Atia Noha N, York Peter, Clark Brian J
Institute of Pharmaceutical Innovation, School of Pharmacy, University of Bradford, Bradford, UK.
J Sep Sci. 2009 Apr;32(7):931-8. doi: 10.1002/jssc.200800655.
A new rapid, sensitive and validated HPLC method has been developed for the determination of methylxanthines and their metabolites in asthmatic patients. The method was initiated by using spiked urine samples on a silica monolithic column as a novel packing material. The mobile phase consisted of 10 mM potassium dihydrogen phosphate buffer/methanol (87.5:12.5 v/v), at a flow rate 1 mL/min. Detection was set at 274 nm. The LOQ for all the compounds ranged from 14 to 41 ng/mL. Excellent linearity was achieved over the studied range of concentration with correlation coefficients 0.9991-0.9998 (n = 6). The developed method was validated by precision and accuracy with RSD <2.55%. On extraction of the drugs and metabolites from the urine samples high recoveries were achieved ranging from 82.06 to 98.34% w/w on RP18 cartridges and methanol/chloroform (20:80 v/v) as the extraction solvent. This method has advantages over other methods using conventional C18 packings.
已开发出一种新的快速、灵敏且经过验证的高效液相色谱法,用于测定哮喘患者体内的甲基黄嘌呤及其代谢物。该方法首先将加标尿液样本注入硅胶整体柱(一种新型填充材料)。流动相由10 mM磷酸二氢钾缓冲液/甲醇(87.5:12.5 v/v)组成,流速为1 mL/min。检测波长设定为274 nm。所有化合物的定量限范围为14至41 ng/mL。在所研究的浓度范围内实现了极佳的线性,相关系数为0.9991 - 0.9998(n = 6)。所开发的方法通过精密度和准确度验证,相对标准偏差<2.55%。从尿液样本中提取药物和代谢物时,使用RP18柱以及甲醇/氯仿(20:80 v/v)作为提取溶剂,回收率较高,范围为82.06至98.34% w/w。该方法相较于其他使用传统C18填料的方法具有优势。