Petrarulo M, Facchini P, Cerelli E, Marangella M, Linari F
Renal Stone Laboratory, Mauriziano Umberto I Hospital, Turin, Italy.
Clin Chem. 1995 Oct;41(10):1518-21.
An enzyme-spectrophotometric method to determine citrate in biological fluids is proposed, based on citrate lyase-catalyzed and phenylhydrazine reactions. The enzyme converts citrate into oxaloacetate, which, in the presence of phenylhydrazine, is transformed into the corresponding phenylhydrazone. The ultraviolet-absorbing product is determined by absorbance measurement at 330 nm. The method is more precise and twice as sensitive as the traditional citrate lyase method and, because it does not require the use of additional enzymes and coenzymes, is cheaper and simpler. Mean analytical recovery of citrate averaged 100.7% +/- 2.2%, imprecision (CV) of the assay for citrate at 0.96 mmol/L (urine) was 2.0%, and the lower limit of quantification was 0.08 mmol/L. Results correlated well with those by both ion-chromatographic and traditional citrate lyase methods.
本文提出了一种基于柠檬酸裂解酶催化和苯肼反应的酶分光光度法来测定生物体液中的柠檬酸盐。该酶将柠檬酸盐转化为草酰乙酸,在苯肼存在的情况下,草酰乙酸会转化为相应的苯腙。通过在330nm处测量吸光度来测定具有紫外吸收的产物。该方法比传统的柠檬酸裂解酶法更精确,灵敏度提高了一倍,并且由于不需要使用额外的酶和辅酶,因此更便宜、更简单。柠檬酸盐的平均分析回收率为100.7%±2.2%,0.96mmol/L(尿液)柠檬酸盐测定的不精密度(CV)为2.0%,定量下限为0.08mmol/L。结果与离子色谱法和传统柠檬酸裂解酶法的结果相关性良好。