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首页> 外文期刊>RSC Advances >Anodic stripping voltammetry of anti-Vi antibody functionalized CdTe quantum dots for the specific monitoring of Salmonella enterica serovar Typhi
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Anodic stripping voltammetry of anti-Vi antibody functionalized CdTe quantum dots for the specific monitoring of Salmonella enterica serovar Typhi

机译:抗Vi抗体功能化CdTe量子点的阳极溶出伏安法,用于肠炎沙门氏菌血清型伤寒的特异性监测

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Recent trends in electrochemical immunoassays have paved the way for metal nanoparticles bursting as a very promising technique for sensitive evaluation. In this work, we report the competence of bioconjugated CdTe quantum dot (QD) and gold nanoparticle (GNP) for the detection of Vi capsular polysaccharide antigen of Salmonella Typhi. The QD and GNP were bioconjugated with anti-Vi antibody and characterized to quantify the loading of respective nanoparticles. Cadmium chloride and gold chloride reference standards were used for the evaluation of the respective metal atoms in the nanobioprobes. The bursting of QD and GNP released 6.91 nmol of cadmium and 83.21 nmol of gold ions in 1 mL each, whereas, the anti-Vi nanobioprobe bursting resulted in the release of 17.29 nmol of cadmium and similar to 34.75 nmol of gold atoms per 1 mu g of antibody. The results are indicative of conjugation of multiple QDs per antibody molecule in marked contrast to the GNPs which can interact and bind with many antibodies owing to its larger size. CdTe-IgG nanobioprobe was, therefore, made use for developing a new sandwich type stripping voltammetry immunoassay in the presence of polymyxin B, a cationic receptor molecule, as a capture molecule. The stripping response observed was much convincing in the range 1 ng to 625 ng of Vi antigen indicating feasibility and reliability of the QD based stripping assay. The results provided an insight into the governing factors of immunostripping inferring the potency of biofunctionalized semiconductor/inorganic nanodots for electroanalytical applications.
机译:电化学免疫测定的最新趋势为金属纳米颗粒的破裂铺平了道路,这是一种非常有前途的灵敏评估技术。在这项工作中,我们报告了生物共轭CdTe量子点(QD)和金纳米颗粒(GNP)检测鼠伤寒沙门氏菌荚膜多糖抗原的能力。 QD和GNP与抗Vi抗体进行生物缀合,并进行表征以量化各个纳米颗粒的负载量。氯化镉和氯化金参考标准品用于评估纳米生物探针中的各个金属原子。 QD和GNP的破裂分别在1 mL中释放出6.91 nmol的镉和83.21 nmol的金离子,而抗Vi纳米生物探针的破裂导致每1亩释放17.29 nmol的镉和大约34.75 nmol的金原子。克抗体。结果表明每个抗体分子具有多个QD,与GNP形成鲜明对比,由于其较大的尺寸,GNP可以与许多抗体相互作用并结合。因此,在多粘菌素B(一种阳离子受体分子)作为捕获分子的存在下,CdTe-IgG纳米生物探针被用于开发一种新型的夹心型溶出伏安法免疫测定。在1 ng至625 ng的Vi抗原范围内观察到的剥离反应非常令人信服,表明基于QD的剥离分析的可行性和可靠性。该结果提供了对免疫条带控制因素的洞察力,这些因素可推断出生物功能化的半导体/无机纳米点在电分析应用中的功效。

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