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Liposomal formulation of a new antifungal hybrid compound provides protection against Candida auris in the ex vivo skin colonization model.
Jaromin, Anna; Zarnowski, Robert; Markowski, Adam; Zagórska, Agnieszka; Johnson, Chad J; Etezadi, Haniyeh; Kihara, Shinji; Mota-Santiago, Pablo; Nett, Jeniel E; Boyd, Ben J; Andes, David R.
Afiliação
  • Jaromin A; Department of Lipids and Liposomes, Faculty of Biotechnology, University of Wroclaw , Wroclaw, Poland.
  • Zarnowski R; Department of Medicine, School of Medicine & Public Health, University of Wisconsin-Madison , Madison, Wisconsin, USA.
  • Markowski A; Department of Medical Microbiology, School of Medicine & Public Health, University of Wisconsin-Madison , Madison, Wisconsin, USA.
  • Zagórska A; Department of Lipids and Liposomes, Faculty of Biotechnology, University of Wroclaw , Wroclaw, Poland.
  • Johnson CJ; Department of Medicinal Chemistry, Jagiellonian University Medical College , Cracow, Poland.
  • Etezadi H; Department of Medicine, University of Wisconsin , Madison, Wisconsin, USA.
  • Kihara S; Department of Pharmacy, University of Copenhagen , Copenhagen, Denmark.
  • Mota-Santiago P; Department of Pharmacy, University of Copenhagen , Copenhagen, Denmark.
  • Nett JE; MAX IV Laboratory, Lund University , Lund, Sweden.
  • Boyd BJ; Department of Medicine, University of Wisconsin , Madison, Wisconsin, USA.
  • Andes DR; Department of Medical Microbiology and Immunology, University of Wisconsin , Madison, Wisconsin, USA.
Antimicrob Agents Chemother ; 68(1): e0095523, 2024 Jan 10.
Article em En | MEDLINE | ID: mdl-38092678
The newly emerged pathogen, Candida auris, presents a serious threat to public health worldwide. This multidrug-resistant yeast often colonizes and persists on the skin of patients, can easily spread from person to person, and can cause life-threatening systemic infections. New antifungal therapies are therefore urgently needed to limit and control both superficial and systemic C. auris infections. In this study, we designed a novel antifungal agent, PQA-Az-13, that contains a combination of indazole, pyrrolidine, and arylpiperazine scaffolds substituted with a trifluoromethyl moiety. PQA-Az-13 demonstrated antifungal activity against biofilms of a set of 10 different C. auris clinical isolates, representing all four geographical clades distinguished within this species. This compound showed strong activity, with MIC values between 0.67 and 1.25 µg/mL. Cellular proteomics indicated that PQA-Az-13 partially or completely inhibited numerous enzymatic proteins in C. auris biofilms, particularly those involved in both amino acid biosynthesis and metabolism processes, as well as in general energy-producing processes. Due to its hydrophobic nature and limited aqueous solubility, PQA-Az-13 was encapsulated in cationic liposomes composed of soybean phosphatidylcholine (SPC), 1,2-dioleoyloxy-3-trimethylammonium-propane chloride (DOTAP), and N-(carbonyl-methoxypolyethylene glycol-2000)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine, sodium salt (DSPE-PEG 2000), and characterized by biophysical and spectral techniques. These PQA-Az-13-loaded liposomes displayed a mean size of 76.4 nm, a positive charge of +45.0 mV, a high encapsulation efficiency of 97.2%, excellent stability, and no toxicity to normal human dermal fibroblasts. PQA-Az-13 liposomes demonstrated enhanced antifungal activity levels against both C. auris in in vitro biofilms and ex vivo skin colonization models. These initial results suggest that molecules like PQA-Az-13 warrant further study and development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Candida / Antifúngicos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Candida / Antifúngicos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article