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首页> 外文期刊>Drug development and industrial pharmacy >pH- and thermo-sensitive MTX-loaded magnetic nanocomposites: synthesis, characterization, and in vitro studies on A549 lung cancer cell and MR imaging
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pH- and thermo-sensitive MTX-loaded magnetic nanocomposites: synthesis, characterization, and in vitro studies on A549 lung cancer cell and MR imaging

机译:pH-和热敏MTX负载磁性纳米复合材料:合成,表征和对A549肺癌细胞和MR成像的体外研究

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摘要

In the current study, we proposed a facile method for fabrication of multifunctional pH- and thermo-sensitive magnetic nanocomposites (MNCs) as a theranostic agent for using in targeted drug delivery and magnetic resonance imaging (MRI). To this end, we decorated Fe3O4 magnetic nanoparticles (MNPs) with N,N-dimethylaminoethyl methacrylate (DMAEMA) and N-isopropylacrylamide (NIPAAm), best known for their pH- and thermo-sensitive properties, respectively. We also conjugated mesoporous silica nanoparticles (MSNs) to polymer matrix acting as drug container to enhance the drug encapsulation efficacy. Methotroxate (MTX) as a model drug was successfully loaded in MNCs (M-MNCs) via surface adsorption onto MSNs and electrostatic interaction between drug and carrier. The pH- and temperature-triggered release of MTX was concluded through the evaluation of in vitro release at both physiological and simulated tumor tissue conditions. Based on in vitro cytotoxicity assay results, M-MNCs significantly revealed higher antitumor activity compared to free MTX. In vitro MR susceptibility experiment showed that M-MNCs relatively possessed high transverse relaxivity (r2) of about 0.15 mM?1·ms?1 and a linear relationship between the transverse relaxation rate (R2) and the Fe concentration in the M-MNCs was also demonstrated. Therefore, the designed MNCs can potentially become smart drug carrier, while they also can be promising MRI negative contrast agent.
机译:在目前的研究中,我们提出了一种用于在靶向药物输送和磁共振成像(MRI)中使用的用于使用靶向药物递送的多功能pH和热敏磁性纳米复合材料(MNC)的容易方法。为此,我们用N,N-二甲基氨基乙基甲基丙烯酸甲酯(DMAEMA)和N-异丙基丙烯酰胺(NIPAAM)装饰Fe3O4磁性纳米颗粒(MNP),分别用于其pH-和热敏性质。我们还共轭介孔二氧化硅纳米颗粒(MSN)至聚合物基质作用作为药物容器以增强药物包封功效。作为模型药物的甲氨酸甲酸(MTX)通过表面吸附在MNC(M-MNCs)中成功地装载到MSN和药物和载体之间的静电相互作用。通过在生理和模拟肿瘤组织条件下的体外释放的评估来结束MTX的pH-和温度触发的释放。基于体外细胞毒性测定结果,与游离MTX相比,M-MNC显着揭示了较高的抗肿瘤活性。在体外MR易感性实验表明,M-MNCs相对具有约0.15mm = 1·MS 2的高横向松弛率(R2)和横向松弛率(R2)与M-MNC中的Fe浓度之间的线性关系也证明。因此,设计的MNC可能成为智能药物载体,而它们也可以是有前途的MRI负造影剂。

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