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Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance

The search for an ocular drug delivery system that could provide long-acting effects without a detriment to the anatomy and physiology of the eye remains a challenge. Polyphenolic compounds (curcumin in particular) have recently gained popularity due to their powerful antioxidant properties; yet cur...

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Autores principales: Abdelkader, Hamdy, Wertheim, David, Pierscionek, Barbara, Alany, Raid G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761359/
https://www.ncbi.nlm.nih.gov/pubmed/33260494
http://dx.doi.org/10.3390/pharmaceutics12121158
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author Abdelkader, Hamdy
Wertheim, David
Pierscionek, Barbara
Alany, Raid G.
author_facet Abdelkader, Hamdy
Wertheim, David
Pierscionek, Barbara
Alany, Raid G.
author_sort Abdelkader, Hamdy
collection PubMed
description The search for an ocular drug delivery system that could provide long-acting effects without a detriment to the anatomy and physiology of the eye remains a challenge. Polyphenolic compounds (curcumin in particular) have recently gained popularity due to their powerful antioxidant properties; yet curcumin suffers poor stability and water solubility. A conventional eye drop formulation of curcumin in the form of a suspension is likely to suffer a short duration of action requiring multiple instillations. On the other hand, polymeric in-situ gelling inserts offer the prospect of overcoming these limitations. The aim of this study was to prepare, characterize and evaluate in vivo, polymeric, in-situ gelling and mucoadhesive inserts for ocular surface delivery of curcumin. Different types and ratios of biocompatible polymers (HPMC, CMC, PL 127 and PVA) and three plasticizers along with the solvent casting method were adopted to prepare curcumin inserts. The inserts were investigated for their physicochemical characteristics, applicability, and suitability of use for potential placement on the ocular surface. The prepared inserts revealed that curcumin was mainly dispersed in the molecular form. Insert surfaces remained smooth and uniform without cracks appearing during preparation and thereafter. Improved mechanical and mucoadhesive properties, enhanced in vitro release (7.5- to 9-fold increases in RRT(300) min) and transcorneal permeation (5.4- to 8.86-fold increases in Papp) of curcumin was achieved by selected in-situ gelling inserts compared to a control curcumin suspension. The developed inserts demonstrated acceptable ocular tolerability, enhanced corneal permeability, and sustained release of curcumin along with retention of insert formulation F7 on the ocular surface for at least two-hours. This insert provides a viable alternative to conventional eye drop formulations of curcumin.
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spelling pubmed-77613592020-12-26 Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance Abdelkader, Hamdy Wertheim, David Pierscionek, Barbara Alany, Raid G. Pharmaceutics Article The search for an ocular drug delivery system that could provide long-acting effects without a detriment to the anatomy and physiology of the eye remains a challenge. Polyphenolic compounds (curcumin in particular) have recently gained popularity due to their powerful antioxidant properties; yet curcumin suffers poor stability and water solubility. A conventional eye drop formulation of curcumin in the form of a suspension is likely to suffer a short duration of action requiring multiple instillations. On the other hand, polymeric in-situ gelling inserts offer the prospect of overcoming these limitations. The aim of this study was to prepare, characterize and evaluate in vivo, polymeric, in-situ gelling and mucoadhesive inserts for ocular surface delivery of curcumin. Different types and ratios of biocompatible polymers (HPMC, CMC, PL 127 and PVA) and three plasticizers along with the solvent casting method were adopted to prepare curcumin inserts. The inserts were investigated for their physicochemical characteristics, applicability, and suitability of use for potential placement on the ocular surface. The prepared inserts revealed that curcumin was mainly dispersed in the molecular form. Insert surfaces remained smooth and uniform without cracks appearing during preparation and thereafter. Improved mechanical and mucoadhesive properties, enhanced in vitro release (7.5- to 9-fold increases in RRT(300) min) and transcorneal permeation (5.4- to 8.86-fold increases in Papp) of curcumin was achieved by selected in-situ gelling inserts compared to a control curcumin suspension. The developed inserts demonstrated acceptable ocular tolerability, enhanced corneal permeability, and sustained release of curcumin along with retention of insert formulation F7 on the ocular surface for at least two-hours. This insert provides a viable alternative to conventional eye drop formulations of curcumin. MDPI 2020-11-28 /pmc/articles/PMC7761359/ /pubmed/33260494 http://dx.doi.org/10.3390/pharmaceutics12121158 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abdelkader, Hamdy
Wertheim, David
Pierscionek, Barbara
Alany, Raid G.
Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title_full Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title_fullStr Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title_full_unstemmed Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title_short Curcumin In Situ Gelling Polymeric Insert with Enhanced Ocular Performance
title_sort curcumin in situ gelling polymeric insert with enhanced ocular performance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761359/
https://www.ncbi.nlm.nih.gov/pubmed/33260494
http://dx.doi.org/10.3390/pharmaceutics12121158
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