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  • 标题:Conventional HPLC Method Used for Simultaneous Determination of the Seven HIV Protease Inhibitors and Nonnucleoside Reverse Transcription Inhibitor Efavirenz in Human Plasma
  • 本地全文:下载
  • 作者:Masaaki Takahashi ; Masao Yoshida ; Tsuyoshi Oki
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2005
  • 卷号:28
  • 期号:7
  • 页码:1286-1290
  • DOI:10.1248/bpb.28.1286
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:We developed a simple HPLC method for the simultaneous quantitative determination of seven HIV protease inhibitors: amprenavir (APV), atazanavir (ATV), indinavir (IDV), lopinavir (LPV), nelfinavir (NFV), ritonavir (RTV), saquinavir (SQV), and a nonnucleoside reverse transcription inhibitor, efavirenz (EFV). This method involves a rapid liquid–liquid drug extraction from plasma, the use of an isocratic elution on a reversed-phase C18 column, and an ultraviolet detection at a single wavelength (205 nm). The mobile phase consisted of 39% 50 m M phosphate buffer (pH 5.9), 22% methanol and 39% acetonitrile. Forty-eight samples could be measured in one day since the runtime of one sample is 30 min. The assay has been validated over a concentration range of 0.05 to 12.20 μg/ml for APV, 0.09 to 12.05 μg/ml for ATV, 0.05 to 12.01 μg/ml for IDV, 0.12 to 12.36 μg/ml for LPV, 0.18 to 12.20 μg/ml for NFV, 0.12 to 12.33 μg/ml for RTV, 0.12 to 12.06 μg/ml for SQV, and 0.05 to 12.17 μg/ml for EFV. Calibration curves were linear in the described concentration ranges. The average accuracy ranged from 97.2 to 106.8%. Both the interday and intraday coefficients of variation for all drugs tested were less than 8.5%. This method provides a simple, accurate, and precise method for the therapeutic drug monitoring of the seven protease inhibitors and EFV in clinical routine use.
  • 关键词:HPCL;therapeutic drug monitoring;HIV protease inhibitor;human immunodeficiency virus (HIV)-1
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