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Updated: Jul 29, 2026

Solubility of Hydrophobic Compounds in Aqueous Solution Using Combinations of Self-assembling Peptide and Amino Acid
Published on: September 20, 2017
Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery
Lin Wang1,2, Xuefeng Shi1, Jian Zhang3
1CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences Beijing 100190 P. R. China jbwang@iccas.ac.cn xfshi@iccas.ac.cn +86-10-62523395 +86-10-62523395 +86-10-62652659.
Abstract:
In this study, a novel supramolecular hydrogel system, abbreviated as AGC16/NTS, prepared by molecular self-assembly of cationic gemini surfactant 1,3-bis(N,N-dimethyl-N-cetylammonium)-2-propylacrylatedibromide (AGC16) 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 AGC16/NTS through hydrophobic interaction, which was confirmed by 1H NMR measurement. The effects of Cur on the mechanical strength, phase transition behaviour and morphology of AGC16/NTS were characterized by rheology and cryogenic scanning electron microscopy (cryo-SEM) methods. The pH-responsive release of Cur from AGC16/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 AGC16/NTS hydrogel is a prospective material for use in encapsulation and controlled-release of hydrophobic drug molecules.
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