摘要
目的:建立高效液相色谱手性添加剂法测定特布他林对映体血药浓度。方法:用Waters Atlantis C18色谱柱(4.6mm×150mm,5μm);流动相为水-乙腈(95:5),其中含8.4mmol·L^-1 β-CD(作为手性流动相添加剂)、0.05mmol·L^-1醋酸铵且pH3.0;流速为0.6mL·min^-1;荧光检测,Ex=280nm,Em=320nm;进样量5山;柱温10℃。结果:特布他林两对映体在0.25—25mg·L^-1的浓度范围内线性良好。结论:该方法简便、快捷,可用于开展临床研究。
Objective: To develop HPLC method for the determination of terbutaline enantiomers in human plasma. Methods: The HPLC condition was column Waters Atlantis C18 (4.6 mm × 150 mm, 5 μm) , and water-acetonitrile (95:5 ) contaning 8.4 mmol·L^-1 β-CD (used as a chiral mobile phase additive), 0.05 mmol·L^-1 ammonium acetate with pH 3.0 as the mobile phase with a flow rate at 0.6 mL·min^-1. The chromatography was monitored by fluorescence detection (Ex = 280 nm, Em = 320 nm); column temperature was 10℃. Results: The linear range were 0.25 -25 mg· L^-1, the recovery was 99.35% - 109.76%, inter-day RSD was less than 4% and intra-day RSD was less than 7%. Conclution: This method is simple and rapid. It provides a suitable method in clinical assay of terbutaline enantiomers.
出处
《药学与临床研究》
2008年第6期460-462,共3页
Pharmaceutical and Clinical Research