Acetaminophen pharmaceutical compositions

• US 20080057122A1
• Filed: 08/31/2006
• Published: 03/06/2008
• Est. Priority Date: 08/31/2006
• Status: Abandoned Application

• Current Assignee: American Capital Limited
• Original Assignee: aaiPharma, Inc.
• Inventors: Toney-Parker, Tania E., James, Jack Lawrence
• Application Number:
  US11/513,906
• Publication Number:
  US 20080057122A1
• Time in Patent Office: Days
• US Class Current: 424/468
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 31/165 having aromatic rings, e.g. colchicine, atenolol, progabide
• CPC Class Codes: A61K 45/06 Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• CPC Class Codes: A61K 9/2077 Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
• CPC Class Codes: A61K 9/5084 Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs tablets containing such a mixture A61K9/2077
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Abstract

Modified release dosage forms for daily oral dosing to a human patient for providing relief from pain are provided. The modified release dosage form comprises an immediate release component and a sustained release component, wherein the immediate release component and the sustained release component collectively contain a therapeutically effective amount of acetaminophen and an optional therapeutically effective amount of active pharmaceutical ingredient such as an opioid or opioid-like analgesic. In one embodiment, the opioid or opioid-like analgesic is propoxyphene napsylate or propoxyphene HCl salt.

Claims

1. A pharmaceutical formulation comprising an immediate release component and an extended release component wherein, when said formulation is administered to a subject, said formulation provides eight-hour bioequivalence of APAP compared to two consecutive administrations of one-half equivalent dose concentrations of APAP at a four-hour interval.

2. A pharmaceutical formulation according to claim 1, wherein APAP is present in said pharmaceutical formation at a dosage strength ranging from about 325 to about 1300 mg in one or more unit dosage forms.

3. A pharmaceutical formulation according to claim 1, wherein APAP is present in the formulation at a dosage strength comprising 325, 500, or 650 mg.

4. A pharmaceutical formulation according to claim 1, wherein at least one active pharmaceutical ingredient is added to at least one of said immediate release component or said extended release component or both.

5. A pharmaceutical formulation according to claim 4, wherein the at least one active pharmaceutical ingredient is selected from the group consisting of an opioid or opioid-like compound, a non-steroidal anti-inflammatory drug (NSAID), a cyclooxygenase-II (COX-2) inhibitor, a glycine receptor antagonist, an antitussive, an expectorant, a decongestant, an antihistamine and mixtures thereof.

6. A pharmaceutical formulation according to claim 5, wherein said active pharmaceutical ingredient is an opioid or opioid-like compound.

7. A pharmaceutical formulation according to claim 6, wherein said opioid or opioid-like compound is selected from the group consisting of alfentanil, allylprodine, alphaprodine, anileridine, benzylmorphine, bezitramide, buprenorphine, butorphanol, clonitazene, codeine, desomorphine, dextromoramide, dezocine, diampromide, diamorphone, dihydrocodeine, dihydromorphine, dimenoxadol, dimepheptanol, dimethylthiambutene, dioxaphetyl butyrate, dipipanone, eptazocine, ethoheptazine, ethylmethylthiambutene, ethylmorphine, etonitazene, fentanyl, heroin, hydrocodone, hydromorphone, hydroxypethidine, isomethadone, ketobemidone, levorphanol, levophenacylmorphan, lofentanil, meperidine, meptazinol, metazocine, methadone, metopon, morphine, myrophine, narceine, nicomorphine, norlevorphanol, normethadone, nalorphine, nalbuphene, normorphine, norpipanone, opium, oxycodone, oxymorphone, papaveretum, pentazocine, phenadoxone, phenomorphan, phenazocine, phenoperidine, piminodine, piritramide, propheptazine, promedol, properidine, propoxyphene, sufentanil, tilidine, tramadol, and salts of any of the foregoing.

8. A pharmaceutical formulation according to claim 7, wherein said opioid or opioid-like compounds is selected from the group consisting of hydrocodone, morphine, hydromorphone, oxycodone, codeine, levorphanol, meperidine, methadone, or salts thereof, and mixtures thereof.

9. A pharmaceutical formulation according to claim 8, wherein said active pharmaceutical ingredient is a propoxyphene salt.

10. A pharmaceutical formulation according to claim 9, wherein the propoxyphene salt is selected from the group consisting of propoxyphene napsylate and propoxyphene hydrochloride.

11. A pharmaceutical formulation according to claim 9, wherein the propoxyphene salt is present in the immediate release and extended release components as a weight ratio comprising 50%IR:

50%ER, 45%IR;

55% ER, or 40%IR;

60%ER.

20. A pharmaceutical formulation according to claim 1, wherein the immediate release component comprises APAP, at least one disintegrant, and, optionally, one or more binders.

24. A pharmaceutical formulation according to claim 1, wherein the extended release component at least one controlled release matrix polymer, and, optionally, one or more APIs.

93. A method of treating pain in a subject in need of such treatment comprising administering a pharmaceutically effective amount of a pharmaceutical formulation of claim 1.

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52. A pharmaceutical formulation in unit dosage form comprising per dosage unit an amount of APAP within a range from about 325 to about 1300 mg of a composition comprising an immediate release component and an extended release component wherein, when said formulation is administered to a subject, said formulation provides eight-hour bioequivalence of APAP compared to two consecutive administrations of one-half equivalent dose concentrations of APAP at a four-hour interval, and wherein said formulation in unit dosage form being adapted for oral administration.

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55. A pharmaceutical formulation comprising a first active ingredient which is APAP and an optional second active ingredient selected from the group consisting of one or more opiod or opiod-like compound wherein, when said formulation is administered to a subject in a single dose and at a total dosage strength of 1300 mg APAP under fasting conditions, the maximum plasma concentration (Cmax) of the APAP following administration is in the range from about 5.89_ug/mL to about 9.52_ug/mL.

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64. A pharmaceutical formulation comprising a blend of (a) an immediate release component comprising acetaminophen, an optional water soluble binder, and at least one disintegrant;

and (b) an extended release component comprising at least one controlled release matrix polymer, and one or more optional fillers, and one or more optional wicking agents.

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87. A pharmaceutical formulation comprising a blend of an immediate release component comprising APAP and an extended release component comprising optional APAP wherein when said formulation is administered to a subject for the treatment of pain for at least 8 hours, providing said formulation is not in the form of a bi-layer tablet.

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94. A method of treating pain and a disease state resulting elevated histamine levels in a subject in need of such treatment comprising administering a pharmaceutically effective amount of a pharmaceutical formulation comprising an immediate release component, an extended release component, APAP, and an antihistimine wherein, when said formulation is administered to a subject, said formulation provides eight-hour bioequivalence of APAP compared to two consecutive administrations of one-half equivalent dose concentrations of APAP at a four-hour interval.

95. A method of treating pain and symptoms of respiratory illness in a subject in need of such treatment comprising administering a pharmaceutically effective amount of a pharmaceutical formulation comprising an immediate release component, an extended release component, APAP and one or more optional decongestants, one or more optional antitussives, and one or more expectorants wherein, when said formulation is administered to a subject, said formulation provides eight-hour bioequivalence of APAP compared to two consecutive administrations of one-half equivalent dose concentrations of APAP at a four-hour interval.

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