Hussain Manzoor, Rehan Touseef, Goh Khang Wen, Shah Sayyed Ibrahim, Khan Abbas, Ming Long Chiau, Shah Nasrullah
Department of Chemistry, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
Department of Food and Nutrition, Shaheed Benazir Bhutto Women University, Peshawar 25000, Pakistan.
Polymers (Basel). 2022 Jun 30;14(13):2681. doi: 10.3390/polym14132681.
There has been very limited work on the control loading and release of the drugs aprepitant and sofosbuvir. These drugs need a significant material for the control of their loading and release phenomenon that can supply the drug at its target site. Magnetic nanoparticles have characteristics that enable them to be applied in biomedical fields and, more specifically, as a drug delivery system when they are incorporated with a biocompatible polymer. The coating with magnetic nanoparticles is performed to increase efficiency and reduce side effects. In this regard, attempts are made to search for suitable materials retaining biocompatibility and magnetic behavior. In the present study, silica-coated iron oxide nanoparticles were incorporated with core-shell particles made of poly(2-acrylamido-2-methylpropane sulfonic acid)@butyl methacrylate to produce a magnetic composite material (MCM-PA@B) through the free radical polymerization method. The as-prepared composite materials were characterized through Fourier-transform infrared (FTIR)spectroscopy, scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), energy-dispersive X-Ray Analysis (EDX), and thermogravimetric analysis (TGA), and were further investigated for the loading and release of the drugs aprepitant and sofosbuvir. The maximum loading capacity of 305.76 mg/g for aprepitant and 307 mg/g for sofosbuvir was obtained at pH 4. Various adsorption kinetic models and isotherms were applied on the loading of both drugs. From all of the results obtained, it was found that MCM-PA@B can retain the drug for more than 24 h and release it slowly, due to which it can be applied for the controlled loading and targeted release of the drugs.
关于阿瑞匹坦和索磷布韦这两种药物的控释载药研究非常有限。这些药物需要一种重要材料来控制其载药和释药现象,以便在靶部位提供药物。磁性纳米颗粒具有一些特性,使其能够应用于生物医学领域,更具体地说,当它们与生物相容性聚合物结合时,可作为药物递送系统。对磁性纳米颗粒进行包衣是为了提高效率并减少副作用。在这方面,人们试图寻找兼具生物相容性和磁性的合适材料。在本研究中,通过自由基聚合法将二氧化硅包覆的氧化铁纳米颗粒与由聚(2-丙烯酰胺-2-甲基丙烷磺酸)@甲基丙烯酸丁酯制成的核壳颗粒相结合,制备出一种磁性复合材料(MCM-PA@B)。通过傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、X射线衍射分析(XRD)、能量色散X射线分析(EDX)和热重分析(TGA)对所制备的复合材料进行了表征,并进一步研究了其对阿瑞匹坦和索磷布韦的载药和释药情况。在pH值为4时,阿瑞匹坦的最大载药量为305.76 mg/g,索磷布韦的最大载药量为307 mg/g。对两种药物的载药过程应用了各种吸附动力学模型和等温线。从所有获得的结果来看,发现MCM-PA@B能够将药物保留超过24小时并缓慢释放,因此它可用于药物的控释载药和靶向释放。