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Core@shell structured ceria@mesoporous silica nanoantibiotics restrain bacterial growth in vitro and in vivo

Due to its modular and flexible design options, mesoporous silica provides ample opportunities when developing new strategies for combinatory antibacterial treatments. In this study, antibacterial ceria (CeO ) nanoparticles (NP) were used as core material, and were further coated with a mesoporous s...

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Bibliographic Details
Published in:Biomaterials advances 2022-02, Vol.133, p.112607-112607, Article 112607
Main Authors: Şen Karaman, Didem, Kietz, Christa, Govardhanam, Prakirth, Slita, Anna, Manea, Alexandra, Pamukçu, Ayşenur, Meinander, Annika, Rosenholm, Jessica M
Format: Article
Language:English
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Summary:Due to its modular and flexible design options, mesoporous silica provides ample opportunities when developing new strategies for combinatory antibacterial treatments. In this study, antibacterial ceria (CeO ) nanoparticles (NP) were used as core material, and were further coated with a mesoporous silica shell (mSiO ) to obtain a core@shell structured nanocomposite (CeO @mSiO ). The porous silica shell was utilized as drug reservoir, whereby CeO @mSiO was loaded with the antimicrobial agent capsaicin (CeO @mSiO /Cap). CeO @mSiO /Cap was further surface-coated with the natural antimicrobial polymer chitosan by employing physical adsorption. The obtained nanocomposite, CeO @mSiO /Cap@Chit, denoted NAB, which stands for "nanoantibiotic", provided a combinatory antibacterial mode of action. The antibacterial effect of NAB on the Gram-negative bacteria Escherichia coli (E.coli) was proven to be significant in vitro. In addition, in vivo evaluations revealed NAB to inhibit the bacterial growth in the intestine of bacteria-fed Drosophila melanogaster larvae, and decreased the required dose of capsaicin needed to eliminate bacteria. As our constructed CeO @mSiO did not show toxicity to mammalian cells, it holds promise for the development of next-generation nanoantibiotics of non-toxic nature with flexible design options.
ISSN:2772-9508
1873-0191
2772-9508
DOI:10.1016/j.msec.2021.112607