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Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer

Fungal infections are an important cause of morbidity and mortality in immunocompromised patients. Amphotericin B (AMB), with broad-spectrum antifungal activity, has long been recognized as a powerful fungicidal drug, but its clinical toxicities mainly nephrotoxicity and poor solubility limit its wi...

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Autores principales: Tang, Xiaolong, Dai, Jingjing, Xie, Jun, Zhu, Yongqiang, Zhu, Ming, Wang, Zhi, Xie, Chunmei, Yao, Aixia, Liu, Tingting, Wang, Xiaoyu, Chen, Li, Jiang, Qinglin, Wang, Shulei, Liang, Yong, Xu, Congjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486495/
https://www.ncbi.nlm.nih.gov/pubmed/26061446
http://dx.doi.org/10.1186/s11671-015-0969-1
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author Tang, Xiaolong
Dai, Jingjing
Xie, Jun
Zhu, Yongqiang
Zhu, Ming
Wang, Zhi
Xie, Chunmei
Yao, Aixia
Liu, Tingting
Wang, Xiaoyu
Chen, Li
Jiang, Qinglin
Wang, Shulei
Liang, Yong
Xu, Congjing
author_facet Tang, Xiaolong
Dai, Jingjing
Xie, Jun
Zhu, Yongqiang
Zhu, Ming
Wang, Zhi
Xie, Chunmei
Yao, Aixia
Liu, Tingting
Wang, Xiaoyu
Chen, Li
Jiang, Qinglin
Wang, Shulei
Liang, Yong
Xu, Congjing
author_sort Tang, Xiaolong
collection PubMed
description Fungal infections are an important cause of morbidity and mortality in immunocompromised patients. Amphotericin B (AMB), with broad-spectrum antifungal activity, has long been recognized as a powerful fungicidal drug, but its clinical toxicities mainly nephrotoxicity and poor solubility limit its wide application in clinical practice. The fungal metabolism along with the host immune response usually generates acidity at sites of infection, resulting in loss of AMB activity in a pH-dependent manner. Herein, we developed pH-responsive AMB-loaded and surface charge-switching poly(d,l-lactic-co-glycolic acid)-b-poly(l-histidine)-b-poly(ethylene glycol) (PLGA-PLH-PEG) nanoparticles for resolving the localized acidity problem and enhance the antifungal efficacy of AMB. Moreover, we modified AMB-encapsulated PLGA-PLH-PEG nanoparticles with anti-Candida albicans antibody (CDA) (CDA-AMB-NPs) to increase the targetability. Then, CDA-AMB-NPs were characterized in terms of physical characteristics, in vitro drug release, stability, drug encapsulation efficiency, and toxicity. Finally, the targetability and antifungal activity of CDA-AMB-NPs were investigated in vitro/in vivo. The result demonstrated that CDA-AMB-NPs significantly improve the targetability and bioavailability of AMB and thus improve its antifungal activity and reduce its toxicity. These NPs may become a good drug carrier for antifungal treatment.
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spelling pubmed-44864952015-07-07 Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer Tang, Xiaolong Dai, Jingjing Xie, Jun Zhu, Yongqiang Zhu, Ming Wang, Zhi Xie, Chunmei Yao, Aixia Liu, Tingting Wang, Xiaoyu Chen, Li Jiang, Qinglin Wang, Shulei Liang, Yong Xu, Congjing Nanoscale Res Lett Nano Commentary Fungal infections are an important cause of morbidity and mortality in immunocompromised patients. Amphotericin B (AMB), with broad-spectrum antifungal activity, has long been recognized as a powerful fungicidal drug, but its clinical toxicities mainly nephrotoxicity and poor solubility limit its wide application in clinical practice. The fungal metabolism along with the host immune response usually generates acidity at sites of infection, resulting in loss of AMB activity in a pH-dependent manner. Herein, we developed pH-responsive AMB-loaded and surface charge-switching poly(d,l-lactic-co-glycolic acid)-b-poly(l-histidine)-b-poly(ethylene glycol) (PLGA-PLH-PEG) nanoparticles for resolving the localized acidity problem and enhance the antifungal efficacy of AMB. Moreover, we modified AMB-encapsulated PLGA-PLH-PEG nanoparticles with anti-Candida albicans antibody (CDA) (CDA-AMB-NPs) to increase the targetability. Then, CDA-AMB-NPs were characterized in terms of physical characteristics, in vitro drug release, stability, drug encapsulation efficiency, and toxicity. Finally, the targetability and antifungal activity of CDA-AMB-NPs were investigated in vitro/in vivo. The result demonstrated that CDA-AMB-NPs significantly improve the targetability and bioavailability of AMB and thus improve its antifungal activity and reduce its toxicity. These NPs may become a good drug carrier for antifungal treatment. Springer US 2015-06-10 /pmc/articles/PMC4486495/ /pubmed/26061446 http://dx.doi.org/10.1186/s11671-015-0969-1 Text en © Tang et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Nano Commentary
Tang, Xiaolong
Dai, Jingjing
Xie, Jun
Zhu, Yongqiang
Zhu, Ming
Wang, Zhi
Xie, Chunmei
Yao, Aixia
Liu, Tingting
Wang, Xiaoyu
Chen, Li
Jiang, Qinglin
Wang, Shulei
Liang, Yong
Xu, Congjing
Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title_full Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title_fullStr Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title_full_unstemmed Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title_short Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer
title_sort enhanced antifungal activity by ab-modified amphotericin b-loaded nanoparticles using a ph-responsive block copolymer
topic Nano Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486495/
https://www.ncbi.nlm.nih.gov/pubmed/26061446
http://dx.doi.org/10.1186/s11671-015-0969-1
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