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Nanoengineered capsules for selective SERS analysis of biological samples

机译:用于生物样品选择性SERS分析的纳米工程胶囊

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Metal nanoparticles conjugated with DNA oligomers have been intensively studied for a variety of applications, including optical diagnostics. Assays based on aggregation of DNA-coated particles in proportion to the concentration of target analyte have not been widely adopted for clinical analysis, however, largely due to the nonspecific responses observed in complex biofluids. While sample pre-preparation such as dialysis is helpful to enable selective sensing, here we sought to prove that assay encapsulation in hollow microcapsules could remove this requirement and thereby facilitate more rapid analysis on complex samples. Gold nanoparticle-based assays were incorporated into capsules comprising polyelectrolyte multilayer (PEMs), and the response to small molecule targets and larger proteins were compared. Gold nanoparticles were able to selectively sense small Raman dyes (Rhodamine 6G) in the presence of large protein molecules (BSA) when encapsulated. A ratiometric based microRNA-17 sensing assay exhibited drastic reduction in response after encapsulation, with statistically-significant relative Raman intensity changes only at a microRNA-17 concentration of 10 nM compared to a range of 0-500 nM for the corresponding solution-phase response.
机译:与DNA低聚物缀合的金属纳米颗粒已被广泛研究用于多种应用,包括光学诊断。基于与目标分析物浓度成比例的DNA包被颗粒聚集的测定尚未广泛用于临床分析,但是,这主要是由于在复杂生物流体中观察到了非特异性反应。尽管样品的预处理(例如透析)有助于实现选择性感测,但在此我们试图证明中空微胶囊中的化验封装可以消除这一要求,从而有助于对复杂样品进行更快速的分析。将基于金纳米颗粒的测定法掺入到包含聚电解质多层(PEM)的胶囊中,并比较了对小分子靶标和较大蛋白的反应。包封时,金纳米颗粒能够在存在大蛋白质分子(BSA)的情况下选择性感知小拉曼染料(若丹明6G)。基于比率的microRNA-17传感测定法在封装后响应显着降低,只有在10nM的microRNA-17浓度下,相对拉曼强度的变化才具有统计学意义,而对于相应的溶液相响应,其范围是0-500nM 。

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