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斑点印迹免疫分析法测定纳米粒子补体调理作用的验证。

Validation of dot blot immunoassay for measurement of complement opsonization of nanoparticles.

机构信息

Department of Pharmaceutical Sciences, The Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Department of Emergency Medicine, the University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

出版信息

J Immunol Methods. 2024 May;528:113668. doi: 10.1016/j.jim.2024.113668. Epub 2024 Apr 2.

Abstract

Complement plays a critical role in the immune response toward nanomaterials. The complement attack on a foreign surface results in the deposition of C3, assembly of C3 convertases, the release of anaphylatoxins C3a and C5a, and finally, the formation of membrane attack complex C5b-9. Various technologies can measure complement activation markers in the fluid phase, but measurements of surface C3 deposition are less common. Previously, we developed an ultracentrifugation-based dot blot immunoassay (DBI) to measure the deposition of C3 and other protein corona components on nanoparticles. Here, we validate the repeatability of the DBI and its correlation with pathway-specific and common fluid phase markers. Moreover, we discuss the advantages of DBI, such as cost-effectiveness and versatility, while addressing potential limitations. This study provides insights into complement activation at the nanosurface level, offering a valuable tool for nanomedicine researchers in the field.

摘要

补体在针对纳米材料的免疫反应中起着关键作用。补体对异物表面的攻击导致 C3 的沉积、C3 转化酶的组装、过敏毒素 C3a 和 C5a 的释放,以及最终膜攻击复合物 C5b-9 的形成。各种技术可用于测量体液中的补体激活标志物,但表面 C3 沉积的测量则不太常见。此前,我们开发了一种基于超速离心的点印迹免疫测定法(DBI)来测量 C3 及其他蛋白冠成分在纳米颗粒上的沉积。在这里,我们验证了 DBI 的可重复性及其与特定途径和常见体液标志物的相关性。此外,我们还讨论了 DBI 的优势,如成本效益和多功能性,同时也探讨了其潜在的局限性。本研究深入了解了纳米表面水平的补体激活,为纳米医学研究人员提供了一个有价值的工具。

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