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硅片上碳纳米管的应用,用于通过免疫聚合酶链反应检测乳腺癌标志物糖类抗原15-3 。

Application of carbon nanotubes layered on silicon wafer for the detection of breast cancer marker carbohydrate antigen 15-3 by immuno-polymerase chain reaction.

作者信息

Sadhasivam S, Chen Jung-Chih, Savitha S, Chang Chun-Wei, Lin Feng-Huei

机构信息

Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, Zhunan, Miaoli, Taiwan, ROC.

出版信息

J Mater Sci Mater Med. 2014 Jan;25(1):101-11. doi: 10.1007/s10856-013-5060-9. Epub 2013 Oct 1.

DOI:10.1007/s10856-013-5060-9
PMID:24081383
Abstract

A highly sensitive detection of breast cancer marker, carbohydrate antigen 15-3 (CA 15-3) by carbon nanotube (CNT) based immuno-polymerase chain reaction was reported. The study was aimed to develop a precise and sensitive method to diagnose breast cancer and its recurrence. The hydrofluoric acid (HF) treated silicon wafer layered with bundled CNT was used as the substrate. The surface was treated with HNO3/H2SO4 to graft carboxyl groups on the tips of CNT. Subsequently, polyoxyethylene bis-amine was grafted to conjugate anti human CA 15-3 antibodies. Water contact angle measurement, scanning electron microscope, Fourier transform infrared spectrometer, Raman spectrometer and sodium dodecyl sulfate polyacrylamide gel electrophoresis were employed to confirm the surface modification. The captured antibodies on the CNT were used to capture the target antigen CA 15-3 and the biotinylated secondary antibodies were subsequently bound with the target antigen. A bi-functional streptavidin was used to link biotinylated DNA to the biotinylated detection antibodies. The biotinylated target DNA was amplified by PCR, and then analyzed by agarose gel electrophoresis. The lower limit of detection of CA 15-3 by the proposed immuno-PCR system was 0.001 U/mL, which is extremely sensitive than the other bioanalytical techniques.

摘要

据报道,基于碳纳米管(CNT)的免疫聚合酶链反应可对乳腺癌标志物糖类抗原15-3(CA 15-3)进行高灵敏度检测。该研究旨在开发一种精确且灵敏的方法来诊断乳腺癌及其复发情况。将涂覆有束状碳纳米管的氢氟酸(HF)处理过的硅片用作底物。用硝酸/硫酸处理表面,以在碳纳米管尖端接枝羧基。随后,接枝聚氧乙烯双胺以偶联抗人CA 15-3抗体。采用水接触角测量、扫描电子显微镜、傅里叶变换红外光谱仪、拉曼光谱仪和十二烷基硫酸钠聚丙烯酰胺凝胶电泳来确认表面改性。碳纳米管上捕获的抗体用于捕获目标抗原CA 15-3,随后生物素化的二抗与目标抗原结合。使用双功能链霉亲和素将生物素化的DNA连接到生物素化的检测抗体上。生物素化的目标DNA通过聚合酶链反应(PCR)进行扩增,然后通过琼脂糖凝胶电泳进行分析。所提出的免疫PCR系统对CA 15-3的检测下限为0.001 U/mL,比其他生物分析技术极其灵敏。

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