Literature DB >> 19904414

A microfluidic cell trap device for automated measurement of quantal catecholamine release from cells.

Yuanfang Gao1, Shantanu Bhattacharya, Xiaohui Chen, Syed Barizuddin, Shubhra Gangopadhyay, Kevin D Gillis.   

Abstract

Neurons and endocrine cells secrete neurotransmitter and hormones in discrete packets in a process called quantal exocytosis. Electrochemical microelectrodes can detect spikes in current resulting from the oxidation of individual quanta of transmitter only if the electrodes are small and directly adjacent to release sites on the cell. Here we report development of a microchip device that uses microfluidic traps to automatically target individual or small groups of cells to small electrochemical electrodes. Microfluidic channels and traps were fabricated by multi-step wet etch of a silicon wafer whereas Pt electrodes were patterned in register with the trap sites. We demonstrate high-resolution amperometric measurement of quantal exocytosis of catecholamines from chromaffin cells on the device. This reusable device is a step towards developing high-throughput lab-on-a-chip instruments for recording quantal exocytosis to increase the pace of basic neuroscience research and to enable screening of drugs that target exocytosis.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19904414     DOI: 10.1039/b913216c

Source DB:  PubMed          Journal:  Lab Chip        ISSN: 1473-0189            Impact factor:   6.799


  15 in total

1.  A microfluidic platform for chemical stimulation and real time analysis of catecholamine secretion from neuroendocrine cells.

Authors:  Igor A Ges; Rebecca L Brindley; Kevin P M Currie; Franz J Baudenbacher
Journal:  Lab Chip       Date:  2013-12-07       Impact factor: 6.799

2.  Single-cell assays.

Authors:  Declan Ryan; Kangning Ren; Hongkai Wu
Journal:  Biomicrofluidics       Date:  2011-04-14       Impact factor: 2.800

3.  Microwell device for targeting single cells to electrochemical microelectrodes for high-throughput amperometric detection of quantal exocytosis.

Authors:  Xin Liu; Syed Barizuddin; Wonchul Shin; Cherian J Mathai; Shubhra Gangopadhyay; Kevin D Gillis
Journal:  Anal Chem       Date:  2011-02-28       Impact factor: 6.986

4.  Automated targeting of cells to electrochemical electrodes using a surface chemistry approach for the measurement of quantal exocytosis.

Authors:  Syed Barizuddin; Xin Liu; Joseph C Mathai; Maruf Hossain; Kevin D Gillis; Shubhra Gangopadhyay
Journal:  ACS Chem Neurosci       Date:  2010-07-01       Impact factor: 4.418

Review 5.  Electrochemical measurement of quantal exocytosis using microchips.

Authors:  Kevin D Gillis; Xin A Liu; Andrea Marcantoni; Valentina Carabelli
Journal:  Pflugers Arch       Date:  2017-09-02       Impact factor: 3.657

6.  Fabrication of two-layer poly(dimethyl siloxane) devices for hydrodynamic cell trapping and exocytosis measurement with integrated indium tin oxide microelectrodes arrays.

Authors:  Changlu Gao; Xiuhua Sun; Kevin D Gillis
Journal:  Biomed Microdevices       Date:  2013-06       Impact factor: 2.838

Review 7.  Microfluidic systems for studying neurotransmitters and neurotransmission.

Authors:  Callie A Croushore; Jonathan V Sweedler
Journal:  Lab Chip       Date:  2013-05-07       Impact factor: 6.799

Review 8.  Microchip-based electrochemical detection for monitoring cellular systems.

Authors:  Alicia S Johnson; Asmira Selimovic; R Scott Martin
Journal:  Anal Bioanal Chem       Date:  2013-01-23       Impact factor: 4.142

9.  Multi-channel PMMA microfluidic biosensor with integrated IDUAs for electrochemical detection.

Authors:  Nongnoot Wongkaew; Peng He; Vanessa Kurth; Werasak Surareungchai; Antje J Baeumner
Journal:  Anal Bioanal Chem       Date:  2013-05-17       Impact factor: 4.142

10.  Two approaches for addressing electrochemical electrode arrays with reduced external connections.

Authors:  J Yao; X A Liu; K D Gillis
Journal:  Anal Methods       Date:  2015-06-22       Impact factor: 2.896

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.