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Multiplexed enrichment and detection of malarial biomarkers using a stimuli-responsive iron oxide and gold nanoparticle reagent system

机译:使用刺激响应性氧化铁和金纳米粒子试剂系统对疟疾生物标志物进行多重富集和检测

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摘要

There is a need for simple yet robust biomarker and antigen purification and enrichment strategies that are compatible with current rapid diagnostic modalities. Here, a stimuli-responsive nanoparticle system is presented for multiplexed magneto-enrichment and non-instrumented lateral flow strip detection of model antigens from spiked pooled plasma. The integrated reagent system allows purification and enrichment of the gold-labeled biomarker half-sandwich that can be applied directly to lateral flow test strips. A linear diblock copolymer with a thermally responsive poly(N-isopropylacrylamide) (pNIPAm) segment and a gold-binding block composed of NIPAm-co-N,N- dimethylaminoethylacrylamide was prepared by reversible addition-fragmentation chain transfer polymerization. The diblock copolymer was used to functionalize gold nanoparticles (AuNPs), with subsequent bioconjugation to yield thermally responsive pNIPAm-AuNPs that were co-decorated with streptavidin. These AuNPs efficiently complexed biotinylated capture antibody reagents that were bound to picomolar quantities of pan-aldolase and Plasmodium falciparum histidine-rich protein 2 (PfHRP2) in spiked pooled plasma samples. The gold-labeled biomarker half-sandwich was then purified and enriched using 10 nm thermally responsive magnetic nanoparticles that were similarly decorated with pNIPAm. When a thermal stimulus was applied in conjunction with a magnetic field, coaggregation of the AuNP half-sandwiches with the pNIPAm-coated iron oxide nanoparticles created large aggregates that were efficiently magnetophoresed and separated from bulk serum. The purified biomarkers from a spiked pooled plasma sample could be concentrated 50-fold into a small volume and applied directly to a commercial multiplexed lateral flow strip to dramatically improve the signal-to-noise ratio and test sensitivity.
机译:需要与当前的快速诊断方式兼容的简单而健壮的生物标志物以及抗原纯化和富集策略。在这里,提出了一种刺激响应纳米颗粒系统,用于对来自加样合并血浆的模型抗原进行多重磁富集和非仪器侧向流条检测。集成的试剂系统可以纯化和富集金标的生物标志物半三明治,该三明治可以直接应用于侧流试纸条。通过可逆加成-断裂链转移聚合反应制备了具有热响应性聚(N-异丙基丙烯酰胺)(pNIPAm)链段和由NIPAm-co-N,N-二甲基氨基乙基丙烯酰胺组成的金结合嵌段的线性二嵌段共聚物。使用二嵌段共聚物对金纳米颗粒(AuNPs)进行功能化,随后进行生物缀合以产生与链霉亲和素共修饰的热响应性pNIPAm-AuNPs。这些AuNPs有效地复合了生物素化的捕获抗体试剂,这些试剂与皮摩尔量的泛醛缩酶和恶性疟原虫富含组氨酸的蛋白质2(PfHRP2)结合。然后,将金标记的生物标志物半三明治用10 nm热响应磁性纳米颗粒进行纯化和富集,该纳米颗粒也用pNIPAm装饰。当结合磁场施加热刺激时,AuNP半三明治与pNIPAm包被的氧化铁纳米颗粒的共聚集产生了大的聚集体,这些聚集体被有效地磁化并与大量血清分离。从加标的混合血浆样品中纯化的生物标志物可以浓缩50倍成小体积,并直接应用于商用的多路侧流试纸条,以显着提高信噪比和测试灵敏度。

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