Dean H G, Bonser J C, Gent J P
Department of Pharmacology, University of Leeds, U.K.
Clin Chem. 1989 Sep;35(9):1945-8.
Two methods are described for determination of octanoic and decanoic acids in plasma and brain homogenate by "high-performance" liquid chromatography with ultraviolet detection. Analysis of the underivatized acids had a detection limit of only 50 mg/L, but formation of the p-bromophenacyl ester increased the sensitivity by 100-fold, to a detection limit of 0.5 mg/L. The latter procedure gave interassay coefficients of variation of 4.1% and 4.8% for octanoic and decanoic acids, respectively. The corresponding intra-assay values were 3.95% and 4.7% (n = 6). The derivative method, applied to samples of plasma from children receiving a medium-chain triglyceride (MCT) diet, gave values in agreement with results by gas-liquid chromatography. Results have also been obtained for samples from mice, either treated with the medium-chain triglyceride diet or given infusions of sodium octanoate.
本文描述了两种通过带紫外检测的“高效”液相色谱法测定血浆和脑匀浆中辛酸和癸酸的方法。对未衍生化的酸进行分析时,检测限仅为50mg/L,但对溴苯甲酰酯的形成使灵敏度提高了100倍,检测限达到0.5mg/L。后一种方法对辛酸和癸酸的批间变异系数分别为4.1%和4.8%。相应的批内变异值分别为3.95%和4.7%(n = 6)。将衍生化方法应用于接受中链甘油三酯(MCT)饮食的儿童的血浆样本,得到的值与气液色谱法的结果一致。对于用中链甘油三酯饮食处理或输注辛酸钠的小鼠样本,也已获得结果。