Yang Ji-Chun, Shang Yue, Li Yu-Hao, Cui Yu, Yin Xue-Bo
State Key Laboratory of Medicinal Chemical Biology , Tianjin Key Laboratory of Biosensing and Molecular Recognition , College of Chemistry , Nankai University , Tianjin , 300071 , China . Email:
Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation , School of Medicine , Nankai University , Tianjin , 300071 , China.
Chem Sci. 2018 Jul 30;9(36):7210-7217. doi: 10.1039/c8sc02305k. eCollection 2018 Sep 28.
Drug-loading often suffers from tedious procedures, limited loading efficiency, slow release, and therefore a low curative effect. Cancer easily recurs and metastasizes even after a solid tumor is removed. Herein, we report a simple strategy with multi-drug co-loading and burst drug release for a high curative effect and anti-recurrence/metastasis. CuS nanoparticles, protoporphyrin IX, and doxorubicin were added to the precursors of ZIF-8 with one-pot co-loading during the formation of ZIF-8 for chemo-, photothermal-, and photodynamic-therapy to eliminate solid tumors. Negative CpG, as a kind of immune adjuvant, was adsorbed on the positive surface of ZIF-8 to inhibit the recurrence and metastasis of tumors with its long-term immune response. Precision treatment with one-pot multi-drug co-loading, controllable drug delivery, and multi-modality therapy may be anticipated by this versatile strategy.
药物负载通常存在操作繁琐、负载效率有限、释放缓慢等问题,因此疗效较低。即使实体瘤被切除,癌症仍容易复发和转移。在此,我们报告了一种简单的策略,即多药共负载和突发药物释放,以实现高疗效和抗复发/转移。在ZIF-8形成过程中,将硫化铜纳米颗粒、原卟啉IX和阿霉素一锅法共负载到ZIF-8的前体中,用于化学疗法、光热疗法和光动力疗法以消除实体瘤。阴性CpG作为一种免疫佐剂,吸附在ZIF-8的阳性表面,通过其长期免疫反应抑制肿瘤的复发和转移。这种通用策略有望实现一锅法多药共负载、可控药物递送和多模态治疗的精准治疗。