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一种基于缺陷相关发光介孔二氧化硅的可追踪且靶向骨的纳米组装体,用于增强成骨分化。

A traceable and bone-targeted nanoassembly based on defect-related luminescent mesoporous silica for enhanced osteogenic differentiation.

作者信息

Ren Huihui, Chen Shizhu, Jin Yanan, Zhang Cuimiao, Yang Xinjian, Ge Kun, Liang Xing-Jie, Li Zhenhua, Zhang Jinchao

机构信息

College of Chemistry & Environmental Science, Chemical Biology Key Laboratory of Hebei Province, Analytical Chemistry Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, P. R. China.

出版信息

J Mater Chem B. 2017 Feb 28;5(8):1585-1593. doi: 10.1039/c6tb02552h. Epub 2017 Feb 3.

Abstract

Osteoporosis is a degenerative bone disorder that affects millions of people worldwide. Despite many novel drugs or therapy strategies that have been developed, the curative effect of current treatments is far from satisfying. Development of effective treatments toward osteoporosis is imminent. Bone mesenchymal stem cells (BMSCs) are one kind of pluripotent stem cells, which are not only easy to separate and purify but also can self-renew and differentiate into osteogenic cells. In this work, a traceable drug delivery system based on gadolinium-labeled defect-related luminescent mesoporous silica nanoparticles (MSNs) was developed for bone marrow homing and enhanced osteogenic differentiation. The results showed that dexamethasone (DEX) could be loaded into nanocarriers and gave a sustained release behaviour. A unique defect-related luminescent property could be utilized to monitor the drug release effectively. In addition, the nanocarriers showed good biocompatibility and were uptaken mainly via an energy-dependent endocytosis process which was mediated by the macropinocytosis pathway. Furthermore, the nanocarriers can be simultaneously used as predominant contrast agents for magnetic resonance imaging. More importantly, DEX-loaded nanocarriers can significantly enhance the alkaline phosphatase activity and promote formation of matrix nodules of the BMSCs.

摘要

骨质疏松症是一种退行性骨疾病,影响着全球数百万人。尽管已经开发了许多新型药物或治疗策略,但目前治疗的疗效仍远不能令人满意。开发针对骨质疏松症的有效治疗方法迫在眉睫。骨髓间充质干细胞(BMSCs)是一种多能干细胞,不仅易于分离和纯化,而且能够自我更新并分化为成骨细胞。在这项工作中,开发了一种基于钆标记的缺陷相关发光介孔二氧化硅纳米颗粒(MSNs)的可追踪药物递送系统,用于骨髓归巢和增强成骨分化。结果表明,地塞米松(DEX)可以负载到纳米载体中并呈现出缓释行为。独特的缺陷相关发光特性可用于有效监测药物释放。此外,纳米载体表现出良好的生物相容性,主要通过巨胞饮途径介导的能量依赖性内吞过程被摄取。此外,纳米载体可同时用作磁共振成像的主要造影剂。更重要的是,负载DEX的纳米载体可以显著提高BMSCs的碱性磷酸酶活性并促进基质结节的形成。

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