, dusting with a powder such as talc and allowing them to dry so as to seal the granules to prevent the enteric coating from penetrating to active ingredients;
5. coating the granules of (4) with a solution of excipients such as an alcoholicsolution of shellac, and preferably dusting with stearic acid or stearic acid salts and allowing to dry to form an enteric-soluble coating.
The enteric coated sealed granules of (5) may be further coated one or more times by additional treatment with the excipient to yield the desired sustained release pharmaceutical preparation.
A wide variety of inert materials, either singly or in combination, which are pharmaceutically acceptable, can be blended with active medicant. They include: l inorganic materials such as salts, for example, carbonates, such as calcium carbonate, magnesium oxide, magnesium carbonate, etc.; (2) phosphates such as calcium phosphate, dicalcium phosphate, tricalcium phosphate, etc.; (3) milk sugars such as milk sugar impalpable, edible or spray dried lactose; (4) film formers; etc.; (5) starch, sugar, combinations of starch and sugar, etc,
The medicant employed in the pharmaceutical preparation is preferably blended with an inert material so that the medicant comprises at least about 5% of the weight of the combined weight of medicant-inert material, such as from about 595%, for example, at least 15%, but preferably at least about 25%, withan optimum of about 30-50%. Preferably the inert material comprises at least about 50% of the combined weight of medicant and inert material.
I have further discovered that where the active medicant is uniformly blended with inert materials prior to the preparation of the sustained release product one obtains a product which has more predictable sustained release properties. For example, where a product is made where the medicant is blended with an inert material as compared to the same material not blended with the inert material, one obtains a product which will consistently deliver to of the medication per capsule. In contrast, a product similarlyprepared without blending with inert materials prior to preparation of the sustained release product may deliver medication inconsistently over a wide range, such as for example.50% of the dosage in one capsule and l607( of the dosage in another capsule, thus causing underdosages, and possible toxic effects due to overdosages.
zein in isopropanol, etc.
Table I 4 stearic acid to 100 parts of sealed particles and then allowed to dry.
EXAMPLE 2 The process of Example 1 was repeated except that the product of Example 1 was coated with calcium stearate/talc enteric coatings instead of one coating and by repeating the (5) Enteric coating step 3 times.
Materials Employed as Film Formers Natural Films Semi-Synthetic Films completely Synthetic Films Tree Exudates and Extracts: Arahic Tragacanth Karaya Larch (ihatti Seed or Root: Locust Bean Guar Psyllium Seed Quince Seed Seaweed Extracts:
Cellulose Derivatives: Carhoxymethylcellulose Methylccllulose Hydroxypropylmethylcellulose Hydroxypropylcellulose Hydroxyethylcellulose Ethylhydroxyethylcellulose Starch Derivatives: Carboxymcthylstarch Hytlroxyethylstareh Hydroxypropylstarch Microbial Fermentation Vinyl Polymers:
Pol \'\'inylpyrrol idone Polyyinylalcohol Carhoxyl inyl Polymer I Acrylic Polymers: Polyacrylic Acid Polyacrylamidc Ethylene Oxide Polymers Agar Gums:
Algin Dextran Carragcenztn Polysaccharidc Fureellaran B-l459 (Kelzan) Others: Others:
Pectin Low Methoxyl Pectin Gelatin and Other Propylene Glycol Proteins Alginate Starch Triethanolamine Alginate Carboxymethyl Locust Bean Gum Carhoxymcthyl Guar Gum Stearic acid. calcium stearate, talc and combinations thereof can also be employed.
The following examples are presented for purposes of illustration and not of limitation.
EXAMPLE 1 l. Blending of Medieant: A medicant (Phenformin HCl) 1 part is uniformly blended with 2 parts of an inert material (starch 25%/sugar 75%).
2. Wetting: This medicant-inert material blend is wetted down with water.
3. Compacting, Drying, Sizing: The wetted medicantinert material is then extruded through an orifice having a diameter of 1/1 6 inch to yield a spaghettilike material which is then dried, broken up and screened to the desired particle size (about l624 mesh).
4. Sealing: These sized, dried, extruded, medicant-inert material particles are then sprayed with an aqueous solution of sugar (89% active) at a ratio of 9 parts of aqueous solution of sugar to 100 parts of particles; and then dusted with a powder (talc) at 10 parts of talc per 100 parts of particles; and then allowed to dry. This seals the particles.
5. Enteric Coating: These sealed particles are then spray coated with an alcoholic solution of shellac (36% shellac) at a ratio of 14 parts of alcoholic shellac to 100 parts of sealed particles and then dusted with a powder (stearic acid) at a ratio of parts of EXAMPLE 3 The process of Example 1 was repeated except that the inert material was not blended with medicant, all other steps being the same.
EXAMPLE 4 The product of Example 1 which contained the inert material in (1) Blending was compared with the product of Example 3 without inert material.
The release of medicant per interval was tested by the following procedures:
1. National Formulary revolving bottle test procedure (NF-XIII);
2. Modified revolving bottle test procedure; 3. Wiley test procedure.
These tests demonstrated that the product of Example 1 containing the inert material consistently released -1 00% of the theoretical medication per unit dosage whereas the product of Example 3 would vary widely, sometimes yielding 50% and other times yielding as high as of theoretical medication per unit dosage. Such control minimizes the possible side effects of over dosages and insures treatment with the desired dosage.
Although Phenformin HCl is employed in the above examples to illustrate a medicant which can be employed in this invention, other medicants can be employed, for example, the following: nitroglycerin, phenylpropanolamine HCl, phenylephrine HCl, chlorpheniramine maleate, caffeine, D-amphetamin S0 amobarbital. pyrilamine maleate, pentaerythritol tetranitrate, isosorbide dinitrate, propantheline bromide, phenobarbital. methapyrilene HCl, theophylline HCl, etc.
3 Other medic-ants which can be employed herein will be obvious to those skilled in the art.
1. A process of preparing a sustained release pharmaceutical preparation of a medicant which comprises l blending a medicant with desired inert materials; (2) wetting the blend with sufficient liquid material so as to act as a binder on compacting; (3) compacting the wetted blend by extruding to form a spaghetti-like material; (4) drying. breaking and screening the extruded material to the desired particle size; (5) spraying the particles with a solution of a film-forming material; (6) dusting the sprayed particles with a powder and drying to form a seal on the particles; and (7) coating the sealed particles with a solution of an excipient so as to form an enteric-soluble coating on the sealed particle.
2. The process of claim 1 wherein the medicant comprises 595% of the medicant-inert material blend.
3. The process of claim 1 where the medicant comprises 30-50% of the medicant-inert material blend.
4. The process of claim 1 where the inert material is a mixture of starch and 75% sugar and there is 1 part medicant to 2 parts inert material.
5. The process of claim 1 where medicant-inert material blend is wetted with water.
6. The process of claim 1 where the wetted blend is extruded through an orifice having a diameter of l/l6 of an inch to form the spaghetti-like material.
7. The process of claim 1 where the dried and broken extruded material is screened to about a 16-24 mesh size.
8. The process of claim 1 where the screened particles are sprayed with an 89% aqueous solution of sugar, as the film-forming material, in a ratio of 9 parts aqueous solution to parts of particles.
9. The process of claim 1 where the sprayed particles are dusted with powdered tale in a ratio of 10 parts talc per 100 parts of particles.
10. The process of claim 1 where the sealed particles are ccated with 14 parts of a 36% alcoholic solution of shellac to 100 parts of particles and then dusted with 25 parts stearic acid per 100 parts sealed particles.
11. The process of claim 1 where the sealed particles are coated with a calcium stearate/talc enteric coating.
12. The process of claim 1 where the enteric coating step is repeated three times.
13. The process of claim 10 where the enteric coating step is repeated three times.
14. The process of claim 12 where the enteric coating step is repeated three times.
15. The product obtained by the process of claim 1.
16. The product obtained by the process of claim 10.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2811483 *||Dec 9, 1954||Oct 29, 1957||Pfizer & Co C||Pharmaceutical composition and process for preparing the same|
|US2895880 *||May 13, 1955||Jul 21, 1959||Smith Kline French Lab||Sustained release pharmaceutical product|
|US3115441 *||Jun 6, 1962||Dec 24, 1963||Hermelin Victor M||Timed release pharmaceutical preparations and method of making the same|
|US3247064 *||Mar 29, 1963||Apr 19, 1966||Shionogi & Co||Multivitamin tablet stabilized with porous silica|
|US3361631 *||Sep 30, 1963||Jan 2, 1968||Sandoz Ag||Method of sugar coating pharmaceutical tablets|
|US3480468 *||Feb 9, 1966||Nov 25, 1969||Farmaceutici Italia||Process of preparing pharmaceutical tablet with orange-peel-like protective sugar coating|
|US3524756 *||May 29, 1967||Aug 18, 1970||Colorcon||Process of coating tablets with alternate tacky and non-tacky layers|
|US3555144 *||May 29, 1969||Jan 12, 1971||American Cyanamid Co||Color-coded jigsaw design tablet compressed from therapeutic extruded cylindrical granules of visibly different colors|
|US3646192 *||Jun 5, 1969||Feb 29, 1972||Hoffmann La Roche||Silica gel stabilizer for sugar coated multivitamin tablets|
|US3728445 *||Oct 19, 1970||Apr 17, 1973||Controlled Medications||Controlled release medicament|
|US3758679 *||Feb 22, 1972||Sep 11, 1973||Lilly Co Eli||Propoxyphene napsylate timed release particles|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4274830 *||Sep 27, 1977||Jun 23, 1981||Colorcon, Inc.||Colored medicinal tablet, natural color pigment and method for using the pigment in coloring food, drug and cosmetic products|
|US4336244 *||Apr 28, 1980||Jun 22, 1982||Colorcon, Inc.||Colored medicinal tablet, natural color pigment and method for using the pigment in coloring food, drug and cosmetic products|
|US4508702 *||Feb 3, 1984||Apr 2, 1985||Key Pharmaceuticals, Inc.||Sustained release aspirin|
|US4555399 *||Mar 8, 1984||Nov 26, 1985||Key Pharmaceuticals, Inc.||Aspirin tablet|
|US4587118 *||Dec 12, 1984||May 6, 1986||Key Pharmaceuticals, Inc.||Dry sustained release theophylline oral formulation|
|US4634587 *||Aug 16, 1984||Jan 6, 1987||Key Pharmaceuticals, Inc.||Sustained release quinidine dosage form|
|US4670251 *||Sep 20, 1984||Jun 2, 1987||Igene Biotechnology, Inc.||Microcrystalline tableting excipient derived from whey|
|US4722815 *||Apr 20, 1987||Feb 2, 1988||Japan Liquid Crystal Co., Ltd.||Process of making a synthetic resin product containing a molecular inclusion compound in cyclodextrin|
|US4786506 *||Mar 2, 1987||Nov 22, 1988||Istituto Gentili S.P.A.||Method for the preparation of granulates suited for the production of sustained release coated tablets for oral use|
|US4834985 *||May 19, 1987||May 30, 1989||Euroceltique S.A.||Controlled release pharmaceutical composition|
|US4849227 *||Mar 3, 1987||Jul 18, 1989||Eurasiam Laboratories, Inc.||Pharmaceutical compositions|
|US4999200 *||Dec 9, 1987||Mar 12, 1991||Marion Laboratories||Psyllium tablet composition, method of manufacture and method of use|
|US5120306 *||Mar 21, 1990||Jun 9, 1992||Gosselin Leon F||Direct delivery of anti-inflammatories to the proximal small bowel|
|US5149542 *||Sep 29, 1987||Sep 22, 1992||Roberto Valducci||Coating membrane and compositions prepared therefrom|
|US5270056 *||Aug 30, 1991||Dec 14, 1993||Aktiebolaget Hassle||Particle having a dyed coke indicator and a pharmaceutical coating for parenteral administration of the pharmaceutical|
|US5275819 *||Apr 26, 1991||Jan 4, 1994||Amer Particle Technologies Inc.||Drug loaded pollen grains with an outer coating for pulsed delivery|
|US5576025 *||Mar 29, 1995||Nov 19, 1996||Takeda Chemical Industries, Ltd.||Gastrointestinal mucosa-adherent matrixes, pharmaceutical preparations and a coating composition|
|US5662935 *||Dec 23, 1993||Sep 2, 1997||Saitec S.R.L.||Process for preparing controlled release pharmaceutical forms and the forms thus obtained|
|US5707636 *||Apr 6, 1995||Jan 13, 1998||Saitec S.R.L.||Apparatus and method for preparing solid forms with controlled release of the active ingredient|
|US5731006 *||Aug 20, 1996||Mar 24, 1998||Takeda Chemical Industries, Ltd.||Gastrointestinal mucosa-adherent granules, pharmaceutical preparations and a coating composition|
|US5882715 *||Jun 19, 1996||Mar 16, 1999||Pharma-Vinci A/S||Method of preparing an oral preparation provided on the outer side with an enteric coating, as well as an oral preparation obtained by the method|
|US6123980 *||Dec 1, 1997||Sep 26, 2000||Imperial Sugar Company||Preparing granulated sugar blends and products|
|US6368635||Dec 18, 1997||Apr 9, 2002||Takeda Chemical Industries, Ltd.||Gastrointestinal mucosa-adherent matrixes pharmaceutical preparations and a coating composition|
|US6613353||Nov 22, 2000||Sep 2, 2003||Pii Drug Delivery, Llc||Pharmaceutical formulations|
|US7846476||May 2, 2002||Dec 7, 2010||Purdue Pharma L.P.||Once-a-day oxycodone formulations|
|US20020142041 *||Feb 20, 2002||Oct 3, 2002||Yohko Akiyama||Gastrointestinal mucosa-adherent matrixes, pharmaceutical preparations and a coating composition|
|US20040096500 *||Nov 12, 2003||May 20, 2004||Benjamin Oshlack||Controlled release oxycodone compositions|
|US20040185098 *||Mar 24, 2004||Sep 23, 2004||Benjamin Oshlack||Controlled release oxycodone compositions|
|US20100291214 *||Jun 25, 2010||Nov 18, 2010||Armark Authentication Technologies, Llc||Three-dimensional microfiber extrudate structure and process for forming three-dimensional microfiber extrudate structure|
|EP0021129A2 *||May 31, 1980||Jan 7, 1981||Kali-Chemie Pharma GmbH||Pancreatin pellets, process for their manufacture and medicines containing these pellets|
|EP0094116A2 *||Apr 27, 1983||Nov 16, 1983||THE PROCTER & GAMBLE COMPANY||Therapeutic granules|
|EP0794769A1 *||Dec 5, 1995||Sep 17, 1997||Pauli, Gunter||Method of drug delivery and coatings for use in the method|
|WO1987005505A1 *||Mar 12, 1987||Sep 24, 1987||Eurosium Lab||Pharmaceutical compositions|
|WO2003028698A2 *||Sep 25, 2002||Apr 10, 2003||Rudolf Schroeder||Method and device for producing granulates that comprise at least one pharmaceutical active substance|
|WO2010151746A2 *||Jun 25, 2010||Dec 29, 2010||Armark Authentication Technologies, Llc||Three-dimensional microfiber extrudate structure and process for forming three-dimensional microfiber extrudate structure|
|U.S. Classification||424/498, 427/2.21, 264/129, 264/131, 424/490, 264/148, 264/118|
|International Classification||A61K9/50, A61K9/22|