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Development of cell metabolite analysis on microfluidic platform()

Cell metabolite analysis is of great interest to analytical chemists and physiologists, with some metabolites having been identified as important indicators of major diseases such as cancer. A high-throughput and sensitive method for drug metabolite analysis will largely promote the drug discovery i...

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Detalles Bibliográficos
Autores principales: Lin, Luyao, Lin, Jin-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762437/
https://www.ncbi.nlm.nih.gov/pubmed/29403948
http://dx.doi.org/10.1016/j.jpha.2015.09.003
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author Lin, Luyao
Lin, Jin-Ming
author_facet Lin, Luyao
Lin, Jin-Ming
author_sort Lin, Luyao
collection PubMed
description Cell metabolite analysis is of great interest to analytical chemists and physiologists, with some metabolites having been identified as important indicators of major diseases such as cancer. A high-throughput and sensitive method for drug metabolite analysis will largely promote the drug discovery industry. The basic barrier of metabolite analysis comes from the interference of complex components in cell biological system and low abundance of target substances. As a powerful tool in biosample analysis, microfluidic chip enhances the sensitivity and throughput by integrating multiple functional units into one chip. In this review, we discussed three critical steps of establishing functional microfluidic platform for cellular metabolism study. Cell in vitro culture model, on chip sample pretreatment, and microchip combined detectors were described in details and demonstrated by works in five years. And a brief summary was given to discuss the advantages as well as challenges of applying microchip method in cell metabolite and biosample analysis.
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spelling pubmed-57624372018-02-05 Development of cell metabolite analysis on microfluidic platform() Lin, Luyao Lin, Jin-Ming J Pharm Anal Review Paper Cell metabolite analysis is of great interest to analytical chemists and physiologists, with some metabolites having been identified as important indicators of major diseases such as cancer. A high-throughput and sensitive method for drug metabolite analysis will largely promote the drug discovery industry. The basic barrier of metabolite analysis comes from the interference of complex components in cell biological system and low abundance of target substances. As a powerful tool in biosample analysis, microfluidic chip enhances the sensitivity and throughput by integrating multiple functional units into one chip. In this review, we discussed three critical steps of establishing functional microfluidic platform for cellular metabolism study. Cell in vitro culture model, on chip sample pretreatment, and microchip combined detectors were described in details and demonstrated by works in five years. And a brief summary was given to discuss the advantages as well as challenges of applying microchip method in cell metabolite and biosample analysis. Xi'an Jiaotong University 2015-12 2015-09-30 /pmc/articles/PMC5762437/ /pubmed/29403948 http://dx.doi.org/10.1016/j.jpha.2015.09.003 Text en © 2015 Xi'an Jiaotong University http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Paper
Lin, Luyao
Lin, Jin-Ming
Development of cell metabolite analysis on microfluidic platform()
title Development of cell metabolite analysis on microfluidic platform()
title_full Development of cell metabolite analysis on microfluidic platform()
title_fullStr Development of cell metabolite analysis on microfluidic platform()
title_full_unstemmed Development of cell metabolite analysis on microfluidic platform()
title_short Development of cell metabolite analysis on microfluidic platform()
title_sort development of cell metabolite analysis on microfluidic platform()
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762437/
https://www.ncbi.nlm.nih.gov/pubmed/29403948
http://dx.doi.org/10.1016/j.jpha.2015.09.003
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