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NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency

OBJECTIVES: NanoDisk–amphotericin B (ND-AMB) is a protein-phospholipid bioparticle containing a “super aggregate” form of antifungal AMB. While lipid-based formulations of AMB, including liposomal AMB (L-AMB), are safer than the deoxycholate (DOC) solubilized form (DOC-AMB), the potency of lipid-bas...

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Autores principales: Burgess, Braydon L, He, Yumin, Baker, Mandie M, Luo, Bing, Carroll, Stephen F, Forte, Trudy M, Oda, Michael N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867322/
https://www.ncbi.nlm.nih.gov/pubmed/24379661
http://dx.doi.org/10.2147/IJN.S50113
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author Burgess, Braydon L
He, Yumin
Baker, Mandie M
Luo, Bing
Carroll, Stephen F
Forte, Trudy M
Oda, Michael N
author_facet Burgess, Braydon L
He, Yumin
Baker, Mandie M
Luo, Bing
Carroll, Stephen F
Forte, Trudy M
Oda, Michael N
author_sort Burgess, Braydon L
collection PubMed
description OBJECTIVES: NanoDisk–amphotericin B (ND-AMB) is a protein-phospholipid bioparticle containing a “super aggregate” form of antifungal AMB. While lipid-based formulations of AMB, including liposomal AMB (L-AMB), are safer than the deoxycholate (DOC) solubilized form (DOC-AMB), the potency of lipid-based formulations is attenuated. We have developed an AMB-based therapy that is both well tolerated and fully efficacious. METHODS: Potency was determined using broth culture growth-inhibition assays and candidacidal kinetics by quantitative culture plating. Toxicology studies were performed in healthy mice. Efficacy was assessed using both immune-competent and leukopenic murine models of systemic Candida albicans infection. RESULTS: ND-AMB C. albicans and Aspergillus fumigatus minimum inhibitory concentrations were fourfold and sixfold lower, respectively, than that observed for L-AMB. ND-AMB exhibited candidacidal activity at 0.125 mg/L, 16-fold lower than L-AMB. In mice, ND-AMB produced no statistically significant kidney or liver toxicity at 15 mg/kg, the highest dose tested. When evaluated in immune-competent mice infected with C. albicans, ND-AMB was at least as effective as DOC-AMB or L-AMB. In a leukopenic model of candidiasis, the 50% effective dose of ND-AMB was around threefold lower than L-AMB. CONCLUSION: These results indicate that ND-AMB exhibits a more favorable safety profile while maintaining uncompromised antifungal properties compared to both DOC-AMB and L-AMB. ND-AMB is a promising therapy for the treatment of invasive fungal infections.
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spelling pubmed-38673222013-12-30 NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency Burgess, Braydon L He, Yumin Baker, Mandie M Luo, Bing Carroll, Stephen F Forte, Trudy M Oda, Michael N Int J Nanomedicine Original Research OBJECTIVES: NanoDisk–amphotericin B (ND-AMB) is a protein-phospholipid bioparticle containing a “super aggregate” form of antifungal AMB. While lipid-based formulations of AMB, including liposomal AMB (L-AMB), are safer than the deoxycholate (DOC) solubilized form (DOC-AMB), the potency of lipid-based formulations is attenuated. We have developed an AMB-based therapy that is both well tolerated and fully efficacious. METHODS: Potency was determined using broth culture growth-inhibition assays and candidacidal kinetics by quantitative culture plating. Toxicology studies were performed in healthy mice. Efficacy was assessed using both immune-competent and leukopenic murine models of systemic Candida albicans infection. RESULTS: ND-AMB C. albicans and Aspergillus fumigatus minimum inhibitory concentrations were fourfold and sixfold lower, respectively, than that observed for L-AMB. ND-AMB exhibited candidacidal activity at 0.125 mg/L, 16-fold lower than L-AMB. In mice, ND-AMB produced no statistically significant kidney or liver toxicity at 15 mg/kg, the highest dose tested. When evaluated in immune-competent mice infected with C. albicans, ND-AMB was at least as effective as DOC-AMB or L-AMB. In a leukopenic model of candidiasis, the 50% effective dose of ND-AMB was around threefold lower than L-AMB. CONCLUSION: These results indicate that ND-AMB exhibits a more favorable safety profile while maintaining uncompromised antifungal properties compared to both DOC-AMB and L-AMB. ND-AMB is a promising therapy for the treatment of invasive fungal infections. Dove Medical Press 2013 2013-12-12 /pmc/articles/PMC3867322/ /pubmed/24379661 http://dx.doi.org/10.2147/IJN.S50113 Text en © 2013 Burgess et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Burgess, Braydon L
He, Yumin
Baker, Mandie M
Luo, Bing
Carroll, Stephen F
Forte, Trudy M
Oda, Michael N
NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title_full NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title_fullStr NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title_full_unstemmed NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title_short NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency
title_sort nanodisk containing super aggregated amphotericin b: a high therapeutic index antifungal formulation with enhanced potency
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867322/
https://www.ncbi.nlm.nih.gov/pubmed/24379661
http://dx.doi.org/10.2147/IJN.S50113
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