光热治疗
光动力疗法
光毒性
癌症研究
癌细胞
血管生成
材料科学
体内
生物相容性
药物输送
转移
癌症
纳米技术
体外
医学
化学
生物
生物化学
冶金
有机化学
生物技术
内科学
作者
Yuanying Zhang,Nan Yang,Zhe Dong,Jiahui Wu,Rui Liao,Yanling Zhang,Gege Zhang,Mingqiang Ren,Feng Wang,Xiaochen Dong,Pingping Liang
标识
DOI:10.1021/acsami.3c03471
摘要
Avoiding the low specificity of phototheranostic reagents at the tumor site is a major challenge in cancer phototherapy. Meanwhile, angiogenesis in the tumor is not only the premise of tumor occurrence but also the basis of tumor growth, invasion, and metastasis, making it an ideal strategy for tumor therapy. Herein, biomimetic cancer cell membrane-coated nanodrugs (mBPP NPs) have been prepared by integrating (i) homotypic cancer cell membranes for evading immune cell phagocytosis to increase drug accumulation, (ii) protocatechuic acid for tumor vascular targeting along with chemotherapy effect, and (iii) near-infrared phototherapeutic agent diketopyrrolopyrrole derivative for photodynamic/photothermal synergetic therapy. The mBPP NPs exhibit high biocompatibility, superb phototoxicity, excellent antiangiogenic ability, and double-trigging cancer cell apoptosis in vitro. More significantly, mBPP NPs could specifically bind to tumor cells and vasculature after intravenous injection, inducing fluorescence and photothermal imaging-guided tumor ablation without recurrence and side effects in vivo. The biomimetic mBPP NPs could cause drug accumulation at the tumor site, inhibit tumor neovascularization, and improve phototherapy efficiency, providing a novel avenue for cancer treatment.
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