3-substituted 2-oxindole-1 carboxamide pharmaceutical compositions
First Claim
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1. A pharmaceutical preparation comprising:
- (A) at least one triglyceride or propylene glycol diester of fractionated coconut oil fatty acids, wherein said coconut oil fatty acids include C8 to C10 fatty acids; and
(B) at least one compound of the formula ##STR2## where R1, R2, and R3 are each independently hydrogen, fluoro, bromo, or chloro, or a pharmaceutically acceptable salt thereof,wherein the ratio of % by weight of (A) to % by weight of (B) ranges from 5.6 to 999.
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Abstract
The present invention relates to a pharmaceutical preparation comprising: (A) at least one triglyceride or propylene glycol diester of fractionated coconut oil fatty acids; and (B) at least one carboxamide compound of the formula I. The composition renders the carboxamides of formula I more storage-stable and less susceptible to hydrolysis. Methods of using the composition to inhibit activation of collagenase, treating inflammatory disease, and eliciting an analgesic response are also disclosed.
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3 Claims
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1. A pharmaceutical preparation comprising:
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(A) at least one triglyceride or propylene glycol diester of fractionated coconut oil fatty acids, wherein said coconut oil fatty acids include C8 to C10 fatty acids; and (B) at least one compound of the formula ##STR2## where R1, R2, and R3 are each independently hydrogen, fluoro, bromo, or chloro, or a pharmaceutically acceptable salt thereof, wherein the ratio of % by weight of (A) to % by weight of (B) ranges from 5.6 to 999. - View Dependent Claims (2, 3)
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Specification