Antimicrobial preservatives to achieve multi-dose formulation using beta-cyclodextrins for liquid dosage forms
View Patent ↗The present invention is directed to pharmaceutical compositions containing a therapeutically effective amount of an Active Pharmaceutical Ingredient (“API”), a pharmaceutically acceptable cyclodextrin and a pharmaceutically acceptable preservative. The invention is also directed to pharmaceutical compositions of the compounds of Formula (I) wherein R 2 is selected from the group consisting of methyl, ethyl, isopropyl, sec-butyl and tert-butyl and a pharmaceutically acceptable cyclodextrin and preservative. Formula (I): In particular, the invention is directed to pharmaceutical compositions of the compound of Formula 1 a , and a pharmaceutically acceptable cyclodextrin and a preservative.
1. A parenteral pharmaceutical composition with injection site toleration comprising a therapeutically effective amount of a compound of Formula (1a),
or a pharmaceutically acceptable salt thereof, a β-cyclodextrin, a pharmaceutically acceptable preservative, a pharmaceutically acceptable vehicle, and an optional pharmaceutically acceptable excipient, wherein the preservative demonstrates pharmaceutically acceptable antimicrobial preservative effectiveness and is selected from the group consisting of thimerosal, propylene glycol, phenol, or meta-cresol.
2. The pharmaceutical composition according to claim 1 wherein the β-cyclodextrin is 2-hydroxypropyl-β-cyclodextrin or sulfobutyl ether-β-cyclodextrin.
3. The pharmaceutical composition according to claim 2 wherein the preservative is about 2.5 to about 3.5 mg/mL of meta-cresol, the cyclodextrin is sulfobutyl ether-β-cyclodextrin, and wherein the pharmaceutically acceptable salt is the citrate monohydrate salt.
4. The pharmaceutical composition according to claim 3 wherein the preservative has a binding value to the cyclodextrin that is less than the binding value of the compound of Formula (1a) to cyclodextrin.
5. The pharmaceutical composition according to claim 4 wherein the binding value of the compound of Formula (1a) to cyclodextrin is between 800 M −1 and 3,000 M.
6. A pharmaceutical composition comprising about 10 mg/mL of a compound of Formula (1a),
about 3.3 mg/mL meta-cresol, about 63 mg/mL sulfobutyl ether-β-cyclodextrin, and a pharmaceutically acceptable vehicle.
7. A method for the treatment of emesis in an animal comprising administering to said animal a composition according to claim 1 .