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    Sulfated cellulose nanofiber hydrogel with mucus-like activities for virus inhibition (2024)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Long, Yanping
    Dimde, Mathias
    Adler, Julia M. (WE 11)
    Vidal, Ricardo Martin (WE 5)
    Povolotsky, Tatyana L.
    Nickl, Philip
    Achazi, Katharina
    Trimpert, Jakob (WE 5)
    Kaufer, Benedikt B. (WE 5)
    Haag, Rainer
    Nie, Chuanxiong
    Quelle
    ACS applied materials & interfaces / American Chemical Society
    Bandzählung: 16
    Heftzählung: 49
    Seiten: 67504 – 67513
    ISSN: 1944-8244
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://pubs.acs.org/doi/10.1021/acsami.4c17998
    DOI: 10.1021/acsami.4c17998
    Pubmed: 39582136
    Kontakt
    Institut für Virologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51833
    virologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Mucus is the first defense barrier against viruses in the human immune system. Inspired by the mucus structure, we designed a highly sulfated hydrogel to bind viruses and prevent infection of the underlying cells. The hydrogel was formed by gelation of sulfated cellulose nanofiber (SCNF) with Ca2+. SCNF exhibited a mucin-like nanofiber structure with high numbers of sulfated groups. Based on the electrostatic interactions with a virus, SCNF could efficiently inhibit herpes simplex virus-1 (HSV-1) infection with a half-maximal inhibitory concentration (IC50) of 0.43 μg/mL, which is comparable to that of heparin (IC50 = 0.30 μg/mL). Benefiting from the multiporous structure and sulfate groups, the Ca2+-SCNF hydrogel could efficiently trap HSV-1 and inhibit the virus from attacking the underlying cells in a transwell model. Furthermore, SCNF also inhibited SARS-CoV-2 infection in a similar experimental setting. By integrating the advantages of high and broad-spectrum virus inhibitory activity as well as low toxicity, it is believed that the Ca2+-SCNF hydrogel can promote the development of highly biocompatible and efficient antiviral material with “binding and inhibition” capability and other diverse strategies.