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Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics

In this work, with the drug oxytetracycline (OTC) released, cell cytotoxicity and antimicrobial studies of dual-responsive sodium alginate and N-Isopropylacrylamide hydrogels (SA/pNIPAAm) with enclosed OTC were investigated. The molecular OTC release was explored with different acid-base conditions...

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Autores principales: Lin, Xuexia, Ma, Qiaoqiao, Su, Jianlong, Wang, Cui, Kankala, Ranjith Kumar, Zeng, Mingrong, Lin, Honggui, Zhou, Shu-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600676/
https://www.ncbi.nlm.nih.gov/pubmed/31159343
http://dx.doi.org/10.3390/molecules24112089
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author Lin, Xuexia
Ma, Qiaoqiao
Su, Jianlong
Wang, Cui
Kankala, Ranjith Kumar
Zeng, Mingrong
Lin, Honggui
Zhou, Shu-Feng
author_facet Lin, Xuexia
Ma, Qiaoqiao
Su, Jianlong
Wang, Cui
Kankala, Ranjith Kumar
Zeng, Mingrong
Lin, Honggui
Zhou, Shu-Feng
author_sort Lin, Xuexia
collection PubMed
description In this work, with the drug oxytetracycline (OTC) released, cell cytotoxicity and antimicrobial studies of dual-responsive sodium alginate and N-Isopropylacrylamide hydrogels (SA/pNIPAAm) with enclosed OTC were investigated. The molecular OTC release was explored with different acid-base conditions and temperature conditions. In order to characterize cell cytotoxicity and antimicrobial efficacy, time-dependent OTC release analysis of different acid-base conditions was performed in SA/pNIPAAm hydrogels. OTC@SA/pNIPAAm hydrogels showed excellent time-dependent antimicrobial efficacy, in which the IC50 values were 50.11 μg mL(−1), 34.27 μg mL(−1), and 22.39 μg mL(−1) among three consecutive days, respectively. Meanwhile, the human cells showed excellent viability at the IC50 dosage of OTC@SA/pNIPAAm (50.11 μg mL(−1)). OTC@SA/pNIPAAm performed in this study indicated that SA/pNIPAAm may serve as drug carriers for sustainable release at a specific concentration and for being employed as substrates for decreasing drug toxicity. Besides, pH-responsive and thermos-responsive SA/pNIPAAm may lead to the better selectivity of drug release in the ideal location or site. Finally, the results demonstrate that the designed, dual-responsive, biocompatible OTC@SA/pNIPAAm hydrogels showed excellent antimicrobial efficacy and may potentially be found to have enormous applicability in the field of pharmaceutics.
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spelling pubmed-66006762019-07-16 Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics Lin, Xuexia Ma, Qiaoqiao Su, Jianlong Wang, Cui Kankala, Ranjith Kumar Zeng, Mingrong Lin, Honggui Zhou, Shu-Feng Molecules Article In this work, with the drug oxytetracycline (OTC) released, cell cytotoxicity and antimicrobial studies of dual-responsive sodium alginate and N-Isopropylacrylamide hydrogels (SA/pNIPAAm) with enclosed OTC were investigated. The molecular OTC release was explored with different acid-base conditions and temperature conditions. In order to characterize cell cytotoxicity and antimicrobial efficacy, time-dependent OTC release analysis of different acid-base conditions was performed in SA/pNIPAAm hydrogels. OTC@SA/pNIPAAm hydrogels showed excellent time-dependent antimicrobial efficacy, in which the IC50 values were 50.11 μg mL(−1), 34.27 μg mL(−1), and 22.39 μg mL(−1) among three consecutive days, respectively. Meanwhile, the human cells showed excellent viability at the IC50 dosage of OTC@SA/pNIPAAm (50.11 μg mL(−1)). OTC@SA/pNIPAAm performed in this study indicated that SA/pNIPAAm may serve as drug carriers for sustainable release at a specific concentration and for being employed as substrates for decreasing drug toxicity. Besides, pH-responsive and thermos-responsive SA/pNIPAAm may lead to the better selectivity of drug release in the ideal location or site. Finally, the results demonstrate that the designed, dual-responsive, biocompatible OTC@SA/pNIPAAm hydrogels showed excellent antimicrobial efficacy and may potentially be found to have enormous applicability in the field of pharmaceutics. MDPI 2019-05-31 /pmc/articles/PMC6600676/ /pubmed/31159343 http://dx.doi.org/10.3390/molecules24112089 Text en © 2019 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
Lin, Xuexia
Ma, Qiaoqiao
Su, Jianlong
Wang, Cui
Kankala, Ranjith Kumar
Zeng, Mingrong
Lin, Honggui
Zhou, Shu-Feng
Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title_full Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title_fullStr Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title_full_unstemmed Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title_short Dual-Responsive Alginate Hydrogels for Controlled Release of Therapeutics
title_sort dual-responsive alginate hydrogels for controlled release of therapeutics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600676/
https://www.ncbi.nlm.nih.gov/pubmed/31159343
http://dx.doi.org/10.3390/molecules24112089
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