Togari A, Sakai J, Matsumoto S, Nagatsu T
J Chromatogr. 1987 Jun 5;417(1):41-6. doi: 10.1016/0378-4347(87)80089-0.
A highly sensitive and specific assay for alkaline and acid phosphatases in biological materials, such as plasma and saliva, has been established. Phenol, formed enzymatically from the substrate phenylphosphate, was determined by high-performance liquid chromatography with electrochemical detection. The retention time of phenol was 7 min and no other peaks were observed. The method is rapid and sensitive with a detection limit for phenol of as little as 5 pmol. Thus, as little as 0.5 microliter of rat plasma or 10 microliters of human saliva is required for both alkaline and acid phosphatase assays. The assay is accurate and reproducible. Using this assay, alkaline and acid phosphatase activities in saliva were found to be 1.12 +/- 0.12 nmol/min/ml and 9.79 +/- 1.23 nmol/min/ml, respectively. This new assay method should be applicable to extremely small biological samples.
已建立一种用于检测生物材料(如血浆和唾液)中碱性磷酸酶和酸性磷酸酶的高灵敏度、高特异性检测方法。通过高效液相色谱-电化学检测法测定由底物磷酸苯酯酶促生成的苯酚。苯酚的保留时间为7分钟,未观察到其他峰。该方法快速、灵敏,苯酚的检测限低至5皮摩尔。因此,碱性磷酸酶和酸性磷酸酶检测分别只需0.5微升大鼠血浆或10微升人唾液。该检测方法准确且可重复。使用此检测方法,发现唾液中碱性磷酸酶和酸性磷酸酶的活性分别为1.12±0.12纳摩尔/分钟/毫升和9.79±1.23纳摩尔/分钟/毫升。这种新的检测方法应适用于极小的生物样本。