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Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections

Chronic fungal infection of the cornea could lead to blindness if not treated properly. Topical amphotericin B (AMP-B) is considered the first treatment of choice for ocular fungal infection. However, factors related to its poor solubility and penetration through intact cornea lead to poor bioavaila...

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Autores principales: Albadr, Alyaa A., Tekko, Ismaiel A., Vora, Lalitkumar K., Ali, Ahlam A., Laverty, Garry, Donnelly, Ryan F., Thakur, Raghu Raj Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888497/
https://www.ncbi.nlm.nih.gov/pubmed/34302273
http://dx.doi.org/10.1007/s13346-021-01032-2
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author Albadr, Alyaa A.
Tekko, Ismaiel A.
Vora, Lalitkumar K.
Ali, Ahlam A.
Laverty, Garry
Donnelly, Ryan F.
Thakur, Raghu Raj Singh
author_facet Albadr, Alyaa A.
Tekko, Ismaiel A.
Vora, Lalitkumar K.
Ali, Ahlam A.
Laverty, Garry
Donnelly, Ryan F.
Thakur, Raghu Raj Singh
author_sort Albadr, Alyaa A.
collection PubMed
description Chronic fungal infection of the cornea could lead to blindness if not treated properly. Topical amphotericin B (AMP-B) is considered the first treatment of choice for ocular fungal infection. However, factors related to its poor solubility and penetration through intact cornea lead to poor bioavailability. Microneedles (MNs) are emerging as a minimally invasive method to enhance ocular drug delivery. This study aims to investigate the potential use of biodegradable poly(vinylpyrrolidone) (PVP) and hyaluronic acid (HA)–based rapidly dissolving MNs for delivery of AMP-B to treat fungal infection. The data obtained illustrates PVP/HA MN arrays’ reproducibility, good mechanical strength, and faster dissolution with 100% drug recovery. Multiphoton microscopic results revealed that MNs successfully penetrate the corneal tissue and enhance AMP-B permeation through corneal layers. Furthermore, PVP/HA MN arrays showed high solubility. Both PVP and HA successfully decreased AMP-B cytotoxicity when compared to free drug. More interestingly, the biocompatible MN formulations preserved the antifungal activity of AMP-B, as demonstrated by significant inhibition of fungal growth. Therefore, this study shows the feasibility of ocular delivery of the poorly soluble AMP-B using a fast-dissolving MN patch. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-88884972022-03-08 Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections Albadr, Alyaa A. Tekko, Ismaiel A. Vora, Lalitkumar K. Ali, Ahlam A. Laverty, Garry Donnelly, Ryan F. Thakur, Raghu Raj Singh Drug Deliv Transl Res Original Article Chronic fungal infection of the cornea could lead to blindness if not treated properly. Topical amphotericin B (AMP-B) is considered the first treatment of choice for ocular fungal infection. However, factors related to its poor solubility and penetration through intact cornea lead to poor bioavailability. Microneedles (MNs) are emerging as a minimally invasive method to enhance ocular drug delivery. This study aims to investigate the potential use of biodegradable poly(vinylpyrrolidone) (PVP) and hyaluronic acid (HA)–based rapidly dissolving MNs for delivery of AMP-B to treat fungal infection. The data obtained illustrates PVP/HA MN arrays’ reproducibility, good mechanical strength, and faster dissolution with 100% drug recovery. Multiphoton microscopic results revealed that MNs successfully penetrate the corneal tissue and enhance AMP-B permeation through corneal layers. Furthermore, PVP/HA MN arrays showed high solubility. Both PVP and HA successfully decreased AMP-B cytotoxicity when compared to free drug. More interestingly, the biocompatible MN formulations preserved the antifungal activity of AMP-B, as demonstrated by significant inhibition of fungal growth. Therefore, this study shows the feasibility of ocular delivery of the poorly soluble AMP-B using a fast-dissolving MN patch. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2021-07-23 2022 /pmc/articles/PMC8888497/ /pubmed/34302273 http://dx.doi.org/10.1007/s13346-021-01032-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Albadr, Alyaa A.
Tekko, Ismaiel A.
Vora, Lalitkumar K.
Ali, Ahlam A.
Laverty, Garry
Donnelly, Ryan F.
Thakur, Raghu Raj Singh
Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title_full Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title_fullStr Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title_full_unstemmed Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title_short Rapidly dissolving microneedle patch of amphotericin B for intracorneal fungal infections
title_sort rapidly dissolving microneedle patch of amphotericin b for intracorneal fungal infections
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888497/
https://www.ncbi.nlm.nih.gov/pubmed/34302273
http://dx.doi.org/10.1007/s13346-021-01032-2
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