Near-infrared light triggered activation of pro-drug combination cancer therapy and induction of immunogenic cell death.
Near-infrared light triggered activation of pro-drug combination cancer therapy and induction of immunogenic cell death.
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近红外光触发前药组合癌症疗法的活化和免疫原性细胞死亡的诱导。
DOI:
10.1016/j.ijpharm.2021.120972
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发表时间:
2021-09-25
影响因子:
5.8
通讯作者:
Li F
中科院分区:
文献类型:
--
作者:
Kang X;Cai Y;Wang Q;Wang C;Chen W;Yang W;Suryawanshi A;Zhou G;Chen P;Li F
Disulfiram copper complex [Cu(DDC)2] nanoparticles have been explored as promising anticancer agents but with concerns of toxic side effects. To improve tumor specificity and enhance anticancer efficacy, we developed a novel [copper sulfide nanoparticle (CuS NP) + disulfiram prodrug (DQ) micelle + near-infrared (NIR) laser] (CDL) combination therapy. DQ, a reactive oxygen species (ROS)-responsive prodrug, can be selectively activated at the tumor site with elevated ROS to release DDC and form Cu(DDC)2 in situ. The CuS NP + NIR laser treatment can effectively increase the intra-tumor ROS levels and efficiently activate the DQ prodrug. The CDL therapy kills cancer cells through multiple mechanisms, including ROS amplification cascade and Cu(DDC)2 chemotherapy. NIR light-triggered tumor-specific “nontoxic-to-toxic” transition can significantly improve the specificity of anticancer effects and reduce systemic toxicity. Also, CDL therapy can effectively induce immunogenic cell death (ICD) and has the potential of eliciting antitumor immunity.
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影响因子:
5.9
作者:
Chu, Zhongyun;Wang, Zhiming;Jia, Nengqin
通讯作者:
Jia, Nengqin
影响因子:
8
作者:
Li, Bin;Jiang, Zhongyin;Lao, Xingzhen
通讯作者:
Lao, Xingzhen
影响因子:
17.1
作者:
Ku, Geng;Zhou, Min;Song, Shaoli;Huang, Qian;Hazle, John;Li, Chun
通讯作者:
Li, Chun
影响因子:
17.1
作者:
Chen, Feng;Hong, Hao;Goel, Shreya;Graves, Stephen A.;Orbay, Hakan;Ehlerding, Emily B.;Shi, Sixiang;Theuer, Charles P.;Nickles, Robert J.;Cai, Weibo
通讯作者:
Cai, Weibo
影响因子:
5.4
作者:
Li, Feng;Danquah, Michael;Mahato, Ram I.
通讯作者:
Mahato, Ram I.