Huebner G H, Huebner G I, Weiss M
Department of Pharmacology, Martin Luther University Halle-Wittenberg, Germany.
Ther Drug Monit. 1996 Oct;18(5):620-3. doi: 10.1097/00007691-199610000-00016.
The standard enzymatic assay for quantification of D-sorbitol in plasma was adapted to the automatic analyzer Cobas Mira S. In the assay, NAD (reagent) in the presence of sorbitoldehydrogenase (SDH; start reagent) converts D-sorbitol to fructose with formation of NADH, which was detected automatically as the difference between the first and last readings at 340 nm. The sample blank values for each specimen were subtracted to exclude both endogenous D-sorbitol and sugars, which also react as substrates for SDH. The method is simple, rapid (40 samples/h), precise down to endogenous concentrations (coefficient of variation < 5%; limit of determination: 0.38 mg/L) and linear up to 100 mg/L. Samples with higher D-sorbitol concentrations were estimated after dilution. The method was used to measure disposition curves of sorbitol in volunteers after a single intravenous dose of 0.8 g sorbitol.
血浆中D-山梨醇定量的标准酶法被应用于自动分析仪Cobas Mira S。在该检测中,在山梨醇脱氢酶(SDH;起始试剂)存在的情况下,NAD(试剂)将D-山梨醇转化为果糖并生成NADH,NADH在340nm处的首次和末次读数之差被自动检测出来。每个样本的样本空白值被减去,以排除内源性D-山梨醇和糖类,它们也作为SDH的底物发生反应。该方法简单、快速(每小时40个样本),对内源性浓度精确(变异系数<5%;测定限:0.38mg/L),在高达100mg/L时呈线性。D-山梨醇浓度较高的样本在稀释后进行测定。该方法用于测量志愿者单次静脉注射0.8g山梨醇后山梨醇的处置曲线。