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Development of a test strip for rapid detection of lactoperoxidase in raw milk

机译:快速检测生乳中乳过氧化物酶的测试条的开发

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摘要

Traditional methods for detecting lactoperoxidase (LP) are complex and time-consuming, so a test strip was made based on the enzymatic reaction principle to enable quick and convenient detection of LP in raw milk. In this study 0.1 mol/L citric acid (CA)/0.2 mol/L disodium hydrogen phosphate (NaP) buffer solution (pH 5.0), 22 mmol/L 3,3',5,5'-tetramethylbenzidine (TMB), 0.6 mmol/L hydrogen peroxide (H2O2), and 0.5% Tween-20 or 0.3% cetyltrimethyl ammonium bromide (CTAB) were optimal for preparing a quick, sensitive, and accurate LP test strip. The coefficient of variation (CV) of the estimated LP concentrations ranged from 2.47% to 6.72% and the minimum LP concentration detected by the test strip was 1–2 mg/L. Estimates of active LP in sixteen raw milk samples obtained using the test strip or the TMB method showed a good correlation (r=0.9776). So the test strip provides a quick, convenient, and accurate method for detecting the LP concentration of raw milk.
机译:传统的检测乳过氧化物酶(LP)的方法复杂且耗时,因此,基于酶促反应原理制备了一个试纸,可以快速,方便地检测生乳中的LP。在本研究中,0.1 mol / L柠檬酸(CA)/0.2 mol / L磷酸氢二钠(NaP)缓冲溶液(pH 5.0),22 mmol / L 3,3',5,5'-四甲基联苯胺(TMB),0.6 mmol / L过氧化氢(H2O2)和0.5%Tween-20或0.3%十六烷基三甲基溴化铵(CTAB)是制备快速,灵敏和准确的LP试纸的最佳选择。估计LP浓度的变异系数(CV)为2.47%至6.72%,试纸检测到的最小LP浓度为1-2 mg / L。使用试纸条或TMB方法获得的16个原奶样品中的活性LP估计值显示出良好的相关性(r = 0.9776)。因此,试纸条提供了一种快速,方便且准确的方法来检测生乳中的LP浓度。

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