Wilhelm J A, Bailey L C, Shepard T A, Venturella V S
Rutgers University, College of Pharmacy, Piscataway, NJ 08855.
J Chromatogr. 1992 Jul 24;578(2):231-8. doi: 10.1016/0378-4347(92)80421-l.
A procedure is described to simultaneously quantitate phenolphthalein and its glucuronide metabolite from dog serum, urine and bile using high-performance liquid chromatography. The major advantages of this over pre-existing methods include direct analysis of the parent compound and glucuronide metabolite without enzymatic hydrolysis, increased sensitivity and the potential for automation of a large number of samples. Analytes were extracted from serum and urine using a combination of liquid- and solid-phase extraction methodology. Bile samples were analyzed directly after a twenty-fold dilution with mobile phase. The components plus internal standard were separated by reversed-phase high-performance liquid chromatography using step gradient elution and quantitated by the absorbance of ultraviolet light at 230 nm. Limits of detection from 1 ml of serum, 0.1 ml of urine and 0.05 ml of bile were 0.1, 0.5 and 10 microgram/ml for phenolphthalein and 0.1, 10 and 50 microgram/ml for phenolphthalein glucuronide, respectively.
本文描述了一种使用高效液相色谱法同时定量犬血清、尿液和胆汁中酚酞及其葡萄糖醛酸代谢物的方法。与现有方法相比,该方法的主要优点包括无需酶水解即可直接分析母体化合物和葡萄糖醛酸代谢物、提高了灵敏度以及大量样品自动化分析的潜力。使用液相和固相萃取方法相结合从血清和尿液中提取分析物。胆汁样品用流动相稀释20倍后直接进行分析。使用梯度洗脱通过反相高效液相色谱法分离各成分和内标,并通过230nm处的紫外吸光度进行定量。从1ml血清、0.1ml尿液和0.05ml胆汁中的检测限来看,酚酞分别为0.1、0.5和10微克/毫升,酚酞葡萄糖醛酸分别为0.1、10和50微克/毫升。