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  1. Article ; Online: M1 Macrophage-Derived Exosome-Mimetic Nanovesicles with an Enhanced Cancer Targeting Ability.

    Baek, Seungki / Jeon, Miyeon / Jung, Han Na / Lee, Wooseung / Hwang, Jee-Eun / Lee, Jeong Seob / Choi, Yeonjeong / Im, Hyung-Jun

    ACS applied bio materials

    2022  Volume 5, Issue 6, Page(s) 2862–2869

    Abstract: Extracellular vesicles (EVs) have been found to be effective therapeutic drug delivery vehicles in a wide range of human diseases, including cancer and neurodegenerative diseases. Proinflammatory (M1) macrophages can modulate the suppressive immune ... ...

    Abstract Extracellular vesicles (EVs) have been found to be effective therapeutic drug delivery vehicles in a wide range of human diseases, including cancer and neurodegenerative diseases. Proinflammatory (M1) macrophages can modulate the suppressive immune environment of tumor tissues to be more inflammatory and have been considered as candidates for cancer immunotherapy. Furthermore, macrophage-derived exosome-mimetic nanovesicles (MNVs) could effectively induce antitumor response and enhance the efficacy of immune checkpoint inhibitors in a recent paper. However, multiple studies indicate that EVs were rapidly cleared by the reticuloendothelial system, and therefore, their tumor targeting efficiencies were limited. Herein, we developed a simple surface modification method of MNVs using polyethylene glycol (PEG) to enhance the in vivo tumor targeting efficiency. PEG-MNVs had 7-fold higher blood circulation than bare MNVs in the animal tumor model. Also, MNVs had a 25-fold higher protein amount than exosomes. Overall, the nanovesicle preparation strategies presented in this study may expedite the clinical translation of EV-based therapeutics in various diseases.
    MeSH term(s) Animals ; Drug Delivery Systems ; Exosomes/metabolism ; Extracellular Vesicles/metabolism ; Macrophages/metabolism ; Neoplasms/drug therapy ; Polyethylene Glycols/pharmacology
    Chemical Substances Polyethylene Glycols (3WJQ0SDW1A)
    Language English
    Publishing date 2022-05-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2576-6422
    ISSN (online) 2576-6422
    DOI 10.1021/acsabm.2c00246
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Development of Spleen Targeting H

    Oh, Chiwoo / Lee, Wooseung / Park, Jeongbin / Choi, Jinyeong / Lee, Somin / Li, Shengjun / Jung, Han Na / Lee, Jeong-Seob / Hwang, Jee-Eun / Park, Jiwoo / Kim, MinKyu / Baek, Seungki / Im, Hyung-Jun

    ACS nano

    2023  Volume 17, Issue 5, Page(s) 4327–4345

    Abstract: Nanoparticles are primarily taken up by immune cells after systemic administration. Thus, they are considered an ideal drug delivery vehicle for immunomodulation. Because the spleen is the largest lymphatic organ and regulates the systemic immune system, ...

    Abstract Nanoparticles are primarily taken up by immune cells after systemic administration. Thus, they are considered an ideal drug delivery vehicle for immunomodulation. Because the spleen is the largest lymphatic organ and regulates the systemic immune system, there have been studies to develop spleen targeting nanoparticles for immunomodulation of cancer and immunological disorders. Inflammatory bowel disease (IBD) includes disorders involving chronic inflammation in the gastrointestinal tract and is considered incurable despite a variety of treatment options. Hydrogen sulfide (H
    MeSH term(s) Humans ; Liposomes/adverse effects ; Spleen ; Inflammatory Bowel Diseases/drug therapy ; Colitis/drug therapy ; Immunomodulation
    Chemical Substances Liposomes
    Language English
    Publishing date 2023-02-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1936-086X
    ISSN (online) 1936-086X
    DOI 10.1021/acsnano.2c08898
    Database MEDical Literature Analysis and Retrieval System OnLINE

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