Bioanalytical method for determination of Nevirapine in-vivo in resource constrained laboratories
Abstract
Simple
high-Performance Liquid Chromatographic method for determination of Nevirapine
in human plasma is hereby reported. Carbamazepine was used as internal standard
(IS). The internal standard and the drug were extracted into basified
di-isopropyl ether, dried with a current of air using hair drier. The dried
sample was reconstituted with 120 μ l of mobile phase followed by injection of
90 μ l of the reconstituted sample into the chromatograph. A reversed phase
column C18 was used and the mobile phase consisted of 250ml acetonitrile and
800 ml phosphate Buffer (pH 7.5). Detection was achieved at 282nm and both NVP
and IS were well separated from endogenous substances.

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