Cargando…

In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study

Systematic administration of painkillers and anti-inflammatory drugs is routinely employed to minimize pain and bodily disorders. Controlled drug delivery has the potential to improve the outcomes of disorders by providing sustained exposure to efficacious drug concentrations. Herein, we report the...

Descripción completa

Detalles Bibliográficos
Autores principales: Gull, Nafisa, Khan, Shahzad Maqsood, Zahid Butt, Muhammad Taqi, Khalid, Syed, Shafiq, Muhammad, Islam, Atif, Asim, Sumreen, Hafeez, Sadaf, Khan, Rafi Ullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072301/
https://www.ncbi.nlm.nih.gov/pubmed/35529386
http://dx.doi.org/10.1039/c9ra05025f
_version_ 1784701030090407936
author Gull, Nafisa
Khan, Shahzad Maqsood
Zahid Butt, Muhammad Taqi
Khalid, Syed
Shafiq, Muhammad
Islam, Atif
Asim, Sumreen
Hafeez, Sadaf
Khan, Rafi Ullah
author_facet Gull, Nafisa
Khan, Shahzad Maqsood
Zahid Butt, Muhammad Taqi
Khalid, Syed
Shafiq, Muhammad
Islam, Atif
Asim, Sumreen
Hafeez, Sadaf
Khan, Rafi Ullah
author_sort Gull, Nafisa
collection PubMed
description Systematic administration of painkillers and anti-inflammatory drugs is routinely employed to minimize pain and bodily disorders. Controlled drug delivery has the potential to improve the outcomes of disorders by providing sustained exposure to efficacious drug concentrations. Herein, we report the fabrication of multi-responsive hydrogels using reactive and functional polymers such as chitosan and polyvinyl pyrrolidone by varying the concentration of a cleavable crosslinker, tetraethyl orthosilicate. The swelling indices of the hydrogels were evaluated in distilled water, solutions with different pH values and different electrolytes. FTIR, WAXRD and TGA were conducted to investigate the structures, crystallinities and thermal stabilities of the prepared multi-responsive hydrogels, respectively. The ultimate tensile strength and elongations at break of the fabricated hydrogels were investigated to assess their mechanical stability. Optical microscopy, biodegradation, antimicrobial and cytotoxicity analyses were further carried out to verify the magnified crosslinked and porous structures, biodegradabilities, biocompatibilities and toxic behaviour of the as-prepared hydrogels, respectively. Drug release analysis was conducted to evaluate their release behaviour in PBS, SGF, SIF and electrolyte solutions. The overall results indicate the successful development of novel, non-toxic and sustained drug deliverable hydrogels, which can be considered as a paramount success towards the fabrication of controlled drug delivery systems.
format Online
Article
Text
id pubmed-9072301
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90723012022-05-06 In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study Gull, Nafisa Khan, Shahzad Maqsood Zahid Butt, Muhammad Taqi Khalid, Syed Shafiq, Muhammad Islam, Atif Asim, Sumreen Hafeez, Sadaf Khan, Rafi Ullah RSC Adv Chemistry Systematic administration of painkillers and anti-inflammatory drugs is routinely employed to minimize pain and bodily disorders. Controlled drug delivery has the potential to improve the outcomes of disorders by providing sustained exposure to efficacious drug concentrations. Herein, we report the fabrication of multi-responsive hydrogels using reactive and functional polymers such as chitosan and polyvinyl pyrrolidone by varying the concentration of a cleavable crosslinker, tetraethyl orthosilicate. The swelling indices of the hydrogels were evaluated in distilled water, solutions with different pH values and different electrolytes. FTIR, WAXRD and TGA were conducted to investigate the structures, crystallinities and thermal stabilities of the prepared multi-responsive hydrogels, respectively. The ultimate tensile strength and elongations at break of the fabricated hydrogels were investigated to assess their mechanical stability. Optical microscopy, biodegradation, antimicrobial and cytotoxicity analyses were further carried out to verify the magnified crosslinked and porous structures, biodegradabilities, biocompatibilities and toxic behaviour of the as-prepared hydrogels, respectively. Drug release analysis was conducted to evaluate their release behaviour in PBS, SGF, SIF and electrolyte solutions. The overall results indicate the successful development of novel, non-toxic and sustained drug deliverable hydrogels, which can be considered as a paramount success towards the fabrication of controlled drug delivery systems. The Royal Society of Chemistry 2019-10-01 /pmc/articles/PMC9072301/ /pubmed/35529386 http://dx.doi.org/10.1039/c9ra05025f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Gull, Nafisa
Khan, Shahzad Maqsood
Zahid Butt, Muhammad Taqi
Khalid, Syed
Shafiq, Muhammad
Islam, Atif
Asim, Sumreen
Hafeez, Sadaf
Khan, Rafi Ullah
In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title_full In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title_fullStr In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title_full_unstemmed In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title_short In vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
title_sort in vitro study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072301/
https://www.ncbi.nlm.nih.gov/pubmed/35529386
http://dx.doi.org/10.1039/c9ra05025f
work_keys_str_mv AT gullnafisa invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT khanshahzadmaqsood invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT zahidbuttmuhammadtaqi invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT khalidsyed invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT shafiqmuhammad invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT islamatif invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT asimsumreen invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT hafeezsadaf invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy
AT khanrafiullah invitrostudyofchitosanbasedmultiresponsivehydrogelsasdrugreleasevehiclesapreclinicalstudy