嵌入镓基液态金属颗粒的可注射复合水凝胶,通过化疗-光热结合治疗实体乳腺癌

IF 9.6 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Wonjeong Lee , Min Joo Shin , Sungjun Kim , Chae Eun Lee , Jonghoon Choi , Hyung-Jun Koo , Min-Jae Choi , Jae Ho Kim , Kyobum Kim
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引用次数: 0

摘要

光热疗法(PTT)通过在肿瘤部位产生局部热量,有望成为一种治疗癌症的方法。在各种光热剂中,镓基液态金属(LM)因其结构的可转换性,已被广泛用作一种新型光热诱导金属化合物。为了克服液态金属颗粒在人体内随机聚集和消散的局限性,我们开发了含液态金属的可注射复合水凝胶平台,能够实现时空 PTT 和化疗。首先用 1,2-二硬脂酰-sn-甘油-3-磷乙醇胺(DSPE)脂类稳定共晶镓铟 LM 粒子。然后,将它们纳入由硫醇明胶与 6-巯基嘌呤(MP)化学药物和聚(乙二醇)-二丙烯酸酯共轭的互穿水凝胶网络中。由此产生的复合水凝胶具有足够的能力通过多步骤机制诱导 MDA-MB-231 乳腺癌细胞死亡:(1) 通过 LM 粒子的近红外激光照射使温度升高导致癌细胞高热死亡,(2) 由于癌细胞被破坏导致谷胱甘肽(GSH)泄漏和二硫键裂解。因此,谷胱甘肽促进了额外的化疗,导致 MP 在肿瘤微环境中加速释放。我们对复合水凝胶系统的有效性进行了评估,结果表明它能显著抑制和杀死肿瘤。这些结果证明了这种可注射复合水凝胶在时空肿瘤治疗方面的潜力。总之,在我们的水凝胶平台中整合 PTT 和化疗可提高疗效,为未来的临床应用提供了广阔的前景。我们的研究开创了癌症治疗的新突破,开发出一种可注射的水凝胶平台,将液态金属(LM)粒子介导的光热疗法和基于 6-巯基嘌呤(MP)的化疗结合在一起。镓基 LM 和 6-巯基嘌呤化疗的结合实现了协同抗癌效果,而我们的可注射复合水凝胶则是这两种治疗剂特异性递送的局部储存库。该平台可诱导多步抗癌机制,将近红外介导的肿瘤热疗死亡与受损癌细胞释放的谷胱甘肽引发的药物释放结合起来。经过体外和体内研究验证的协同疗效凸显了显著的肿瘤抑制作用。这种具有协同疗效的可注射复合水凝胶为生物材料介导的实体瘤时空治疗带来了巨大前景,为三阴性乳腺癌提供了一种有效的靶向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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.

Statement of significance

Our research pioneers a breakthrough in cancer treatments by developing an injectable hydrogel platform incorporating liquid metal (LM) particle-mediated photothermal therapy and 6-mercaptopurine (MP)-based chemotherapy. The combination of gallium-based LM and MP achieves synergistic anticancer effects, and our injectable composite hydrogel acts as a localized reservoir for specific delivery of both therapeutic agents. This platform induces a multi-step anticancer mechanism, combining NIR-mediated hyperthermic tumor death and drug release triggered by released glutathione from damaged cancer populations. The synergistic efficacy validated in vitro and in vivo studies highlights significant tumor suppression. This injectable composite hydrogel with synergistic therapeutic efficacy holds immense promise for biomaterial-mediated spatiotemporal treatment of solid tumors, offering a potent targeted therapy for triple negative breast cancers.

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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
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