MWCNT-Fe3O4-based immuno-PCR for the early screening of nasopharyngeal carcinoma

被引:10
作者
Liu Chia-Ching [1 ,2 ]
Subramaniam, Sadhasivam [3 ]
Sivasubramanian, Savitha [5 ]
Lin Feng-Huei [1 ,2 ,4 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Biomed Engn, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Engn, Taipei 100, Taiwan
[3] Bharathiar Univ, Dept Microbial Biotechnol, Coimbatore 641046, Tamil Nadu, India
[4] Natl Hlth Res Inst, Div Biomed Engn & Nanomed Res, Miaoli 350, Taiwan
[5] Sree Sastha Inst Engn & Technol, Dept Biotechnol, Madras, Tamil Nadu, India
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2016年 / 61卷
关键词
NPC; iPCR; MWCNT; EBNA1; antigen; Nanocomposites; CARBON NANOTUBES; ANTIGEN;
D O I
10.1016/j.msec.2015.12.055
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Nasopharyngeal carcinoma (NPC) is the most prevalent form of malignancy in southeast China and its development is meticulously related to EBV pathogenesis. The current screening techniques are unsatisfactory in terms of the sensitivity and hence most of the NPC patients are diagnosed at an advanced stage. Herein, we report the multi-walled carbon nanotubes (MWCNTs) combined with iron oxide nanoparticles as a sensing surface for the early screening of nasopharyngeal carcinoma (NPC) by immuno-PCR (iPCR). The MWCNT-Fe3O4 nanocomposite was characterized by Fourier transform infrared spectra (FTIR), Raman spectra, X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HR-TEM). The characterization techniques had confirmed the successful formation of MWCNT-Fe3O4 nanocomposites. The MWCNT-Fe3O4-based iPCR was effectively tested for the quantification of anti-EBV antibodies in human serum and the limit of detection (LOD) was compared with ELISA. The limit of detection by iPCR was valid until 1:10,000,000 fold dilution of NPC+ve human serum, whereas ELISA can detect the anti-EBV antibodies in human serum up to 1:100,000 fold dilution. The MWCNT-Fe3O4 offers an excellent surface area for the antigen-antibody binding and hence greater sensitivity was achieved. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:422 / 428
页数:7
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