首页> 外文会议>International Seminar on Chemistry >Gold Nanoparticles Modified Screen-Printed Immunosensor for Cancer Biomarker HER2 Determination Based on Anti HER2 Bioconjugates
【24h】

Gold Nanoparticles Modified Screen-Printed Immunosensor for Cancer Biomarker HER2 Determination Based on Anti HER2 Bioconjugates

机译:基于抗HER2生物缀合物进行癌症生物标志物HER2测定的金纳米颗粒改性丝网印刷免疫传感器

获取原文

摘要

Human epidermal growth factor receptor 2 (HER2) is a biomarker of breast cancer plays a major role in the proliferation of breast cancer cells. The determination of HER2 concentration is one of the ways of early detection of breast cancer. In this study we have developed a label free immunosensor for the detection of HER2 using an anti HER2- gold nanoparticles (GNP) bioconjugates. Anti HER2-GNP bioconjugates synthesized by adding anti HER2 on the GNPs that already reacted with APTMS and PEG-NHS-Maleimide. GNP-APTMS characterized using FTIR and cyclic voltammetry with a potassium ferrisianide system. The anti HER2-GNP bioconjugates immobilized on the screen printed carbon electrode-GNP (SPCE-GNP) surface with covalent bonding systems (amine coupling). The result of this study showed FTIR spectra that anti HER2-GNP bioconjugates successfully synthesized. The cyclic voltammograms of GNP-SPCE without and with anti HER2-GNP bioconjugates showed the increase of fericyanide redox pair peak current from 51.946 μA to 121.891 μA. The anti HER2 bioconjugates binds HER2 then the fericyanide peak current decreases in proportion with the addition of HER2. Optimal response of current signal was generated at concentration 5.0 μg/mL anti HER2 and the incubation time of anti HER2-GNP was 1 hour. Limit of detection of HER2 from developed immunosensor is 1.02 × 10~(-2) ng/mL.
机译:人表皮生长因子受体2(HER2)是乳腺癌的生物标志物在乳腺癌细胞的增殖中发挥着重要作用。 HER2浓度的测定是早期检测乳腺癌的方法之一。在这项研究中,我们使用抗HER2-金纳米颗粒(GNP)生物缀合出来的免疫免疫传感器用于检测HER2。通过在已经与APTMS和PEG-NHS-马来酰亚胺反应的GNP上添加抗HER2来合成抗HER2-GNP生物缀合物。使用FTIR和循环伏安法用钾铁司体系的循环伏安特征的GNP-APPTM。用共价键合系统(胺偶联)固定在筛网印刷碳电极-GNP(SPCE-GNP)表面上的抗HER2-GNP生物缀合物。该研究的结果表明,成功合成的抗HER2-GNP生物缀合物的FTIR光谱。 GNP-SPCE的循环伏安图没有和抗HER HER2-GNP生物缀合物显示氧化铈氧化还原对峰值电流从51.946μA至121.891μA的增加。抗HER2生物缀合物与HER2结合,然后通过添加HER2比例降低了偏心锰沸点。在浓度5.0μg/ ml抗HER2处产生电流信号的最佳响应,抗HER2-GNP的孵育时间为1小时。来自发育免疫传感器的HER2检测极限为1.02×10〜(-2)Ng / ml。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号