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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),...

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Detalles Bibliográficos
Autores principales: Wang, Lin, Shi, Xuefeng, Zhang, Jian, Zhu, Yuejun, Wang, Jinben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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
Descripción
Sumario: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.