| Literature DB >> 29883792 |
Junya de Lacorte Singulani1, Liliana Scorzoni1, Natália Manuela Strohmayer Lourencetti1, Luana Rossi Oliveira1, Rosana Silva Conçolaro1, Patricia Bento da Silva1, Ana Carolina Nazaré2, Carlos Roberto Polaquini2, Francesca Damiani Victorelli1, Marlus Chorilli1, Luis Octávio Regasini2, Ana Marisa Fusco Almeida1, Maria José Soares Mendes Giannini3.
Abstract
Paracoccidioidomycosis (PCM) is a systemic mycosis endemic in Latin America, caused by Paracoccidioides spp. A limited number of antifungal agents are available and the search for new compounds has increased. Additionally, nanostructured lipid system (NLS) has emmerged as an interesting strategy to carrier compounds for the treatment of mycosis. In this work, the antifungal efficacy and toxicity of dodecyl gallate (DOD) associated with a NLS was evaluated through in vitro and in vivo tests. DOD showed good in vitro antifungal activity and low toxicity in lung fibroblasts and zebrafish embryos, but no antifungal efficacy in infected mice, which may have been a result of low bioavailability. On the other hand, the association of DOD + NLS was beneficial and resulted in lower toxicity in lung fibroblasts and zebrafish embryos. In addition, NLS + DOD promoted a significant reduction in the fungal burden of mice lungs and could be a potential therapeutic option against PCM.Entities:
Keywords: Antifungal compound; In vivo models; Lipid nanoparticles; Paracoccidioides sp.; Systemic mycosis
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Year: 2018 PMID: 29883792 DOI: 10.1016/j.ijpharm.2018.06.013
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875