Upreti G C
Anal Biochem. 1984 Mar;137(2):485-92. doi: 10.1016/0003-2697(84)90117-9.
A simple method of inorganic phosphate determination for colored and/or turbid biological samples is described. The procedure is mild, and so is suitable for routine phosphohydrolase assays. Following deproteinization by ice-cold trichloroacetic (or silicotungstic) acid, the sample was treated with acid-washed charcoal to remove interference due to color. The phosphate in the colorless supernatant was assayed either by measuring the phosphomolybdate spectrophotometrically at 310 nm, following its extraction in organic solvents or by a modified Fiske and Subbarow method. The turbidity interference in the latter case was eliminated either by centrifugation, by sodium dodecyl sulfate treatment, or by extraction of reduced phosphomolybdate blue color by cyclohexanone. Though deproteinization by silicotungstic acid eliminated the turbidity problem, its use in conjunction with charcoal treatment was not convenient.
本文描述了一种用于测定有色和/或浑浊生物样品中无机磷酸盐的简单方法。该方法温和,适用于常规磷酸水解酶分析。用冰冷的三氯乙酸(或硅钨酸)进行脱蛋白处理后,样品用酸洗过的活性炭处理以去除颜色干扰。无色上清液中的磷酸盐可通过以下两种方法测定:一是在有机溶剂中萃取后,于310 nm处用分光光度法测定磷钼酸盐;二是采用改良的Fiske和Subbarow方法。在后一种情况下,通过离心、十二烷基硫酸钠处理或用环己酮萃取还原的磷钼酸蓝颜色来消除浊度干扰。虽然用硅钨酸脱蛋白消除了浊度问题,但将其与活性炭处理结合使用并不方便。