Shenzhen Key Laboratory of Smart Healthcare Engineering, Guangdong Provincial Key Laboratory of Advanced Biomaterials, Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen 518055, China.
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
ACS Biomater Sci Eng. 2024 Apr 8;10(4):2270-2281. doi: 10.1021/acsbiomaterials.3c01887. Epub 2024 Mar 27.
Tumor hypoxia-associated drug resistance presents a major challenge for cancer chemotherapy. However, sustained delivery systems with a high loading capability of hypoxia-inducible factor-1 (HIF-1) inhibitors are still limited. Here, we developed an ultrastable iodinated oil-based Pickering emulsion (PE) to achieve locally sustained codelivery of a HIF-1 inhibitor of acriflavine and an anticancer drug of doxorubicin for tumor synergistic chemotherapy. The PE exhibited facile injectability for intratumoral administration, great radiopacity for in vivo examination, excellent physical stability (>1 mo), and long-term sustained release capability of both hydrophilic drugs (i.e., acriflavine and doxorubicin). We found that the codelivery of acriflavine and doxorubicin from the PE promoted the local accumulation and retention of both drugs using an acellular liver organ model and demonstrated significant inhibition of tumor growth in a 4T1 tumor-bearing mouse model, improving the chemotherapeutic efficacy through the synergistic effects of direct cytotoxicity with the functional suppression of HIF-1 pathways of tumor cells. Such an iodinated oil-based PE provides a great injectable sustained delivery platform of hydrophilic drugs for locoregional chemotherapy.
肿瘤乏氧相关的耐药性是癌症化疗的主要挑战。然而,具有高载氧诱导因子-1(HIF-1)抑制剂能力的持续释放系统仍然有限。在这里,我们开发了一种超稳定的碘油基 Pickering 乳液(PE),以实现局部持续共递送吖啶黄素作为 HIF-1 抑制剂和阿霉素作为抗癌药物,用于肿瘤协同化疗。PE 具有可注射用于瘤内给药、体内检查的高放射密度、出色的物理稳定性(>1 个月)和两种亲水性药物(即吖啶黄素和阿霉素)的长期持续释放能力。我们发现,从 PE 共递送吖啶黄素和阿霉素促进了在非细胞肝脏器官模型中两种药物的局部积累和保留,并在 4T1 荷瘤小鼠模型中显示出显著的肿瘤生长抑制作用,通过与肿瘤细胞的 HIF-1 途径的功能抑制的直接细胞毒性协同作用,提高了化疗疗效。这种碘油基 PE 为局部化疗提供了一种可注射的亲水性药物持续释放平台。