Document Detail

Single-cell chemical lysis on microfluidic chips with arrays of microwells.
MedLine Citation:
PMID:  22368473     Owner:  NLM     Status:  MEDLINE    
Many conventional biochemical assays are performed using populations of cells to determine their quantitative biomolecular profiles. However, population averages do not reflect actual physiological processes in individual cells, which occur either on short time scales or nonsynchronously. Therefore, accurate analysis at the single-cell level has become a highly attractive tool for investigating cellular content. Microfluidic chips with arrays of microwells were developed for single-cell chemical lysis in the present study. The cellular occupancy in 30-μm-diameter microwells (91.45%) was higher than that in 20-μm-diameter microwells (83.19%) at an injection flow rate of 2.8 μL/min. However, most of the occupied 20-μm-diameter microwells contained individual cells. The results of chemical lysis experiments at the single-cell level indicate that cell membranes were gradually lysed as the lysis buffer was injected; they were fully lysed after 12 s. Single-cell chemical lysis was demonstrated in the proposed microfluidic chip, which is suitable for high-throughput cell lysis.
Chun-Ping Jen; Ju-Hsiu Hsiao; Nikolay A Maslov
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2011-12-30
Journal Detail:
Title:  Sensors (Basel, Switzerland)     Volume:  12     ISSN:  1424-8220     ISO Abbreviation:  Sensors (Basel)     Publication Date:  2012  
Date Detail:
Created Date:  2012-02-27     Completed Date:  2012-06-13     Revised Date:  2013-06-26    
Medline Journal Info:
Nlm Unique ID:  101204366     Medline TA:  Sensors (Basel)     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  347-58     Citation Subset:  IM    
Department of Mechanical Engineering and Advanced Institute of Manufacturing with High-Tech Innovation, National Chung Cheng University, Chia Yi 62102, Taiwan.
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MeSH Terms
Chemical Fractionation / methods*
HeLa Cells
Microfluidic Analytical Techniques / instrumentation*,  methods*
Microscopy, Fluorescence
Single-Cell Analysis / methods*
Time Factors

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