前药
光热治疗
提拉帕扎明
化学
体内
生物物理学
介孔二氧化硅
体外
缺氧(环境)
肿瘤缺氧
癌症研究
纳米技术
放射治疗
介孔材料
氧气
催化作用
材料科学
生物化学
有机化学
医学
生物
生物技术
内科学
细胞毒性
作者
Wenting Li,Shikai Liu,Shuming Dong,Shili Gai,Fangmei Zhang,Yushan Dong,Dan Yang,Fei He,Lei Zhong,Piaoping Yang
标识
DOI:10.1016/j.cej.2020.127027
摘要
Synergistic therapy with different treatment mechanisms is an emerging strategy to improve antitumor efficiency. Here, a diversified nanoplatform (Ag2[email protected]) is synthesized by coating mesoporous silica on Ag2S nanoparticles (NPs), followed by loading hypoxia-active prodrug (tirapazamine) insides the mesoporous silica and coating glucose oxidase (GOx) on the surface. Considering that the degree of hypoxia in tumors is not high enough, GOx is combined with hypoxia-active tirapazamine prodrug, and two important functions are realized. One is the consumption of oxygen to enhance the hypoxic environment and promote the curative effect of tirapazamine, and the other is the consumption of glucose to achieve starvation treatment. Additionally, we take the lead in using Ag2S NPs for second near-infrared (NIR-II, 1064 nm) excited photothermal therapy (PTT). The photothermal conversion efficiency (44.7%) of Ag2[email protected] is even better than that under 808 nm laser irradiation (38.2%). Finally, in vivo NIR-II fluorescence imaging well demonstrated that Ag2[email protected] can offer an obvious tracking effect for the therapeutic process. Therefore, superior to any single therapeutic mode, our designed Ag2[email protected] demonstrates an excellent tumor inhibition effect in vitro and in vivo due to synergistic starvation, hypoxia-active prodrug treatment and PTT effect, suggesting the significant prospect of NIR-II imaging guided antitumor therapy.
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