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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 >Novel label-free and high-throughput microchip electrophoresis platform for multiplex antibiotic residues detection based on aptamer probes and target catalyzed hairpin assembly for signal amplification
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Novel label-free and high-throughput microchip electrophoresis platform for multiplex antibiotic residues detection based on aptamer probes and target catalyzed hairpin assembly for signal amplification

机译:基于适体探针的多重抗生素残留物检测新的无标记和高通量微芯片电泳平台,用于信号放大的靶催化发夹组件

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摘要

Novel label-free and multiplex aptasensors have been developed for simultaneous detection of several antibiotics based on a microchip electrophoresis (MCE) platform and target catalyzed hairpin assembly (CHA) for signal amplification. Kanamycin (Kana) and oxytetracycline (OTC) were employed as models for testing the system. These aptasensors contained six DNA strands termed as Kana aptamer-catalysis strand (Kana apt-C), Kana inhibit strand (Kana inh), OTC aptamer-catalysis strand (OTC apt-C), OTC inhibit strand (OTC inh), hairpin structures H1 and H2 which were partially complementary. Upon the addition of Kana or OTC, the binding event of aptamer and target triggered the self-assembly between H1 and H2, resulting in the formation of many H1-H2 complexes. They could show strong signals which represented the concentration of Kana or OTC respectively in the MCE system. With the help of the well-designed and high-quality CHA amplification, the assay could yield 300-fold amplified signal comparing that from non-amplified system. Under optimal conditions, this assay exhibited a linear correlation in the ranges from 0.001 ng mL(-1) to 10 ng mL(-1) with the detection limits of 0.7 pg mL(-1) and 0.9 pg mL(-1) (S/N=3) toward Kana and OTC, respectively. The platform has the following advantages: firstly, the aptamer probes can be fabricated easily without labeling signal tags for MCE detection; Secondly, the targets can just react with probes and produce the amplified signal in one-pot. Finally, the targets can be simultaneously detected within 10 min in different channels, thus high-throughput measurement can be achieved. Based on this work, it is estimated that this detection platform will be universally served as a simple, sensitive and portable platform for antibiotic contaminants detection in biological and environmental samples.
机译:已经开发了新的无标记和多重的Aptasensors,用于同时检测基于微芯片电泳(MCE)平台和靶催化发夹组件(CHA)的几种抗生素进行信号放大。 Kanamycin(Kana)和催产素(OTC)用作测试系统的模型。这些Aptasectors含有六条DNA链作为Kana Aptamer-催化链(Kana Apt-C),Kana抑制链(Kana Inh),OTC Aptamer-催化链(OTC APT-C),OTC抑制链(OTC INH),发夹结构H1和H2部分互补。在添加Kana或OTC后,适体和靶的结合事件触发H1和H2之间的自组装,导致许多H1-H2复合物的形成。它们可以显示出强的信号,该信号分别在MCE系统中分别表示Kana或OTC的浓度。借助于精心设计和高质量的CHA扩增,测定可以产生300倍的放大信号,比较非放大系统。在最佳条件下,该测定在0.001ng ml(-1)至10ng ml(-1)的范围内显示出线性相关性,检测限为0.7pg ml(-1)和0.9 pg ml(-1)( S / n = 3)分别向Kana和OTC。该平台具有以下优点:首先,可以轻松地制造适体探针而无需标记MCE检测的信号标签;其次,目标可以与探针反应并在一锅中产生放大的信号。最后,可以在不同通道的10分钟内同时检测目标,因此可以实现高通量测量。基于这项工作,据估计,该检测平台将被普遍存在,作为生物和环境样品中的抗生素污染物检测的简单,灵敏和便携式平台。

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