Si Xinghui, Ji Guofeng, Ma Sheng, Xu Yudi, Zhao Jiayu, Huang Zichao, Zhang Yu, Song Wantong, Tang Zhaohui
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. China.
University of Science and Technology of China, Hefei 230026, P. R. China.
ACS Biomater Sci Eng. 2020 Sep 14;6(9):5281-5289. doi: 10.1021/acsbiomaterials.0c00840. Epub 2020 Aug 11.
Peritoneal seeding represents one of the most frequent sites of metastasis for late-stage gastrointestinal and gynecological cancer. At present, the major treatment method for peritoneal metastatic carcinoma (PMC) is the combination of cytoreductive surgery (CRS) with hyperthermic intraperitoneal chemotherapy (HIPEC). Nevertheless, the 5 year survival rate of patients after these treatments is still far from satisfactory. Here, we report a biodegradable implant co-loaded with doxorubicin (DOX) and anti-PD-1 monoclonal antibody (aPD-1) (BI@DOX+aPD-1) for a combination of immunogenic chemotherapy and immune checkpoint therapy for PMC postoperative treatment. The bio-implant is fabricated with oxidized dextran (ODEX) and 4-arm poly(ethylene glycol) amine (4-arm PEG-NH) by Schiff's base reaction at mild conditions, with DOX and aPD-1 loaded inside during and after the fabrication process, respectively. studies confirmed the slow and sustained release of DOX and aPD-1 from the bio-implants. studies showed that the bio-implants could be gradually degraded and maintain relatively high concentrations of therapeutic agents in the mouse abdomen. In a murine CT26 PMC model, the BI@DOX+aPD-1 resulted in a 89.7% tumor-suppression rate after peritoneal implantation. Importantly, the combination therapy of DOX and aPD-1 in the bio-implant showed an excellent synergistic effect with a value of 2.35. This easy-fabricated bio-implant combined with DOX and aPD-1 should be promising for clinical PMC postoperative treatment.
腹膜种植是晚期胃肠道和妇科癌症最常见的转移部位之一。目前,腹膜转移癌(PMC)的主要治疗方法是减瘤手术(CRS)联合腹腔内热灌注化疗(HIPEC)。然而,这些治疗后患者的5年生存率仍远不尽人意。在此,我们报道一种可生物降解的植入物,其共负载阿霉素(DOX)和抗PD-1单克隆抗体(aPD-1)(BI@DOX+aPD-1),用于PMC术后免疫原性化疗和免疫检查点治疗的联合应用。该生物植入物是在温和条件下通过席夫碱反应由氧化葡聚糖(ODEX)和四臂聚乙二醇胺(4臂PEG-NH)制备而成,在制备过程中和制备后分别将DOX和aPD-1负载于其中。研究证实了DOX和aPD-1从生物植入物中的缓慢持续释放。研究表明,该生物植入物可在小鼠腹腔内逐渐降解并维持较高浓度的治疗药物。在小鼠CT26 PMC模型中,腹膜植入BI@DOX+aPD-1后肿瘤抑制率达89.7%。重要的是,生物植入物中DOX和aPD-1的联合治疗显示出优异的协同效应,协同指数为2.35。这种易于制备的联合DOX和aPD-1的生物植入物在PMC术后临床治疗中应具有广阔前景。