Affiliation:
1. Beijing National Laboratory for Molecular Sciences Laboratory of Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
2. University of Chinese Academy of Sciences Beijing 100049 P. R. China
Abstract
AbstractSelective activation of Pt(IV) prodrugs within tumors is particularly attractive because of their low damage to normal tissues. However, current common activation via chemical/photoreduction of Pt(IV) prodrugs into Pt(II) counterparts is limited by undesirable spatial–temporal control over this reduction process and the ineffective tissue penetration depth of undesirable light. Here, a pseudo‐conjugated‐polymer is designed via Stille polymerization, resulting in PSP‐Pt with a Pt(IV) prodrug of oxaliplatin (Oxa(IV)) in the polymer main chain that can be activated by NIR‐II light. PSP‐Pt can co‐assemble with a commercially available lipid polymer, namely mPEG2k‐DSPE, into NPPSP‐Pt. Under 1064 nm light irradiation, NPPSP‐Pt can be photoactivated to accelerate the Pt(IV) reduction to release oxaliplatin, thereby killing the cancer cells by photothermal effect and chemo‐immunotherapy inside a mouse model with CT26 colon cancer. This work reports the application of NIR‐II light for accelerating Pt(IV) reduction for cancer tumor therapy.
Funder
National Natural Science Foundation of China
Subject
Mechanical Engineering,Mechanics of Materials,General Materials Science
Cited by
12 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献