Nakagawa T, Haginaka J, Yamaoka K, Uno T
J Antibiot (Tokyo). 1978 Aug;31(8):769-75. doi: 10.7164/antibiotics.31.769.
A rapid and accurate high speed liquid chromatographic method has been developed for the determination of cephalexin in human plasma and urine. The method involves micropore filtration of urine specimens and methanol extraction of plasma samples followed by HSLC separation on a bonded reverse phase column utilizing a mobile phase of methanol-water containing acetic acid. The quantitativity of UV response at 254 nm covered a wide range of cephalexin concentrations down to 0.5 microgram/ml, and no metabolite peaks were detected. The time courses of plasma level and urinary excretion were determined until 6 hours after oral administration of cephalexin capsules to healthy volunteers. The pharmacokinetic parameters were estimated using a two compartment open model.
已开发出一种快速准确的高速液相色谱法,用于测定人血浆和尿液中的头孢氨苄。该方法包括对尿液标本进行微孔过滤,对血浆样品进行甲醇萃取,然后在键合反相柱上进行高速液相色谱分离,流动相为含乙酸的甲醇 - 水。在254nm处的紫外响应定量范围涵盖低至0.5微克/毫升的广泛头孢氨苄浓度,且未检测到代谢物峰。对健康志愿者口服头孢氨苄胶囊后直至6小时的血浆水平和尿排泄的时间过程进行了测定。使用二室开放模型估算药代动力学参数。