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Microfluidic flow cytometry: The role of microfabrication methodologies, performance and functional specification

期刊

TECHNOLOGY
卷 6, 期 1, 页码 1-23

出版社

WORLD SCIENTIFIC PUBL CO PTE LTD
DOI: 10.1142/S2339547818300019

关键词

Flow Cytometry; Microfluidics; Florescence-Based Detection; Flow Focusing; Optical Detection; Impedance Spectroscopy; Electrochemical Detection; Micropump; Microvalves

资金

  1. NIH [P41EB002503, R01EB020036, T32GM008339]
  2. NSF IDBR [DBI1353918]
  3. Div Of Biological Infrastructure [1353918] Funding Source: National Science Foundation
  4. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB020036, P41EB002503] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM008339] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Flow cytometry is an invaluable tool utilized in modern biomedical research and clinical applications requiring high throughput, high resolution particle analysis for cytometric characterization and/or sorting of cells and particles as well as for analyzing results from immunocytometric assays. In recent years, research has focused on developing microfluidic flow cytometers with the motivation of creating smaller, less expensive, simpler, and more autonomous alternatives to conventional flow cytometers. These devices could ideally be highly portable, easy to operate without extensive user training, and utilized for research purposes and/or point-of-care diagnostics especially in limited resource facilities or locations requiring on-site analyses. However, designing a device that fulfills the criteria of high throughput analysis, automation and portability, while not sacrificing performance is not a trivial matter. This review intends to present the current state of the field and provide considerations for further improvement by focusing on the key design components of microfluidic flow cytometers. The recent innovations in particle focusing and detection strategies are detailed and compared. This review outlines performance matrix parameters of flow cytometers that are interdependent with each other, suggesting trade offs in selection based on the requirements of the applications. The ongoing contribution of microfluidics demonstrates that it is a viable technology to advance the current state of flow cytometry and develop automated, easy to operate and cost-effective flow cytometers.

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