首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Electrogenerated chemiluminescence biosensing method based on 5-hydroxymethylcytosine antibody and PDDA-CNTs nanocomposites for the determination of 5-hydroxymethylcytosine double-stranded DNA
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Electrogenerated chemiluminescence biosensing method based on 5-hydroxymethylcytosine antibody and PDDA-CNTs nanocomposites for the determination of 5-hydroxymethylcytosine double-stranded DNA

机译:基于5-羟甲基胞嘧啶抗体和PDDA-CNT纳米复合材料的电化学化学发光生物传感方法,用于测定5-羟甲基胞嘧啶双链DNA

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摘要

A highly sensitive electrogenerated chemiluminescence (ECL) method was developed for trace analysis of 5-hydroxymethylcytosine double-stranded DNA (5-hmC-dsDNA). The poly-(dimethyldiallyl ammonium chloride)/multiwalled carbon nanotubes composite was assembled on a bare glassy carbon electrode (GCE) to provide high specific surface area on which the loadable capacity of 5-hmC-dsDNA and 5-hmC antibody can be greatly increased. The derivative of ruthenium (II) bibyridine, Ru (bpy)(2) (dcbpy)NHS, coupled with 5-hmC antibody to activate an ECL reaction when the applied potential was biased at 1.4 V vs. Ag/AgCl. The loading ratio of substrates were optimized to enhance the detection sensitivity of 5-hmC-dsDNA. It was found that the ECL intensity was a piecewise linear function of the concentration of 5-hmC-dsDNA over the range of 1.0 x 10(-11)-2.0 x 10(-9) M. A linear relationship of I = 6850.3 C-(nM) + 863.8 (R = 0.9954) was obtained from 0.01 to 0.2 nM, while the fitting equation of I = 3840.0 C-(nM) + 1392.4 (R = 0.9974) is for the concentration range of 0.2 - 2.0 nM. The detectable low limit can reach to 2.3 x 10(-12) M. Formation of the antigen-antibody immunocomplex in highly concentrated solutions should undertake most of the responsibility for a decrease in slope. Furthermore, reliability, reproducibility and practicability of the ECL method have been proved to perform well, even in real bio-tissues, suggesting promising prospect in early diagnosis of cancer.
机译:开发了一种高敏感的电化学化学发光(ECL)方法,用于痕量分析5-羟甲基胞嘧啶双链DNA(5-HMC-DSDNA)。将聚 - (二甲基甲基氯化铵)/多晶碳纳米管复合材料组装在裸露的玻璃碳电极(GCE)上,以提供高比表面积,可容纳5-HMC-DSDNA和5-HMC抗体的可加载能力大大增加。钌(II)苯吡啶,Ru(BPY)(2)(DCBPY)NH的衍生物,与5-HMC抗体相结合,以激活ECL反应,当施加的电位偏置为1.4V与Ag / AgCl时。优化基材的负载比以增强5-HMC-DSDNA的检测灵敏度。结果发现,在ECL强度为5-HMC-双链DNA以上范围内的浓度的分段线性函数1.0×10(-11)-2.0×10(-9)M的线性的关系我= 6850.3Ç - (nm)+ 863.8(r = 0.9954)得到0.01至0.2nm,而i = 3840.0 c-(nm)+ 1392.4(r = 0.9974)的拟合方程为0.2-2.0nm的浓度范围。可检测的低限度可达到2.3×10(-12)米,抗原抗体免疫混合物在高度浓缩的溶液中的形成应承担大部分倾斜度的责任。此外,ECL方法的可靠性,再现性和实用性已被证明是甚至在真实生物组织中表现出良好的,这表明早期诊断癌症的有希望的前景。

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