Musson D G, Vincek W C, Dobrinska M R, Vickers S, Leidy H L
J Chromatogr. 1984 Jun 8;308:251-9. doi: 10.1016/s0021-9673(01)87551-8.
The pivaloyloxyethyl ester of methyldopa is an antihypertensive prodrug possessing improved bioavailability properties over methyldopa. A sensitive cation-exchange, high-performance liquid chromatographic assay using electrochemical detection has been developed for the ester in plasma and urine in order to determine the extent of its hydrolysis after oral administration. The chromatographic conditions involve two Altex Partisil 10 SCX columns (25 cm X 4.6 mm) in series; a mobile phase consisting of methanol, potassium phosphate buffer, pH 3.0, and EDTA disodium dihydrate; and an electrochemical detector set at 0.5 V. The pivaloyloxyethyl ester in plasma or urine is extracted into ethyl acetate, back-extracted into 0.1 M sulfuric acid, and analyzed directly by high-performance liquid chromatography. For urine, the ethyl acetate extract is washed with a buffer (pH 8.0) prior to the back-extraction step. The assay gives a linear response over the concentration range of 10-160 ng/ml in plasma and 20-400 ng/ml in urine.
甲基多巴的特戊酰氧基乙酯是一种前体抗高血压药,与甲基多巴相比,其生物利用度有所提高。已开发出一种灵敏的阳离子交换高效液相色谱法,采用电化学检测血浆和尿液中的酯,以确定口服给药后其水解程度。色谱条件包括两根串联的Altex Partisil 10 SCX柱(25 cm×4.6 mm);流动相由甲醇、pH 3.0的磷酸钾缓冲液和乙二胺四乙酸二钠组成;电化学检测器设置为0.5 V。血浆或尿液中的特戊酰氧基乙酯用乙酸乙酯萃取,再反萃取到0.1 M硫酸中,然后直接用高效液相色谱分析。对于尿液,在反萃取步骤之前,乙酸乙酯萃取液先用缓冲液(pH 8.0)洗涤。该测定法在血浆浓度范围为10 - 160 ng/ml和尿液浓度范围为20 - 400 ng/ml时呈线性响应。