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蛋白 G'-接枝介孔硅纳米粒子的孔径对作为体外过敏诊断的血清预处理系统的影响。

Influence of Pore Size in Protein G'-Grafted Mesoporous Silica Nanoparticles as a Serum Pretreatment System for In Vitro Allergy Diagnosis.

机构信息

Allergy Research Group, Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma BIONAND. RICORS "Enfermedades inflamatorias", Málaga, 29590, Spain.

Facultad de Ciencias, Universidad de Málaga, Málaga, 29010, Spain.

出版信息

Adv Healthc Mater. 2023 Jun;12(15):e2203321. doi: 10.1002/adhm.202203321. Epub 2023 Mar 8.

DOI:10.1002/adhm.202203321
PMID:36847336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11468951/
Abstract

Particles with the capacity to bind to immunoglobulin G (IgG) can be used for the purification of IgG or to process clinical samples for diagnostic purposes. For in vitro allergy diagnosis, the high IgG levels in serum can interfere with the detection of allergen-specific IgE, the main diagnostic biomarker. Although commercially available, current materials present a low IgG capture capacity at large IgG concentrations or require complex protocols, preventing their use in the clinic. In this work, mesoporous silica nanoparticles are prepared with different pore sizes, to which IgG-binding protein G' is grafted. It is found that for one particular optimal pore size, the IgG capture capacity of the material is greatly enhanced. The capacity of this material to efficiently capture human IgG in a selective way (compared to IgE) is demonstrated in both solutions of known IgG concentrations as well as in complex samples, like serum, from healthy controls and allergic patients using a simple and fast incubation protocol. Interestingly, IgG removal using the best-performing material enhances in vitro IgE detection in sera from patients allergic to amoxicillin. These results highlight the great translation potential of this strategy to the clinic in the context of in vitro allergy diagnosis.

摘要

具有结合免疫球蛋白 G(IgG)能力的颗粒可用于 IgG 的纯化或用于临床样本的处理以进行诊断目的。对于体外过敏诊断,血清中高浓度的 IgG 会干扰过敏原特异性 IgE 的检测,而 IgE 是主要的诊断生物标志物。尽管已有商业化产品,但目前的材料在 IgG 浓度较高时 IgG 捕获能力较低,或者需要复杂的方案,从而阻止了它们在临床上的应用。在这项工作中,制备了具有不同孔径的介孔硅纳米颗粒,并将 IgG 结合蛋白 G'接枝到这些颗粒上。研究发现,对于一个特定的最佳孔径,材料的 IgG 捕获能力大大增强。该材料在已知 IgG 浓度的溶液中以及在复杂样本(如来自健康对照者和过敏患者的血清)中以简单快速的孵育方案,以选择性方式(与 IgE 相比)高效捕获人 IgG 的能力得到了证明。有趣的是,使用性能最佳的材料去除 IgG 可增强对阿莫西林过敏患者血清中的体外 IgE 检测。这些结果突出了该策略在体外过敏诊断背景下向临床应用的巨大转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/e0f0e7a4f25e/ADHM-12-2203321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/1dc6f79024b7/ADHM-12-2203321-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/cbad575cb2cf/ADHM-12-2203321-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/8ce1ec2f682e/ADHM-12-2203321-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/421e4e3bdcb6/ADHM-12-2203321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/e0f0e7a4f25e/ADHM-12-2203321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/1dc6f79024b7/ADHM-12-2203321-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/cbad575cb2cf/ADHM-12-2203321-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/8ce1ec2f682e/ADHM-12-2203321-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/421e4e3bdcb6/ADHM-12-2203321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8897/11468951/e0f0e7a4f25e/ADHM-12-2203321-g005.jpg

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