Conventional HPLC Method Used for Simultaneous Determination of the Seven HIV Protease Inhibitors and Nonnucleoside Reverse Transcription Inhibitor Efavirenz in Human Plasma
| Autor: | Masao Yoshida, Tsuyoshi Oki, Tatsuo Suzuki, Masaaki Takahashi, Naoya Okumura, Tsuguhiro Kaneda |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
Cyclopropanes
Efavirenz Pharmaceutical Science chemistry.chemical_compound Amprenavir Indinavir Oxazines medicine Humans Chromatography High Pressure Liquid Pharmacology Chromatography Chemistry Reproducibility of Results Lopinavir HIV Protease Inhibitors General Medicine Reference Standards Benzoxazines Atazanavir Nelfinavir Alkynes Reverse Transcriptase Inhibitors Spectrophotometry Ultraviolet Ritonavir Saquinavir medicine.drug |
| Zdroj: | Biological and Pharmaceutical Bulletin. 28:1286-1290 |
| ISSN: | 1347-5215 0918-6158 |
| Popis: | 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 mM 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 microg/ml for APV, 0.09 to 12.05 microg/ml for ATV, 0.05 to 12.01 microg/ml for IDV, 0.12 to 12.36 microg/ml for LPV, 0.18 to 12.20 microg/ml for NFV, 0.12 to 12.33 microg/ml for RTV, 0.12 to 12.06 microg/ml for SQV, and 0.05 to 12.17 microg/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. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|