A MgAl-LDH-CuS nanosheet-based thermo-responsive composite hydrogel with nir-responsive angiogenesis inhibitor releasing capability for multimode starvation therapy

被引:2
|
作者
Liu, Xueyan [1 ,2 ,3 ]
Hu, Tingting [5 ]
Jia, Yijiang [1 ,2 ]
Yang, Shuqing [3 ]
Yang, Yu [3 ]
Cui, Zhuolin [3 ]
Wang, Tao [3 ]
Liang, Ruizheng [3 ,4 ]
Tan, Chaoliang [5 ]
Wang, Yuji [1 ,2 ,3 ]
机构
[1] Capital Med Univ, Sch Pharmaceut Sci, 10 Xitoutiao, Beijing 100069, Peoples R China
[2] Minist Educ China, Engn Res Ctr Endogenous Prophylact, Lab Clin Med, Beijing Lab Biomed Mat, Beijing 100069, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[4] Quzhou Inst Innovat Resource Chem Engn, Quzhou 324000, Peoples R China
[5] Univ Hong Kong, Dept Elect & Elect Engn, Pokfulam Rd, Hong Kong 999077, Peoples R China
基金
中国国家自然科学基金;
关键词
Layered double hydroxides; Thermo-sensitive hydrogels; Angiogenesis inhibitor; NIR-responsive releases; Starvation therapy; NANOMEDICINE;
D O I
10.1186/s12951-024-02384-w
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The rapid proliferation of tumors is highly dependent on the nutrition supply of blood vessels. Cutting off the nutrient supply to tumors is an effective strategy for cancer treatment, known as starvation therapy. Although various hydrogel-based biomaterials have been developed for starvation therapy through glucose consumption or intravascular embolization, the limitations of single-mode starvation therapy hinder their therapeutic effects. Herein, we propose a dual-function nutrition deprivation strategy that can block the nutrients delivery through extravascular gelation shrinkage and inhibit neovascularization through angiogenesis inhibitors based on a novel NIR-responsive nanocomposite hydrogel. CuS nanodots-modified MgAl-LDH nanosheets loaded with angiogenesis inhibitor (sorafenib, SOR) are incorporated into the poly(n-isopropylacrylamide) (PNIPAAm) hydrogel by radical polymerization to obtain the composite hydrogel (SOR@LDH-CuS/P). The SOR@LDH-CuS/P hydrogel can deliver hydrophobic SOR with a NIR-responsive release behavior, which could decrease the tumor vascular density and accelerate cancer cells apoptosis. Moreover, the SOR@LDH-CuS/P hydrogel exhibits higher (3.5 times) compressive strength than that of the PNIPAAm, which could squeeze blood vessels through extravascular gelation shrinkage. In vitro and in vivo assays demonstrate that the interruption of nutrient supply by gelation shrinkage and the prevention of angiogenesis by SOR is a promising strategy to inhibit tumor growth for multimode starvation therapy.
引用
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页数:14
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