| Literature DB >> 30991089 |
Barbara Giordani1, Paolo Emidio Costantini2, Stefano Fedi3, Martina Cappelletti4, Angela Abruzzo5, Carola Parolin6, Claudio Foschi7, Giulia Frisco8, Natalia Calonghi9, Teresa Cerchiara10, Federica Bigucci11, Barbara Luppi12, Beatrice Vitali13.
Abstract
Staphylococcus aureus is the major causative agent of skin and soft tissue infections, whose prevention and treatment have become more difficult due to the emergence of antibiotic-resistant strains. In this regard, the development of an effective treatment represents a challenge that can be overcome by delivering new antibiofilm agents with appropriate nanocarriers. In this study, a biosurfactant (BS) isolated from Lactobacillus gasseri BC9 and subsequently loaded in liposomes (LP), was evaluated for its ability to prevent the development and to eradicate the biofilm of different methicillin resistant S. aureus (MRSA) strains. BS from L. gasseri BC9 was not cytotoxic and was able to prevent formation and to eradicate the biofilm of different MRSA strains. BS loaded liposomes (BS-LP) presented a mean diameter (lower than 200 nm) suitable for topical administration and a low polydispersity index (lower than 0.2) that were maintained over time for up 28 days. Notably, BS-LP showed higher ability than free BS to inhibit S. aureus biofilm formation and eradication. BS-LP were loaded in lyophilized matrices able to quickly dissolve (dissolution time lower than 5 s) upon contact with exudate, thus allowing vesicle reconstitution. In conclusion, in this work, we demonstrated the antibiofilm activity of Lactobacillus-derived BS and BS-LP against clinically relevant MRSA strains. Furthermore, the affordable production of lyophilized matrices containing BS-LP for local prevention of cutaneous infections was established.Entities:
Keywords: Biofilm; Cutaneous infections; Fast dissolving solid matrices; Lactobacilli biosurfactants; Liposomes; Methicillin resistant Staphylococcus aureus
Mesh:
Substances:
Year: 2019 PMID: 30991089 DOI: 10.1016/j.ejpb.2019.04.011
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571