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Delivery strategies of amphotericin B for invasive fungal infections.

作者信息

Wang Xiaochun, Mohammad Imran Shair, Fan Lifang, Zhao Zongmin, Nurunnabi Md, Sallam Marwa A, Wu Jun, Chen Zhongjian, Yin Lifang, He Wei

机构信息

Department of Pharmaceutics, China Pharmaceutical University, Nanjing 211198, China.

School of Pharmaceutical Sciences, Sun Yat-sen University, University Town, Guangzhou 510006, China.

出版信息

Acta Pharm Sin B. 2021 Aug;11(8):2585-2604. doi: 10.1016/j.apsb.2021.04.010. Epub 2021 Apr 29.


DOI:10.1016/j.apsb.2021.04.010
PMID:34522599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8424280/
Abstract

Invasive fungal infections (IFIs) represent a growing public concern for clinicians to manage in many medical settings, with substantial associated morbidities and mortalities. Among many current therapeutic options for the treatment of IFIs, amphotericin B (AmB) is the most frequently used drug. AmB is considered as a first-line drug in the clinic that has strong antifungal activity and less resistance. In this review, we summarized the most promising research efforts on nanocarriers for AmB delivery and highlighted their efficacy and safety for treating IFIs. We have also discussed the mechanism of actions of AmB, rationale for treating IFIs, and recent advances in formulating AmB for clinical use. Finally, this review discusses some practical considerations and provides recommendations for future studies in applying AmB for combating IFIs.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/06b131286d9f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/757251fc7b24/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/a60d58c430ed/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/361ccb11e422/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/76119e5e508b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/0a127b3bb0fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/3ea3afed9cdf/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/a8eeca52b37b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/06b131286d9f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/757251fc7b24/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/a60d58c430ed/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/361ccb11e422/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/76119e5e508b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/0a127b3bb0fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/3ea3afed9cdf/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/a8eeca52b37b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7795/8424280/06b131286d9f/gr7.jpg

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Delivery strategies of amphotericin B for invasive fungal infections.

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引用本文的文献

[1]
Antifungal Drugs for the Treatment of Invasive Fungal Infections-A Limited Therapeutic Toolbox Facing Growing Resistances.

Pharmaceuticals (Basel). 2025-8-19

[2]
Transcriptomics Insights into Targeting CK2 Complex in : Implications for Large-Scale Antifungal Virtual Screening.

Curr Med Mycol. 2024-12-9

[3]
Advancing fungal keratitis treatment: transitioning from conventional amphotericin B therapy to nanocarrier-based delivery systems.

Naunyn Schmiedebergs Arch Pharmacol. 2025-5-17

[4]
Pathology-inspired collagen-binding thermosensitive micelle drops enable prolonged and efficient treatment of fungal keratitis.

Bioact Mater. 2025-4-22

[5]
Molecular Mechanism of Aflatoxin B Synthesis Related AfVerB Regulating the Development, AFB Biosyntheis and Virulence of Mainly Through Its CYP Domain.

J Fungi (Basel). 2025-4-9

[6]
Foam-Based Drug Delivery Systems for Skin Disorders: A Comprehensive Review.

AAPS PharmSciTech. 2025-4-4

[7]
In Vitro Efficacy and Toxicity Assessment of an Amphotericin B Gel for the Treatment of Cutaneous Leishmaniasis.

Pharmaceuticals (Basel). 2025-3-18

[8]
Beyond Conventional Antifungals: Combating Resistance Through Novel Therapeutic Pathways.

Pharmaceuticals (Basel). 2025-3-4

[9]
Genomics insights of candidiasis: mechanisms of pathogenicity and drug resistance.

Front Microbiol. 2025-2-27

[10]
iPSC-derived exosomes as amphotericin B carriers: a promising approach to combat cryptococcal meningitis.

Front Microbiol. 2025-2-10

本文引用的文献

[1]
Drug Nanorod-Mediated Intracellular Delivery of microRNA-101 for Self-sensitization via Autophagy Inhibition.

Nanomicro Lett. 2019-9-25

[2]
Recent advances in drug delivery systems for targeting cancer stem cells.

Acta Pharm Sin B. 2021-1

[3]
Nanomedicine-based drug delivery towards tumor biological and immunological microenvironment.

Acta Pharm Sin B. 2020-11

[4]
Deliver Anti-inflammatory Drug Baicalein to Macrophages by Using a Crystallization Strategy.

Front Chem. 2020-9-11

[5]
Intracellular codelivery of anti-inflammatory drug and anti-miR 155 to treat inflammatory disease.

Acta Pharm Sin B. 2020-8

[6]
Ultradeformable Lipid Vesicles Localize Amphotericin B in the Dermis for the Treatment of Infectious Skin Diseases.

ACS Infect Dis. 2020-10-9

[7]
Copolymeric Micelles Overcome the Oral Delivery Challenges of Amphotericin B.

Pharmaceuticals (Basel). 2020-6-11

[8]
Preparation, Characterization, and Formulation Optimization of Ionic-Liquid-in-Water Nanoemulsions toward Systemic Delivery of Amphotericin B.

Mol Pharm. 2020-6-1

[9]
Switchable release nano-reservoirs for co-delivery of drugs via a facile micelle-hydrogel composite.

J Mater Chem B. 2017-5-21

[10]
Lyophilized Iron Oxide Nanoparticles Encapsulated in Amphotericin B: A Novel Targeted Nano Drug Delivery System for the Treatment of Systemic Fungal Infections.

Pharmaceutics. 2020-3-10

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