Folic Acid-Conjugated MnO Nanoparticles as a T1 Contrast Agent for Magnetic Resonance Imaging of Tiny Brain Gliomas

被引:68
作者
Chen, Ning [1 ]
Shao, Chen [2 ]
Qu, Yanming [1 ]
Li, Shuai [2 ]
Gu, Wei [2 ]
Zheng, Tingting [2 ]
Ye, Ling [2 ]
Yu, Chunjiang [1 ]
机构
[1] Capital Med Univ, Beijing Sanbo Brain Hosp, Dept Neurosurg, Beijing 100093, Peoples R China
[2] Capital Med Univ, Sch Chem Biol & Pharmaceut Sci, Beijing 100069, Peoples R China
关键词
manganese oxide nanoparticles (MnO NPs); tiny brain glioma; magnetic resonance imaging (MRI); folic acid (FA); MANGANESE OXIDE NANOPARTICLES; IN-VIVO; DRUG-DELIVERY; MRI CONTRAST; PROBES; CELLS; FUNCTIONALIZATION; RELAXIVITY; PLATFORM; VITRO;
D O I
10.1021/am505223t
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Detection of brain gliomas at the earliest stage is of great importance to improve outcomes, but it remains a most challenging task. In this study, oleic acid capped manganese oxide (MnO) nanoparticles (NPs) were prepared by the thermal decomposition of manganese oleate precursors and then transformed to water-dispersible MnO NPs by replacing oleic acid with N-(trimethoxysilylpropyl) ethylene diamine triacetic acid (TETT) silane. The covalently bonded TETT silane offers MnO NPs colloidal stability and abundant carboxylic functional groups allowing the further conjugation of the glioma-specific moiety, folic acid (FA). Moreover, the thin layer of TETT silane ensures a short distance between external Mn ion and water proton, which endows the FA-conjugated, TETT modified MnO (MnO-TETT-FA) NPs a longitudinal relaxivity as high as 4.83 mM(-1) s(-1). Accordingly, the in vivo magnetic resonance (MR) images demonstrated that MnO-TETT-FA NPs could efficiently enhance the MRI contrast for tiny brain gliomas. More importantly, due to the specificity of FA, MnO-TETT-FA NPs led to a clearer margin of the tiny glioma. This together with the good biocompatibility discloses the great potential of MnO-TETT-FA NPs as effective MRI contrast agents for the early diagnosis of brain gliomas.
引用
收藏
页码:19850 / 19857
页数:8
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