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US4837030A Expired / Lapsed US ⏱️ 0.0 years remaining

Novel controlled release formulations of tetracycline compounds

Assignee: Wyeth Holdings LLC
•
Filing: 1987-10-06
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Granted: 1989-06-06
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Expires: 2007-10-06
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Abstract

Abstract Pharmaceutical compositions comprising spherical granules including thereon or therein a 7- or 9-akylamino-6-deoxy-6-demethyltetracycline or an acid-addition salt thereof blended with at least one excipient are adapted to control the rate of drug release in the stomach and in the intenstine in order not to produce nausea or dizziness upon oral administration during antibacterial therapy.

Inventors

  • 👤 Joseph J. Valorose, Jr.
  • 👤 Raymond J. Biehl
  • 👤 Nitin V. Sheth
  • 👤 Walter A. Strathy
  • 👤 Michael K. Doelling

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 16:17
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/65; A61K9/00; A61K9/14; A61K9/16; A61K9/1605; A61K9/1629; A61K9/1652; A61K9/20; A61K9/48; A61K9/50; A61K9/5073; A61K9/5078; A61P; A61P31/00; A61P31/04

Claims Analysis

Total Claims: 44
Claim 1
Independent Claim 68 words
A spheronized pharmaceutical composition spherical comprising granules which include on or in said granules an effective antibacterial amount of a 7- or 9-(lower)alkylamino-6-deoxy-6-demethyltetracycline or a non-toxic acid addition said thereof blended with an effective amount of at least one pharmaceutically acceptable excipient, said granules being adapted to control the rate of release of said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline in the human stomach and human intesting upon oral administration.
Claim 2
Dependent Claim 68 words
A spheronized pharmaceutical composition spherical comprising granules which include on or in said granules an effective antibacterial amount of a 7- or 9-(lower)alkylamino-6-deoxy-6-demethyltetracycline or a non-toxic acid addition said thereof blended with an effective amount of at least one pharmaceutically acceptable excipient, said granules being adapted to control the rate of release of said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline in the human stomach and human intesting upon oral administration.
Claim 3
Dependent Claim 44 words
A pharmaceutical composition as defined in claim 1 wherein controlling the rate comprises retarding the rate of release of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound in the human stomach and promoting rapid release of said tetracycline compound in the human intestine upon oral administration.
Claim 4
Dependent Claim 49 words
A pharmaceutical composition as defined in claim 1 wherein each of said spherical granules includes an ultrathin layer of a polymer substantially uniformly coating each of said spherical granules, said polymer being slowly erodable in the human stomach and rapidly erodable in the human small intestine upon oral administration.
Claim 5
Dependent Claim 57 words
A pharmaceutical composition as defined in claim 1 wherein said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline compound is substantially completely released from said spherical granules in not less than about 20 minutes nor more than about 90 minutes when suspended in deionized water at ambient temperature at a drug concentration of about 100 mg of drug/900 ml of water.
Claim 6
Dependent Claim 55 words
A pharmaceutical composition as defined in claim 3 wherein said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline compound is substantially completely released from said spherical granules in not less than about 20 minutes nor more than about 90 minutes when suspended in deionized water at ambient temperature at a drug concention of about 100 mg/900 ml of water.
Claim 7
Dependent Claim 45 words
A pharmaceutical composition as defined in claim 1 wherein said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline is selected from (a) 7-dimethylamino-6-deoxy-6-demethyl tetracyline; (b) 7-methylamino-6-deoxy-6-demethyltetracycline; (c) 9-methylamino-6-deoxy-6-demethyltetracycline; (d) 7-ethylamino-6-deoxy-6-demethyltetracycline; (e) 7-iospropylamino-6-deoxy-6-demethyltetracyline; (f) a non-toxic acid addition salt of (a)-(e) inclusive; or (g) a mixture of any of (a)-(f).
Claim 8
Dependent Claim 25 words
A pharmaceutical composition as defined in claim 6 wherein said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline compound is selected from 7-dimethylamino-6-deoxy-6-demethyltetracycline or an acid addition salt thereof.
Claim 9
Dependent Claim 18 words
A pharmaceutical composition as defined in claim 7 wherein said 7- or 9-(lower)alkylamino-6-deoxy-6-demethyl tetracycline compound comprises 7-dimethylamino-6-deoxy-6-demethyltetracycline hydrochloride.
Claim 10
Dependent Claim 41 words
A pharmaceutical composition as defined in claim 1 wherein said pharmaceutical excipient comprises microcrystalline cellulose, polyvinylpyrrolidone, hydroxypropylmethyl cellulose, microcrystalline cellulose in combination with lactose, microcrystalline cellulose in combination with sodium carboxymethyl cellulose, or a mixture of any of said pharmaceutical excipients.
Claim 11
Dependent Claim 15 words
A pharmaceutical composition as defined in claim 9 wherein said pharmaceutical excipient comprises microcrystalline cellulose.
Claim 12
Dependent Claim 39 words
A pharmaceutical composition as defined in claim 3 wherein said pharmaceutical excipient comprises microcrystalline cellulose, polyvinylpyrrolidone, hydroxypropylmethyl cellulose, microcrystalline cellulose in combination with lactose, microcrystalline cellulose in combination with sodium carboxymethylcellulose, or a mixture of any of the foregoing.
Claim 13
Dependent Claim 15 words
A pharmaceutical composition as defined in claim 11 wherein said pharmaceutical excipient comprises microcrystalline cellulose.
Claim 14
Dependent Claim 53 words
A pharmaceutical composition as defined in claim 1 wherein said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound comprises from about 10 to about 70 parts by weight and said excipient comprises from about 90 to about 30 parts by weight per 100 parts by weight of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound and said excipient.
Claim 15
Dependent Claim 48 words
A pharmaceutical composition as defined in claim 3 wherein wherein said tetracycline compound comprises from about 10 to about 70 parts by weight and said excipient comprises from about 90 to about 30 parts by weight per 100 parts by weight of said tetracycline compound and said excipient.
Claim 16
Dependent Claim 72 words
A pharmaceutical composition as defined in claim 3 wherein said polymer is selected from (a) methylcellulose; (b) ethylcellulose; (c) hydroxyethyl cellulose; (d) hydroxypropyl cellulose; (e) hydroxypropyl methylcellulose; (f) hydroxypropyl methylcellulose phthalate; (g) cellulose acetate phthalate (h) hydroxypropyl methylcellulose succinate (i) a polymer or copolymer of (meth)acrylic acid or an ester thereof; or (j) a mixture of any of (a)-(i) alone or in further combination with a plasticizer, a colorant or a pigment.
Claim 17
Dependent Claim 27 words
A pharmaceutical composition as defined in claim 3 which also includes an ultrathin top layer of the same or a different polymer over an intermediate polymer layer.
Claim 18
Dependent Claim 19 words
A pharmaceutical composition as defined in claim 16 wherein the intermediate layer and the top layer comprise hydroxypropyl methylcellulose.
Claim 19
Dependent Claim 32 words
A pharmaceutical composition as defined in claim 3 wherein said polymer comprises from about 2 to less than about 10 percent by weight of the total weight of said polymer-coated spherical granules.
Claim 20
Dependent Claim 29 words
A pharmaceutical composition as defined in claim 18 wherein said polymer comprises from about 2 to about 5 percent by weight of the weight of said polymer-control spherical granules.
Claim 21
Dependent Claim 27 words
A pharmaceutical composition as defined in claim 1 wherein the spherical granules have an average diameter in the range of from about 0.1 to about 2.5 millimeters.
Claim 22
Dependent Claim 24 words
A pharmaceutical composition as defined in claim 20 wherein the spherical granules have an average diameter of from about 0.8 to about 1.2 millimeters.
Claim 23
Dependent Claim 106 words
A controlled release pharmaceutical composition in oral dosage unit form comprising A. A gelatin capsule filled solely with B. beads having an average diameter of from about 0.1 to about 2.5 millimeters, each bead being similar in composition and comprising spherical granules which include on or in said granules an effective antibacterial amount of a 7- or 9-(lower)alkylamino-6-deoxy-6-demethyltetracycline or a non-toxic acid addition salt thereof blended with an effective amount of at least one pharmaceutically acceptable excipient, said granules being adapted to control the rate of release of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound in the human stomach and in the human intestine upon oral administration.
Claim 24
Dependent Claim 106 words
A controlled release pharmaceutical composition in oral dosage unit form comprising A. A gelatin capsule filled solely with B. beads having an average diameter of from about 0.1 to about 2.5 millimeters, each bead being similar in composition and comprising spherical granules which include on or in said granules an effective antibacterial amount of a 7- or 9-(lower)alkylamino-6-deoxy-6-demethyltetracycline or a non-toxic acid addition salt thereof blended with an effective amount of at least one pharmaceutically acceptable excipient, said granules being adapted to control the rate of release of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound in the human stomach and in the human intestine upon oral administration.
Claim 25
Dependent Claim 49 words
A control release pharmaceutical composition as defined in claim 22 wherein controlling the rate comprises retarding the rate of release of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound in the human stomach and promoting rapid release of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound in the human intesting upon oral administration.
Claim 26
Dependent Claim 51 words
A controlling release pharmaceutical composition as defined in claim 22 wherein each of said spherical granules includes an ultrathin layer of a polymer substantially uniformly coating each of said spherical granules, said polymer being slowly erodable in the human stomach and rapidly erodable in the human small intestine upon oral administration.
Claim 27
Dependent Claim 48 words
A controlled release pharmaceutical composition as defined in claim 22 wherein said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound is selected from (a) 7-dimethylamino-6-deoxy-6-demethyl tetracyline; (b) 7-methylamino-6-deoxy-6-dimethyltetracycline; (c) 9-methylamino-6-deoxy-6-demethyltetracycline; (d) 7-ethylamino-6-deoxy-6-demethyltetracycline; (e) 7-isopropylamino-6-deoxy-6-demethyltetracycline; (f) a non-toxic acid addition salt of (a)-(e), inclusive; or (g) a mixture of any of (a)-(f).
Claim 28
Dependent Claim 28 words
A controlled release pharmaceutical composition as defined in claim 25 wherein said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound is selected from 7-dimethylamino6-deoxy-6-demethyl tetracycline or an acid addition salt thereof.
Claim 29
Dependent Claim 19 words
A controlled release pharmaceutical composition as defined in claim 26 wherein said 7- or 9-(lower)alkyl-amino-6-deoxy-6-tetracycline compound comprises 7-dimethylamino-6-deoxy-6-demethyltetracycline hydrochloride.
Claim 30
Dependent Claim 42 words
A controlled release pharmaceutical composition as defined in claim 22 wherein said pharmaceutical excipient comprises microcrystalline cellulose, polyvinylpyrrolidone, hydroxypropylmethyl cellulose, microcrystalline cellulose in combination with lactose, microcrystalline cellulose in combination with sodium carboxymethyl-cellulose, or a mixture of any of said pharmaceutical excipients.
Claim 31
Dependent Claim 17 words
A controlled release pharmaceutical composition as defined in claim 28 wherein said pharmaceutical excipient comprises microcrystalline cellulose.
Claim 32
Dependent Claim 43 words
A controlled release pharmaceutical composition as defined in claim 24 wherein said pharmaceutical excipient comprises microcrystalline cellulose, polyvinyl pyrrolidone, hydroxypropylmethyl cellulose, microcrystalline cellulose in combination with lactose, microcrystalline cellulose in combination with sodium carboxymethyl-cellulose, or a mixture of any of said pharmaceutical excipients.
Claim 33
Dependent Claim 17 words
A controlled release pharmaceutical composition as defined in claim 30 wherein said pharmaceutical excipient comprises microcrystalline cellulose.
Claim 34
Dependent Claim 58 words
A controlled release pharmaceutical composition as defined in claim 22 wherein in beads B said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound comprises from about 10 to about 70 parts by weight and said excipient comprises from about 90 to about 30 parts by weight per 100 parts by weight of said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound and said excipient.
Claim 35
Dependent Claim 54 words
A controlled release composition as defined in claim 24 wherein said beads B said 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound comprises from about 10 to about 70 parts by weight and said excipient comprises from about 90 to about 30 parts by weight per 100 parts by weight of said tetracycline compound and said excipient.
Claim 36
Dependent Claim 74 words
A controlled release pharmaceutical composition as defined in claim 22 wherein wherein said polymer is selected from (a) methylcellulose; (b) ethylcellulose; (c) hydroxyethyl cellulose; (d) hydroxypropyl cellulose; (e) hydroxypropyl methylcellulose; (f) hydroxypropyl methylcellulose phthalate; (g) cellulose acetate phthalte (h) hydroxypropyl methylcellulose succinate (i) a polymer or copolymer of (meth)acrylic acid or an ester thereof; or (j) a mixture of any of (a)-(i), or in further combination with a plasticizer, a colorant or a pigment.
Claim 37
Dependent Claim 29 words
A controlled release pharmaceutical composition as defined in claim 24 wherein beads B also include an ultrathin top layer of the same or a different polymer over intermediate layer.
Claim 38
Dependent Claim 21 words
A controlled release pharmaceutical composition as defined in claim 35 wherein the intermediate layer and the top layer comprise hydroxypropyl methylcellulose.
Claim 39
Dependent Claim 34 words
A controlled release pharmaceutical composition as defined in claim 24 wherein said polymer comprises from about 2 to less than about 10 percent by weight of the total weight of said polymer coated spheres.
Claim 40
Dependent Claim 28 words
A controlled release pharmaceutical composition as defined in claim 37 wherein said polymer comprises from about 2 to about 5 percent by weight of said polymer coated spheres.
Claim 41
Dependent Claim 25 words
A controlled release pharmaceutical composition as defined in claim 22 wherein said beads have an average diameter of from about 0.1 to about 2.5 millimeters.
Claim 42
Dependent Claim 27 words
A controlled release pharmaceutical composition as defined in claim 22 wherein each capsule contains from about 25 to about 200 mg of 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound.
Claim 43
Dependent Claim 26 words
A controlled release pharmaceutical composition as defined in claim 24 wherein each capsule contains from about 25 to about 200 of 7- or 9-(lower)alkyl-amino-6-deoxy-6-demethyl tetracycline compound.
Claim 44
Dependent Claim 18 words
A controlled release pharmaceutical composition as defined in claim 1 in oral dosage unit form comprising a tablet.

References Cited (Backward Citations)

US4207258A Cited
US4038315A Cited
US3901942A Cited
US3960757A Cited
US4154827A Cited
US4622244A Cited
US4500458A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-06-05 1992-12-05 1993-06-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-06-05 1996-12-05 1997-06-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-06-05 2000-12-05 2001-06-06 $7700.00 Window Closed / Lapsed

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