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Cited 7 time in webofscience Cited 8 time in scopus
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Label-Free Exosome Analysis by Surface-Enhanced Raman Scattering Spectroscopy with Laser-Ablated Silver Nanoparticle Substrate

Authors
Park, Jong-EunNam, HyeonoHwang, June SikKim, SeunggyuKim, Seong JaeKim, SanhaJeon, Jessie S.Yang, Minyang
Issue Date
Dec-2024
Publisher
Wiley-Blackwell
Keywords
breast cancer; exosomes; nanofabrication; point-of-care testing (POCT); rapid and label-free detection; selective laser ablation and melting (SLAM); surface-enhanced raman scattering (SERS) spectroscopy
Citation
Advanced Healthcare Materials, v.13, no.32
Indexed
SCIE
SCOPUS
Journal Title
Advanced Healthcare Materials
Volume
13
Number
32
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/74166
DOI
10.1002/adhm.202402038
ISSN
2192-2640
2192-2659
Abstract
Early diagnostics of breast cancer is crucial to reduce the risk of cancer metastasis and late relapse. Exosome, which contains distinct information of its origin, can be the target object as a liquid biopsy. However, its low sensitivity and inadequate diagnostic tools interfere with the point-of-care testing (POCT) of the exosome. Recently, Surface-enhanced Raman Scattering (SERS) spectroscopy, which amplifies the Raman scattering, has been proved as a promising tool for exosome detection. However, the fabrication process of SERS probe or substrate is still inefficient and far from large-scale production. This study proposes rapid and label-free detection of breast cancer-derived exosomes by statistical analysis of SERS spectra using silver-nanoparticle-based SERS substrate fabricated by selective laser ablation and melting (SLAM). Employing silver nanowires and optimizing laser process parameters enable rapid and low-energy fabrication of SERS substrate. The functionalities including sensitivity, reproducibility, stability, and renewability are evaluated using rhodamine 6G as a probe molecule. Then, the feasibility of POCT is examined by the statistical analysis of SERS spectra of exosomes from malignant breast cancer cells and non-tumorigenic breast epithelial cells. The presented framework is anticipated to be utilized in other biomedical applications, facilitating cost-effective and large-scale production performance.
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Hwang, June Sik
대학원 (기계항공우주공학부)
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