作者: Erin R. Lepper , Sandra M. Swain , Antoinette R. Tan , William D. Figg , Alex Sparreboom
DOI: 10.1016/J.JCHROMB.2003.08.015
关键词: Quantitative analysis (chemistry) 、 Erlotinib Hydrochloride 、 Spectrophotometry 、 Chromatography 、 Acetonitrile 、 Hydrochloride 、 High-performance liquid chromatography 、 Erlotinib 、 Chemistry 、 Extraction (chemistry)
摘要: A high-performance liquid-chromatographic (HPLC) assay with UV detection has been developed for the quantitative determination of erlotinib (OSI-774) in human plasma. Quantitative extraction was achieved by a single-solvent involving mixture acetonitrile and n-butyl chloride (1:4, v/v). Erlotinib internal standard hydrochloride salt (OSI-597) were separated on column packed Nova-Pak C18 material mobile phase composed water, pH 2.0 (60:40, The effluent monitored dual at wavelengths 348 nm (erlotinib) 383 (OSI-597). calibration graph linear range 100-4500 ng/ml, values accuracy precision ranging from 87.9 to 96.2% 2.13 5.10%, respectively, three different sets quality control samples. method successfully applied study pharmacokinetics cancer patient recommended daily dose 150 mg.