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高效液相色谱法测定血浆中NG-硝基-L-精氨酸和NG-硝基-L-精氨酸甲酯

Determination of NG-nitro-L-arginine and NG-nitro-L-arginine methyl ester in plasma by high-performance liquid chromatography.

作者信息

Whiting M J, Rutten A J, Williams P, Bersten A D

机构信息

Department of Biochemistry and Chemical Pathology, Flinders Medical Centre, Adelaide, Australia.

出版信息

J Chromatogr B Biomed Appl. 1994 Oct 3;660(1):170-5. doi: 10.1016/0378-4347(94)00257-6.

Abstract

An HPLC method has been developed for the measurement of the nitric oxide synthase inhibitors, NG-nitro-L-arginine (L-NOLA) and NG-nitro-L-arginine methyl ester (L-NAME), in sheep plasma. Using an ion-exchange HPLC column (JWAS 150, 100 x 3.9 mm I.D., Millipore-Waters, Australia) and post-column ninhydrin detection, L-NOLA was separated from valine and other plasma amino acids. When added to sheep plasma, good recovery (mean 102%) and precision (mean coefficient of variation 2.7%) in the measurement of L-NOLA was obtained over the range 2-50 mg/l. L-NAME was unstable in sheep plasma at 37 degrees C, and was converted to L-NOLA with a half-life of 250 min. This method will permit pharmacokinetic parameters to be determined for these potential drugs, and will allow plasma drug concentrations to be correlated with the pharmacodynamic effects of these compounds.

摘要

已开发出一种高效液相色谱(HPLC)方法,用于测定绵羊血浆中的一氧化氮合酶抑制剂NG-硝基-L-精氨酸(L-NOLA)和NG-硝基-L-精氨酸甲酯(L-NAME)。使用离子交换HPLC柱(JWAS 150,内径100×3.9 mm,澳大利亚密理博-沃特世公司)和柱后茚三酮检测,L-NOLA与缬氨酸及其他血浆氨基酸得以分离。当添加到绵羊血浆中时,在2-50 mg/l范围内测定L-NOLA时,回收率良好(平均102%)且精密度高(平均变异系数2.7%)。L-NAME在37℃的绵羊血浆中不稳定,会转化为L-NOLA,半衰期为250分钟。该方法将能够确定这些潜在药物的药代动力学参数,并使血浆药物浓度与这些化合物的药效学效应相关联。

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