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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Direct detection of small molecules using a nano-molecular imprinted polymer receptor and a quartz crystal resonator driven at a fixed frequency and amplitude
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Direct detection of small molecules using a nano-molecular imprinted polymer receptor and a quartz crystal resonator driven at a fixed frequency and amplitude

机译:使用纳米分子印迹聚合物受体直接检测小分子,并以固定频率和幅度驱动的石英晶体谐振器

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摘要

Small molecule detection is of wide interest in clinical and industrial applications. However, its accessibility is still limited as miniaturisation and system integration is challenged in reliability, costs and complexity. Here we combined a 14.3 MHz quartz crystal resonator (QCR), actuated and analysed using a fixed frequency drive (FFD) method, with a nanomolecular imprinted polymer for label-free, realtime detection of N-hexanoyl-L-homoserine lactone (199 Da), a gram-negative bacterial infection biomarker. The lowest concentration detected (1 mu M) without any optimisation was comparable with that of a BIAcore SPR system, an expensive laboratory gold standard, with significant enhancement in sensitivity and specificity beyond the state-of-the-art QCR. The analytical formula-based FFD method can potentially allow a multiplexed "QCR-on-chip" technology, bringing a paradigm shift in speed, accessibility and affordability of small molecule detection.
机译:小分子检测对临床和工业应用具有广泛兴趣。 然而,它的可访问性仍然有限,因为小型化和系统集成在可靠性,成本和复杂性方面受到质疑。 在这里,我们使用固定频率驱动(FFD)方法组合14.3 MHz石英晶体谐振器(QCR),致动和分析,用纳米压印聚合物进行标记,实时检测N-己酰基-L-HomoSerine内酯(199Da ),革兰氏阴性细菌感染生物标志物。 没有任何优化的检测到(1μm)的最低浓度与Biacore SPR系统,昂贵的实验室金标准的浓度相当,其敏感性和特异性超出了最先进的QCR的显着增强。 基于分析式的FFD方法可能允许多路复用的“QCR型”技术,使得速度,可访问性和小分子检测的负担能力的范式转变。

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