壳聚糖
药物输送
纳米颗粒
硫化铜
化学
铜
硫化物
化学工程
自愈水凝胶
控制释放
高分子化学
材料科学
纳米技术
核化学
有机化学
工程类
作者
Jiayao Wang,Jingguo Li,Shaokui Cao,Yingliang Liu,Jun Shi
摘要
ABSTRACT In recent years, the remotely multi‐responsive chitosan (CS) hydrogel has been garnering extensive attention owing to its remarkable potential in biomedical applications. Meanwhile, it presents a wide range of uses in the realm of controlled drug delivery and photothermal chemical combination therapy. In this paper, the CS/β‐glycerophosphate disodium salt (β‐GP) physical crosslinked network was employed as the framework to encapsulate near‐infrared (NIR) responsive hollow copper sulfide (CuS)/polydopamine (PDA) nanoparticles, and the NIR/pH synergistic responsive CS/CuS/PDA hydrogel was fabricated. The negatively charged β‐GP, along with the hollow CuS/PDA nanoparticles, played a key role in promoting the creation of abundant electronegative cavities. As a result, the hybrid hydrogel achieved an impressively high DOX loading rate, reaching up to 95.5%. The CS/CuS/PDA hydrogel exhibits excellent pH responsiveness, which could be attributed to the disintegration of the CS/β‐GP network under acidic buffer solution. In addition, hollow CuS/PDA nanoparticles embedded in the hydrogel endow the hydrogel with excellent NIR photothermal responsiveness, which significantly promotes the release of DOX. Consequently, the CS/CuS/PDA hydrogel reveals excellent synergistically enhanced NIR, pH, and thermal triple‐responsiveness, indicating its tremendous promise in the field of controlled drug release.
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