Abstract
The ability to fabricate microfluidic systems with complex structures and with compatible dimensions between the microfluidics and biological cells have attracted significant attention in the development of microchips for analyzing the biophysical and biochemical functions of cells. Just as cell-based microfluidics have become a versatile tool for biosensing, diagnostics, drug screening and biological research, detector modules for cell-based microfluidics have also undergone major development over the past decade. This review focuses on detection methods commonly used in cell-based microfluidic systems, and provides a general survey and an in-depth look at recent developments in optical and electrochemical detection methods for microfluidic applications for biological systems, particularly cell analysis. Selected examples are used to illustrate applications of these detection systems and their advantages and weaknesses.
Abbreviations
- MS:
-
mass spectrometric
- NMR:
-
nuclear magnetic resonance
- CE:
-
capillary electrophoresis
- ECARs:
-
extracellular acidification rates
- LIF:
-
laser-induced fluorescence
- CL:
-
chemiluminescence
- BL:
-
bioluminescence
- HRP:
-
horseradish peroxidase
- ATP:
-
adenosine triphosphate
- ADP:
-
adenosine diphosphate
- AMP:
-
adenosine monophosphate
- PDMS:
-
poly(dimethyl siloxane)
- PCR:
-
polymerase chain reaction
- TLM:
-
thermal lens microscopy
- PIN:
-
positive-intrinsic-negative
- C4D:
-
capacitively coupled contactless conductivity detector
- UME:
-
ultramicroelectrode
- QDs:
-
quantum dots
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Acknowledgements
This work was supported by the Research Grants Council, Hong Kong (CityU Project No. 9040983) and the National Hi-Tech 863 Program, China (2003AA2Z2052).
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Yi, C., Zhang, Q., Li, CW. et al. Optical and electrochemical detection techniques for cell-based microfluidic systems. Anal Bioanal Chem 384, 1259–1268 (2006). https://doi.org/10.1007/s00216-005-0252-x
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DOI: https://doi.org/10.1007/s00216-005-0252-x