As a drug delivery system with vast potential applications, hydrogels have garnered significant attention due to their unique drug loading mechanisms and effectiveness. In this paper, a novel reversible thermosensitive hydrogel polymer, synthesized through copolymerization of mono-6-allyl-β-cyclodextrin, N-isopropylacrylamide, and acrylamide, is introduced. This hydrogel polymer formed a three-dimensional network structure in water, featuring β-cyclodextrin hydrophobic cavities. The encapsulated drug molecules could be slowly and progressively released from both the three-dimensional network and the β-cyclodextrin hydrophobic cavities. IR and XRD analysis confirmed the successful encapsulation of the target drug molecules, sodium salicylate and naproxen sodium, within the β-cyclodextrin cavity of the hydrogel polymer and its three-dimensional network space. Specifically, when the mass ratio of N-isopropylacrylamide/acrylamide/mono-6-allyl-β-cyclodextrin was 9.8/0.2/0.5, the polymer hydrogel demonstrated an initial gelation temperature of 34.9 °C and a final gelation temperature of 37 °C. The expansion rate of the blank hydrogel was slightly higher than that of the drug-loaded hydrogel. Both drugs undergo sustained release through the hydrogel, adhering to Fick’s diffusion law, ensuring consistent drug release within 8 h and maintaining this release for over 24 h, regardless of the drug loading rate. Within 30 days, the degradation rate of the drug-loaded hydrogels in PBS exceeded 15%, while the degradation rate in the presence of lysozyme was more than 40%. These properties render the hydrogel a versatile candidate for targeted drug delivery and biomedical applications, offering novel strategies for treating chronic diseases and other conditions.
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