Lee Hye Won, Ji Hye Young, Kim Hoi Yun, Lee Kang Choon, Lee Hye Suk
Drug Metabolism and Bioanalysis Laboratory, College of Pharmacy, Wonkwang University, Iksan 570-749, Korea.
Bioanalysis. 2009 Apr;1(1):63-70. doi: 10.4155/bio.09.10.
To develop and validate a rapid, sensitive and selective liquid chromatography-electrospray ionization mass spectrometric method for the determination of meloxicam and its metabolite 5-carboxymeloxicam in human plasma.
A liquid extraction method was chosen for sample clean-up. Meloxicam, 5-carboxymeloxicam and isoxicam (internal standard) were analyzed on an XBridge™ C18 column with 65% methanol in 10 mM ammonium formate (pH 3.0) and detected in selected reaction monitoring mode. The standard curves were linear over the concentration range 10-2500 ng/ml for meloxicam and 2-100 ng/ml for 5-carboxymeloxicam. Matrix effects were practically absent.
This method has been successfully applied to the pharmacokinetic study of meloxicam and 5-carboxymeloxicam after oral administration of meloxicam (15 mg) to 30 volunteers.
建立并验证一种快速、灵敏且具选择性的液相色谱 - 电喷雾电离质谱法,用于测定人血浆中的美洛昔康及其代谢物5 - 羧基美洛昔康。
选择液液萃取法进行样品净化。美洛昔康、5 - 羧基美洛昔康和异恶酰胺(内标)在XBridge™ C18柱上进行分析,流动相为含65%甲醇的10 mM甲酸铵(pH 3.0),采用选择反应监测模式进行检测。美洛昔康在10 - 2500 ng/ml浓度范围内、5 - 羧基美洛昔康在2 - 100 ng/ml浓度范围内标准曲线呈线性。几乎不存在基质效应。
该方法已成功应用于30名志愿者口服美洛昔康(15 mg)后美洛昔康和5 - 羧基美洛昔康的药代动力学研究。