| Literature DB >> 26012928 |
Yanyan Liu1, Yong Liu2, Wenbo Bu3, Chao Cheng4, Changjing Zuo4, Qingfeng Xiao1, Yong Sun2, Dalong Ni1, Chen Zhang1, Jianan Liu1, Jianlin Shi5.
Abstract
Local hypoxia in tumors is an undesirable consequence of photodynamic therapy (PDT), which will lead to greatly reduced effectiveness of this therapy. Bioreductive pro-drugs that can be activated at low-oxygen conditions will be highly cytotoxic under hypoxia in tumors. Based on this principle, double silica-shelled upconversion nanoparticles (UCNPs) nanostructure capable of co-delivering photosensitizer (PS) molecules and a bioreductive pro-drug (tirapazamine, TPZ) were designed (TPZ-UC/PS), with which a synergetic tumor therapeutic effect has been achieved first by UC-based (UC-) PDT under normal oxygen environment, immediately followed by the induced cytotoxicity of activated TPZ when oxygen is depleted by UC-PDT. Treatment with TPZ-UC/PS plus NIR laser resulted in a remarkably suppressed tumor growth as compared to UC-PDT alone, implying that the delivered TPZ has a profound effect on treatment outcomes for the much-enhanced cytotoxicity of TPZ under PDT-induced hypoxia.Entities:
Keywords: bioreductive pro-drugs; hypoxia; photodynamic therapy; synergetic therapy; upconversion nanoparticles
Mesh:
Substances:
Year: 2015 PMID: 26012928 DOI: 10.1002/anie.201500478
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336