光动力疗法
光敏剂
体内
肿瘤微环境
化学
癌症研究
缺氧(环境)
肿瘤缺氧
活性氧
生物相容性
医学
药品
药物输送
氧气
生物物理学
药理学
生物化学
光化学
放射治疗
肿瘤细胞
外科
有机化学
生物
生物技术
作者
Xingchao Wang,Zhiqiang Wang,Wei Ma,Xiaodan Wu,Wen Fang,Changhong Guo,Yingxue Jin
标识
DOI:10.1016/j.jphotobiol.2021.112274
摘要
Photodynamic therapy (PDT) has gained much attention in tumor therapy because of its special advantages. PDT heavily depends on the oxygen, yet the tumor microenvironment (TME) is a hypoxic and acid milieu, which weakens the PDT effect. Based on the consideration that the TME deteriorated by the PDT oxygen consumption could activate the hypoxic-sensitive small-molecule drug, we designed and prepared an integrated nanocomposite including zirconium ion metal organic framework (carrier), pyropheophorbide-a (PPa, photosensitizer), and 6-amino flavone (AF, hypoxic-sensitive drug), aiming to exert a cascaded PDT-chemotherapy (CT) antitumor effect and to solve the hypoxic challenge. The prepared nanocomposite showed great stability under the physiological (pH 7.4) condition and could continuously release PPa and AF under slightly acidic pH condition (pH 6.4), suggesting a tumor microenvironment responsive feature. Systematical in vitro and in vivo researches under various conditions (light, dark, hypoxic and normoxic) have showed that the obtained [email protected]/[email protected] nanoparticles (NPs) had good biocompatibility and could achieve efficient antitumor effects based on PDT- chemotherapy (CT) cascade process. Finally, bright red fluorescence was observed in the tumor cells after internalization implying an application potential in tumor imaging.
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