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Ocular penetration of chloramphenicol. Effects of route of administration.

作者信息

George F J, Hanna C

出版信息

Arch Ophthalmol. 1977 May;95(5):879-82. doi: 10.1001/archopht.1977.04450050157020.

DOI:10.1001/archopht.1977.04450050157020
PMID:558746
Abstract

Chloramphenicol was applied topically to the eye in ointment, as a powder, or injected subconjunctivally and intravenously in rabbits. Aqueous humor samples were taken at varying time intervals up to six hours and analyzed for chloramphenicol using gas-liquid chromatography. The topical route using ointment and the subconjunctival injection route produced bacteriostatic concentrations of chloramphenicol in the aqueous humor lasting for several hours, while the topical powder and intravenous routes yielded relatively low concentrations. As compared with the other means of drug delivery, ointment was the most efficient in that it provided the highest aqueous concentration per total amount of drug administered.

摘要

相似文献

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Antimicrob Agents Chemother. 1991 Sep;35(9):1791-8. doi: 10.1128/AAC.35.9.1791.
2
Systemic absorption of topically applied chloramphenicol eyedrops.局部应用氯霉素眼药水的全身吸收。
Br J Ophthalmol. 1979 Oct;63(10):690-1. doi: 10.1136/bjo.63.10.690.