Hisaka A, Kasamatsu S, Takenaga N, Ohtawa M
Central Research Laboratories, Banyu Pharmaceutical Co., Ltd, Tokyo, Japan.
J Chromatogr. 1989 Sep 29;494:183-9. doi: 10.1016/s0378-4347(00)82667-5.
A new and rapid high-performance liquid chromatographic assay has been developed for the determination of L-3-(3-hydroxy-4-pivaloyloxyphenyl)alanine (NB-355,I), a novel prodrug of L-DOPA. The method involves precolumn derivatization of the drug in biological samples with o-phthalaldehyde (OPA) and N-acetyl-L-cysteine (NAC) in a triethanolamine buffer (pH 8.0), giving a fluorescent compound that is stable for 2 h at 4 degrees C. Use of an internal standard improved the assay in accuracy and reliability. A programmable injector allowed automatic derivatization of large numbers of samples. Chromatographic separation was performed on a reversed-phase column (Capcell Pak C18) in which the silica gel was coated with silicone polymer. The peaks corresponding to compound I and the internal standard were eluted within 16 min with a mobile phase of acetonitrile-phosphate buffer (pH 7.1). The reliable limit of quantification was 0.5 pmol per injection (0.05 micrograms equivalents of L-DOPA per ml in plasma). The method was successfully applied for the measurements of dog plasma concentrations after oral dosing of compound I.
已开发出一种新型快速高效液相色谱法,用于测定L-3-(3-羟基-4-新戊酰氧基苯基)丙氨酸(NB-355,I),一种左旋多巴的新型前药。该方法包括在三乙醇胺缓冲液(pH 8.0)中,用邻苯二甲醛(OPA)和N-乙酰-L-半胱氨酸(NAC)对生物样品中的药物进行柱前衍生化,生成一种在4℃下2小时内稳定的荧光化合物。使用内标提高了测定的准确性和可靠性。可编程进样器可对大量样品进行自动衍生化。在硅胶涂覆有硅氧烷聚合物的反相柱(Capcell Pak C18)上进行色谱分离。化合物I和内标的峰在16分钟内用乙腈-磷酸盐缓冲液(pH 7.1)的流动相洗脱。定量可靠限为每次进样0.5皮摩尔(血浆中每毫升相当于0.05微克左旋多巴)。该方法成功应用于犬口服化合物I后的血浆浓度测定。