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

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作者
Xiaolong Tang
Jingjing Dai
Jun Xie
Yongqiang Zhu
Ming Zhu
Zhi Wang
Chunmei Xie
Aixia Yao
Tingting Liu
Xiaoyu Wang
Li Chen
Qinglin Jiang
Shulei Wang
Yong Liang
Congjing Xu
机构
[1] Anhui University of Science and Technology,Stem Cell Engineering Research Center
[2] Anhui University of Science and Technology,Department of Respiration, Tumour Hospital of Affiliated Huainan Oriental Hospital Group
[3] Southern Medical University,School of Biotechnology
[4] Yantai City Center for Disease Control and Prevention,Clinical Laboratory, Department of Nephrology
[5] Huai’an Hospital Affiliated of Xuzhou Medical College,undefined
来源
Nanoscale Research Letters | 2015年 / 10卷
关键词
Amphotericin B; Targetability; Nanocarrier;
D O I
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学科分类号
摘要
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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