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Intestinal absorption of sodium cefoxitin in rats: effect of formulation.

作者信息

Nishihata T, Yoshitomi H, Higuchi T

出版信息

J Pharm Pharmacol. 1986 Jan;38(1):69-70. doi: 10.1111/j.2042-7158.1986.tb04472.x.

Abstract

The absorption of cefoxitin from rat intestine, rectum and small intestine was greater when the powdered form was administered than when an aqueous solution was given. Cefoxitin absorption from the small intestine was significantly increased after its administration in suppository form prepared with a triglyceride base, although rectal absorption from the suppository did not differ from that of the drug in powdered form. The increase in absorption by the small intestine from the suppository form may be due to fatty acids produced from triglyceride by lipase.

摘要

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