4.8 Article

Eradicating intracellular MRSA via targeted delivery of lysostaphin and vancomycin with mannose-modified exosomes

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 329, Issue -, Pages 454-467

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2020.11.045

Keywords

Exosomes; Surface functionalization; Antibiotics; Targeted delivery; Intracellular infection

Funding

  1. National Natural Science Foundation of China [21572027, 81703424]
  2. Ministry of Science and Technology [2019ZX09301164]
  3. Chongqing Science and Technology Bureau [csts2019jcyj-zdxmX0021]

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MExos is a promising novel antibiotic delivery platform for eradicating intracellular MRSA, rapidly accumulating in the mouse liver and spleen, the target organs of intracellular MRSA.
Intracellular methicillin-resistant Staphylococcus aureus (MRSA) is extremely difficult to remove by common antibiotics, leading to infection recurrence and resistance. Herein we report a novel exosome-based antibiotic delivery platform for eradicating intracellular MRSA, where mannosylated exosome (MExos) is employed as the drug carrier and preferentially taken up by macrophages, delivering lysostaphin (MExoL) and vancomycin (MExoV) to intracellular pathogens. Combination of MExoL and MExoV eradicated intracellular quiescent MRSA. Moreover, MExos rapidly accumulated in mouse liver and spleen, the target organs of intracellular MRSA, after intravenous (IV) administration. Thus, the MExos antibiotic delivery platform is a promising strategy for combating intracellular infection.

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