Gluth W P, Sörgel F
IBMP-Institute for Biomedical and Pharmaceutical Research, Nürnberg-Heroldsberg.
Pharmazie. 1991 May;46(5):336-9.
A HPLC assay is presented for the determination of oxprenolol (1) and its glucuronic acid conjugate (2) in human plasma and urine. The procedure employs a selective re-extraction using alprenolol (3) as the internal standard, followed by reversed-phase chromatography and UV-detection. The minimal detectable concentration is 10 ng/ml in plasma and 50 ng/ml in urine, using 1.0 and 0.5 ml of plasma and urine, respectively. Within-run and day-to-day variations are below 10% at all concentrations examined. Plasma and urine samples of either healthy volunteers or patients with renal failure are free of interferences from endogenous compounds and drugs frequently used in these patients. The glucuronic acid conjugate of oxprenolol is determined as the parent compound after hydrolytic cleavage with beta-glucuronidase/arylsulfatase. The specificity and selectivity of this cleavage are also demonstrated.
本文介绍了一种用于测定人血浆和尿液中氧烯洛尔(1)及其葡萄糖醛酸结合物(2)的高效液相色谱法。该方法采用以烯丙洛尔(3)为内标的选择性再萃取,随后进行反相色谱和紫外检测。分别使用1.0和0.5 ml血浆及尿液时,血浆中的最低检测浓度为10 ng/ml,尿液中的最低检测浓度为50 ng/ml。在所检测的所有浓度下,批内和日间变异均低于10%。健康志愿者或肾衰竭患者的血浆和尿液样本不受内源性化合物及这些患者常用药物的干扰。氧烯洛尔的葡萄糖醛酸结合物在用β-葡萄糖醛酸酶/芳基硫酸酯酶水解裂解后作为母体化合物进行测定。还证明了这种裂解的特异性和选择性。