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首页> 外文期刊>Annals of laboratory medicine. >Development and Evaluation of an Immunoglobulin Y-Based ELISA for Measuring Prostate Specific Antigen in Human Serum
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Development and Evaluation of an Immunoglobulin Y-Based ELISA for Measuring Prostate Specific Antigen in Human Serum

机译:基于免疫球蛋白Y的ELISA检测人体血清前列腺特异性抗原的开发和评估

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Background: Measurement of serum prostate specific antigen (PSA) concentrations remains one of the leading methods for diagnosing prostate cancer. We developed and evaluated an immunoglobulin Y (IgY)-based ELISA to measure total PSA (tPSA) concentrations in human serum that could be used as an alternative to commercially available in vitro diagnostic assays that rely on mouse monoclonal IgG. Methods: A sandwich ELISA based on an anti-PSA IgY antibody was developed. We evaluated the ability of the anti-PSA IgY antibody to detect free and complexed PSA at the same molar ratio. The assay was optimized, and its analytical performance was verified by calculating limit of background (LoB), limit of detection (LoD), and limit of quantification (LoQ). We performed correlation and regression analyses between tPSA concentrations measured by our ELISA and those from commercial assays: Cobas 6000 (Roche Diagnostics, Warszawa, Poland) and PSA total ELISA (IBL International, Hamburg, Germany). Results: LoB, LoD, and LoQ, were 0.061, 0.083, and 0.100 ng/mL, respectively, and linearity range was 0.100–3.375 ng/mL. tPSA concentrations from our IgY-based ELISA strongly correlated with those from the commercial assays. Conclusions: Our IgY-based ELISA is an efficient equivalent to the above commercial assays. The use of IgY as the detecting agent could reduce the risk of false positive results, as well as decrease the overall cost of analysis.
机译:背景:血清前列腺特异性抗原(PSA)浓度的测量仍然是诊断前列腺癌的主要方法之一。我们开发并评估了一种基于免疫球蛋白Y(IgY)的ELISA试剂盒,以测量人血清中的总PSA(tPSA)浓度,可以用作依赖小鼠单克隆IgG的体外诊断方法的替代方法。方法:建立了基于抗PSA IgY抗体的夹心ELISA。我们评估了抗PSA IgY抗体在相同摩尔比下检测游离和复合PSA的能力。优化了测定方法,并通过计算背景极限(LoB),检测极限(LoD)和定量极限(LoQ)验证了其分析性能。我们对通过ELISA测定的tPSA浓度与商业测定的tPSA浓度之间进行了相关性和回归分析:Cobas 6000(Roche Diagnostics,华沙,波兰)和PSA总ELISA(IBL International,汉堡,德国)。结果:LoB,LoD和LoQ分别为0.061、0.083和0.100 ng / mL,线性范围为0.100-3.375 ng / mL。我们基于IgY的ELISA中的tPSA浓度与商业化检测中的浓度高度相关。结论:我们的基于IgY的ELISA与上述商业化测定有效等效。使用IgY作为检测剂可以降低假阳性结果的风险,并降低总体分析成本。

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