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基于泮库溴铵对胆碱酯酶的抑制作用对其动力学测定方法的一种改进。

A modification of the kinetic determination of pancuronium bromide based on its inhibitory effect on cholinesterase.

作者信息

Stankov-Jovanovic V P, Nikolic-Mandic S D, Mandic Lj M, Mitic V D

机构信息

Faculty of Science and Mathematics, Department of Chemistry, University of Nis Visegradska, Nis, Serbia.

出版信息

J Clin Lab Anal. 2007;21(2):124-31. doi: 10.1002/jcla.20162.

Abstract

A modification of the existing spectrophotometric kinetic method for the determination of pancuronium bromide (PCBr), based on pooled human serum cholinesterase (ChE, EC 3.1.1.8 acylcholine acylhydrolase) inhibition, was developed. Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as substrate and determination was performed at pH 7.6. Essential basic kinetic parameters were also determined: Michaelis-Menten's constant KM=0.33 mmol/L, maximal reaction rate Vmax=42.29 micromol/L min, inhibition constant KI=0.34 micromol/L, and IC50=0.235 micromol/L. Linear dependence between the reaction rate and the inhibitor concentration exists in PCBr concentration range 8.29-265.28 nmol/L, which corresponds to the real sample concentrations from 0.166 to 5.306 micromol/L. The method detection limit was established to be 1.86 nmol/L and the quantification limit was 6.18 nmol/L. Precision of the method was tested for three pancuronium concentrations (16.58, 99.48, and 198.96 nmol/L). The relative standard deviation (RSD) was in the range 0.78-5.13%. Accuracy was examined by the standard addition method. The influence of substances usually present in serum and urine on the reaction rate was determined. The method developed was applied for PCBr determination in spiked serum and urine samples and in the urine taken during surgery. The method was proven to have good sensitivity, accuracy, and precision and can be considered suitable for clinical practice.

摘要

基于人血清胆碱酯酶(ChE,EC 3.1.1.8 酰基胆碱酰基水解酶)抑制作用,开发了一种用于测定泮库溴铵(PCBr)的现有分光光度动力学方法的改进方法。碘化丁酰硫代胆碱(浓度为 1.667 mmol/L)用作底物,在 pH 7.6 条件下进行测定。还测定了基本的动力学参数:米氏常数 KM = 0.33 mmol/L,最大反应速率 Vmax = 42.29 μmol/L·min,抑制常数 KI = 0.34 μmol/L,半数抑制浓度 IC50 = 0.235 μmol/L。在 8.29 - 265.28 nmol/L 的 PCBr 浓度范围内,反应速率与抑制剂浓度呈线性关系,这对应于实际样品浓度为 0.166 至 5.306 μmol/L。该方法的检测限确定为 1.86 nmol/L,定量限为 6.18 nmol/L。对三种泮库溴铵浓度(16.58、99.48 和 198.96 nmol/L)测试了该方法的精密度。相对标准偏差(RSD)在 0.78 - 5.13%范围内。通过标准加入法检验了准确度。测定了血清和尿液中通常存在的物质对反应速率的影响。所开发的方法应用于加标血清和尿液样品以及手术期间采集的尿液中 PCBr 的测定。该方法被证明具有良好的灵敏度、准确度和精密度,可认为适用于临床实践。

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