An LC-MS-MS method for the determination of nevirapine, a non-nucleoside reverse transcriptase inhibitor, in human plasma

J Pharm Biomed Anal. 2003 Apr 1;31(5):953-9. doi: 10.1016/s0731-7085(02)00708-2.

Abstract

A sensitive and rapid liquid chromatography tandem mass spectrometry (LC-MS-MS) method has been developed to measure the levels of the HIV-1 non-nucleoside reverse transcriptase inhibitor nevirapine (NVP) in human plasma. The analyte and internal standard (IS) are isolated from plasma by a simple perchloric acid precipitation of plasma proteins followed by centrifugation. LC-MS-MS in positive mode used pairs of ions at m/z of 267/226 for NVP and 628/421 for the IS, respectively. Two linear calibration curves were established for quantitation of NVP with the low curve ranging from 25 to 1000 ng/ml and the high curve ranging from 1000 to 10,000 ng/ml. Mean inter- and intra-assay coefficients of variation (CVs) over the ranges of the two standard curves were less than 10%. The overall recovery of NVP was 92.4%.

MeSH terms

  • Anti-HIV Agents / blood*
  • Calibration / standards
  • Chromatography, High Pressure Liquid / methods
  • Drug Stability
  • Humans
  • Mass Spectrometry / methods
  • Nevirapine / blood*
  • Reverse Transcriptase Inhibitors / blood*
  • Sensitivity and Specificity

Substances

  • Anti-HIV Agents
  • Reverse Transcriptase Inhibitors
  • Nevirapine