Cumulative IgG reagent carryover detected in carryover evaluation of urinary total protein testing using AU5800 biochemistry analyzer.

IF 1.8
Biochemia medica Pub Date : 2025-06-15 Epub Date: 2025-04-15 DOI:10.11613/BM.2025.020702
Jialu Li, Guoxiang Bao
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Abstract

Introduction: Accurate measurement of urinary total protein (UTP) is crucial for diagnosing renal and systemic diseases. This study aims to comprehensively evaluate potential carryover scenarios in UTP testing using AU5800 biochemistry analyzer and to identify factors influencing assay accuracy.

Materials and methods: High-concentration quality control materials and pure water was used to evaluate specific sample probe carryover. Additionally, 24-hour mixed urine samples from patients were used to evaluate specific carryover from the reagent probe, mixbars, and cuvettes. For cumulative sample carryover evaluation, pure water was used as reagent and mixed serum as sample for continuous testing. During the process, 24-hour urine samples were interspersed, and UTP concentrations were measured at 0, 10, 20, and 30 minutes. Cumulative reagent carryover was evaluated by testing pure water sequentially with eight reagents sharing the same analytical unit and inner cuvettes as UTP, with UTP concentrations of 24-hour urine samples recorded at 0, 10, 20, and 30 minutes.

Results: Specific carryover from the sample probe, reagent probe, mixbars, and cuvettes was not detected during carryover evaluation of UTP testing. However, a significant cumulative reagent carryover of Immunoglobulin G (IgG) reagent was observed, while no cumulative sample carryover was identified.

Conclusions: The full range of possible carryover scenarios in UTP testing was evaluated using AU5800 biochemistry analyzer. Our data provide valuable references for evaluating carryover in laboratories, ensuring the accuracy and reliability of laboratory results.

AU5800生化分析仪检测尿总蛋白携带评价中的累积IgG试剂携带。
尿总蛋白(UTP)的准确测定对肾脏和全身性疾病的诊断至关重要。本研究旨在综合评价AU5800生化分析仪检测UTP的潜在携带情况,并确定影响检测准确性的因素。材料与方法:采用高浓度质控材料和纯净水评价特定样品探针携带率。此外,24小时患者混合尿液样本用于评估试剂探针、混合棒和比色皿的特异性携带。累积留样评价以纯净水为试剂,混合血清为样品连续检测。在此过程中,将24小时尿液样本分散,并在0、10、20和30分钟测量UTP浓度。累积试剂携带量通过连续测试纯水来评估,使用8种试剂共享相同的分析单元和与UTP相同的内比色皿,并记录24小时尿液样本在0,10,20和30分钟的UTP浓度。结果:在UTP检测的携带性评估中,未检测到样品探针、试剂探针、混合棒和试管的特定携带性。然而,观察到免疫球蛋白G (IgG)试剂的显著累积携带,而未发现累积样本携带。结论:使用AU5800生化分析仪对UTP检测中可能的携带情况进行了全面评估。我们的数据为实验室结转评价提供了有价值的参考,保证了实验室结果的准确性和可靠性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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