首页> 外文期刊>Applied biochemistry and biotechnology, Part A. enzyme engineering and biotechnology >The Rapid and Sensitive Quantitative Determination of Galactose by Combined Enzymatic and Colorimetric Method: Application in Neonatal Screening
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The Rapid and Sensitive Quantitative Determination of Galactose by Combined Enzymatic and Colorimetric Method: Application in Neonatal Screening

机译:酶联比色法快速灵敏定量测定半乳糖:在新生儿筛查中的应用

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摘要

The quantitative measurement of galactose in blood is essential for the early diagnosis, treatment, and dietary monitoring of galactosemia patients. In this communication, we aimed to develop a rapid, sensitive, and cost-effective combined method for galactose determination in dry blood spots. This procedure was based on the combination of enzymatic reactions of galactose dehydrogenase (GalDH), dihydrolipoyl dehydrogenase (DLD), and alkaline phosphates with a colorimetric system. The incubation time and the concentration of enzymes used in new method were also optimized. The analytical performance was studied by the precision, recovery, linearity, and sensitivity parameters. Statistical analysis was applied to method comparison experiment. The regression equation and correlation coefficient (R (2)) were Y = 0.0085x + 0.032 and R (2) = 0.998, respectively. This assay exhibited a recovery in the range of 91.7-114.3 % and had the limit detection of 0.5 mg/dl for galactose. The between-run coefficient of variation (CV) was between 2.6 and 11.1 %. The within-run CV was between 4.9 and 9.2 %. Our results indicated that the new and reference methods were in agreement because no significant biases exist between them. Briefly, a quick and reliable combined enzymatic and colorimetric assay was presented for application in newborn mass screening and monitoring of galactosemia patients.
机译:血液中半乳糖的定量测量对于半乳糖血症患者的早期诊断,治疗和饮食监测至关重要。在此交流中,我们旨在开发一种快速,灵敏且经济高效的联合方法来测定干血斑中的半乳糖。该程序基于半乳糖脱氢酶(GalDH),二氢脂酰脱氢酶(DLD)和碱性磷酸盐的酶促反应与比色系统的组合。还优化了新方法的孵育时间和酶浓度。通过精密度,回收率,线性和灵敏度参数研究了分析性能。统计分析应用于方法比较实验。回归方程和相关系数(R(2))分别为Y = 0.0085x + 0.032和R(2)= 0.998。该测定法的回收率在91.7-114.3%范围内,半乳糖的极限检测值为0.5 mg / dl。行程间变异系数(CV)在2.6和11.1%之间。批内CV在4.9%和9.2%之间。我们的结果表明,新方法和参考方法是一致的,因为它们之间没有明显的偏差。简而言之,提出了一种快速,可靠的酶法和比色法联合检测方法,用于半乳糖血症患者的新生儿大规模筛查和监测。

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