Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China.
Wuxi School of Medicine, Jiangnan University, Lihu Avenue1800, Wuxi 214122, China.
Acta Biomater. 2022 Aug;148:206-217. doi: 10.1016/j.actbio.2022.06.012. Epub 2022 Jun 11.
Very limited treatment options are available to fight hepatocellular carcinoma (HCC), a serious global health concern with high morbidity and mortality. The integration of multiple therapies into one nanoplatform to exert synergistic therapeutic effects offers advantages over monotherapies. Here, we describe the construction of the nanoplatform Sor@GR-COF-366 for synergistic chemotherapy and photodynamic therapy (PDT) for HCC using a porphyrin-based covalent organic framework (COF-366) coated with N-acetyl-galactosamine (GalNAc) and rhodamine B (RhB), and loaded with the first-line agent, Sorafenib (Sor). The nanoplatform is targeted towards ASGPR-overexpressed HCC cells and liver tissues by GalNAc and observed by real-time imaging of RhB in vitro and in vivo. The nanoplatform Sor@GR-COF-366 exerts an enhanced synergistic tumor suppression effect in a subcutaneous HCC mouse model with a tumor inhibition rate (TGI) of 97% while significantly prolonging survival at very low toxicity. The potent synergistic therapeutic outcome is confirmed in an orthotopic mouse model of HCC with the TGI of 98% with a minimally invasive interventional PDT (IPDT). Sor@GR-COF-366 is a promising candidate to be combined with chemo-IPDT for the treatment of HCC. STATEMENT OF SIGNIFICANCE: This work describes the construction of covalent-organic frameworks (COFs) modified with glyco-moieties to serve as hepato-targeted multitherapy delivery systems. They combine minimally invasive interventional photodynamic therapy (IPDT) triggered synergism with chemotherapy treatment for hepatocellular carcinoma (HCC). With the aid of minimally invasive intervention, PDT can elicit potent anti-cancer activity for deep solid tumors. This platform shows strong therapeutic outcomes in both subcutaneous and orthotopic mouse models, which can significantly prolong survival. This work showed an effective combination of a biomedical nano-formulation with the clinical operational means in cancer treatment, which is greatly promising in clinical translation.
用于治疗肝细胞癌 (HCC) 的治疗选择非常有限,HCC 是一种严重的全球健康问题,具有高发病率和死亡率。将多种疗法整合到一个纳米平台中以发挥协同治疗效果优于单药治疗。在这里,我们描述了使用基于卟啉的共价有机框架 (COF-366) 构建纳米平台 Sor@GR-COF-366,用于协同化疗和光动力疗法 (PDT) 治疗 HCC,该 COF-366 用 N-乙酰半乳糖胺 (GalNAc) 和罗丹明 B (RhB) 进行了涂层,并负载了一线药物索拉非尼 (Sor)。纳米平台通过 GalNAc 靶向过表达 ASGPR 的 HCC 细胞和组织,并通过体外和体内 RhB 的实时成像进行观察。纳米平台 Sor@GR-COF-366 在皮下 HCC 小鼠模型中表现出增强的协同肿瘤抑制作用,肿瘤抑制率 (TGI) 为 97%,同时在非常低的毒性下显著延长了生存期。在 HCC 的原位小鼠模型中,通过微创介入光动力疗法 (IPDT) 证实了强大的协同治疗效果,TGI 为 98%。Sor@GR-COF-366 是一种很有前途的候选药物,可与化疗-IPDT 联合用于治疗 HCC。
本工作描述了用糖基修饰的共价有机框架 (COFs) 构建作为肝靶向多疗法递送系统。它们结合微创介入光动力疗法 (IPDT) 触发的协同作用与化疗治疗肝细胞癌 (HCC)。借助微创干预,PDT 可以为深部实体肿瘤引发强大的抗癌活性。该平台在皮下和原位小鼠模型中均显示出强大的治疗效果,可显著延长生存期。这项工作展示了生物医学纳米制剂与癌症治疗中的临床操作手段的有效结合,在临床转化中具有很大的应用前景。