| Literature DB >> 26313660 |
Na Sun1, Jine Wang1, Liya Ji1, Shanni Hong1, Jingjin Dong1, Yahui Guo1, Kunchi Zhang1, Renjun Pei1.
Abstract
Circulating tumor cell (CTC) isolation has attracted a great deal of research interest in recent years. However, there are still some challenges, including purity as well as viability of the captured CTCs, resulting from nanoscale structures and inorganic nanomaterials. Here, a chitosan nanoparticle surface is first fabricated by electrospray to provide a cellular compatible interface. The "soft" substrate, further modified by polyethylene glycol (PEG) as an antifouling molecule and DNA aptamer as a specific capture molecule, has a hydrophilic nature and is capable of specific capture of viable rare CTCs from artificial white blood cell (WBC) samples. Furthermore, a subsequent in situ culture strategy based on the developed cellular compatible soft interface is introduced for further purification and proliferation of the captured rare number target cells. The WBCs are weeded out after 2 d, and after a 7 d proliferation nearly 200 MCF-7 cells are obtained from 7 target cells with more than 90% purity. This work provides a promising strategy for viable isolation and purification of rare CTCs and it has great potential for achieving clinical validity.Entities:
Keywords: biomaterials; chitosan; circulating tumor cells; in situ culture; nanoparticles
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Year: 2015 PMID: 26313660 DOI: 10.1002/smll.201501718
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281