Injectable composite hydrogels embedded with gallium-based liquid metal particles for solid breast cancer treatment via chemo-photothermal combination

被引:9
|
作者
Lee, Wonjeong [1 ]
Shin, Min Joo [2 ]
Kim, Sungjun [1 ]
Lee, Chae Eun [1 ]
Choi, Jonghoon [3 ]
Koo, Hyung-Jun [4 ]
Choi, Min-Jae [1 ]
Kim, Jae Ho [2 ]
Kim, Kyobum [1 ]
机构
[1] Dongguk Univ, Dept Chem & Biochem Engn, Seoul 04620, South Korea
[2] Pusan Natl Univ, Sch Med, Dept Physiol, Yangsan 50612, South Korea
[3] Chung Ang Univ, Sch Integrat Engn, Seoul 06974, South Korea
[4] Seoul Natl Univ Sci & Technol, Dept Chem & Biomol Engn, Seoul 01811, South Korea
基金
新加坡国家研究基金会;
关键词
Liquid metal; Hydrogel; Combinational therapy; Photothermal therapy; Chemotherapy; DRUG-DELIVERY; MESOPOROUS SILICA; THERAPY; RELEASE; NANOPARTICLES; REGENERATION; SYSTEM;
D O I
10.1016/j.actbio.2024.04.011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Photothermal therapy (PTT) holds great promise as a cancer treatment modality by generating localized heat at the tumor site. Among various photothermal agents, gallium -based liquid metal (LM) has been widely used as a new photothermal-inducible metallic compound due to its structural transformability. To overcome limitations of random aggregation and dissipation of administrated LM particles into a human body, we developed LM -containing injectable composite hydrogel platforms capable of achieving spatiotemporal PTT and chemotherapy. Eutectic gallium-indium LM particles were first stabilized with 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine (DSPE) lipids. They were then incorporated into an interpenetrating hydrogel network composed of thiolated gelatin conjugated with 6-mercaptopurine (MP) chemodrug and poly(ethylene glycol)-diacrylate. The resulted composite hydrogel exhibited sufficient capability to induce MDA-MB-231 breast cancer cell death through a multi -step mechanism: (1) hyperthermic cancer cell death due to temperature elevation by near -infrared laser irradiation via LM particles, (2) leakage of glutathione (GSH) and cleavage of disulfide bonds due to destruction of cancer cells. As a consequence, additional chemotherapy was facilitated by GSH, leading to accelerated release of MP within the tumor microenvironment. The effectiveness of our composite hydrogel system was evaluated both in vitro and in vivo , demonstrating significant tumor suppression and killing. These results demonstrate the potential of this injectable composite hydrogel for spatiotemporal cancer treatment. In conclusion, integration of PTT and chemotherapy within our hydrogel platform offers enhanced therapeutic efficacy, suggesting promising prospects for future clinical applications.
引用
收藏
页码:140 / 153
页数:14
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