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Determination of valproic acid in human serum by high-performance liquid chromatography with fluorescence detection.

机译:高效液相色谱-荧光检测法测定人血清中丙戊酸的含量。

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摘要

A simple and highly sensitive high-performance liquid chromatographic method is described for the determination of valproic acid in human serum. The method is based on the direct derivatization of serum sample with 6,7-methylenedioxy-1-methyl-2-oxo-1,2-dihydroquinoxaline-3-ylpr opionohydrazide. The derivatization reaction proceeds in aqueous solution in the presence of pyridine and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide at 37 degrees C. The resulting derivatives were separated on a reversed-phase column (YMC Pack ODS-A) with isocratic elution and were fluorimetrically detected at 440 nm with excitation at 365 nm. The detection limit (signal-to-noise ratio=3) for valproic acid added to serum sample was 0.1 microg (700 fmol)/ml serum sample (2.3 fmol on column). The method was applied to determine the unbound- and total-valproic acid levels in the serum obtained from three healthy volunteers after oral administration of the drug (600 mg).
机译:描述了一种简单高效的高效液相色谱法,用于测定人血清中的丙戊酸。该方法基于将血清样品直接与6,7-亚甲基二氧基-1-甲基-2-甲基-2-氧代1,2-二氢喹喔啉-3-基丙基Opionohydrazide衍生化。在吡啶和1-乙基-3-(3-二甲基氨基丙基)碳二亚胺存在下,在水溶液中于37°C进行衍生化反应。将所得衍生物在反相柱(YMC Pack ODS-A)上用等度分离。洗脱,并在365 nm激发下于440 nm荧光检测。添加到血清样品中的丙戊酸的检出限(信噪比= 3)为0.1微克(700 fmol)/ ml血清样品(柱上2.3 fmol)。该方法用于测定口服药物(600 mg)后从三名健康志愿者那里获得的血清中未结合的丙戊酸和总丙戊酸水平。

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