Filist Monika, Buś-Kwaśnik Katarzyna, Ksycińska Hanna, Rudzki Piotr J
Pharmaceutical Research Institute, Pharmacology Department, 8 Rydygiera, 01-793 Warsaw, Poland.
Pharmaceutical Research Institute, Pharmacology Department, 8 Rydygiera, 01-793 Warsaw, Poland.
J Pharm Biomed Anal. 2014 Nov;100:184-189. doi: 10.1016/j.jpba.2014.07.015. Epub 2014 Aug 8.
A sensitive liquid chromatographic-tandem mass spectrometric method was developed and validated to study the pharmacokinetics of a low dose of azithromycin in human plasma. The sample preparation was based on liquid-liquid extraction with the low volume of methyl t-butyl ether. The chromatographic separation was performed on a Symmetry C18 column (50×2.1mm, 3.5μm). Gradient elution with ammonium acetate-acetonitrile and ammonium acetate-methanol was applied. Positive electrospray ionisation tandem mass spectrometry in the multiple reaction monitoring mode was used for the detection of azithromycin. The influence of a major metabolite, including the possibility of its back-conversion, on the quantification of azithromycin was evaluated. Isotope labelled azithromycin was used as the internal standard. The calibration curve was linear in the range of 0.5-250.0ng/mL. The new validated method was successfully applied to a pharmacokinetic study in humans following a single 100mg oral dose.
建立并验证了一种灵敏的液相色谱-串联质谱法,用于研究低剂量阿奇霉素在人血浆中的药代动力学。样品制备基于用少量甲基叔丁基醚进行液-液萃取。色谱分离在Symmetry C18柱(50×2.1mm,3.5μm)上进行。采用醋酸铵-乙腈和醋酸铵-甲醇梯度洗脱。在多反应监测模式下采用正电喷雾电离串联质谱法检测阿奇霉素。评估了主要代谢物对阿奇霉素定量的影响,包括其逆向转化的可能性。使用同位素标记的阿奇霉素作为内标。校准曲线在0.5-250.0ng/mL范围内呈线性。新验证的方法成功应用于单次口服100mg剂量后的人体药代动力学研究。