| Literature DB >> 19904763 |
Bong-Hyun Jun1, Mi Suk Noh, Jaeyun Kim, Gunsung Kim, Homan Kang, Min-Soo Kim, Young-Tae Seo, Jongho Baek, Jong-Ho Kim, Juyoung Park, Seongyong Kim, Yong-Kweon Kim, Taeghwan Hyeon, Myung-Haing Cho, Dae Hong Jeong, Yoon-Sik Lee.
Abstract
In this study, surface-enhanced Raman spectroscopy (SERS)-encoded magnetic nanoparticles (NPs) are prepared and utilized as a multifunctional tagging material for cancer-cell targeting and separation. First, silver-embedded magnetic NPs are prepared, composed of an 18-nm magnetic core and a 16-nm-thick silica shell with silver NPs formed on the surface. After simple aromatic compounds are adsorbed on the silver-embedded magnetic NPs, they are coated with silica to provide them with chemical and physical stability. The resulting silica-encapsulated magnetic NPs (M-SERS dots) produce strong SERS signals and have magnetic properties. In a model application as a tagging material, the M-SERS dots are successfully utilized for targeting breast-cancer cells (SKBR3) and floating leukemia cells (SP2/O). The targeted cancer cells can be easily separated from the untargeted cells using an external magnetic field. The separated targeted cancer cells exhibit a Raman signal originating from the M-SERS dots. This system proves to be an efficient tool for separating targeted cells. Additionally, the magnetic-field-induced hot spots, which can provide a 1000-times-stronger SERS intensity due to aggregation of the NPs, are studied.Entities:
Mesh:
Substances:
Year: 2010 PMID: 19904763 DOI: 10.1002/smll.200901459
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281