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一种智能pH响应性磁性纳米复合材料的合成,作为药物的高负载载体。

Synthesis of a smart pH-responsive magnetic nanocomposite as high loading carrier of pharmaceutical agents.

作者信息

Berah Razieh, Ghorbani Mohsen, Moghadamnia Ali Akbar

机构信息

Babol University of Technology, Babol, Iran.

Department of Chemical Engineerng, Babol Noshirvani University of Technolgy, Shariati Ave., Babol, 47148-71167, Iran.

出版信息

Int J Biol Macromol. 2017 Jun;99:731-738. doi: 10.1016/j.ijbiomac.2017.03.039. Epub 2017 Mar 8.

Abstract

To create facile external controlled drug delivery system, a magnetic porous carrier based on Tin oxide nanoparticles was synthesized by an inexpensive and versatile hydrothermal strategy and used for in-vitro process. Magnetic nanocomposites were qualified by Fourier Transform Infrared (FTIR), Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Vibrational Sample Magnetometer (VSM) and Transmission Electron Microscopy (TEM). Results showed that nanoparticles were synthesized successfully with good dispersion of magnetic nanoparticles in cavity, uniform particle size distribution with average size of 65nm and high magnetization of 33.75 emu/mg. Furthermore, the nano-porosity and magnetism allowed high efficiency and remote controlled drug release. In this study, anti-migraine Sumatriptan was used as drug sample and the effect of drug concentration, Fe/Sn ratio and loading time on drug absorption were investigated. The best result was checked for stability at body temperature and different body pH. The sample with drug concentration of 0.25(mg/ml), Fe/Sn=0.22 and loading time of 1.5h had the highest drug efficiency (70%). Finally, in order to simulate the in vivo process for in-vitro step, Amnion was used and drug diffusion rate was measured in different intervals and different pH values. The result illustrated that after 25h, diffusion reached 65% at pH=2 and 56% at pH=7, and then became constant. Based on the above mentioned results, the carrier has an acceptable in vitro yield and therefore could be chosen for future in vivo researches.

摘要

为了构建简便的外部可控药物递送系统,采用一种廉价且通用的水热法合成了基于氧化锡纳米颗粒的磁性多孔载体,并将其用于体外实验。通过傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、X射线衍射(XRD)、振动样品磁强计(VSM)和透射电子显微镜(TEM)对磁性纳米复合材料进行了表征。结果表明,成功合成了纳米颗粒,磁性纳米颗粒在空腔中分散良好,粒径分布均匀,平均粒径为65nm,磁化强度高达33.75emu/mg。此外,纳米孔隙率和磁性使得药物能够高效且远程可控释放。在本研究中,以抗偏头痛药物舒马曲坦作为药物样本,研究了药物浓度、铁/锡比和负载时间对药物吸收的影响。检测了在体温和不同人体pH值下最佳结果的稳定性。药物浓度为0.25(mg/ml)、铁/锡=0.22且负载时间为1.5h的样品具有最高的药物效率(70%)。最后,为了模拟体外步骤中的体内过程,使用了羊膜,并在不同时间间隔和不同pH值下测量了药物扩散速率。结果表明,25小时后,在pH=2时扩散率达到65%,在pH=7时达到56%,然后趋于恒定。基于上述结果,该载体具有可接受的体外产率,因此可用于未来的体内研究。

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