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通过叶酸修饰的表面工程化多壁碳纳米管将药物靶向递送至关节炎区域。

Drug targeting to arthritic region via folic acid appended surface-engineered multi-walled carbon nanotubes.

作者信息

Kayat Jitendra, Mehra Neelesh Kumar, Gajbhiye Virendra, Jain Narendra Kumar

机构信息

a Pharmaceutics Research Laboratory, Department of Pharmaceutical Sciences , Dr. Hari Singh Gour University , Sagar , Madhya Pradesh , India .

b Pharmaceutical Nanotechnology Research Laboratory, Department of Pharmaceutics , ISF College of Pharmacy , Moga , Punjab , India , and.

出版信息

J Drug Target. 2016;24(4):318-27. doi: 10.3109/1061186X.2015.1077846. Epub 2015 Aug 18.

Abstract

This study was aimed at developing and investigating folate anchored carbon nanotubes for targeting an anti-arthritic drug, Methotrexate (MTX) to inflammatory arthritic region. The folic acid (FA) was conjugated to amidated multi-walled carbon nanotubes (MWCNTs) and confirmed by Fourier transform infrared (FTIR), (1)H NMR spectroscopy and X-ray diffraction analysis. The MTX was loaded into the pristine and functionalized-MWCNTs and extensively characterized in vitro and in vivo studies. The drug entrapment efficiency was found high in folate conjugated MWCNTs. In vitro drug release in PBS (pH 7.4) from pristine MWCNTs and folate conjugated MWCNTs formulation was found to be 66.35 ± 2.3 and 56.88 ± 1.9% in 24 h, respectively. Folate conjugated MWCNTs significantly increased (p < 0.005) the percentage inhibition of arthritis, biological half-life and volume of distribution of MTX as compared to MTX-loaded naked MWCNTs as well as free MTX. In in vivo biodistribution studies, MTX was found to be significantly higher (p < 0.005) in arthritic joints from folate functionalized MWCNTs as compared to free drug as well as drug-loaded naked MWCNTs. The present outcomes highlights the propensity of drug-loaded functionalized MWCNTs to alter the pharmacokinetics as well as sustained and targeted drug delivery system as well.

摘要

本研究旨在开发并研究叶酸锚定的碳纳米管,用于将抗关节炎药物甲氨蝶呤(MTX)靶向递送至炎性关节炎区域。将叶酸(FA)与酰胺化多壁碳纳米管(MWCNTs)偶联,并通过傅里叶变换红外光谱(FTIR)、氢核磁共振(¹H NMR)光谱和X射线衍射分析进行确认。将MTX载入原始的和功能化的MWCNTs中,并在体外和体内研究中进行广泛表征。发现在叶酸偶联的MWCNTs中药物包封效率较高。在PBS(pH 7.4)中,原始MWCNTs和叶酸偶联MWCNTs制剂的体外药物释放率在24小时内分别为66.35±2.3%和56.88±1.9%。与载有MTX的裸MWCNTs以及游离MTX相比,叶酸偶联的MWCNTs显著提高了(p<0.005)关节炎的抑制百分比、MTX的生物半衰期和分布容积。在体内生物分布研究中,与游离药物以及载药裸MWCNTs相比,发现叶酸功能化MWCNTs在关节炎关节中的MTX含量显著更高(p<​0.005)。目前的研究结果突出了载药功能化MWCNTs改变药代动力学的倾向以及持续和靶向给药系统的特性。

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