期刊
MATERIALS ADVANCES
卷 3, 期 3, 页码 1459-1471出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ma00848j
关键词
-
资金
- Australian Research Council [DP160102836, DP210103151]
- Commonwealth Scientific and Industrial Research Organisation (CSIRO)
- National Health and Medical Research Council [APP1173669, APP1175047]
Liquid biopsy in precision oncology offers dynamic assessment of tumor heterogeneity, minimally invasive procedures, and cost-effective tests. Microfluidic techniques integrated with surface enhanced Raman scattering (SERS) provide a powerful strategy for simultaneous detection of multiple cancer biomarkers in liquid biopsy, supporting precision oncology.
Liquid biopsy-based diagnosis in precision oncology exhibits significant advantages over the traditional tissue biopsies by offering dynamic assessment of tumour heterogeneity, minimally invasive procedures for frequent sampling, and cost-effective tests. Implementation of liquid biopsy-based diagnosis for precision oncology could be the key to provide a confident cancer screening with tailored risk assessment, patient stratification, and real-time monitoring of cancer therapies. To achieve precision oncology with liquid biopsy, the simultaneous analysis of multiple circulating tumour biomarkers is a powerful strategy to establish an accurate signature for each individual patient. Among various developed approaches for tumour biomarker detection, microfluidic devices integrated with surface enhanced Raman scattering (SERS) are emerging as one of the powerful techniques to support precision oncology based on its potential to provide multiplexing and high sensitivity. Particularly, the microfluidic devices provide miniaturised channels for parallel reactions and SERS has the extremely narrow spectra for intrinsic multiplexing. This mini review will focus on recently reported SERS microfluidic techniques, which are capable of simultaneous detection of multiple cancer biomarkers in liquid biopsy and have the promise to be integrated into precision oncology.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据