人血清中Hepcidin-25自动ELISA检测方法的验证

T. Rolić, S. Mandić, I. Lukic, V. Horvat, I. Banjari
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引用次数: 0

摘要

hepcidin -25是hepcidin的生物活性形式,是调节铁稳态的主蛋白。不同方法测定的血清浓度往往无法比较,且结果解释复杂。材料和方法:目的是验证第一个全自动酶联免疫吸附测定(ELISA)方法,使用DRG Hybrid XL分析仪(DRG Instruments, Marburg, Germany)与质谱法标准化。使用市售的低(C1)和高(C2)浓度对照,进行了测定内(CVi)和测定间(CVg)的精度和偏倚。通过分析20名健康男性的血清样本,验证了参考区间。结果:CVi = 9.1% (C1), 4.5% (C2);CVg = 8.9% (C1), 5.6% (C2);C1和C2的计算偏差分别为33%和20%。结论:全自动ELISA检测血清中hepcidin-25的方法在DRG Hybrid XL分析仪上验证符合分析验收标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Verification of the Automated ELISA Assay for Hepcidin-25 in Human Serum
Introduction: Hepcidin-25, the bioactive form of hepcidin, is the master protein in regulating iron homeostasis. Serum concentrations, measured by different methods, are often incomparable and complicate results interpretation.Materials and Methods: The aim was to verify the first fully automated enzyme-linked immunosorbent assay (ELISA) method, using the DRG Hybrid XL analyzer (DRG Instruments, Marburg, Germany) standardized against the mass spectrometry method. Intra- (CVi) and inter-assay (CVg) precision and bias were performed using commercially available controls with low (C1) and high (C2) concentrations. The reference interval was verified by analyzing serum samples of 20 healthy males.Results: CVi = 9.1% (C1), 4.5% (C2); CVg = 8.9% (C1), 5.6% (C2); calculated bias was 33% for C1 and 20% for C2, respectively.Conclusion: Verification of the fully automated ELISA method for hepcidin-25 in serum on the DRG Hybrid XL analyzer met the analytical acceptance criteria.
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