| Literature DB >> 29696813 |
Elita Montanari1, Angela Oates2, Chiara Di Meo1, Josephine Meade3, Rugiada Cerrone1, Antonio Francioso4, Deirdre Devine5, Tommasina Coviello1, Patrizia Mancini6, Luciana Mosca4, Pietro Matricardi1.
Abstract
Staphylococcus aureus is one of the most significant human pathogens that is frequently isolated in a wide range of superficial and systemic infections. The ability of S. aureus to invade and survive within host cells such as keratinocytes and host immune cells has been increasingly recognized as a potential factor in persistent infections and treatment failures. The incorporation of antibiotics into hyaluronan-cholesterol nanohydrogels represents a novel paradigm in the delivery of therapeutic agents against intracellular bacteria. The work presented herein shows that NHs quickly enter human keratinocytes and accumulate into lysosomes. When used for targeting intracellular S. aureus the antimicrobial activity of loaded levofloxacin is enhanced, possibly changing the antibiotic intracellular fate from cytosol to lysosome. Indeed, gentamicin, an antibiotic that predominantly accumulates in lysosomes, shows significant and equal antibacterial activity when entrapped into NHs. These results strongly suggest that lysosomal formulations may display preferential activity toward intracellular S. aureus, opening new avenues for the use of HA-based NHs for treatment of such skin infections.Entities:
Keywords: antibiotic delivery; hyaluronan; intracellular infections; keratinocytes; nanohydrogels
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Year: 2018 PMID: 29696813 DOI: 10.1002/adhm.201701483
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933