Self-adaptive hydrogel for breast cancer therapy via accurate tumor elimination and on-demand adipose tissue regeneration

脂肪组织 透明质酸 化学 再生(生物学) 生物物理学 纳米载体 自愈水凝胶 阿霉素 药物输送 生物医学工程 细胞生物学 生物化学 化疗 高分子化学 外科 有机化学 解剖 生物 医学
作者
Ran Tian,Xinyu Qiu,Wenyun Mu,Bolei Cai,Zhongning Liu,Shiyu Liu,Xin Chen
出处
期刊:Chinese Chemical Letters [Elsevier]
卷期号:35 (1): 108343-108343 被引量:11
标识
DOI:10.1016/j.cclet.2023.108343
摘要

The irregular defects and residual tumor tissue after surgery are challenges for effective breast cancer treatment. Herein, a smart hydrogel with self-adaptable size and dual responsive cargos release was fabricated to treat breast cancer via accurate tumor elimination, on-demand adipose tissue regeneration and effective infection inhibition. The hydrogel consisted of thiol groups ended polyethylene glycol (SH-PEG-SH) and doxorubicin encapsulated mesoporous silica nanocarriers ([email protected]) double crosslinked hyaluronic acid (HA) after loading of antibacterial peptides (AP) and adipose-derived stem cells (ADSCs). A pH-cleavable unsaturated amide bond was pre-introduced between MSNs and HA frame to perform the tumor-specific acidic environment dependent [email protected] release, meanwhile an esterase degradable glyceryl dimethacrylate cap was grafted on MSNs, which contributed to the selective chemotherapy in tumor cells with over-expressed esterase. The bond cleavage between MSNs and HA would also cause the swelling of the hydrogel, which not only provide sufficient space for the growth of ADSCs, but allows the hydrogel to fully fill the irregular defects generated by surgery and residual tumor atrophy, resulting in the on-demand regeneration of adipose tissue. Moreover, the sustained release of AP could be simultaneously triggered along with the size change of hydrogel, which further avoided bacterial infection to promote tissue regeneration.
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