Actively Targeted In Vivo Multiplex Detection of Intrinsic Cancer Biomarkers Using Biocompatible SERS Nanotags

被引:157
作者
Dinish, U. S. [1 ]
Balasundaram, Ghayathri [1 ]
Chang, Young-Tae [1 ,2 ,3 ]
Olivo, Malini [1 ,4 ]
机构
[1] ASTAR, Singapore Bioimaging Consortium, Singapore 138667, Singapore
[2] Natl Univ Singapore, Dept Chem, Singapore, Singapore
[3] Natl Univ Singapore, Inst Life Sci, MedChem Program, Singapore, Singapore
[4] Natl Univ Ireland Galway, Sch Phys, Galway, Ireland
关键词
ENHANCED RAMAN-SCATTERING; GROWTH-FACTOR RECEPTOR; CELLS; BIODISTRIBUTION; NANOPARTICLES; IMMUNOASSAY; DIAGNOSIS; DOTS;
D O I
10.1038/srep04075
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Surface-enhanced Raman scattering (SERS) technique is becoming highly popular for multiplex biosensing due to the 'fingerprint' Raman spectra from every molecule. As a proof-of-concept, we demonstrated the actively targeted multiplex in vitro and in vivo detection of three intrinsic cancer biomarkers - EGFR, CD44 and TGF beta RII in a breast cancer model using three multiplexing capable, biocompatible SERS nanoparticles/nanotags. Intra-tumorally injected antibody conjugated nanotags specifically targeting the three biomarkers exhibited maximum signal at 6 hours and no detectable signal at 72 hours. However, nanotags without antibodies showed no detectable signal after 6 hours. This difference could be due to the specific binding of the bioconjugated nanotags to the receptors on the cell surface. Thus, this study establishes SERS nanotags as an ultrasensitive nanoprobe for the multiplex detection of biomarkers and opens up its potential application in monitoring tumor progression and therapy and development into a theranostic probe.
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页数:7
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