Titus D C, August T F, Yeh K C, Eisenhandler R, Bayne W F, Musson D G
Merck Sharp & Dohme Research Laboratories, West Point, PA 19486.
J Chromatogr. 1990 Dec 14;534:87-100. doi: 10.1016/s0378-4347(00)82151-9.
Two assay procedures are described for the analysis of levodopa, carbidopa and 3-O-methyldopa in plasma and levodopa, carbidopa and dopamine in urine. The methods are suitable for quantifying the analytes following therapeutic administration of levodopa and carbidopa. Both were based on reversed-phase high-performance liquid chromatography (HPLC) with electrochemical detection and with methyldopa as the internal standard. Plasma samples were prepared by perchloric acid precipitation followed by the direct injection of the supernatant. Urine was prepared by alumina adsorption, and the analytes were desorbed with perchloric acid solution containing disodium EDTA and sodium metabisulfite prior to injection into the HPLC system. The methods have been utilized to evaluate the pharmacokinetics and bioavailability of oral dosage forms containing levodopa and carbidopa.
本文描述了两种分析血浆中左旋多巴、卡比多巴和3 - O - 甲基多巴以及尿液中左旋多巴、卡比多巴和多巴胺的检测方法。这些方法适用于在左旋多巴和卡比多巴治疗给药后对分析物进行定量。两种方法均基于反相高效液相色谱(HPLC)并采用电化学检测,以甲基多巴作为内标。血浆样品通过高氯酸沉淀制备,然后直接进样上清液。尿液通过氧化铝吸附制备,在注入HPLC系统之前,分析物用含有乙二胺四乙酸二钠和焦亚硫酸钠的高氯酸溶液解吸。这些方法已用于评估含左旋多巴和卡比多巴口服剂型的药代动力学和生物利用度。