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原位微乳液法合成羟基磷灰石 - 镁铁氧体纳米复合材料作为磁性药物递送系统

In situ microemulsion synthesis of hydroxyapatite-MgFe2O4 nanocomposite as a magnetic drug delivery system.

作者信息

Foroughi Firoozeh, Hassanzadeh-Tabrizi S A, Bigham Ashkan

机构信息

Young Researchers and Elite Club, Najafabad Branch, Islamic Azad University, Najafabad, Iran.

Young Researchers and Elite Club, Najafabad Branch, Islamic Azad University, Najafabad, Iran.

出版信息

Mater Sci Eng C Mater Biol Appl. 2016 Nov 1;68:774-779. doi: 10.1016/j.msec.2016.07.028. Epub 2016 Jul 14.

DOI:10.1016/j.msec.2016.07.028
PMID:27524079
Abstract

In this study, an innovative synthesis process has been developed to produce hydroxyapatite-magnesium ferrite (HA-MgFe2O4) nanocomposite. In addition, the effect of calcination temperature on drug delivery behavior of produced samples was investigated. HA-MgFe2O4 nanocomposite was prepared via one-step modified reverse microemulsion synthesis route. The resulting products were characterized by X-ray Diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), and Brunauer-Emmett-Teller surface area analysis (BET). The calcined samples at 500 and 700°C demonstrated mesoporous characteristics and large specific surface areas of 88 and 32m(2)/g, respectively. TEM and VSM results showed that the nanocomposite calcined at 700°C has core-shell morphology and a maximum saturation magnetization of 9.47emug(-1).

摘要

在本研究中,已开发出一种创新的合成工艺来制备羟基磷灰石-镁铁氧体(HA-MgFe2O4)纳米复合材料。此外,还研究了煅烧温度对所制备样品药物递送行为的影响。HA-MgFe2O4纳米复合材料通过一步改性反相微乳液合成路线制备。所得产物通过X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、场发射扫描电子显微镜(FESEM)、透射电子显微镜(TEM)、振动样品磁强计(VSM)和布鲁诺尔-埃米特-泰勒表面积分析(BET)进行表征。在500和700°C煅烧的样品分别表现出介孔特性和88和32m(2)/g的大比表面积。TEM和VSM结果表明,在700°C煅烧的纳米复合材料具有核壳形态,最大饱和磁化强度为9.47emug(-1)。

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