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Sustained release matrix for high-dose insoluble drugs

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US20040121012A1
US20040121012A1 US10731859 US73185903A US2004121012A1 US 20040121012 A1 US20040121012 A1 US 20040121012A1 US 10731859 US10731859 US 10731859 US 73185903 A US73185903 A US 73185903A US 2004121012 A1 US2004121012 A1 US 2004121012A1
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Prior art keywords
release
gum
sustained
ibuprofen
dosage
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US10731859
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Anand Baichwal
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Penwest Pharmaceuticals Co
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Penwest Pharmaceuticals Co
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic, hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/192Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-arylpropionic acids, ethacrynic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic, hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S514/00Drug, bio-affecting and body treating compositions
    • Y10S514/96Significant, tablet formulation, e.g. designated excipient, disintegrant, glydent or lubricant

Abstract

Sustained release dosage forms of high dose insoluble drugs such as ibuprofen and methods for their manufacture are disclosed.

Description

    BACKGROUND OF THE INVENTION
  • [0001]
    The advantages of controlled release products are well known in the pharmaceutical field and include the ability to maintain a desired blood level of a medicament over a comparatively longer period of time while increasing patient compliance by reducing the number of administrations necessary to achieve the same. These advantages have been attained by a wide variety of methods.
  • [0002]
    Oral controlled release delivery systems should ideally be adaptable so that release rates and profiles can be matched to physiological and chronotherapeutic requirements. While many oral controlled and sustained release formulations are already known, certain drugs that are relatively insoluble in water and which further have relatively high dose requirements (based on weight) present formulation difficulties which render them unsuitable for inclusion in sustained release formulations. Difficulties in preparing suitable sustained release formulations of insoluble drugs are increased when the dose of the insoluble drug to be delivered to render a therapeutic effect over the desired period of time is relatively high, e.g., 500 mg or greater.
  • [0003]
    An example of a high dose, insoluble drug is ibuprofen, which is a non-steroidal anti-inflammatory agent (“NSAID”). Several immediate release forms of ibuprofen are commercially available, e.g., Motrin® (available from Upjohn) and Brufen® (available from The Boots Company PLC), and a sustained release ibuprofen formulation, Brufen Retard™, is commercially available from the Boots Company PLC. Indomethacin, another high dose insoluble NSAID, is commercially available in sustained release form as Indocin SR™ from Merck & Co., Inc.
  • [0004]
    There is still a need in the art for sustained release dosage forms of insoluble NSAIDs that are bioavailable and provide suitable release profiles of the NSAID from the dosage form over a sustained period of time, e.g. for about 12 to about 24 hours.
  • OBJECTS AND SUMMARY OF THE INVENTION
  • [0005]
    It is an object of the present invention to provide sustained release dosage forms of insoluble NSAIDs that provide an early onset of action and a sustained release of the NSAID.
  • [0006]
    It is a further object of the present invention to provide a method for preparing such bioavailable sustained release NSAID dosage forms.
  • [0007]
    It is a further object of the present invention to provide a sustained release excipient which is suitable for providing sustained release insoluble NSAID dosage forms.
  • [0008]
    The aforementioned objects and others are achieved by virtue of the present invention, which relates in part to a sustained release dosage form comprising from about 500 mg to about 1000 mg of an insoluble NSAID and an effective amount of a sustained release carrier to release the NSAID over a desired sustained period of time, which releases at least about 6 percent by weight of the NSAID at about 2 hours and provides a too (i.e., releases 50% by weight of the NSAID) at from about 12 to about 16 hours, after exposure of the dosage form to simulated gastrointestinal fluid.
  • [0009]
    The present invention is also directed to a sustained release oral dosage form containing ibuprofen as the active agent, which dosage form provides an, early onset of action, e.g., the dosage form releases at least about 6 percent of the ibuprofen by weight about 2 hours, and/or the dosage form releases at least about 20 percent of the ibuprofen by weight about 4 hours, after exposure to simulated gastrointestinal conditions (such-as via an in-vitro dissolution testing method), and which on the other hand provides a t50 at about 12 to about 16 hours.
  • [0010]
    The present invention is also directed to an sustained release oral solid dosage form including from-about 500 mg to about 1000 mg of an insoluble NSAID and a sustained release carrier, and which releases at least 20 percent by weight of the NSAID after about 4 hours-and provides a t50 at about 12 to about 16 hours, after exposure of the dosage form to simulated gastric fluid.
  • [0011]
    Sustained release dosage forms of NSAIDs according to the present invention have the desireable inventive advantage of providing a rapid onset of therapeutic effect of the insoluble NSAID and still provide sustained release of the NSAID so as to provide effective blood plasma levels of the ibuprofen over the entire dosing interval, e.g., about 24 hours. Such sustained release oral ibuprofen dosage forms provide an in-vitro dissolution rate, when measured, e.g., by the USP Dissolution Apparatus (Paddle Type II) of at least 6 percent by weight ibuprofen released after 2 hours, and/or at least about 20 percent by weight ibuprofen released after 4 hours, and which provides a t50 after about 12 to about 16 hours.
  • [0012]
    In preferred embodiments, the insoluble NSAID is ibuprofen, which preferably comprises from about 500 mg to about 1000 mg of the dosage forms. A non-limiting list of other insoluble NSAIDs that may be used in accordance with the pre sent invention include etodolac, fenoprofen (as the calcium salt), naproxen, mefenamic acid, nabumetone, tolmetin, and the like.
  • [0013]
    In other preferred embodiments, the sustained release carrier includes xanthan gum and a crosslinking agent, e.g., a galactomannan. In preferred embodiments, the sustained release carrier includes xanthan gum and locust bean gum in a 1:20 to about a 20:1 weight ratio. In preferred embodiments, the xanthan gum comprises from about 5 to about 95 percent by weight of the sustained release carrier. In other preferred embodiments, locust bean gum comprises from about 50 to about 95% by weight of the sustained release carrier.
  • [0014]
    In preferred embodiments, the dosage forms include from about 500 mg to about 1000 mg of the insoluble NSAID are suitable for dosing on a twice daily basis. In other preferred embodiments, the dosage forms include from about 500 mg to about 1000 mg of the insoluble NSAID and are suitable for dosing on a once daily basis. When administered on a once daily basis, it is preferred that more than one tablet containing 500 mg to 1000 mg of the insoluble NSAID are administered as a single dose to a patient.
  • [0015]
    In each of the embodiments set forth above, the dosage form is preferably a tablet.
  • [0016]
    The present invention is also directed to a method of preparing an oral sustained release dosage form of a high dose insoluble NSAID tablet comprising the steps of wet granulating a mixture of xanthan gum, locust bean gum, an inert diluent and insoluble NSAID to form a granulate; and tableting the resultant granulate into tablets containing from about 500 to about 1000 mg insoluble NSAID; wherein the ratio of the total weight of the insoluble NSAID in the tablet to the combined weight of xanthan gum and locust bean gum is from about 1:0.06 to about 1:0.4.
  • [0017]
    Another aspect of the invention is directed to a sustained release pharmaceutical excipient for use in sustained release oral solid dosage forms of insoluble NSAIDs, including xanthan gum, a crosslinking agent, and from about 20 to about 35 percent by weight of an inert diluent, e.g., dextrose.
  • [0018]
    In a preferred embodiment, the total combined weight of the xanthan gum and the crosslinking agent is from about 65 to about 80 percent of the excipient. In particularly preferred embodiments, the crosslinking agent is locust bean gum.
  • [0019]
    In another preferred embodiment of the invention, a sustained release ibuprofen tablet is provided comprising from about 500 to about 1000 mg ibuprofen, and from about 7 to about 40 percent of a hydrophilic gum matrix comprising xanthan gum and a cross-linking agent capable of cross-linking the xanthan gum when said tablet is exposed to an aqueous environment. In preferred embodiments, the cross-linking agent is, e.g., a homopolysaccharide such as locust bean gum, an ionizable gel strength enhancing agent, or mixtures thereof.
  • [0020]
    Yet another embodiment of the invention is directed to a sustained release tablet containing-from about 500 mg to about 1000 mg of an insoluble NSAID in a sustained release matrix including xanthan gum and a crosslinking agent, wherein the total weight of the tablet is from about 110 percent to about 140 percent by weight of the insoluble NSAID, and the xanthan gum and the crosslinking agent comprise from about 7 to about 40 percent of the tablet by weight. In certain embodiments where the weight of NSAID, e.g., ibuprofen in the tablet is about 800 mg, the combined gum weight is from about 119 percent to about 136 percent of the insoluble NSAID.
  • [0021]
    The invention also provides a method of retarding the release of ibuprofen from a sustained release ibuprofen tablet containing xanthan gum when the tablet is exposed to an aqueous environment comprising replacing from about 5 to about 95 percent by weight of the xanthan gum in a sustained release ibuprofen tablet with a weight equivalent amount of a crosslinking agent, e.g., locust bean gum, wherein the ratio of said xanthan gum to said locust bean gum is from about 1:20 to about 20:1.
  • [0022]
    In embodiments where the cross-linking agent comprises an ionizable gel strength enhancing agent as defined herein, the ionizable gel strength enhancing agent may comprise from about 1 to about 20% of the total weight of sustained release carrier, e.g., xanthan gum galactomannan gum and ionizable gel strength enhancing agent.
  • [0023]
    Yet another aspect of the invention is directed to a sustained release insoluble NSAID tablet comprising from about 500 to about 1000 mg insoluble NSAID; xanthan gum; locust bean gum; and an inert diluent; wherein the combined weight of the xanthan gum and the locust bean gum is from about 7 to about 40 percent by weight of the final tablet weight and the ratio of insoluble NSAID to the combined weight of the xanthan gum and the locust bean gum is from about 1:0.08 to about 1:0.25. In preferred embodiments where the sustained release formulation is dosed on a twice-a-day basis, the tablet releases at least 6% by weight at about 2 hours after exposure of the dosage form to simulated gastrointestinal fluid and releases 50% by weight of the insoluble from about 5 to about 8 hours after such exposure. In other preferred embodiments, the sustained release ibuprofen tablet releases at least 20% at about 4 hours after exposure of the dosage form to simulated gastrointestinal fluid arid releases 50% by weight of the insoluble NSAID at between from about 12 to about 16 hours after said exposure.
  • [0024]
    By “sustained release” it is meant for purposes of the present invention that the therapeutically active agent, e.g. a high dose insoluble drug such as ibuprofen, is released from the formulation at a controlled rate such that therapeutically beneficial blood levels (but below toxic levels) of the medicament are maintained over an extended period of time, e.g., providing a 12 hour or a 24 hour dosage form.
  • [0025]
    By “bioavailable” it is meant for purposes of the present invention that the therapeutically active agent, e.g. ibuprofen, is absorbed from the sustained release formulation and becomes available in the body at the intended site of drug action.
  • [0026]
    By “insoluble”, it is meant that the therapeutically active medicament has an aqueous solubility of less than about 10 grains per liter (g/l).
  • [0027]
    The term “environmental fluid” is meant for purposes of the present invention to encompass, e.g., an aqueous solution such as in-vitro dissolution media, or gastrointestinal fluid.
  • [0028]
    The term “insoluble NSAID” for purposes of the present invention includes insoluble NSAID, pharmaceutically acceptable salts, complexes, esters, pharmaceutically acceptable isomers thereof, and crystalline forms thereof; with the caveat that the particular form of insoluble NSAID is insoluble as defined herein. All documents cited in this specification are hereby incorporated by reference in their entireties.
  • [0029]
    The term “high dose” for purposes of the present invention, when referring to an insoluble NSAID, refers to a total daily dose of NSAID. When referring to a dosage form or a formulation, the term “high dose” mean that the dosage form or formulation contains from about 500 mg to about 1000 mg of the insoluble NSAID.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • [0030]
    [0030]FIG. 1 is a graphical representation of the dissolution profiles for sustained release ibuprofen tablets prepared according to Examples 4, 5 and 6, Brufen Retard™ 800 mg tablet (available from The Boots Company PLC) and the ibuprofen formulation set forth in Example 1 of EP 234 670 A2; and
  • [0031]
    [0031]FIG. 2 is a graphical representation of the dissolution profiles for sustained release ibuprofen tablets prepared according to Examples 7, 8 and 9, and the ibuprofen formulation set forth in Example 1 of EP 234 670 A2.
  • DETAILED DESCRIPTION
  • [0032]
    Non-steroidal anti-inflammatory drugs exhibits analgesic, anti-inflammatory and antipyretic activity. They are used to treat a variety of diseases and conditions, e.g., rheumatoid arthritis, inflammation.
  • [0033]
    Ibuprofen (α-methyl-4-(2-methylpropyl) benzene acetic acid) is a frequently prescribed NSAID. Typically, ibuprofen is administered in immediate-release form in adult doses ranging from 200 mg to 800 mg three or four times daily, i.e., about 600 mg to about 3200 mg ibuprofen/day. Ibuprofen is often used in chronic treatment regimens, and sustained release dosage forms are desirable to, e.g., reduce the number of necessary daily doses and to increase patient compliance. Ibuprofen, is practically insoluble in water and, as noted above, is a high dose drug, characteristics that present substantial challenges to even the skilled pharmaceutical formulator, especially when sustained release dosage forms of a particular NSAID are desired.
  • [0034]
    U.S. Pat. Nos. 4,994,276; 5,128,143; 5,135,757; 5,554,387; 5,512,297; 5,478,574; 5,472,711; 5,399,362; 5,399,359; 5,399,358 and 5,169,639, all assigned to the Assignee of the instant invention, describe sustained release pharmaceutical formulations and sustained release excipients suitable for use in sustained release dosage forms comprising a gelling agent of both hetero- and homo- polysaccharides which exhibit synergism, e.g., the combination of two or more polysaccharide gums produce a higher viscosity and faster hydration than that which would be expected by either of the gums alone, the resultant gel being faster-forming and more rigid. U.S. Pat. No. 5,455,046, also assigned to the Assignee of the present invention, discloses sustained release heterodisperse hydrogel systems for insoluble drugs. Suitable formulations according to the '046 patent including a gelling agent, an inert pharmaceutical diluent, a cationic cross-linking agent (e.g. calcium sulfate) and a medicament having moderate to poor solubility, e.g., less than 10 g/l. All of the aforementioned references and all references cited herein are incorporated by references in their entireties.
  • [0035]
    Attempts have been made in the art to provide pharmaceutically acceptable sustained release ibuprofen formulations. European Patent Application Publication No. 0 234 670 A2 and its United States counterpart, U.S. Pat. No. 5,415,871 incorporated by reference, (both of which are assigned to The Boots Company PLC, Nottingham, England), describe solid sustained release pharmaceutical formulations comprising a compressed mixture of a pharmacologically active ingredient, e.g. ibuprofen, and 7.5 to 28% by weight of the formulation of a sustained release carrier comprising a major proportion of xanthan gum. The formulations purportedly require lower levels of sustained release carrier than previously suggested in the art and yet still provide release of the active agent into ,he body over a prolonged period. The formulations described therein are said to be suitable for once or twice daily administration to a patient.
  • [0036]
    The Examples in both the EP Publication '670 and the U.S. '871 patent suggest that to provide a suitable sustained release ibuprofen formulation it is preferred that xanthan gum is included as the only gum in the sustained release carrier. The Examples in these documents show that when a portion of the xanthan gum is replaced with another gum, e.g. sodium alginate, the rate of ibuprofen release from the dosage form is increased (compare, e.g. Examples 7 (15% xanthan gum) and 11 (10% xanthan gum and 5% sodium alginate). Dissolution data provided for the sustained release ibuprofen formulation indicate that the t50 for the exemplified sustained release ibuprofen formulations ranges from 3.5 to 9.5 hours and that the formulations release from 0.6 to 2.7 hours.
  • [0037]
    In contrast, preferred sustained release insoluble NSAID dosage forms of, e.g., according to ibuprofen, the present invention release at least 6% of the insoluble NSAID by weight at about 2 hours after exposure of the dosage form to simulated gastrointestinal fluid and yet provide a prolonged and sustained release of ibuprofen from the dosage form as evidenced by a t50 of from about 12 to about 16 hours. The unique dissolution profile provides a rapid onset of action coupled with an extended, release of insoluble NSAID from the dosage form. Preferably, the dosage form is suitable for dosing on a twice daily or once daily basis. When administered on a once-a-day basis, it is preferred that two or more dosage forms, e.g., tablets, are administered as a single dose.
  • [0038]
    It has been suggested that the unique dissolution profile, e.g. the initial release of ibuprofen at only 2 hours after in-vitro and the much slower prolonged release of the remaining ibuprofen is caused by the “swelling” and “gelling” properties of the xanthan gum and the cross-linking agent upon exposure to an environmental fluid. It is hypothesized that upon contact with an environmental fluid, the sustained release insoluble NSAID formulations prepared according to the present invention swell and gel to form a hydrophilic gel matrix from which the drug is released. The initial relatively faster release rate during the two hour period after exposure of the dosage form to environmental fluid. It is suggested that during the initial time period of exposure to an environmental fluid, the xanthan gum hydrates and form a gel matrix causing release of the active agent. As hydration continues, cross-linking of the xanthan gum occurs due to interaction with the cross-linking agent, causing an increase in gel strength and a decrease in the rate of release of drug from the dosage form. This explanation is for discussion only, and is in no way intended to limit the scope of the present invention.
  • [0039]
    Xanthan gum, the preferred heteropolysaccharide, is produced by microorganisms, for instance, by fermentation with the organism xanthomonas compestris. Most preferred is xanthan gum which is a high molecular weight (>106) heteropolysaccharide. Xanthan gum contains D-glucose, D-mannose, D-glucuronate in the molar ratio of 2.8:2.0:20, and is partially acetylated with about 4.7% acetyl. Xanthan gum also includes about 3% pyruvate, which is attached to a single unit D-glucopyromosyl side chain as a metal. It dissolves in hot or cold water and the viscosity of aqueous solutions of xanthan gum is only slightly affected by changes in the pH of a solution between 1 and 11.
  • [0040]
    The term “heteropolysaccharide” as used in the present invention is defined as a water-soluble polysaccharide containing two or more kinds of sugar units, the heteropolysaccharide having a branched or helical configuration, and having excellent water-wicking properties and immense thickening properties. When admixed with an appropriate ionizable gel strength enhancing agent capable of enhancing the gel strength of the hydrophilic matrix upon exposure to an aqueous solution, e.g. gastric fluid, etc., the gum packs closely and many intermolecular attachments are formed which make the structure strong and provide a hydrophilic gum matrix having high gel strength. The ionizable gel strength enhancing agent is therefore an agent capable of enhancing the gel strength of a gel formed by exposure of the heteropolysaccharide to an aqueous environment, thus affecting the rate of release of the active medicament.
  • [0041]
    The galactomannans used in the present invention which are capable of cross-linking with the xanthan gum are polysaccharides which are composed solely-of mannose and galactose. Galactomannans which have higher proportions of unsubstituted mannose regions have been found to achieve more interaction with the heteropolysaccharide. Locust bean gum, which has a higher ratio of mannose to the galactose, is especially preferred as compared to other galactomannans such as guar and hydroxypropyl guar.
  • [0042]
    The cross-linking agent may be, e.g., a galactomannan such as locust bean gum or an ionizable gel strength enhancing agent. The ionizable gel strength enhancing agent may be monovalent, divalent or multivalent ionizable salts. Preferred salts are the inorganic salts, including various alkali metal and/or alkaline earth metal sulfates, chlorides, borates, bromides, etc. Ionizable alkaline earth organic salts such as citrates, acetates, lactates, etc. may also be used in accordance with the present invention. Specific examples of suitable ionizable gel strength enhancing agents include calcium sulfate, sodium chloride, potassium sulfate, sodium carbonate, lithium chloride, tripotassium phosphate, sodium borate, potassium bromide, potassium fluoride, sodium bicarbonate, calcium chloride, magnesium chloride, sodium citrate, sodium acetate, calcium lactate, magnesium sulfate, alkali metal chlorides, magnesium chloride, calcium chloride, organic acids such as citric, succinic, fumaric, malic, maleic, glutaric, lactic and the like, alkali metal sulfates such as sodium sulfate, alkali metal alkyl sulfates wherein the alkyl group is from 1 to 14 carbon atoms, such as sodium methyl sulfate, sodium lauryl sulfate and the like as well as dioctyl sodium sulfosuccinate, dihydrogen sodium phosphate, monohydrogen sodium phosphate, disodium hydrogen phosphate, sodium chloride, sodium fluoride and mixtures thereof. Multivalent metal cations may also be utilized.
  • [0043]
    However, the preferred ionizable gel strength enhancing agents are bivalent. Particularly preferred salts are calcium sulfate and sodium chloride.
  • [0044]
    It is to be understood that the ionizable compound may be a single compound or a mixture of two or more materials that provide the desired release characteristics. The ionizable gel strength enhancing agents of the present invention are added in an amount effective to obtain a desirable increased gel strength of a gel formed by exposure of the heteropolysaccharide to an aqueous environment.
  • [0045]
    In other embodiments of the invention, the ionizable gel enhancing agent may comprise a surfactant or wetting agent such as pharmaceutically acceptable anionic surfactants, cationic surfactants, amphoteric (amplipathic/amphophilic) surfactants, and non-ionic surfactants. Examples of suitable surfactant or wetting agents include alkali metal chlorides, magnesium chloride, calcium chloride, organic acids such as citric, succinic, fumaric, malic, maleic, glutaric, lactic and the like, alkali metal sulfates such as sodium sulfate, alkali metal alkyl sulfates wherein the alkyl group is from 1 to 14 carbon atoms, such as sodium methyl sulfate, sodium lauryl sulfate and the like as well as dioctyl sodium sulfosuccinate, dihydrogen sodium phosphate, monohydrogen sodium phosphate, disodium hydrogen phosphate, sodium chloride, sodium fluoride and mixtures thereof. It is to be understood that the ionizable compound may be a single compound or a mixture of two or more materials that provide the desired release characteristics. Other examples of suitable surfactants and/or suitable wetting agents are disclosed in U.S. Pat. No. 5,478,574, assigned to the assignee of the present invention.
  • [0046]
    The controlled release properties of the controlled release formulations of the present invention may be optimized when xanthan gum comprises from about 1 to 99% by weight of the sustained release carrier. In where the sustained release carrier comprises a crosslinking preferably comprises from about 1 to about 99% by weight of the sustained release carrier. In embodiments where the crosslinking agent is a galactomannan, e.g., locust bean gum, xanthan gum preferably comprises from about 5 to 95% by weight of the sustained release carrier. In other embodiments where the crosslinking agent is an ionizable gel strength enhancing agent, e.g., calcium sulfate, the ionizable gel strength enhancing agent comprises from about 1 to about 20% by weight of the sustained release carrier. Combinations of crosslinking agents, e.g., a galactomannan and an ionizable gel strength enhancing agents may also be included in the sustained release carrier. The skilled artisan will understand that the above ratios will vary according to, e.g., the type of crosslinking agent or combinations of crosslinking agents present in the formulation, so long as the desired dissolution parameters of the dosage form is maintained.
  • [0047]
    Other acceptable gelling agents may optionally be included in sustained release formulations of the present invention include those gelling agents well-known in the art. Examples include vegetable gums such as alginates, carrageenan, pectin, guar gum, xanthan gum, modified starch, hydroxypropylmethylcellulose, methylcellulose, and other cellulosic materials such-as sodium carboxymethylcellulose and hydroxypropyl cellulose. This list is not meant to be exclusive.
  • [0048]
    The formulations of the present invention also include an inert diluent. Any generally accepted soluble or insoluble inert diluent material can be used. Preferably, the inert diluent comprises a monosaccharide, a disaccharide, a polyhydric alcohol, a cellulose (such as microcrystalline cellulose), starches, and/or mixtures thereof. Examples of suitable inert pharmaceutical fillers include sucrose, dextrose, lactose, microcrystalline cellulose, xylitol, fructose, sorbitol, mixtures thereof and the like. However, it is preferred that a soluble pharmaceutical filler such as dextrose, sucrose, or mixtures thereof be used.
  • [0049]
    Examples of such pre-manufactured direct compression excipients include Emcocel® (microcrystalline cellulose, N.F.), Emdex® (dextrates, N.F.), and Tab-Fine® (a number of direct-compression sugars including sucrose, fructose, and dextrose), all of which are commercially available from Edward Mendell Co., Inc., Patterson, N.Y.). Other direct compression diluents include Anhydrous lactose (Lactose N.F. anhydrous direct tableting) from Sheffield Chemical, Union, N.J. 07083; Elcems® G-250 (Powdered cellulose, N.F.) from Degussa, D-600 Frankfurt (Main) Germany; Fast-Flo Lactose® (Lactose, N.F., spray dried) from Foremost Whey Products, Banaboo, Wis. 53913; Maltrin® (Agglomerated maltrodextrin) from Grain Processing Corp., Muscatine, Iowa 52761; Neosorb 60® (Sorbitol, N.F., direct-compression) from Roquette Corp., 645 5th Ave., New York, N.Y. 10022; Nu-Tab® (Compressible sugar, N.F.) from Ingredient Technology, Inc., Pennsauken, N.J. 08110; Poly-plasdone XL® (Crospovidone, N.F., cross-linked polyvinylpyrrolidone) from GAF Corp., New York, N.Y. 10020; Primojel® (Sodium starch glycolate, N.F., carboxymethyl starch) from Generichem Corp., Little Falls, N.J. 07424; Solka Floc® (Cellulose floc) from Edward Mendell Co., Carmel, N.Y. 10512; Spray-dried-lactose® (Lactose N.F., spray dried) from Foremost Whey Products, Baraboo, Wis. 53913 and DMV Corp., Vehgel, Holland; and Sta-Rx 1500® (Starch 1500) (Pregelatinized starch, N.F., compressible) from Colorcon, Inc., West Point, Pa. 19486. Pre-manufactured directed compression excipients may also comprise all or a portion of the inert diluent.
  • [0050]
    In further alternative embodiments of the invention, a therapeutically active agent-can be incorporated (admixed, granulated, etc.) with any of the ingredients of the sustained release excipient, if so desired. The remaining formulation steps would remain essentially the same as would be understood by one skilled in the art.
  • [0051]
    In further embodiments of the present invention, the inert diluent which is used in conjunction with the sustained release pharmaceutical excipient of the present invention is an augmented microcrystalline cellulose as disclosed in U.S. patent application Ser. No. 5,585,115 entitled “PHARMACEUTICAL EXCIPIENT HAVING IMPROVED COMPRESSIBILITY”, inventors B. Sherwood, J. Staniforth and E. Hunter, hereby: incorporated by reference.
  • [0052]
    In certain embodiments of the invention, the sustained release carrier also includes a hydrophobic material in an amount effective to slow the hydration of the gum without disrupting the hydrophilic matrix formed by the heteropolysaccharide when the formulation is exposed to fluids in an environment of use. This may be accomplished by granulating the sustained release carrier with a solution or dispersion of hydrophobic material prior to the incorporation of the medicament. The hydrophobic material may be selected from alkylcelluloses, acrylic and/or methacrylic acid polymers or copolymers, hydrogenated vegetable oils, zein, as well as other pharmaceutically acceptable hydrophobic materials known to those skilled in the art. A preferred hydrophobic cellulosic material is ethylcellulose. The amount of hydrophobic material incorporated into the sustained release matrix is that which is effective to slow the hydration of the gums without disrupting the hydrophilic matrix formed upon exposure to an environmental-fluid, e.g. a gastric fluid.
  • [0053]
    In certain embodiments of the present invention, the hydrophobic material may be included in the sustained release carrier in an amount from about 1% to about 20% by weight. More preferably, the hydrophobic material may be included in the sustained release matrix in an amount from about 3% to about 12%, and most preferably from about 5% to about 10%, by weight of the final formulation. The hydrophobic material may be dissolved in an organic solvent or dispersed in an aqueous solution for incorporation into the formulation.
  • [0054]
    The combination of the xanthan gum with the cross-linking agent and inert diluent provides a ready to use sustained release excipient in which a formulator need only blend the desired active medicament and an optional lubricant with the excipient and then make an oral solid dosage form. The sustained release excipient may thus comprise a physical admix of the xanthan gum with the cross-linking agent and inert diluent.
  • [0055]
    The sustained release pharmaceutical excipient prepared in accordance with the present invention is preferably wet granulated prior to addition of the medicament. In this technique, the desired amounts of the xanthan gum cross-linking agent, and inert diluent are mixed together and moistened with a wet granulating aid such as water, propylene glycol, glycerol, alcohol or the like is added to prepare a moistened mass. The moistened mass is dried, and then milled with, e.g., conventional equipment, into granules. The resultant sustained release excipient is ready to use. The sustained release excipient has certain advantages including it is free-flowing, good cohesive properties, and can be directly admixed with the insoluble NSAID, e.g., via wet granulation, formed into the desired dosage form such as a tablet. On the other hand, the granulate can be formulated into a capsule, used in the granulate form, extruded, and/or spheronized with an active medicament to form pellets, etc. In alternative preferred embodiments, the individual ingredients of the sustained release excipient may be wet granulated with all or part of the insoluble NSAID.
  • [0056]
    In a preferred embodiment of the invention, sustained release ibuprofen tablets are prepared by wet granulating together the requisite amounts of ibuprofen, crosslinking agent (e.g. locust bean gum) and inert diluent in the presence of a wet granulating aid, e.g. water or ethyl alcohol. The resultant mixture may then be dried, e.g. in a fluid bed dryer, and compressed into tablets.
  • [0057]
    Optionally, lubricants such as those described above may be mixed with the granulation prior to tableting. Other tableting or processing aids may be added as required.
  • [0058]
    The dosage forms of the present invention are preferably tablets. However, as noted above, the ingredients may also be formulated in a capsule, extruded and spheronized with an active medicament to form pellets, etc.
  • [0059]
    For example, the complete mixture, in an amount sufficient to make a uniform batch of tablets, is subjected to tableting in a conventional production scale tableting machine at normal compression pressure, i.e. about 2000-1600 lbs/sq in. However, the mixture should not be compressed to such a degree that there is subsequent difficulty in its hydration when exposed to gastric fluid. An effective amount of any generally accepted pharmaceutical lubricant, including the calcium or magnesium soaps may be added to the above-mentioned ingredients of the excipient be added at the time the medicament is added, or in any event prior to compression into a said dosage form. One preferred lubricant is Pruv, e.g., in the amount of about 3.0 percent of the solid dosage form.
  • [0060]
    The tablets may be optionally coated with an overcoat containing, e.g., hydroxypropylmethylcellulose, colorants and the like.
  • [0061]
    In preferred embodiments of the invention where the NSAID is ibuprofen and the crosslinking agent is locust bean gum, the weight ratio of ibuprofen to the combined weight of the gums, i.e. xanthan gum and locust bean gum, is from about 1:0.06 to about 1:0.4, and preferably from about 1:0.08 to about 1:0.25. The ibuprofen:gum ratio is indicative of the reduced amount of gum required compared to prior art sustained release ibuprofen formulations. The dosage forms of the present invention are economically advantageous in that less gum is required to produce a suitable dosage form, with the added advantages of smaller tablet size and once or twice daily dosing.
  • [0062]
    Variables which may affect the release rate and the compressibility of tablets prepared with the excipient of the present invention are the drug to gum ratio; the method of incorporation of excipient (method of granulation); the relative amount of the gum to ionizable gel strength enhancing agent; and the ratio of active medicament to the sustained release excipient.
  • [0063]
    An effective amount of a wetting agent may be included in the formulation in order to, increase the bioavailability of the ibuprofen. The wetting agent may be added, e.g., by spraying while mixing the granulate.
  • [0064]
    Suitable wetting agents for use in conjunction with the present invention include polyethyleneglycols as esters or ethers. Examples include polyethoxylated castor oil, polyethoxylated hydrogenated castor oil, polyethoxylated fatty acid from castor oil or polyethoxylated fatty acid from castor oil or polyethoxylated fatty acid from hydrogenated castor oil. Commercially available wetting agents which can be used are known under trade names Cremophor, Myrj, Polyoxyl 40 stearate, Emerest 2675, Lipal 395 and PEG 3350. An especially preferred wetting agent is polyethyleneglycol having a molecular weight of 3,350 (i.e., PEG 3350).
  • [0065]
    When included in the formulation, the wetting agent is dissolved in a suitable solvent such as water, and is thereafter added to the blended mixture of the sustained release excipient and the medicament. This allows the wetting agent to wet the particles of the excipient such that when the solvent evaporates the particles of the medicament which precipitate are tiny and do not aggregate. A granulate of the medicament and the wetting agent is obtained which is preferably finely and homogeneously dispersed in the excipient.
  • [0066]
    The wetting agent is preferably included in an amount effective to provide a final sustained release product having acceptable bioavailability. For example, in certain embodiments of the present invention wherein the medicament is ibuprofen, the wetting agent is included in an amount front about 5% to about 10% of the final product, by weight.
  • [0067]
    In certain embodiments of the embodiment a hydrophobic polymer such as those described hereinabove is added to the mixture of wetting agent and ibuprofen.
  • [0068]
    The hydrophobic material may be dissolved in an organic solvent or dispersed in an aqueous solution. Thereafter, the hydrophobic material may be used to coat the granulate of ibuprofen/wetting agent/sustained release excipient. The granulate may be coated with the hydrophobic coating to a weight gain of, e.g., from about 1 to about 20 percent, and preferably from about 5 to about 10 percent. The granulation is then preferably dried. Thereafter, the granulate may be further formulated into an appropriate, oral dosage form, for example, by compression of the resulting granulate into appropriately sized tablets, by filling gelatin capsules with an appropriate amount of the granulate (with or without compression of the granulate), as well as use in the manufacture of other oral dosage forms known to those skilled in the art. This embodiment may be particularly beneficial to control the amount of ibuprofen released during the initial phases of dissolution when the formulation is exposed to fluid in an environment of use, e.g., in-vitro dissolution or in the gastrointestinal tract.
  • [0069]
    In certain embodiments of the present invention, the tablet core includes a portion of the total dose of the insoluble NSAID or an additional dose of the insoluble NSAID in either the hydrophobic or enteric coating, or in an additional overcoating coated on the outer surface of the tablet core (without the hydrophobic or enteric coating) or as a second coating layer coated on the surface of the base coating comprising the hydrophobic or enteric coating material. This may be desired when, for example, a loading dose of ibuprofen is needed to provide therapeutically effective blood levels of the active agent when the formulation is first exposed to gastric fluid. The loading dose of medicament included in the coating layer may be, e.g., from about 10% to about 40% of the total amount of medicament included in the formulation. It is particularly preferred to include all or a portion of the total dose of the insoluble NSAID as a coating around the tablet core when the sustained release carrier comprises from about 40 to about 100% by weight xanthan gum, e.g. from about 45 to about 99% by weight. In such embodiments, it is preferable that the dosage form and/or the tablet core is coated with a sustained and/or release coating an enteric coating containing a hydrophobic polymer.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • [0070]
    The following examples illustrate various aspects of the present invention. They are not to be construed to limit the claims in any manner whatsoever.
  • EXAMPLES 1-3
  • [0071]
    In Examples 1-3, a sustained release excipient is prepared as set forth below:
    TABLE 1
    Preparation of a Sustained Release Excipient
    Component (%) Ex. 1 Ex. 2 Ex. 3
    Xanthan Gum 35  5 65
    Locust Bean Gum 35 65  5
    Dextrose 30 30 30
    Water*  28%  37%  21%
  • [0072]
    Processing Steps: 1.5 kg batch
  • [0073]
    1. Weigh out xanthan gum, locust bean gum and dextrose.
  • [0074]
    2. Charge high shear mixer/granulator with xanthan gum, locust bean gum and dextrose and dry blend for 3 minutes.
  • [0075]
    3. Add water and granulate until desirable granules are formed.
  • [0076]
    4. Dry granules in fluid bed dryer at 70° C. until LOD is less than 5%.
  • [0077]
    5. Pass granules through Fitzmill @3500 rpm, hammers forward.
  • EXAMPLES 4-9 Preparation of Tablets
  • [0078]
    The sustained release excipients prepared in Examples 4-6 are mixed with the drug (ibuprofen) and sustained release ibuprofen tablets are prepared as set forth below:
    TABLE 2
    Tablets of Examples 4-6
    Component (%) Ex. 4 Ex. 5 Ex. 6
    Sustained release excipient 280 280 280
    Ibuprofen 800 800 800
    Mg Stearate 10 10 10
  • [0079]
    Processing Steps: 1.5 kg batch
  • [0080]
    1. Screen drug through 25 mesh.
  • [0081]
    2. Weigh out sustained release excipient and drug.
  • [0082]
    3. Charge high shear mixer/granulator with sustained release excipient and drug and dry blend for 3 minutes.
  • [0083]
    4. Add water while mixing and granulate until desirable granules are formed.
  • [0084]
    5. Pass granules through Fitzmill @2500 rpm, blades forward.
  • [0085]
    6. Dry granules in fluid bed dryer at 55° C. until LOD is less than 3%.
  • [0086]
    7. Pass granules through 16 mesh screen on an oscillating granulator.
  • [0087]
    8. Using a V-Blender, blend granules and Magnesium Stearate for 5 minutes.
  • [0088]
    9. Compress into tablets using 0.3750×0.8300 in. capsule shaped punches to a hardness of about 15 kP.
  • [0089]
    The final composition of the tablets of Examples 4-6 are set forth in Tables 3-5 below:
    TABLE 3
    Tablet Composition of Example 4
    Component (%) mg/Tablet %
    Excipient (Ex. 1)  280  25.7
    (Xanthan Gum) (98) (9.0)
    (Locust Bean Gum) (98) (9.0)
    (Dextrose) (84) (7.7)
    Ibuprofen  800  73.3
    Mg Stearate  10  1
    Total 1090 100.0
  • [0090]
    [0090]
    TABLE 4
    Tablet Composition of Example 5
    Component (%) mg/Tablet %
    Excipient (Ex. 2)  280  25.7
    (Xanthan Gum) (14) (1.3)
    (Locust Bean Gum) (182) (16.7)
    (Dextrose) (84) (7.7)
    Ibuprofen  800  73.3
    Mg Stearate  10  1
    Total 1090 100.0
  • [0091]
    [0091]
    TABLE 5
    Tablet Composition of Example 6
    Component (%) mg/Tablet %
    Excipient (Ex. 3)  280  25.7
    (Xanthan Gum) (14) (16.7)
    (Locust Bean Gum) (182) (1.3)
    (Dextrose) (84) (7.7)
    Ibuprofen  800  73.3
    Mg Stearate  10  1
    Total 1090 100.0
  • EXAMPLES 7-9
  • [0092]
    Sustained release ibuprofen tablets are prepared in accordance using the excipients of Examples 1-3 using the process described in Examples 4-6 except that the total amount of excipient in the tablet was reduced from 280 mg to 140 mg. The composition of the tablets according to Examples 7-9 are set forth in Tables 6-8 below:
    TABLE 6
    Tablet Composition of Example 7
    Component (%) mg/Tablet %
    Sustained release excipient 140  14.7
    (Xanthan Gum) (49) (5.2)
    (Locust Bean Gum) (49) (5.2)
    (Dextrose) (42) (4.4)
    Ibuprofen 800  84.2
    Mg Stearate  10  1.1
    Total 950 100.0
  • [0093]
    [0093]
    TABLE 7
    Tablet Composition of Example 8
    Component (%) mg/Tablet %
    Sustained release excipient 140  14.7
    (Xanthan Gum) (7) (0.7)
    (Locust Bean Gum) (91) (9.6)
    (Dextrose) (42) (4.4)
    Ibuprofen 800  84.2
    Mg Stearate  10  1.1
    Total 950 100.0
  • [0094]
    [0094]
    TABLE 8
    Tablet Composition of Example 9
    Component (%) mg/Tablet %
    Sustained release excipient 140  14.7
    (Xanthan Gum) (91) (9.6)
    (Locust Bean Gum) (7) (0.7)
    (Dextrose) (42) (4.4)
    Ibuprofen 800  84.2
    Mg Stearate  10  1.1
    Total 950 100.0
  • EXAMPLES 10-11 - Dissolution Testing EXAMPLE 10
  • [0095]
    Tablets prepared in accordance with Examples 4-6 are tested with respect to in-vitro dissolution. The dissolution tests are conducted in an automated USP dissolution apparatus (Paddle Type 11), and the amount of drug released was analyzed via UV analysis. In Comparative Example A, Brufen Retard™, sustained release ibuprofen tablets commercially available from The Boots Company were also tested according to the same method. In Comparative Example B, the dissolution of Example 1 (a sustained release ibuprofen tablet) set forth in EP 234670 A2 is composed. Example 1 of EP 234670 is a sustained release ibuprofen tablet containing 800 mg ibuprofen, 196.9 mg xanthan gum (Keltrol F), 3.1 mg colloidal silicon dioxide (Aerosil 200) 25.9 mg polyvinylpyrollidone (Plasdone K29-32) and 10.4 mg stearic acid. The dissolution of Example 1 of EP 234670 A2 was undertaken in accordance with the general procedures set forth herein, and the dissolution results are taken from the results provided in that publication.
    TABLE 9
    Dissolution Method
    Dissolution Results Hours pH
    Type II 0 2.5
    900 ml 1 4.5
    100 rpm 2 4.5
    3 6.8
    4-24 6.8
  • [0096]
    [0096]
    TABLE 10
    Dissolution Results
    Time (Hr) Ex. 4 Ex. 5 Ex. 6 Ex. A Ex. B
    0 0 0 0 0 0
    1 2.4 4.1 2.3 1.3 0.2
    2 3.2 11.0 5.8 3.1 1.1
    3 4.4 12.4 7.7 5.9 2.5
    4 6.9 22.7 14.2 16.3 11.4
    6 10.4 26.7 17.5 29.9 23.3
    8 14 31.4 21.8 46.5 36.5
    12 23.8 47.3 37.3 62.8 69.3
    16 44.5 59.6 65.5 73.3 85.2
    18 61.2 63.3 77.2 79.8 91.5
    24 84.3 76.8 87.2 88.1
  • [0097]
    The dissolutions results are also graphically depicted in FIG. 1. The dissolution results indicate that the tablets of Examples 4-6 provide sustained release of the ibuprofen from the dosage form.
  • EXAMPLE 11
  • [0098]
    Dissolution tests are conducted on the tablets of Examples 7, 8 and 9 in accordance with the method described in Example 10 above. The results are set forth in Table 11 below:
    TABLE 11
    Dissolution Results
    Time (Hr) Ex. 7 Ex. 8 Ex. 9 Ex. A Ex. B
    0 0 0 0 0 0
    1 1.7 3.5 2.3 1.3 0.2
    2 3.6 10.2 8.1 3.1 1.1
    3 4.8 11.8 10.1 5.9 2.5
    4 11.0 22.0 26.0 16.3 11.4
    6 15.3 27.9 32.4 29.9 23.3
    8 19.1 34.4 41.4 46.5 36.5
    12 27.7 48.8 72.7 62.8 69.3
    16 46.6 58.5 98.3 73.3 85.2
    18 56.4 61.6 100.2 79.8 91.5
    24 67.4 70.0 100.9 88.1
  • [0099]
    The dissolution results are also graphically depicted in FIG. 2.
  • [0100]
    The results show that a suitable sustained release of ibuprofen is still obtained although the tablet formulations of Examples 7-9 contain 50% less sustained release excipient than Examples 4-6.
  • [0101]
    The Examples provided above are not meant to be exclusive. Many other variations of the present invention will be apparent to those skilled in the art, and are contemplated to be within the scope of the present invention.

Claims (28)

What is claimed is:
1. A sustained release dosage form, comprising from about 500 mg to about 1000 mg of an insoluble NSAID and an effective amount of a sustained release carrier, said dosage form releasing providing a dissolution or said NSAID in-vitro when measured by the USP Type II (Paddle) Method, of from about 6 percent by weight of said NSAID released after about 2 hours and a t50 after about 12 to about 16 hours.
2. The dosage form of claim 1, wherein said sustained release carrier comprises xanthan gum and a crosslinking agent.
3. The dosage form of claim 2, wherein said crosslinking agent is a galactomannan.
4. The dosage form of claim 3, wherein said galactomannan is locust bean gum.
5. The dosage form of claim 1, further comprising an inert diluent.
6. The dosage form of claim 1, wherein said NSAID is selected from the group consisting of ibuprofen, calcium fenoprofen, naproxen, etodolac, mefenamic acid, tolmetin, and mixtures thereof.
7. The dosage form of claim 1, wherein said NSAID is ibuprofen.
8. The dosage form of claim 1, which is in the form of a tablet.
9. The dosage form of claim 2, wherein said cross-linking agent comprises a galactomannan gum, an ionizible gel strength enhancing agent, or a combination thereof.
10. A sustained release dosage form, comprising from about 500 mg to about 1000 mg of an insoluble NSAID and an effective amount of a sustained release carrier, said dosage form releasing providing a dissolution of said NSAID in-vitro when measured by the USP Type II (Paddle) Method, of from about 20 percent by weight of said ibuprofen released after about 4 hours and a t50 after about 12 to about 16 hours.
11. The dosage form of claim 10, wherein said sustained release carrier comprises xanthan gum and a crosslinking agent.
12. The dosage form of claim 11, wherein said crosslinking agent is a galactomannan.
13. The dosage form of claim 12, wherein said galactomannan is locust bean gum.
14. The dosage form of claim 11, further comprising an inert diluent.
15. The dosage form of claim 10, wherein the said NSAID is selected from the group consisting of ibuprofen, calcium fenoprofen, naproxen, etodolac, mefenamic acid, tolmetin, and mixtures thereof.
16. The dosage form of claim 10, wherein the said NSAID is ibuprofen.
17. The dosage form of claim 12, wherein said cross-linking agent comprises a galactomannan gum, an ionizible gel strength enhancing agent, or a combination thereof.
18. A sustained release ibuprofen dosage form comprising about 500 mg to about 1000 mg ibuprofen; a sustained release coating comprising a hydrophobic material; and a tablet core comprising xanthan gum; wherein from about 1 to about 20 percent by weight of said ibuprofen is coated on said tablet, said dosage form releasing providing a dissolution of said NSAID in-vitro when measured by the USP Type II (Paddle) Method, of from about 6 percent by weight of said NSAID released after about 2 hours and a t50 after about 12 to about 16 hours.
19. An oral sustained release dosage form, comprising
a matrix comprising from about 500 to about 1000 mg of ibuprofen and a sustained release carrier comprising about 5 to about 95% xanthan gum and a crosslinking agent comprising locust bean gum; wherein the weight ratio of said ibuprofen to the combined weight of said xanthan gum and said locust bean gum is from about 1:0.06 to about 1:0.4.
20. The oral sustained release dosage form of claim 19, comprising wherein the weight ratio of said NSAID to the combined weight of said xanthan gum and said locust bean gum is from about 0.08 to about 0.25.
21. The oral sustained release tablet of claim 19 composing from about 800 to about 1000 mg ibuprofen.
22. A method of preparing an oral sustained release dosage form comprising the steps of
wet granulating a mixture of xanthan gum, locust bean gum, an inert diluent and an insoluble ibuprofen in a ratio of xanthan gum to locust bean gum is from about 1:20 to about 20:1 and in a ratio of the total weight of ibuprofen to the combined weight of said xanthan gum and said locust bean gum is from about 1:0.06 to about 1:0.4; and
tableting the resulting granulate into tablets containing from about 500 to about 1000 mg of ibuprofen.
23. A sustained release pharmaceutical excipient for use in oral solid dosage forms, comprising xanthan gum, a galactomannan capable of cross-linking said xanthan gum in the presence of aqueous solutions, and from about 20 to about 35 percent by weight of an inert diluent.
24. A sustained release tablet comprising
from about 500 mg to about 1000 mg of an insoluble NSAID in a sustained release matrix comprising xanthan gum and locust bean gum, wherein the total weight of said tablet is from about 110 percent to about 140 percent by weight of said insoluble NSAID, said xanthan gum and said locust bean gum comprising from about 7 to about 40 percent by weight of the tablet.
25. The sustained release tablet of claim 24, wherein said NSAID is ibuprofen and the combined weight of said xanthan gum and said locust bean gum is from about 119 percent to about 136 percent of ibuprofen.
26. A method of retarding the release of ibuprofen from a sustained release ibuprofen tablet containing xanthan gum when the tablet is exposed to an aqueous environment comprising replacing from about 5 to about 95 percent by weight of the xanthan gum in the sustained release ibuprofen tablet with a weight equivalent amount of locust bean gum, wherein the ratio of said xanthan gum to said locust bean gum ranges from about 1:20 to about 20:1.
27. A sustained release ibuprofen tablet comprising
from about 600 to about 1000 mg ibuprofen;
xanthan gum;
locust bean gum; and
an inert diluent;
wherein the combined weight of said xanthan gum and said locust bean gum is from about 7 to about 40 percent by weight of the final tablet weight and the ratio of ibuprofen to the combined weight of said xanthan gum and said locust bean gum is from about 1:0.06 to about 1:0.4.
28. A sustained release ibuprofen tablet of claim 27 wherein the ratio of ibuprofen to the combined weight of said xanthan gum and said locust bean gum is from about 1:0.08 to about 1:0.25.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030046834A1 (en) * 2001-09-12 2003-03-13 Jitsumi Hanafusa Self-propelled snowplow vehicle
US20070077297A1 (en) * 2004-09-30 2007-04-05 Scolr Pharma, Inc. Modified release ibuprofen dosage form
US20080131507A1 (en) * 2006-12-04 2008-06-05 Michael Hite Method of forming a tablet
US9452135B2 (en) 2012-03-20 2016-09-27 Particle Dynamics International, Llc Gelling agent-based dosage form

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6726930B1 (en) 1993-09-09 2004-04-27 Penwest Pharmaceuticals Co. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5773025A (en) 1993-09-09 1998-06-30 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems--amorphous drugs
US5912268A (en) * 1995-05-22 1999-06-15 Alza Corporation Dosage form and method for treating incontinence
US6262115B1 (en) * 1995-05-22 2001-07-17 Alza Coporation Method for the management of incontinence
ES2322405T3 (en) * 1996-07-08 2009-06-19 Penwest Pharmaceuticals Co. Matrix controlled to high doses insoluble drugs release.
WO1999009988A1 (en) * 1997-08-27 1999-03-04 Hexal Ag New pharmaceutical compositions of meloxicam with improved solubility and bioavailability
US6056977A (en) 1997-10-15 2000-05-02 Edward Mendell Co., Inc. Once-a-day controlled release sulfonylurea formulation
JP4545927B2 (en) * 1998-04-07 2010-09-15 アルコン ラボラトリーズ, インコーポレイテッド Gelling ophthalmic compositions containing xanthan gum
JP2002525311A (en) * 1998-10-01 2002-08-13 エラン ファーマ インターナショナル,リミティド Controlled release nanoparticle composition
US8293277B2 (en) * 1998-10-01 2012-10-23 Alkermes Pharma Ireland Limited Controlled-release nanoparticulate compositions
US8236352B2 (en) * 1998-10-01 2012-08-07 Alkermes Pharma Ireland Limited Glipizide compositions
US6419960B1 (en) * 1998-12-17 2002-07-16 Euro-Celtique S.A. Controlled release formulations having rapid onset and rapid decline of effective plasma drug concentrations
US7083808B2 (en) * 1998-12-17 2006-08-01 Euro-Celtique S.A. Controlled/modified release oral methylphenidate formulations
US6673367B1 (en) 1998-12-17 2004-01-06 Euro-Celtique, S.A. Controlled/modified release oral methylphenidate formulations
EP1135106B1 (en) * 1999-09-30 2008-04-09 Penwest Pharmaceuticals Co. Sustained release matrix systems for highly soluble drugs
US20050037073A1 (en) * 2000-01-13 2005-02-17 Alpharx Inc. Solid self-emulsifying dosage form for improved delivery of poorly soluble hydrophobic compounds and the process for preparation thereof
US20040013613A1 (en) * 2001-05-18 2004-01-22 Jain Rajeev A Rapidly disintegrating solid oral dosage form
US7198795B2 (en) * 2000-09-21 2007-04-03 Elan Pharma International Ltd. In vitro methods for evaluating the in vivo effectiveness of dosage forms of microparticulate of nanoparticulate active agent compositions
CA2440641A1 (en) * 2001-03-13 2002-09-19 Anand R. Baichwal Chronotherapeutic dosage forms containing glucocorticosteroid
US8329216B2 (en) * 2001-07-06 2012-12-11 Endo Pharmaceuticals Inc. Oxymorphone controlled release formulations
EP1406630A1 (en) * 2001-07-06 2004-04-14 Endo Pharmaceuticals Inc. Parenteral administration of 6-hydroxy-oxymorphone for use as an analgesic
DE60223254D1 (en) * 2001-07-06 2007-12-13 Penwest Pharmaceuticals Co The sustained release formulations of oxymorphone
JP2005523876A (en) * 2001-09-26 2005-08-11 ペンウェスト ファーマシューティカルズ カンパニー Opioid formulations potential for abuse is reduced
DK1439829T3 (en) * 2001-10-24 2005-10-10 Gruenenthal Gmbh Medicament containing 3- (3-dimethylamino-1-ethyl-2-methyl-propyl) phenol with delayed release of the active substance
CA2409552A1 (en) * 2001-10-25 2003-04-25 Depomed, Inc. Gastric retentive oral dosage form with restricted drug release in the lower gastrointestinal tract
US20030104052A1 (en) * 2001-10-25 2003-06-05 Bret Berner Gastric retentive oral dosage form with restricted drug release in the lower gastrointestinal tract
US20030091630A1 (en) * 2001-10-25 2003-05-15 Jenny Louie-Helm Formulation of an erodible, gastric retentive oral dosage form using in vitro disintegration test data
US20030152622A1 (en) * 2001-10-25 2003-08-14 Jenny Louie-Helm Formulation of an erodible, gastric retentive oral diuretic
US7459283B2 (en) * 2002-02-04 2008-12-02 Elan Pharma International Limited Nanoparticulate compositions having lysozyme as a surface stabilizer
US20040101566A1 (en) * 2002-02-04 2004-05-27 Elan Pharma International Limited Novel benzoyl peroxide compositions
DE60309300D1 (en) * 2002-03-20 2006-12-07 Elan Pharma Int Ltd Nanoparticle compositions of angiogenesis inhibitors
WO2003086353A1 (en) * 2002-04-05 2003-10-23 Penwest Pharmaceuticals Co. Sustained release metoprolol formulations
US7776314B2 (en) 2002-06-17 2010-08-17 Grunenthal Gmbh Abuse-proofed dosage system
US20030232097A1 (en) * 2002-06-17 2003-12-18 Strides Inc. Oily wax matrix suspension formulation comprising ibuprofen free acid and potassium salt of ibuprofen
JP4776229B2 (en) * 2002-07-16 2011-09-21 エラン ファーマ インターナショナル,リミティド Liquid dosage compositions of stable nanoparticulate active agent
EP1549296A4 (en) * 2002-08-02 2006-08-09 Penwest Pharmaceuticals Co Sustained release formulations of metformin
KR20060002922A (en) * 2003-03-31 2006-01-09 알자 코포레이션 Non-aqueous single phase vehicles and formulations utilizing such vehicles
US20050042289A1 (en) * 2003-04-29 2005-02-24 Yamanouchi Pharma Technologies, Inc. Tablets and methods for modified release of hydrophylic and other active agents
US20070048228A1 (en) 2003-08-06 2007-03-01 Elisabeth Arkenau-Maric Abuse-proofed dosage form
JP2007505921A (en) * 2003-09-19 2007-03-15 ペンウェスト ファーマシューティカルズ カンパニー Delayed release dosage form
US20050118267A1 (en) * 2003-09-19 2005-06-02 Penwest Pharmaceuticals Co. Chronotherapeutic dosage forms
CA2542755A1 (en) * 2003-10-17 2005-04-28 Medrx Co., Ltd. Biguanide drug-containing jelly preparation
JP2009500317A (en) * 2005-06-29 2009-01-08 パナセア バイオテック リミテッド Modified release pharmaceutical compositions and methods of manufacturing
WO2007069874A1 (en) * 2005-12-16 2007-06-21 Hanmi Pharm. Co., Ltd. Solid dispersion comprising an active ingredient having a low melting point and tablet for oral administration comprising same
US20070212414A1 (en) * 2006-03-08 2007-09-13 Penwest Pharmaceuticals Co. Ethanol-resistant sustained release formulations
GB0708375D0 (en) * 2006-05-19 2007-06-06 Norbrook Lab Ltd Stable aqueous suspension
US9023381B2 (en) * 2007-01-26 2015-05-05 Michelle Chow Enhanced medicinal delivery system processes and products thereby especially useful for children
US20090124650A1 (en) * 2007-06-21 2009-05-14 Endo Pharmaceuticals, Inc. Method of Treating Pain Utilizing Controlled Release Oxymorphone Pharmaceutical Compositions and Instructions on Effects of Alcohol
WO2009092601A1 (en) 2008-01-25 2009-07-30 Grünenthal GmbH Pharmaceutical dosage form
CN102316864B (en) * 2009-01-22 2015-04-01 雅培医疗保健私人有限公司 Chronotherapeutic pharmaceutical composition
RU2607499C2 (en) 2010-09-02 2017-01-10 Грюненталь Гмбх Destruction-resistant dosage form containing anionic polymer
US20130225697A1 (en) 2012-02-28 2013-08-29 Grunenthal Gmbh Tamper-resistant dosage form comprising pharmacologically active compound and anionic polymer
CA2913209A1 (en) 2013-05-29 2014-12-04 Grunenthal Gmbh Tamper resistant dosage form with bimodal release profile
CA2949422A1 (en) * 2014-05-26 2015-12-03 Grunenthal Gmbh Multiparticles safeguarded against ethanolic dose-dumping
CA2983642A1 (en) 2015-04-24 2016-10-27 Grunenthal Gmbh Tamper-resistant dosage form with immediate release and resistance against solvent extraction

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5096714A (en) * 1988-06-28 1992-03-17 Hauser-Kuhrts, Inc. Prolonged release drug tablet formulations
US5330761A (en) * 1993-01-29 1994-07-19 Edward Mendell Co. Inc. Bioadhesive tablet for non-systemic use products
US5455046A (en) * 1993-09-09 1995-10-03 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5662933A (en) * 1993-09-09 1997-09-02 Edward Mendell Co., Inc. Controlled release formulation (albuterol)
US5773025A (en) * 1993-09-09 1998-06-30 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems--amorphous drugs
US6056977A (en) * 1997-10-15 2000-05-02 Edward Mendell Co., Inc. Once-a-day controlled release sulfonylurea formulation
US6093420A (en) * 1996-07-08 2000-07-25 Edward Mendell Co., Inc. Sustained release matrix for high-dose insoluble drugs

Family Cites Families (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1670827C3 (en) * 1967-03-20 1974-10-24 Bayer Ag, 5090 Leverkusen
US3784684A (en) * 1971-08-24 1974-01-08 Bayer Ag Coronary dilator in a pharmaceutical dosage unit form
DE2714065A1 (en) * 1977-03-30 1978-10-12 Boehringer Mannheim Gmbh Instillationszubereitung
GB1579818A (en) * 1977-06-07 1980-11-26 Yamanouchi Pharma Co Ltd Nifedipine-containing solid preparation composition
CA1146866A (en) * 1979-07-05 1983-05-24 Yamanouchi Pharmaceutical Co. Ltd. Process for the production of sustained release pharmaceutical composition of solid medical material
DE3033919A1 (en) * 1980-09-09 1982-04-22 Bayer Ag Solid pharmaceutical preparations containing Nifedipin and methods for their preparation
US5264446A (en) * 1980-09-09 1993-11-23 Bayer Aktiengesellschaft Solid medicament formulations containing nifedipine, and processes for their preparation
US4346709A (en) * 1980-11-10 1982-08-31 Alza Corporation Drug delivery devices comprising erodible polymer and erosion rate modifier
JPH0122245B2 (en) * 1981-09-14 1989-04-25 Kanebo Ltd
JPH0220611B2 (en) * 1982-12-02 1990-05-10 Takada Seiyaku Kk
US4765989A (en) * 1983-05-11 1988-08-23 Alza Corporation Osmotic device for administering certain drugs
DE3318649A1 (en) * 1983-05-21 1984-11-22 Bayer Ag Biphasic formulation
DE3320582A1 (en) * 1983-06-08 1984-12-13 Thomae Gmbh Dr K Gliquidonhaltige preparation form and methods for their production
US4851229A (en) * 1983-12-01 1989-07-25 Alza Corporation Composition comprising a therapeutic agent and a modulating agent
JPS60139688A (en) * 1983-12-28 1985-07-24 Tokyo Tanabe Co Ltd Amorphous dihydropyridine powder pharmaceutical
DE3400106A1 (en) * 1984-01-04 1985-07-11 Bremecker Klaus Dieter Dr Pharmaceutical compositions with controlled release of medicinal substance
WO1985004100A1 (en) * 1984-03-21 1985-09-26 American Home Products Corporation Sustained release pharmaceutical capsules
NL194389C (en) * 1984-06-14 2002-03-04 Novartis Ag A process for the preparation of a solid dispersion of a pharmaceutically active agent which has a low solubility in water, in a solid matrix of a water-soluble polyalkylene glycol as a carrier.
DE3438830C2 (en) * 1984-10-23 1991-04-11 Dr. Rentschler Arzneimittel Gmbh & Co, 7958 Laupheim, De
DE3586713D1 (en) * 1984-11-15 1992-11-05 Hercon Lab Device for the controlled release of active pharmaceutical ingredients.
GB8514665D0 (en) * 1985-06-11 1985-07-10 Eroceltique Sa Oral pharmaceutical composition
ES2040209T3 (en) * 1985-10-15 1993-10-16 Eurand Italia S.P.A. Process for preparing solid formulations nifedipine high availability biological and sustained effect, and the formulations obtained.
GB8601204D0 (en) * 1986-01-18 1986-02-19 Boots Co Plc Therapeutic agents
ES2060593T3 (en) * 1986-02-03 1994-12-01 Elan Corp Plc Drug delivery system.
ES2031929T3 (en) * 1986-04-11 1993-01-01 Aktiebolaget Hassle Procedure for obtaining a solid preparation with extended release.
GB8608818D0 (en) * 1986-04-11 1986-05-14 Reckitt & Colmann Prod Ltd Pharmaceutical compositions
US4803076A (en) * 1986-09-04 1989-02-07 Pfizer Inc. Controlled release device for an active substance
DE3636123C2 (en) * 1986-10-23 1989-06-01 Dr. Rentschler Arzneimittel Gmbh & Co, 7958 Laupheim, De
ES2040697T3 (en) * 1986-12-18 1993-11-01 Kurt H. Prof. Dr. Bauer Nifedipine concentrate stabilized against the influence of light, and process for their preparation.
US5015479A (en) * 1987-02-02 1991-05-14 Seamus Mulligan Sustained release capsule or tablet formulation comprising a pharmaceutically acceptable dihydropyridine
GB8705083D0 (en) * 1987-03-04 1987-04-08 Euro Celtique Sa Spheroids
US5288500A (en) * 1987-03-13 1994-02-22 Benzon Pharma A/S Oral composition containing particles comprising an active substance
DE3862337D1 (en) * 1987-04-13 1991-05-16 Ono Pharmaceutical Co Pharmaceutical preparations which contain esters or amides as active ingredients.
US4808413B1 (en) * 1987-04-28 1991-09-10 Squibb & Sons Inc
US4792448A (en) * 1987-06-11 1988-12-20 Pfizer Inc. Generic zero order controlled drug delivery system
DE3720757A1 (en) * 1987-06-24 1989-01-05 Bayer Ag Dhp-coat tablet
FR2618073B1 (en) * 1987-07-16 1990-09-07 Pf Medicament type tablets hydrophilic matrix base of salbutamol and their method of preparing
US4792452A (en) * 1987-07-28 1988-12-20 E. R. Squibb & Sons, Inc. Controlled release formulation
GB8722306D0 (en) * 1987-09-22 1987-10-28 Aps Research Ltd Sustained-release formulation
DE3877492T2 (en) * 1987-10-08 1993-05-13 Haessle Ab A pharmaceutical preparation with delayed release of a dihydropyridine and a beta-adrenergic receptor antagonists and methods of manufacture thereof.
GB8723896D0 (en) * 1987-10-12 1987-11-18 Aps Research Ltd Controlled-release formulation
US5160734A (en) * 1987-11-25 1992-11-03 American Cyanamid Company Sustained release delivery system for substituted dihydropyridine calcium channel blockers
JP2670680B2 (en) * 1988-02-24 1997-10-29 株式会社ビーエムジー Physiologically active substance-containing polylactic acid microspheres and their preparation
JP2668730B2 (en) * 1988-03-09 1997-10-27 雪印乳業株式会社 Sustained-release formulation using natural polymer
US5211957A (en) * 1988-03-25 1993-05-18 Ciba-Geigy Corporation Solid rapidly disintegrating dosage form
US5019397A (en) * 1988-04-21 1991-05-28 Alza Corporation Aqueous emulsion for pharmaceutical dosage form
JP2528706B2 (en) * 1988-05-30 1996-08-28 ゼリア新薬工業株式会社 Pharmaceutical compositions of the dihydropyridine compounds
US5128143A (en) * 1988-09-19 1992-07-07 Edward Mendell Co., Inc. Sustained release excipient and tablet formulation
US5169639A (en) * 1988-09-19 1992-12-08 Edward Mendell Co., Inc. Controlled release verapamil tablets
US4994276A (en) * 1988-09-19 1991-02-19 Edward Mendell Co., Inc. Directly compressible sustained release excipient
US5135757A (en) * 1988-09-19 1992-08-04 Edward Mendell Co., Inc. Compressible sustained release solid dosage forms
GB8903328D0 (en) * 1989-02-14 1989-04-05 Ethical Pharma Ltd Nifedipine-containing pharmaceutical compositions and process for the preparation thereof
DE59008160D1 (en) * 1989-03-14 1995-02-16 Egyt Gyogyszervegyeszeti Gyar Solid pharmaceutical preparations and methods for their preparation.
US5007790A (en) * 1989-04-11 1991-04-16 Depomed Systems, Inc. Sustained-release oral drug dosage form
US5133974A (en) * 1989-05-05 1992-07-28 Kv Pharmaceutical Company Extended release pharmaceutical formulations
US5091190A (en) * 1989-09-05 1992-02-25 Alza Corporation Delivery system for administration blood-glucose lowering drug
US5024843A (en) * 1989-09-05 1991-06-18 Alza Corporation Oral hypoglycemic glipizide granulation
EP0438249B1 (en) 1990-01-15 1995-08-09 Elan Corporation, Plc Controlled absorption naproxen formulation for once-daily administration
EP0468392A1 (en) * 1990-07-27 1992-01-29 Jagotec Ag Process for preparing pharmaceutical compositions having an increased active substance dissolution rate, and the compositions obtained
GB9022788D0 (en) * 1990-10-19 1990-12-05 Cortecs Ltd Pharmaceutical formulations
US5215758A (en) * 1991-09-11 1993-06-01 Euroceltique, S.A. Controlled release matrix suppository for pharmaceuticals
US5169638A (en) * 1991-10-23 1992-12-08 E. R. Squibb & Sons, Inc. Buoyant controlled release powder formulation
US5273760A (en) * 1991-12-24 1993-12-28 Euroceltigue, S.A. Stabilized controlled release substrate having a coating derived from an aqueous dispersion of hydrophobic polymer
GB9200607D0 (en) * 1992-01-13 1992-03-11 Ethical Pharma Ltd Pharmaceutical compositions containing nifedipine and process for the preparation thereof
US5286493A (en) * 1992-01-27 1994-02-15 Euroceltique, S.A. Stabilized controlled release formulations having acrylic polymer coating
CA2086989A1 (en) * 1992-02-17 1993-08-18 Sabine Compassi Dosage forms having prolonged active ingredient release
US5292534A (en) 1992-03-25 1994-03-08 Valentine Enterprises, Inc. Sustained release composition and method utilizing xanthan gum and an active ingredient
US5518730A (en) * 1992-06-03 1996-05-21 Fuisz Technologies Ltd. Biodegradable controlled release flash flow melt-spun delivery system
US5264459A (en) * 1992-07-13 1993-11-23 Arch Development Corporation Use of β-adrenergic agonists to treat patients with demyelinating or autoimmune diseases
US5472711A (en) * 1992-07-30 1995-12-05 Edward Mendell Co., Inc. Agglomerated hydrophilic complexes with multi-phasic release characteristics
EP0582169A3 (en) * 1992-08-05 1995-09-27 Bayer Italia Spa Pharmaceutical preparations for the oral administration of dihydropyridines in beverage form
US5324351A (en) * 1992-08-13 1994-06-28 Euroceltique Aqueous dispersions of zein and preparation thereof
BE1006990A5 (en) * 1993-04-22 1995-02-07 Univ Gent METHOD AND COMPOSITION TO MAKE AN ACTIVE INGREDIENT IN A solid dosage form.
US5543099A (en) * 1994-09-29 1996-08-06 Hallmark Pharmaceutical, Inc. Process to manufacture micronized nifedipine granules for sustained release medicaments
CA2205442C (en) * 1994-12-01 2003-01-21 David R. Friend Nsaid delivery employing a powdered hydrocolloid gum obtainable from higher plants
US5845563A (en) * 1997-01-10 1998-12-08 Sunbeam Products, Inc. Rotisserie cooker

Patent Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5096714A (en) * 1988-06-28 1992-03-17 Hauser-Kuhrts, Inc. Prolonged release drug tablet formulations
US5330761A (en) * 1993-01-29 1994-07-19 Edward Mendell Co. Inc. Bioadhesive tablet for non-systemic use products
US5958456A (en) * 1993-09-09 1999-09-28 Edward Mendell Co., Inc. Controlled release formulation (albuterol)
US5512297A (en) * 1993-09-09 1996-04-30 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5554387A (en) * 1993-09-09 1996-09-10 Edward Mendell Co., Ltd. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5662933A (en) * 1993-09-09 1997-09-02 Edward Mendell Co., Inc. Controlled release formulation (albuterol)
US5667801A (en) * 1993-09-09 1997-09-16 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5773025A (en) * 1993-09-09 1998-06-30 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems--amorphous drugs
US5846563A (en) * 1993-09-09 1998-12-08 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5455046A (en) * 1993-09-09 1995-10-03 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US6048548A (en) * 1993-09-09 2000-04-11 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems-amorphous drugs
US20010046516A1 (en) * 1993-09-09 2001-11-29 Anand Baichwal Sustained release heterodisperse hydrogel systems-amorphous drugs
US6245356B1 (en) * 1993-09-09 2001-06-12 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems-amorphous drugs
US6136343A (en) * 1993-09-09 2000-10-24 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US6093420A (en) * 1996-07-08 2000-07-25 Edward Mendell Co., Inc. Sustained release matrix for high-dose insoluble drugs
US6056977A (en) * 1997-10-15 2000-05-02 Edward Mendell Co., Inc. Once-a-day controlled release sulfonylurea formulation
US6537578B1 (en) * 1997-10-15 2003-03-25 Penwest Pharmaceuticals Co. Once-a-day controlled release sulfonylurea formulation
US20030219481A1 (en) * 1997-10-15 2003-11-27 Dileep Bhagwat Novel once-a-day controlled release sulfonylurea formulation

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030046834A1 (en) * 2001-09-12 2003-03-13 Jitsumi Hanafusa Self-propelled snowplow vehicle
US20070077297A1 (en) * 2004-09-30 2007-04-05 Scolr Pharma, Inc. Modified release ibuprofen dosage form
US20100143466A1 (en) * 2004-09-30 2010-06-10 Scolr Pharma, Inc. Modified release ibuprofen dosage form
US9028869B2 (en) 2004-09-30 2015-05-12 Shasun Pharmaceuticals Limited Modified release ibuprofen dosage form
US9730895B2 (en) 2004-09-30 2017-08-15 Shasun Pharmaceuticals Limited Method for providing modified release of ibuprofen
US20080131507A1 (en) * 2006-12-04 2008-06-05 Michael Hite Method of forming a tablet
US7749537B2 (en) 2006-12-04 2010-07-06 Scolr Pharma, Inc. Method of forming a tablet
US9452135B2 (en) 2012-03-20 2016-09-27 Particle Dynamics International, Llc Gelling agent-based dosage form

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