布法林
体内
药物输送
纳米颗粒
PLGA公司
化学
肿瘤微环境
体外
材料科学
生物物理学
细胞凋亡
纳米技术
癌症研究
有机化学
生物化学
生物
肿瘤细胞
医学
生物技术
作者
Haijun Wang,David H. Bremner,Kunhua Wu,Xiarong Gong,Qing Fan,Xiaotian Xie,Hongmei Zhang,Junzi Wu,Li‐Min Zhu
标识
DOI:10.1016/j.cej.2019.122848
摘要
In this study, platelet membrane (PLTM) biomimetic hollow MnO2 nanoparticles were prepared and these were investigated for delivery of bufalin. Additionally, these nanoparticles, in response to the tumor microenvironment, showed rapid drug release and generated the hydroxyl radicals (HO) by the Fenton reaction between Mn2+ and endogenous H2O2 for use in MRI-guided anti-tumor activity. Firstly, poly(lactic-co-glycolic acid) (PLGA) nanoparticles were used to reduce KMnO4 to HMnO2 nanoparticles followed by acetone etching. After bufalin loading, these NPs were biomimetically cloaked with PLTM to form PLTM-HMnO2@Bu NPs. In vitro release profiles showed that the NPs responded to acid pH and glutathione (GSH) to induce decomposition of MnO2, resulting in rapid release of bufalin and yielding the MRI contrast agent Mn2+. In vivo MRI studies revealed an obvious T1 contrast enhancement at the tumor site because of a combination of the EPR and active targeting effects. The PLTM-HMnO2 NPs led to effective inhibition of tumor growth, attributing to Fenton-like Mn2+ conversion of endogenous H2O2 in the tumor to highly toxic HO and this anti-tumor efficacy was enhanced when combined with chemotherapy. These results indicate that the PLTM biomimetic HMnO2 nanoparticles are promising drug delivery systems for MRI-monitoring and enhanced targeted treatment of tumors.
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