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Negative interference of icteric serum on a bichromatic biuret total protein assay.

机译:黄疸血清对双色缩二脲总蛋白测定的负面影响。

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摘要

Background: Bilirubin is stated to be a negative interferent in some biuret assays and thus could contribute to pseudohypoproteinemia in icteric samples.Objective: The purpose of the study was to evaluate the magnitude of and reason for a falsely low total protein concentration in icteric serum when the protein concentration is measured with a bichromatic spectrophotometric biuret assay.Methods: Commercially available bilirubin was dissolved in 0.1 M NaOH and then mixed with sera from 2 dogs to achieve various bilirubin concentrations of up to 40 mg/dL (first set of samples) and 35 mg/dL (second set of samples, for confirmation of first set of results and to explore the interference). Biuret total protein and bilirubin concentrations were determined with a chemistry analyzer (Cobas® 6000 with c501 module). Line graphs were drawn to illustrate the effects of increasing bilirubin concentrations on the total protein concentrations. Specific spectrophotometric absorbance readings were examined to identify the reason for the negative interference.Results: High bilirubin concentrations created a negative interference in the Cobas biuret assay. The detectable interference occurred with a spiked bilirubin concentration of 10.7 mg/dL in one set of samples and 20.8 mg/dL in a second set. The interference was due to a greater secondary absorbance reading at the second measuring point in the samples spiked with bilirubin, which possibly had converted to biliverdin.Conclusion: Marked hyperbilirubinemia is associated with a falsely low serum total protein concentrations when measured with a bichromatic spectrophotometric biuret assay. This can result in pseudohypoproteinemia and pseudohypoglobulinemia in icteric serum.
机译:背景:胆红素在某些缩二脲测定中被认为是阴性干扰物,因此可能导致黄疸样品中的假性低蛋白血症。目的:本研究的目的是评估黄疸时总血清中总蛋白浓度虚假降低的程度和原因。方法:将市售的胆红素溶解在0.1 M NaOH中,然后与来自两只狗的血清混合,以达到高达40 mg / dL的各种胆红素浓度(第一批样品),并通过双色分光光度法测定两种样品中的蛋白质浓度。 35 mg / dL(第二组样品,用于确认第一组结果并探讨干扰)。使用化学分析仪(带有c501模块的Cobas®6000)测定缩二脲总蛋白和胆红素的浓度。绘制线图以说明增加胆红素浓度对总蛋白浓度的影响。检查特定的分光光度法吸光度读数,以确定产生负干扰的原因。结果:高胆红素浓度在Cobas缩二脲测定法中产生了负干扰。可检测到的干扰发生在一组样品中的胆红素浓度为10.7 mg / dL,而在第二组样品中为20.8 mg / dL。干扰是由于加标了胆红素的样品中第二个测量点的二级吸光度读数较高,该样品可能已转化为胆绿素。结论:当使用双色分光光度计双缩脲测定时,明显的高胆红素血症与血清总蛋白浓度错误地相关。分析。这可能会导致黄疸血清中的伪低蛋白血症和伪低球蛋白血症。

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