光动力疗法
材料科学
光敏剂
阿霉素
乙二醇
肿瘤缺氧
肿瘤微环境
纳米医学
纳米颗粒
癌症研究
纳米技术
化疗
光化学
化学
医学
有机化学
放射治疗
肿瘤细胞
外科
作者
Haiyang Wang,Wenbo Wang,Lu Liu,Meng Wang,Guowei Li,Hang Li,Bo Li,Siming Yu,Dong Ma,Wei Xue
标识
DOI:10.1021/acsami.1c18601
摘要
Photodynamic therapy (PDT) has attracted extensive attention in the clinical treatment of malignant tumor. However, the acidic and hypoxic conditions of the tumor microenvironment (TME) limit the further application of PDT in the clinic. Herein, we fabricate a new nanoplatform─HPDA@MnO2@Ce6/DOX@PEG-RGD (HPMRCD)─by means of coating hollow polydopamine nanoparticles (HPDA) with manganese dioxide (MnO2), which is modified by cyclic RGD functionalized poly(ethylene glycol) (PEG) and further co-loaded with a photosensitizer, Chlorin e6 (Ce6), and a chemotherapy drug, doxorubicin (DOX). This nanoplatform could be enriched in tumor tissues, then instantly dissociated under an acidic and H2O2-rich TME. The dual-responsive release of Mn2+ ions and oxygen (O2) can relieve tumor hypoxia, which can be used as a magnetic resonance contrast agent and the latter can enhance the PDT effect. Furthermore, the degradation of HPMRCD leads to an efficient loaded therapeutic molecule release, thus yielding a potential therapy to enhance tumor suppression by adopting the combined chemo-photodynamic therapy.
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