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在SPAPLUS™免疫比浊分析仪上对Freelite™人游离κ轻链和人游离λ轻链进行分析性能评估。

The analytical performance evaluation of Freelite™ Human Kappa Free and Human Lambda Free on the SPAPLUS™ immunoturbidimetric analyzer.

作者信息

Cha Kyong-Ho, Sim Yang Bo, Chae Hyojin, Park Hae-il, Kim Myungshin, Kim Yonggoo

机构信息

Department of Laboratory Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea.

出版信息

J Clin Lab Anal. 2014 May;28(3):229-36. doi: 10.1002/jcla.21671. Epub 2014 Jan 29.

Abstract

BACKGROUND

SPAPLUS™ is a turbidimetric immunoassay analyzer for detection of excess free light chain (FLC) antigens in serum. Here, we evaluated the analytical performance of Freelite™ Human Kappa Free and Lambda Free on a SPAPLUS™ instrument.

METHODS

We evaluated the precision, linearity, sample carryover, and drift of the SPAPLUS™ instrument and compared it with Hitachi 7600 and BN™ II instruments. We evaluated the detection of antigen excess for 12 specimens from patients with monoclonal gammopathy.

RESULTS

The coefficients of variations of κFLC and λFLC were below 5.0%. Linearity was shown in the range of 9.68-152.25 mg/l for κFLC and 4.96-171.09 mg/l for λFLC, and no drift was observed. The κFLC sample carryover was statistically significant, but much smaller than the optimum allowable bias. Agreement rates with the two comparative methods were 87.1, 87.1, and 97.1% or higher for κFLC, λFLC, and the κ/λ ratio, respectively. Antigen excess signals were observed for all 12 antigen excess specimens.

CONCLUSIONS

The Freelite™ on the SPAPLUS™ exhibited appropriate precision, linearity, and relative comparability to the reagents on the other instruments. It was good at detecting specimens that had previously demonstrated the hook effect due to antigen excess.

摘要

背景

SPAPLUS™是一种用于检测血清中过量游离轻链(FLC)抗原的比浊免疫分析仪器。在此,我们评估了Freelite™人κ游离轻链和λ游离轻链在SPAPLUS™仪器上的分析性能。

方法

我们评估了SPAPLUS™仪器的精密度、线性、样本携带污染和漂移,并将其与日立7600和BN™ II仪器进行比较。我们评估了12例单克隆丙种球蛋白病患者标本的抗原过量检测情况。

结果

κFLC和λFLC的变异系数均低于5.0%。κFLC的线性范围为9.68 - 152.25 mg/l,λFLC的线性范围为4.96 - 171.09 mg/l,且未观察到漂移。κFLC样本携带污染具有统计学意义,但远小于最佳允许偏差。与两种比较方法的符合率,κFLC、λFLC和κ/λ比值分别为87.1%、87.1%和97.1%或更高。所有12个抗原过量标本均观察到抗原过量信号。

结论

SPAPLUS™上的Freelite™表现出适当的精密度、线性,并且与其他仪器上的试剂具有相对可比性。它擅长检测先前因抗原过量而出现钩状效应的标本。

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