| Literature DB >> 22414137 |
Ajay M Shah1, Min Yu, Zev Nakamura, Jordan Ciciliano, Matthew Ulman, Kenneth Kotz, Shannon L Stott, Shyamala Maheswaran, Daniel A Haber, Mehmet Toner.
Abstract
Microfluidic systems for affinity-based cell isolation have emerged as a promising approach for the isolation of specific cells from complex matrices (i.e., circulating tumor cells in whole blood). However, these technologies remain limited by the lack of reliable methods for the innocuous recovery of surface captured cells. Here, we present a biofunctional sacrificial hydrogel coating for microfluidic chips that enables the highly efficient release of isolated cells (99% ± 1%) following gel dissolution. This covalently cross-linked alginate biopolymer system is stable in a wide variety of physiologic solutions (including EDTA treated whole blood) and may be rapidly degraded via backbone cleavage with alginate lyase. The capture and release of EpCAM expressing cancer cells using this approach was found to have no significant effect on cell viability or proliferative potential, and recovered cells were demonstrated to be compatible with downstream immunostaining and FISH analysis.Entities:
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Year: 2012 PMID: 22414137 PMCID: PMC3328665 DOI: 10.1021/ac300190j
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986