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Amphotericin B and micafungin duo-loaded nanoemulsion as a potential strategy against Candida auris biofilms
Gabriel Davi Marena1,2, André Luiz Carneiro Soares do Nascimento2, Gabriela Corrêa Carvalho1,2
1Department of Biological Sciences, São Paulo State University (UNESP), School of Pharmaceutical Sciences, São Paulo State, Brazil.
Abstract:
Candida auris is a multidrug-resistant yeast that has seen a worrying increase during the COVID-19 pandemic. Give7/n this, new therapeutic options, such as controlled-release nanomaterials, may be promising in combating the infection. Therefore, this study aimed to develop amphotericin B (AmB) and micafungin (MICA)-loaded nanoemulsions (NEMA) and evaluated against biofilms of C. auris. Nanoemulsions (NEs) were characterized and determined minimum inhibitory concentration MIC90, checkerboard and anti-biofilm. NEMA presented a size of 53.7 and 81.4 nm for DLS and NTA, respectively, with good stability and spherical morphology. MICAmB incorporated efficiency was 88.4 and 99.3%, respectively. The release results show that AmB and MICA obtained a release of 100 and 63.4%, respectively. MICAmB and NEMA showed MIC90 values of 0.015 and 0.031 ug/mL, respectively and synergism. NEMA showed greater metabolic inhibition and morphological changes in mature biofilms. This drugs combination and co-encapsulation proved to be a promising therapy against C. auris biofilms.
Insights
Controlled-release nanoemulsions loaded with amphotericin B and micafungin show promise against multidrug-resistant Candida auris biofilms. This combination therapy offers a potential new strategy to combat this growing public health threat.
Area of Science:
- * Pharmaceutical Sciences
- * Infectious Diseases
- * Nanotechnology
Background:
- * Candida auris is a multidrug-resistant yeast with increasing prevalence, particularly noted during the COVID-19 pandemic.
- * Novel therapeutic strategies are urgently needed to combat C. auris infections.
- * Controlled-release nanomaterials offer a promising avenue for drug delivery against resistant pathogens.
Purpose of the Study:
- * To develop and characterize amphotericin B (AmB) and micafungin (MICA)-loaded nanoemulsions (NEMA).
- * To evaluate the efficacy of NEMA against Candida auris biofilms.
- * To assess the synergistic potential of combined AmB and MICA in nanoemulsion formulation.
Main Methods:
- * Development and characterization of nanoemulsions (NEs) using Dynamic Light Scattering (DLS) and Nanoparticle Tracking Analysis (NTA).
- * Determination of encapsulation efficiency, drug release profiles, and minimum inhibitory concentration (MIC90).
- * Evaluation of anti-biofilm activity using checkerboard assays, metabolic inhibition, and morphological analysis.
Main Results:
- * NEMA exhibited optimal size (53.7-81.4 nm), good stability, and spherical morphology.
- * High encapsulation efficiencies for AmB (88.4%) and MICA (99.3%) were achieved.
- * NEMA demonstrated synergistic activity against C. auris biofilms, with low MIC90 values (0.015 µg/mL for AmB, 0.031 µg/mL for NEMA) and significant metabolic inhibition.
Conclusions:
- * Co-encapsulation of AmB and MICA into nanoemulsions is a viable and promising strategy.
- * NEMA effectively inhibits C. auris biofilm formation and viability.
- * This combination nanoemulsion therapy presents a potent new option for treating Candida auris infections.
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