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开发一种 Abbott ARCHITECT 环孢素免疫分析法,无代谢物交叉反应。

Development of an Abbott ARCHITECT cyclosporine immunoassay without metabolite cross-reactivity.

机构信息

Abbott Diagnostics, Abbott Park, IL 60064, USA.

出版信息

Clin Biochem. 2010 Sep;43(13-14):1152-7. doi: 10.1016/j.clinbiochem.2010.06.007. Epub 2010 Jun 21.

Abstract

OBJECTIVE

We investigated the mechanism by which the ARCHITECT cyclosporine (CsA) chemiluminescent microparticle immunoassay (CMIA) eliminates cross-reactivity to CsA metabolites AM1 and AM9, despite its use of a monoclonal antibody which shows cross-reactivity in fluorescence polarization immunoassays.

DESIGN AND METHODS

The CMIA was accomplished by incubating an extracted blood sample with magnetic microparticles coated with a very low amount of anti-CsA antibody. After a wash step the microparticles were incubated with a chemiluminescent CsA tracer, followed by a second wash step and measurement of chemiluminescence. The reagent concentrations of salt and detergent were optimized to maximize CsA binding and minimize metabolite interference.

RESULTS

Elimination of CsA metabolite cross-reactivity was shown using purified metabolites and blood samples containing native CsA metabolites. The CMIA demonstrated precision and sensitivity acceptable for use in a clinical setting.

CONCLUSION

We conclude that it is possible to eliminate CsA metabolite immuno-cross-reactivity by careful assay design.

摘要

目的

我们研究了 ARCHITECT 环孢素(CsA)化学发光微粒子免疫分析(CMIA)消除与 CsA 代谢物 AM1 和 AM9 交叉反应的机制,尽管它使用的单克隆抗体在荧光偏振免疫分析中显示出交叉反应。

设计和方法

CMIA 通过将提取的血液样本与涂有极低量抗 CsA 抗体的磁性微粒子孵育来完成。在洗涤步骤后,将微粒子与化学发光 CsA 示踪剂孵育,然后进行第二次洗涤步骤并测量化学发光。优化了盐和洗涤剂的试剂浓度,以最大限度地提高 CsA 结合并最小化代谢物干扰。

结果

使用纯化的代谢物和含有天然 CsA 代谢物的血液样本证明了消除 CsA 代谢物免疫交叉反应的效果。CMIA 表现出可接受的临床应用的精密度和灵敏度。

结论

我们得出结论,通过仔细的测定设计,可以消除 CsA 代谢物的免疫交叉反应。

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