Chai B L, Minkler P E, Hoppel C L
Medical Research, VA Medical Center, Cleveland, OH 44106.
J Chromatogr. 1988 Aug 19;430(1):93-101. doi: 10.1016/s0378-4347(00)83137-0.
A sensitive and selective high-performance liquid chromatographic assay for free and total ibuprofen and its major metabolites in human urine is described. Urine is acidified, drug and metabolites are extracted into hexane-propanol, back-extracted into sodium bicarbonate, neutralized and chromatographed. Ibufenac (4-isobutylphenylacetic acid) and 2-phenylpropionic acid were employed as internal standards. The extraction efficiencies were 94-100% for all compounds. The two metabolites and their internal standard were separated using an isocratic chromatographic system, followed by an abrupt step gradient to a second eluent for separation of ibuprofen and its internal standard with a total run time of 18 min. Detection was by a fixed-wavelength detector (214 nm). Sample-to-sample and day-to-day reproducibility studies yielded coefficients of variability of less than 9% for all compounds. The sensitivity was sufficient to determine 2.5 micrograms/ml free ibuprofen in 100 microliters urine.
本文描述了一种灵敏且具选择性的高效液相色谱法,用于测定人尿中游离和总布洛芬及其主要代谢物。尿液经酸化处理后,药物及其代谢物被萃取至己烷 - 丙醇中,再反萃取至碳酸氢钠溶液中,经中和后进行色谱分析。以异丁苯乙酸(ibufenac)和2 - 苯丙酸作为内标。所有化合物的萃取效率为94 - 100%。两种代谢物及其内标采用等度色谱系统进行分离,随后以突然的阶跃梯度切换至第二种洗脱液,用于分离布洛芬及其内标,总运行时间为18分钟。采用固定波长检测器(214 nm)进行检测。样品间和不同日期的重现性研究表明,所有化合物的变异系数均小于9%。该方法的灵敏度足以测定100微升尿液中2.5微克/毫升的游离布洛芬。