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用于快速纯化、富集和检测生物标志物的混合刺激响应磁性和金纳米粒子系统。

Mixed stimuli-responsive magnetic and gold nanoparticle system for rapid purification, enrichment, and detection of biomarkers.

机构信息

Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.

出版信息

Bioconjug Chem. 2010 Dec 15;21(12):2197-204. doi: 10.1021/bc100180q. Epub 2010 Nov 11.

Abstract

A new diagnostic system for the enrichment and detection of protein biomarkers from human plasma is presented. Gold nanoparticles (AuNPs) were surface-modified with a diblock copolymer synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization. The diblock copolymer contained a thermally responsive poly(N-isopropylacrylamide) (pNIPAAm) block, a cationic amine-containing block, and a semi-telechelic PEG₂-biotin end group. When a mixed suspension of 23 nm pNIPAAm-modified AuNPs was heated with pNIPAAm-coated 10 nm iron oxide magnetic nanoparticles (mNPs) in human plasma, the thermally responsive pNIPAAm directed the formation of mixed AuNP/mNP aggregates that could be separated efficiently with a magnet. Model studies showed that this mixed nanoparticle system could efficiently purify and strongly enrich the model biomarker protein streptavidin in spiked human plasma. A 10 ng/mL streptavidin sample was mixed with the biotinylated pNIPAAm-modified AuNPs and magnetically separated in the mixed nanoparticle system with pNIPAAm mNPs. The aggregates were concentrated into a 50-fold smaller fluid volume at room temperature where the gold nanoparticle reagent redissolved with the streptavidin target still bound. The concentrated gold-labeled streptavidin could be subsequently analyzed directly using lateral flow immunochromatography. This rapid capture and enrichment module thus utilizes the mixed stimuli-responsive nanoparticle system to achieve concentration of a gold-labeled biomarker that can be directly analyzed using lateral flow or other rapid diagnostic strategies.

摘要

一种用于从人血浆中富集和检测蛋白质生物标志物的新型诊断系统。金纳米粒子(AuNPs)经两亲嵌段共聚物表面修饰,该嵌段共聚物使用可逆加成-断裂链转移(RAFT)聚合合成。两亲嵌段共聚物包含热响应性聚(N-异丙基丙烯酰胺)(pNIPAAm)嵌段、含阳离子胺的嵌段和半遥爪聚乙二醇 2-生物素末端基团。当加热含有 pNIPAAm 涂层的 10nm 氧化铁磁性纳米粒子(mNPs)的 23nm pNIPAAm 修饰的 AuNPs 的混合悬浮液在人血浆中时,热响应性 pNIPAAm 指导形成混合的 AuNP/mNP 聚集体,这些聚集体可以通过磁铁有效地分离。模型研究表明,这种混合纳米粒子系统可以有效地纯化和强烈富集缀合生物素的模型生物标志物蛋白链霉亲和素。将 10ng/mL 的链霉亲和素样品与生物素化的 pNIPAAm 修饰的 AuNPs 混合,并在含有 pNIPAAm mNPs 的混合纳米粒子系统中通过磁分离。在室温下,将混合物浓缩到 50 倍更小的流体体积,其中金纳米粒子试剂与仍结合的链霉亲和素靶标重新溶解。浓缩的金标记的链霉亲和素随后可以直接使用侧向流动免疫层析法进行分析。因此,这种快速捕获和富集模块利用混合刺激响应纳米粒子系统实现了金标记生物标志物的浓缩,该生物标志物可以直接使用侧向流动或其他快速诊断策略进行分析。

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