干血斑中总半乳糖的测定——ce标记试剂盒的广泛测定评价

R. Fingerhut, T. Torresani
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引用次数: 3

摘要

大多数新生儿筛查实验室使用ce标记或fda批准的检测试剂盒,就像常规临床化学一样。如果检测试剂盒按照制造商指定的方式使用,国家法规只要求客户进行最低限度的评估。基于微量滴度的试剂盒概念通常是基于这样一种观念,即实验室总是处理整个微量滴度板。然而,在日常工作中,这是一个相当罕见的例外,这导致每个新生儿的成本远高于检测试剂盒中每次检测的成本。此外,浪费资源的数量相当高。测试了Perkin Elmer公司新生儿总半乳糖试剂盒的性能。确定了特异性、检出限(LOD)、定量限(LOQ)、组内和组间变异、回收率、测量信号和试剂的稳定性。结果还与阿斯托利亚太平洋抽查系统进行了比较。此外,我们(偶然)有机会测试2个已经过期超过3年的套件。根据LOD/LOQ的定义,LOD为165 ~ 306 μmol/L, LOQ为475 ~ 703 μmol/L。在220、590、1200和2060 μmol/L下,平均回收率为112.8%,法内CVs分别为11.3、7.3、4.0和3.0,法间CVs分别为28.7、15.9、7.8和9.3。重组和混合试剂必须在几小时内使用,即使在-20℃下保存也不稳定。而若将重组半乳糖底物试剂与半乳糖氧化酶试剂仅按日用量混合,其余分别在-20℃下单独存放,则至少能稳定存放12天。过期测试包的性能与其他测试包没有区别。总半乳糖试剂盒的性能可与用于新生儿筛查的其他测试相媲美。然而,通过彻底验证和修改分析程序,我们可以显著降低每个新生儿的成本并减少不必要的废物产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of total galactose from dried blood spots—extensive assay evaluation of a CE-marked test-kit
Most newborn screening laboratories use CE-marked or FDA-approved test-kits, like in routine clinical chemistry. National regulations require only minimal evaluation from the customer, if the test-kits are used as specified by the manufacturer. The microtiter-based kit-concept is often based on the perception, that the laboratory always processes whole microtiter plates. However, in the daily routine, this is rather a rare exception, which leads to much higher costs per newborn, compared to the costs per assay in the test-kits. In addition the amount of wasted resources is quite high. Performance of the Neonatal Total Galactose kit from Perkin Elmer was tested. We have determined specificity, limit of detection (LOD), limit of quantitation (LOQ), intra and inter assay variation, recovery, stability of measuring signal and reagents. Results were also compared with the Astoria Pacific Spot Check System. In addition, we had (by chance) the opportunity to test 2 kits, which were already expired for more than 3 years. LOD was 165 - 306 μmol/L and LOQ 475 - 703 μmol/L, depending on the definition of LOD/LOQ. Mean recovery was 112.8%, intra assay CVs were 11.3, 7.3, 4.0, and 3.0, and inter assay CVs 28.7, 15.9, 7.8, and 9.3, at 220, 590, 1200, and 2060 μmol/L respectively. Reconstituted and mixed reagents must be used within some hours, and were unstable even if stored at -20℃. However, if the reconstituted galactose substrate reagent and galactose oxidase reagent were only mixed according to the daily requirements, and the rest stored separately at -20℃, they were stable for at least 12 days. The performance of the expired test-kits did not differ from the others. The performance of the Total Galactose kit is comparable to other tests used for newborn screening. However, we could significantly reduce the costs per newborn and reduce unnecessary production of waste, by thorough validation and modification of the assay procedures.
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