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Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir

Acyclovir has a short half-life and offers poor bioavailability. Its daily dose is 200 mg five times a day. A tamarind gum and β-cyclodextrin-based pH-responsive hydrogel network for sustained delivery of acyclovir was developed using the free-radical polymerization technique. Developed networks wer...

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Autores principales: Shafiq, Kanza, Mahmood, Asif, Salem-Bekhit, Mounir M., Sarfraz, Rai Muhammad, Algarni, Alanood S., Taha, Ehab I., Mansour, Ahd A., Al Zahrani, Sami, Benguerba, Yacine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785578/
https://www.ncbi.nlm.nih.gov/pubmed/36558978
http://dx.doi.org/10.3390/ph15121527
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author Shafiq, Kanza
Mahmood, Asif
Salem-Bekhit, Mounir M.
Sarfraz, Rai Muhammad
Algarni, Alanood S.
Taha, Ehab I.
Mansour, Ahd A.
Al Zahrani, Sami
Benguerba, Yacine
author_facet Shafiq, Kanza
Mahmood, Asif
Salem-Bekhit, Mounir M.
Sarfraz, Rai Muhammad
Algarni, Alanood S.
Taha, Ehab I.
Mansour, Ahd A.
Al Zahrani, Sami
Benguerba, Yacine
author_sort Shafiq, Kanza
collection PubMed
description Acyclovir has a short half-life and offers poor bioavailability. Its daily dose is 200 mg five times a day. A tamarind gum and β-cyclodextrin-based pH-responsive hydrogel network for sustained delivery of acyclovir was developed using the free-radical polymerization technique. Developed networks were characterized by FTIR, DSC, TGA, PXRD, EDX, and SEM. The effect of varying feed ratios of polymers, monomers, and crosslinker on the gel fraction, swelling, and release was also investigated. FTIR findings confirmed the compatibility of the ingredients in a new complex polymer. The thermal stability of acyclovir was increased within the newly synthesized polymer. SEM photomicrographs confirmed the porous texture of hydrogels. The gel fraction was improved (from 90.12% to 98.12%) with increased reactant concentrations. The pH of the dissolution medium and the reactant contents affected swelling dynamics and acyclovir release from the developed carrier system. Based on the R2 value, the best-fit model was zero-order kinetics with non-Fickian diffusion as a release mechanism. The biocompatibility of the developed network was confirmed through hematology, LFT, RFT, lipid profile, and histopathological examinations. No sign of pathology, necrosis, or abrasion was observed. Thus, a pH-responsive and biocompatible polymeric system was developed for sustained delivery of acyclovir to reduce the dosing frequency and improve patient compliance.
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spelling pubmed-97855782022-12-24 Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir Shafiq, Kanza Mahmood, Asif Salem-Bekhit, Mounir M. Sarfraz, Rai Muhammad Algarni, Alanood S. Taha, Ehab I. Mansour, Ahd A. Al Zahrani, Sami Benguerba, Yacine Pharmaceuticals (Basel) Article Acyclovir has a short half-life and offers poor bioavailability. Its daily dose is 200 mg five times a day. A tamarind gum and β-cyclodextrin-based pH-responsive hydrogel network for sustained delivery of acyclovir was developed using the free-radical polymerization technique. Developed networks were characterized by FTIR, DSC, TGA, PXRD, EDX, and SEM. The effect of varying feed ratios of polymers, monomers, and crosslinker on the gel fraction, swelling, and release was also investigated. FTIR findings confirmed the compatibility of the ingredients in a new complex polymer. The thermal stability of acyclovir was increased within the newly synthesized polymer. SEM photomicrographs confirmed the porous texture of hydrogels. The gel fraction was improved (from 90.12% to 98.12%) with increased reactant concentrations. The pH of the dissolution medium and the reactant contents affected swelling dynamics and acyclovir release from the developed carrier system. Based on the R2 value, the best-fit model was zero-order kinetics with non-Fickian diffusion as a release mechanism. The biocompatibility of the developed network was confirmed through hematology, LFT, RFT, lipid profile, and histopathological examinations. No sign of pathology, necrosis, or abrasion was observed. Thus, a pH-responsive and biocompatible polymeric system was developed for sustained delivery of acyclovir to reduce the dosing frequency and improve patient compliance. MDPI 2022-12-08 /pmc/articles/PMC9785578/ /pubmed/36558978 http://dx.doi.org/10.3390/ph15121527 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shafiq, Kanza
Mahmood, Asif
Salem-Bekhit, Mounir M.
Sarfraz, Rai Muhammad
Algarni, Alanood S.
Taha, Ehab I.
Mansour, Ahd A.
Al Zahrani, Sami
Benguerba, Yacine
Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title_full Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title_fullStr Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title_full_unstemmed Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title_short Development and Optimization of Tamarind Gum-β-Cyclodextrin-g-Poly(Methacrylate) pH-Responsive Hydrogels for Sustained Delivery of Acyclovir
title_sort development and optimization of tamarind gum-β-cyclodextrin-g-poly(methacrylate) ph-responsive hydrogels for sustained delivery of acyclovir
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785578/
https://www.ncbi.nlm.nih.gov/pubmed/36558978
http://dx.doi.org/10.3390/ph15121527
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