Please use this identifier to cite or link to this item: https://doi.org/10.1002/advs.201500118
Title: Rational Design of Materials Interface for Efficient Capture of Circulating Tumor Cells
Authors: Li, Y.-Q
Chandran, B.K
Lim, C.T 
Chen, X
Issue Date: 2015
Citation: Li, Y.-Q, Chandran, B.K, Lim, C.T, Chen, X (2015). Rational Design of Materials Interface for Efficient Capture of Circulating Tumor Cells. Advanced Science 2 (11) : 1500118. ScholarBank@NUS Repository. https://doi.org/10.1002/advs.201500118
Rights: Attribution 4.0 International
Abstract: Originating from primary tumors and penetrating into blood circulation, circulating tumor cells (CTCs) play a vital role in understanding the biology of metastasis and have great potential for early cancer diagnosis, prognosis and personalized therapy. By exploiting the specific biophysical and biochemical properties of CTCs, various material interfaces have been developed for the capture and detection of CTCs from blood. However, due to the extremely low number of CTCs in peripheral blood, there exists a need to improve the efficiency and specificity of the CTC capture and detection. In this regard, a critical review of the numerous reports of advanced platforms for highly efficient and selective capture of CTCs, which have been spurred by recent advances in nanotechnology and microfabrication, is essential. This review gives an overview of unique biophysical and biochemical properties of CTCs, followed by a summary of the key material interfaces recently developed for improved CTC capture and detection, with focus on the use of microfluidics, nanostructured substrates, and miniaturized nuclear magnetic resonance-based systems. Challenges and future perspectives in the design of material interfaces for capture and detection of CTCs in clinical applications are also discussed. © 2015 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Source Title: Advanced Science
URI: https://scholarbank.nus.edu.sg/handle/10635/183461
ISSN: 21983844
DOI: 10.1002/advs.201500118
Rights: Attribution 4.0 International
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