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首页> 外文期刊>Scientific reports. >Surface plasmon resonance based sensor for the detection of glycopeptide antibiotics in milk using rationally designed nanoMIPs
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Surface plasmon resonance based sensor for the detection of glycopeptide antibiotics in milk using rationally designed nanoMIPs

机译:基于表面等离子共振的传感器,使用合理设计的nanoMIP检测牛奶中的糖肽抗生素

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Glycopeptide antibiotics are known as the last resort for the treatment of serious infections caused by Gram-positive bacteria. The use of milk products contaminated with these antibiotic residues leads to allergic reactions and sensitivity in human. Also, long-term consumption of milk products containing low levels of these antibiotics may cause the relevant bacteria to build up resistance to these last resort antibiotics. Sensitive, rapid and effective quantification and monitoring systems play a key role for their determination in milk products. Hence, molecularly imprinted nanostructures were rationally designed in this work to produce high affinity synthetic receptors to be coupled with a surface plasmon resonance sensor for the analysis of glycopeptide antibiotics in milk samples. The nanoMIP-SPR sensor enabled vancomycin quantification with the LODs of 4.1?ng?mL?1 and 17.7?ng?mL?1 using direct and competitive assays, respectively. The recoveries rates for two sensor methods ranged in 85–110% with RSDs below 7%. The affinity between the nanoMIP receptors and the target molecule (dissociation constant: 1.8?×?10?9?M) is mostly superior to natural receptors and other synthetic receptors. Unlike other methods commonly employed for the detection of milk contaminants this approach is extremely simple, fast and robust, and do not require pre-sample treatment.
机译:糖肽抗生素被认为是治疗由革兰氏阳性细菌引起的严重感染的最后手段。使用受这些抗生素残留污染的奶制品会导致人体过敏反应和敏感性。此外,长期食用含有低含量这些抗生素的乳制品可能会导致相关细菌对这些最后使用的抗生素产生抗药性。灵敏,快速,有效的定量和监测系统在乳制品中的测定中起着关键作用。因此,在这项工作中合理设计了分子印迹的纳米结构,以产生高亲和力的合成受体,并与表面等离子体共振传感器耦合以分析牛奶样品中的糖肽抗生素。 nanoMIP-SPR传感器分别使用直接和竞争性检测方法对万古霉素的LOD分别为4.1?ng?mL?1和17.7?ng?mL?1进行定量。两种传感器方法的回收率在85–110%之间,RSD低于7%。 nanoMIP受体与靶分子之间的亲和力(解离常数:1.8?×?10?9?M)大多优于天然受体和其他合成受体。与通常用于检测牛奶污染物的其他方法不同,此方法极其简单,快速且可靠,并且不需要进行样品前处理。

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