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用于局部经皮给药治疗类风湿性关节炎的纳米控释甲氨蝶呤递送系统的构建

Construction of a Nano-Controlled Release Methotrexate Delivery System for the Treatment of Rheumatoid Arthritis by Local Percutaneous Administration.

作者信息

Guo Tingting, Kang Xu, Ren Sifan, Ouyang Xianjin, Chang Mingming

机构信息

College of Bioscience and Resource Environment, Beijing University of Agriculture, Beijing 102206, China.

Key Laboratory of Urban Agriculture (North China) Ministry of Agriculture, Beijing University of Agriculture, Beijing 102206, China.

出版信息

Nanomaterials (Basel). 2021 Oct 23;11(11):2812. doi: 10.3390/nano11112812.

Abstract

A drug delivery system was specifically designed for the treatment of rheumatoid arthritis (RA) by local percutaneous administration and the nano-controlled release of methotrexate (MTX). The release behavior of MTX from the synthesized MTX-mSiO@PDA system was investigated in vitro and in vivo. The obtained results show that after 48 h, twice as much MTX (cumulative amount) is released at pH 5.5 than at pH 7.4. This suggests that the MTX-mSiO@PDA system exhibits a good pH sensitivity. In vitro local percutaneous administration experiments revealed that the cumulative amount of MTX transferred from MTX-mSiO@PDA to pH 5.0 receptor fluid through the whole skin was approximately three times greater than the amount transferred to pH 7.4 receptor fluid after 24 h. Moreover, in vivo experiments conducted on a complete induced arthritis (CIA) model in DBA/1 mice demonstrated that the thickness of a mouse's toes decreases to nearly 65% of the initial level after 27 days of local percutaneous MTX-mSiO@PDA administration. Compared to the mice directly injected with MTX, those administered with MTX-mSiO@PDA by local percutaneous application exhibit much lower toe thickness deviation, which indicates that the latter group experiences a better cure stability. Overall, these results demonstrate that the local percutaneous administration of MTX delivery systems characterized by nano-controlled release may play an important role in RA therapy.

摘要

一种药物递送系统专门设计用于通过局部经皮给药和甲氨蝶呤(MTX)的纳米控释来治疗类风湿性关节炎(RA)。研究了MTX从合成的MTX-mSiO@PDA系统中的体外和体内释放行为。所得结果表明,48小时后,在pH 5.5时释放的MTX(累积量)是pH 7.4时的两倍。这表明MTX-mSiO@PDA系统表现出良好的pH敏感性。体外局部经皮给药实验表明,经24小时后,MTX从MTX-mSiO@PDA通过全皮转移到pH 5.0受体液中的累积量约为转移到pH 7.4受体液中的量的三倍。此外,在DBA/1小鼠的完全诱导性关节炎(CIA)模型上进行的体内实验表明,局部经皮给予MTX-mSiO@PDA 27天后,小鼠脚趾厚度降至初始水平的近65%。与直接注射MTX的小鼠相比,通过局部经皮应用给予MTX-mSiO@PDA的小鼠的脚趾厚度偏差要低得多,这表明后一组具有更好的治愈稳定性。总体而言,这些结果表明,以纳米控释为特征的MTX递送系统的局部经皮给药可能在RA治疗中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2777/8624172/68bfa7b53854/nanomaterials-11-02812-g001a.jpg

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