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Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery
In this study, a novel supramolecular hydrogel system, abbreviated as AGC(16)/NTS, prepared by molecular self-assembly of cationic gemini surfactant 1,3-bis(N,N-dimethyl-N-cetylammonium)-2-propylacrylatedibromide (AGC(16)) and anionic aromatic compound trisodium 1,3,6-naphthalenetrisulfonate (NTS),...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085726/ https://www.ncbi.nlm.nih.gov/pubmed/35548234 http://dx.doi.org/10.1039/c8ra06064a |
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author | Wang, Lin Shi, Xuefeng Zhang, Jian Zhu, Yuejun Wang, Jinben |
author_facet | Wang, Lin Shi, Xuefeng Zhang, Jian Zhu, Yuejun Wang, Jinben |
author_sort | Wang, Lin |
collection | PubMed |
description | In this study, a novel supramolecular hydrogel system, abbreviated as AGC(16)/NTS, prepared by molecular self-assembly of cationic gemini surfactant 1,3-bis(N,N-dimethyl-N-cetylammonium)-2-propylacrylatedibromide (AGC(16)) and anionic aromatic compound trisodium 1,3,6-naphthalenetrisulfonate (NTS), was used to encapsulate hydrophobic model drug curcumin (Cur), constructing a pH-responsive drug delivery system. Cur was effectively encapsulated into the hydrophobic domains of AGC(16)/NTS through hydrophobic interaction, which was confirmed by (1)H NMR measurement. The effects of Cur on the mechanical strength, phase transition behaviour and morphology of AGC(16)/NTS were characterized by rheology and cryogenic scanning electron microscopy (cryo-SEM) methods. The pH-responsive release of Cur from AGC(16)/NTS was obtained and the release amount of Cur ascended with pH value decreasing from 7.4 to 3.0. The hydrodynamic sizes of the released Cur-aggregates determined by dynamic light scattering (DLS) were used to analyse the release process of Cur at different pH. The cell viability assay and cell imaging experiment demonstrated that Cur-loaded hydrogel has much higher cytotoxicity and better cell uptake compared to free Cur. Overall, the AGC(16)/NTS hydrogel is a prospective material for use in encapsulation and controlled-release of hydrophobic drug molecules. |
format | Online Article Text |
id | pubmed-9085726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90857262022-05-10 Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery Wang, Lin Shi, Xuefeng Zhang, Jian Zhu, Yuejun Wang, Jinben RSC Adv Chemistry In this study, a novel supramolecular hydrogel system, abbreviated as AGC(16)/NTS, prepared by molecular self-assembly of cationic gemini surfactant 1,3-bis(N,N-dimethyl-N-cetylammonium)-2-propylacrylatedibromide (AGC(16)) and anionic aromatic compound trisodium 1,3,6-naphthalenetrisulfonate (NTS), was used to encapsulate hydrophobic model drug curcumin (Cur), constructing a pH-responsive drug delivery system. Cur was effectively encapsulated into the hydrophobic domains of AGC(16)/NTS through hydrophobic interaction, which was confirmed by (1)H NMR measurement. The effects of Cur on the mechanical strength, phase transition behaviour and morphology of AGC(16)/NTS were characterized by rheology and cryogenic scanning electron microscopy (cryo-SEM) methods. The pH-responsive release of Cur from AGC(16)/NTS was obtained and the release amount of Cur ascended with pH value decreasing from 7.4 to 3.0. The hydrodynamic sizes of the released Cur-aggregates determined by dynamic light scattering (DLS) were used to analyse the release process of Cur at different pH. The cell viability assay and cell imaging experiment demonstrated that Cur-loaded hydrogel has much higher cytotoxicity and better cell uptake compared to free Cur. Overall, the AGC(16)/NTS hydrogel is a prospective material for use in encapsulation and controlled-release of hydrophobic drug molecules. The Royal Society of Chemistry 2018-09-10 /pmc/articles/PMC9085726/ /pubmed/35548234 http://dx.doi.org/10.1039/c8ra06064a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wang, Lin Shi, Xuefeng Zhang, Jian Zhu, Yuejun Wang, Jinben Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title | Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title_full | Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title_fullStr | Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title_full_unstemmed | Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title_short | Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery |
title_sort | self-assembled ph-responsive supramolecular hydrogel for hydrophobic drug delivery |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085726/ https://www.ncbi.nlm.nih.gov/pubmed/35548234 http://dx.doi.org/10.1039/c8ra06064a |
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