Abstract | BACKGROUND: Staphylococcus aureus survival inside phagocytes is considered to provide a reservoir of bacteria that are relatively protected from antibiotics, thus enabling long-term colonization of the host and explaining clinical failures and relapses after antibiotic therapy. PURPOSE: The objective of this study was to develop a nanovesicle using exosomes loaded with linezolid to overcome intracellular infections by pathogenic bacteria. METHODS: Exosomes were collected from the culture supernatants of RAW 264.7 cells. Their size distribution and zeta potential were characterized by dynamic light scattering, their morphology was characterized by transmission electron microscopy, and their protein content (CD63 and Flotillin 1) was assessed by Western blotting. Linezolid was incorporated into exosomes by co-incubation at 37°C and it's accumulation in RAW264.7 cells and release in vitro were determined by high performance liquid chromatography. The intracellular bactericidal effect was evaluated in methicillin-resistant S. aureus (MRSA)-infected macrophages in vitro and MRSA peritonitis model in vivo. RESULTS: We prepared a nanoformulation of the antibiotic linezolid using exosomes harvested from mouse RAW264.7 macrophages. The exosomal formulation of linezolid was more effective against intracellular MRSA infections in vitro and in vivo than the free linezolid. Our data also showed no signs of cytotoxicity in macrophages. CONCLUSION:
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Authors | Xiaohong Yang, Gongming Shi, Jian Guo, Chenhui Wang, Yun He |
Journal | International journal of nanomedicine
(Int J Nanomedicine)
Vol. 13
Pg. 8095-8104
( 2018)
ISSN: 1178-2013 [Electronic] New Zealand |
PMID | 30555228
(Publication Type: Journal Article)
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Chemical References |
- Anti-Bacterial Agents
- Anti-Infective Agents
- Linezolid
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Topics |
- Animals
- Anti-Bacterial Agents
(therapeutic use)
- Anti-Infective Agents
(administration & dosage, pharmacology)
- Cells, Cultured
- Drug Delivery Systems
- Exosomes
(chemistry)
- Female
- Humans
- Linezolid
(administration & dosage, pharmacology)
- Macrophages
(cytology, drug effects, microbiology)
- Methicillin-Resistant Staphylococcus aureus
(drug effects)
- Mice
- Peritonitis
(drug therapy, microbiology)
- Staphylococcal Infections
(drug therapy, microbiology)
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