English  |  正體中文  |  简体中文  |  Items with full text/Total items : 17901/22917 (78%)
Visitors : 7561070      Online Users : 147
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/19901


    Title: Advances in exosomes technology
    Authors: Chen, B.-Y.
    Lin, D.P.-C.
    Huang, C.-T.
    Hsu, M.-Y.
    Contributors: 圖書館
    Date: 2019-03
    Issue Date: 2019-03-12T03:33:02Z (UTC)
    ISSN: 00098981
    Abstract: Exosomes, also called extracellular vesicles (EVs), are membranous structures measuring between 40 and 100 nm. Exosomes, secreted by various cells of the human body into body fluids, contain protein, mRNA, miRNA, and signaling molecules. Physiologically, exosomes assist in the intercellular transport of protein and RNA. Immunologically, exosomes exhibit antigen-presenting capability. In recent studies, exosomes were found to be associated with the pathophysiology of cardiovascular, renal, neurological, and ocular diseases. In addition, exosomes may play a major role in cancer metastasis. Due to the extremely small size and scarcity of exosomes in living samples, many early studies utilized sucrose density gradient ultracentrifugation for exosome collection. However, sucrose density gradient ultracentrifugation is rather time consuming and requires large biological sample quantities. Newer exosome studies combined immunoaffinity and microfluidic system approaches for more efficient exosome collection. Our review summarizes existing methods for EV isolation and notes their advantages and disadvantages. These promising approaches are all characterized by isolation efficiency, and savings in cost, labor, and time. Optimization of current methods is a necessary step toward clinically-relevant diagnostic product production, but the fact that EVs are already widely used in disease diagnosis and treatment encourages continued efforts. © 2019
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/19901
    Relation: Clinica Chimica Acta Volume 493, June 2019, Pages 14-19
    Appears in Collections:[視光學系暨碩士班] 期刊論文

    Files in This Item:

    File Description SizeFormat
    Advances-in-exosomes-technology2019Clinica-Chimica-Acta.pdf1136KbAdobe PDF488View/Open


    SFX Query

    All items in CSMUIR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback