Department of Chemical & Biochemical Engineering, Dongguk University, Seoul 04620, Republic of Korea.
Department of Physiology, School of Medicine, Pusan National University, Yangsan 50612, Republic of Korea.
Acta Biomater. 2024 May;180:140-153. doi: 10.1016/j.actbio.2024.04.011. Epub 2024 Apr 10.
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.
光热疗法(PTT)通过在肿瘤部位产生局部热量,有望成为一种癌症治疗方法。在各种光热剂中,基于镓的液态金属(LM)由于其结构可变形性,已被广泛用作新型光热诱导金属化合物。为了克服随机聚集和管理 LM 颗粒在人体内消散的局限性,我们开发了含有 LM 的可注射复合水凝胶平台,能够实现时空 PTT 和化学疗法。首先用 1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺(DSPE)脂质稳定镓-铟共晶液态金属(LM)颗粒。然后将它们掺入由巯基化明胶与 6-巯基嘌呤(MP)化学药物和聚乙二醇-二丙烯酸酯共轭而成的互穿水凝胶网络中。所得复合水凝胶通过多步机制表现出足够的诱导 MDA-MB-231 乳腺癌细胞死亡的能力:(1)由于近红外激光照射通过 LM 颗粒引起的温度升高导致过热的癌细胞死亡,(2)由于癌细胞的破坏导致谷胱甘肽(GSH)泄漏和二硫键断裂。结果,GSH 促进了额外的化学治疗,导致 MP 在肿瘤微环境中加速释放。我们的复合水凝胶系统的有效性在体外和体内进行了评估,证明了对肿瘤的显著抑制和杀伤作用。这些结果表明,这种可注射复合水凝胶在时空癌症治疗方面具有潜力。总之,在我们的水凝胶平台中整合 PTT 和化学疗法提供了增强的治疗效果,为未来的临床应用提供了有希望的前景。意义声明:我们的研究通过开发一种包含液态金属(LM)颗粒介导的光热疗法和基于 6-巯基嘌呤(MP)的化学疗法的可注射水凝胶平台,在癌症治疗方面取得了突破。基于镓的 LM 和 MP 的组合实现了协同抗癌效果,我们的可注射复合水凝胶作为两种治疗剂的局部储库。该平台诱导多步抗癌机制,结合近红外介导的热肿瘤死亡和由受损癌细胞群释放的谷胱甘肽触发的药物释放。在体外和体内研究中验证的协同功效强调了显著的肿瘤抑制作用。这种具有协同治疗效果的可注射复合水凝胶为生物材料介导的实体瘤时空治疗提供了巨大的潜力,为三阴性乳腺癌提供了一种有效的靶向治疗方法。