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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method.
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Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method.

机译:通过酶法终点法测定血清胆固醇的四种来源的胆固醇氧化酶的性能。

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BACKGROUND: Cholesterol oxidase is used for the determination of serum cholesterol. It can be derived from Streptomyces, Pseudomonas fluorescens, Cellulomonas, and Brevibacterium. This study compared the performance characteristics of four enzymes in the endpoint cholesterol determination. METHODS: Using the Mega analyzer, we studied assay optimization, linearity, precision, recovery, interference, stability, and compared 110 patient samples. RESULTS: The linearity for the four enzymes was up to 13.0 mmol/l at the optimal enzyme activity. The average within-run CVs ranged from 1.6% to 1.9% and between-day ranged from 2.8% to 3.0%, within the NCEP analytical criteria. The analytical recoveries obtained from four reagents ( approximately 96.5%) were excellent. The assays using these enzyme sources compared favorably with the commercial method and appeared accurate near the clinical decision cut-points. Hemoglobin concentration at 1.9 g/l interfered with the P. fluorescens cholesterol oxidase. Bilirubin caused a negative interference while lipemia generated a positive interference with all enzyme sources. Reagents were stable up to 6 weeks. CONCLUSIONS: Streptomyces, Cellulomonas, and Brevibacterium were essentially analytically equivalent. Streptomyces and Cellulomonas cholesterol oxidase are one-quarter as expensive Brevibacterium. Cellulomonas is a new source of cholesterol oxidase for determining serum cholesterol by the endpoint method.
机译:背景:胆固醇氧化酶用于测定血清胆固醇。它可以衍生自链霉菌,荧光假单胞菌,纤维单胞菌和短杆菌属。这项研究比较了四种酶在终点胆固醇测定中的性能特征。方法:使用Mega分析仪,我们研究了分析的优化,线性,精度,回收率,干扰,稳定性,并比较了110个患者样品。结果:在最佳酶活性下,四种酶的线性最高可达13.0 mmol / l。在NCEP分析标准内,平均运行中CV范围为1.6%至1.9%,日间范围为2.8%至3.0%。从四种试剂(约96.5%)获得的分析回收率极高。使用这些酶源的测定与商业方法相比具有优势,并且在临床决策切点附近显得准确。 1.9 g / l的血红蛋白浓度干扰了荧光假单胞菌胆固醇氧化酶。胆红素引起负面干扰,而血脂对所有酶源产生积极干扰。试剂稳定至6周。结论:链霉菌,纤维单胞菌和短杆菌属在分析上基本相同。链霉菌和纤维单胞菌胆固醇氧化酶是昂贵的短杆菌的四分之一。纤维单胞菌素是通过终点法测定血清胆固醇的胆固醇氧化酶的新来源。

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