首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Synthesis of Fe_3O_4@silica/poly(N-isopropylacrylamide) as a novel thermo-responsive system for controlled release of H3PMo12O40 nano drug in AC magnetic field
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Synthesis of Fe_3O_4@silica/poly(N-isopropylacrylamide) as a novel thermo-responsive system for controlled release of H3PMo12O40 nano drug in AC magnetic field

机译:Fe_3O_4 @二氧化硅/聚(N-异丙基丙烯酰胺)的合成作为AC磁场中H3PMO12O40纳米药物控制释放的新型热响应系统

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摘要

In this work, a new method is introduced for synthesis of nano drug for the first time. H3PMo12O40 and Fe_3O_4@SiO_2/poly(N-isopropylacrylamide), were prepared as nano drug and magneto thermally responsive nano-carrier respectively. Then the released behavior of H3PMo12O40 nano-drug from this thermo-responsive carrier was investigated in an AC magnetic field. When a drug particle is broken up to nanometer range, the total surface area is increased; therefore the rate of dissolution and the rate of release are increased. The as-synthesized nanostructures were characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), and Fourier transform infrared spectroscopy (FT-IR). Furthermore, experimental condition which lead to the released profile of H_3PMo_(12)O_(40) nano-drug from Fe_3O_4@SiO_2/poly(N-isopropylacrylamide), such as strength of magnetic field (H), temperature (T), particle size of drug and content of loaded drug were tested. Increasing the strength of magnetic field, temperature and content of loaded drug, the rate of drug release was also increased.
机译:在这项工作中,首次引入了一种新方法,用于合成纳米药物。 H3PMO12O40和Fe_3O_4 / @ SiO_2 / Poly(N-异丙基丙烯酰胺)分别作为纳米药物和磁热响应纳米载体制备。然后在AC磁场中研究了来自该热响应载体的H3PMO12O40纳米药物的释放行为。当药物颗粒被破坏到纳米范围时,总表面积增加;因此,增加溶解和释放速率。通过扫描电子显微镜(SEM),X射线粉末衍射(XRD),透射电子显微镜(TEM),振动样品仪(VSM)和傅里叶变换红外光谱(FT-IR),表征了如合成的纳米结构。此外,导致H_3PMO_(12)o_(40)纳米药物的释放型材的实验条件来自Fe_3O_4 / poly_2 / poly(n-异丙基丙烯酰胺),例如磁场(h)的强度,温度(t),颗粒测试了药物的尺寸和载药的含量。增加磁场的强度,负载药物的温度和含量,药物释放速率也增加。

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