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基于 MgAl-LDH-CuS 纳米片的热响应复合水凝胶,具有近红外响应性血管生成抑制剂释放能力,用于多模式饥饿治疗。

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

机构信息

School of Pharmaceutical Sciences, Capital Medical University, No.10 Xitoutiao, You An Men, Beijing, 100069, P. R. China.

Laboratory for Clinical Medicine, Engineering Research Center of Endogenous Prophylactic of Ministry of Education of China, Beijing Laboratory of Biomedical Materials, Beijing, 100069, P. R. China.

出版信息

J Nanobiotechnology. 2024 Mar 23;22(1):127. doi: 10.1186/s12951-024-02384-w.

Abstract

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.

摘要

肿瘤的快速增殖高度依赖于血管的营养供应。切断肿瘤的营养供应是癌症治疗的一种有效策略,称为饥饿疗法。尽管已经开发出各种基于水凝胶的生物材料通过消耗葡萄糖或血管内栓塞来进行饥饿疗法,但单一模式饥饿疗法的局限性限制了它们的治疗效果。在此,我们提出了一种双重功能的营养剥夺策略,该策略可以通过血管外凝胶收缩来阻断营养物质的输送,并通过基于新型近红外响应纳米复合材料水凝胶的血管生成抑制剂来抑制新血管生成。将载有血管生成抑制剂(索拉非尼,SOR)的 CuS 纳米点修饰的 MgAl-LDH 纳米片通过自由基聚合掺入聚(N-异丙基丙烯酰胺)(PNIPAAm)水凝胶中,得到复合水凝胶(SOR@LDH-CuS/P)。SOR@LDH-CuS/P 水凝胶可以递送疏水性 SOR,并具有近红外响应的释放行为,从而降低肿瘤血管密度并加速癌细胞凋亡。此外,SOR@LDH-CuS/P 水凝胶的压缩强度比 PNIPAAm 高 3.5 倍,可以通过血管外凝胶收缩挤压血管。体外和体内实验表明,通过凝胶收缩中断营养供应和通过 SOR 预防血管生成是抑制肿瘤生长的多模式饥饿疗法的一种有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a512/10960490/ad60ad439ceb/12951_2024_2384_Fig1_HTML.jpg

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