Benzonatate modified release solid tablets and capsules
View Patent ↗A 12-hour anti-tussive modified release solid tablet or capsule is described which comprises a benzonatate adsorbate in a matrix with a sufficient amount of one or more pharmaceutically acceptable modified release pH-independent, substances to provide a 12-hour modified release profile to the benzonatate, wherein there is substantially no benzonatate release from the tablet or capsule in the buccal cavity and no more than about 25% release of the benzonatate within 1 hour as determined in an in vitro dissolution assay.
1. A modified release benzonatate solid oral composition comprising (a) a homogenous solid dispersion comprising (i) benzonatate adsorbed onto one or more of a silica, silicon dioxide or silicate to form a benzonatate adsorbate and (ii) at least one pharmaceutically acceptable modified release pH-independent, hydrophilic or hydrophobic matrix-forming substance in an amount effective to provide a modified release profile to the benzonatate, and (b) a coating over said homogenous solid dispersion,
wherein there is substantially no benzonatate release from the composition in the buccal cavity, and
wherein the composition provides a pharmacokinetic profile for benzonatate, based on an equivalent of about a 300 mg dose of benzonatate administered at 12 hour intervals in a 24 hour period, of one or more of: a geometric mean area under the curve (AUC) inf of about 110 ng-h/mL to about 170 ng-h/mL, a geometric mean maximum plasma concentration (C max ) of about 28 ng/mL to about 34 ng/mL and/or a T max of about 12 hours to 20 hours.
2. The modified release benzonatate composition according to claim 1 , wherein the composition provides a pharmacokinetic profile for benzonatate, based on an equivalent of about a 300 mg dose of benzonatate administered at 12 hour intervals in a 24 hour period, comprising one or more of: a geometric mean C max of about 30 ng/mL and/or a geometric mean AUC inf of about 150 ng-h/mL.
3. The modified release benzonatate composition according to claim 1 , wherein the composition provides a pharmacokinetic profile for benzonatate, based on an equivalent of about a 300 mg dose of benzonatate administered at 12 hour intervals in a 24 hour period, comprising one or more of: an arithmetic mean C max of about 30 ng/mL to about 35 ng/mL and/or an arithmetic mean AUC inf of about 180 ng-h/mL to about 185 ng-h/mL.
4. The modified release benzonatate composition according to claim 1 , wherein no more than about 25% of the benzonatate is released within 1 hour as determined in an in vitro dissolution assay.
5. The modified release benzonatate composition according to claim 1 , wherein the coating is a pH-independent coating.
6. The modified release benzonatate composition according to claim 1 , wherein the coating is a reverse enteric coating.
7. The modified release benzonatate composition according to claim 6 , wherein said reverse enteric coating comprises (a) a pH-dependent methyl methacrylate and diethylaminoethyl methacrylate copolymer or (b) a pH-dependent cationic copolymer based on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate.
8. The modified release benzonatate composition according to claim 6 , wherein said reverse enteric coating comprises a pH-dependent cationic copolymer based on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate.
9. The modified release benzonatate composition according to claim 6 , wherein said reverse enteric coating comprises about 5% to about 40% weight of the composition.
10. The modified release benzonatate composition according to claim 1 , wherein the weight ratio of benzonatate to silica, silicon dioxide, or silicate is in the range of about 5:1 to about 1:10, or about 3:1 to about 1:1.
11. The modified release benzonatate according to claim 1 , wherein the benzonatate adsorbate comprises about 60% w/w benzonatate.
12. The modified release benzonatate composition according to claim 1 , in which the matrix-forming substance is a hydrophilic polymer, wherein the composition comprises about 5% w/w to about 35% w/w, or about 5% w/w to about 30% w/w of the at least one hydrophilic polymer, based on the weight of the composition prior to coating.
13. The modified release benzonatate composition according to claim 12 , wherein the hydrophilic polymer is a low viscosity polymer.
14. The modified release benzonatate composition according to claim 13 , wherein the low viscosity, hydrophilic polymer is a hydroxypropyl methylcellulose having a viscosity of about 4000 mPa-s to about 100,000 mPa-s, or a blend of polymers containing said hydroxypropyl methycellulose.
15. The modified release benzonatate composition according to claim 1 which is a compressed tablet.
16. The modified release benzonatate composition according to claim 15 , wherein the tablet further comprises at least one excipient selected from one or more of bulking agents, binders, and lubricants.
17. The modified release benzonatate composition according to claim 1 , wherein the solid oral composition further comprises at least one or more additional pharmaceutically active components.
18. The modified release benzonatate composition according to claim 17 , wherein said at least one or more additional active components is selected from an anti-pyretic, an analgesic, an anti-histamine, an expectorant and a decongestant.
19. The modified release benzonatate composition according to claim 17 , wherein said at least one or more additional active components are independently in immediate release form, in modified release form, or both.
20. The modified release benzonatate composition according claim 18 , wherein said expectorant is guaifenesin.
21. The modified release benzonatate composition according to claim 18 , which comprises one or more additional active components in the matrix.