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    Home > Medical News > Medical Science News > Aiming at tumor cells to set up a "direct attack" channel

    Aiming at tumor cells to set up a "direct attack" channel

    • Last Update: 2021-09-11
    • Source: Internet
    • Author: User
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    Based on the high-throughput nanofluidic chip, the exosomes are loaded with drugs and kill the tumor process.


    Based on the high-throughput nanofluidic chip, the exosomes are loaded with drugs and kill the tumor process.


    On September 2, the team of Researcher Yang Hui from Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences developed a nanofluidic chip technology, which realized the high-throughput preparation of exosomal drug carriers, and experimentally verified the new exosomal drug carriers.


    Exosomes are nano-sized particles that can be secreted into extracellular space or body fluids by almost all cell types, with a diameter of about 30 to 200 nanometers.


    The traditional methods of loading exogenous substances into exosomes, such as electroporation, have always had the disadvantages that the loading efficiency is too low and the integrity and functionality of the exosomes are easily destroyed, making exosomes useful in biomedicine.


    With the help of nanofluid chip technology, the "Exosomal Nanoperforator" can precisely control the characteristics of the fluid at the nanoscale, and achieve highly controllable conditions for the preparation of exosomal drug carriers


    As a class of antibiotics, doxorubicin is often used as a treatment for various types of cancers such as glioma, malignant lymphoma, breast cancer and lung cancer


    "The research results show that the developed nanofluidic chip ensures the activity of drug-containing exosomes, and at the same time sets up a "direct channel" against cancer cells, tumor cells, etc.


    At present, the research team is striving to standardize the production of this nanofluidic system


    Related paper information: https://doi.


    https://doi.
    org/10.
    1002/smll.
    202102150
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