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Facile One-Pot Synthesis of Magnetic Targeted Polymers for Drug Delivery and Study on Thermal Decomposition Kinetics

机译:轻松的一锅合成磁性靶向聚合物用于药物输送和研究热分解动力学的研究

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摘要

Magnetic targeting materials are the hot topic of research in the current study of targeted drug carrier. However, the complexity of the preparation method has hindered its further development. In this paper, a facile one-pot strategy was developed to synthesize a novel amphiphilic drug carrier (Fe3O4-PVA@SH). We determined that Fe3O4-PVA@SH drug carrier with uniform size and excellent superparamagnetic properties can be fabricated on the simultaneous formation of magnetic Polyvinyl alcohol(PVA) polymer-linked branches of thiohydrazide-iminopropyltriethoxysilane (TIPTS) by mixing Fe3O4, PVA, and TIPTS in a DMSO alkaline aqueous solution. The Fe3O4-PVA@SH drug carrier were subsequently characterised by FTIR, XPS, SEM, EDS, size and VSM. It was found that the drug carrier Fe3O4-PVA@SH could achieve 83% aspirin loading and 85% DOX?HCl loading. In vitro simulated drug release experi- ments showed that Aspirin could achieved 86.9% at pH 7.2 and DOX?HCl could achieved 81.6% at pH 4.7 for 80 h. Additionally, we measured the thermal stability and enthalpy of thermal decomposition of the Fe3O4-PVA@SH coupling agent using a differential scanning calorimeter (DSC) and a non-isothermal decomposition method. This research offers the potential for the industrialization of magnetic drug carriers as a means of increasing its cost-effectiveness and leveraging magnetic targeted drug carriers for drug delivery and other applications.
机译:磁靶材料是当前对靶向药物载体研究的研究的热门话题。但是,制备方法的复杂性阻碍了其进一步的发展。在本文中,制定了一种简单的单锅策略,以合成一种新型的两亲药载体(FE3O4-PVA@SH)。 We determined that Fe3O4-PVA@SH drug carrier with uniform size and excellent superparamagnetic properties can be fabricated on the simultaneous formation of magnetic Polyvinyl alcohol(PVA) polymer-linked branches of thiohydrazide-iminopropyltriethoxysilane (TIPTS) by mixing Fe3O4, PVA, and TIPTS在DMSO碱性水溶液中。 FE3O4-PVA@SH药物载体随后以FTIR,XPS,SEM,EDS,大小和VSM为特征。发现药物载体FE3O4-PVA@SH可以达到83%的阿司匹林加载和85%的DOX?HCl加载。体外模拟的药物释放实验表明,阿司匹林在pH 7.2时可以达到86.9%,而dox?hcl可以在80 h时在pH 4.7时达到81.6%。此外,我们使用差分扫描量热仪(DSC)和非等温分解方法测量了Fe3O4-PVA@SH耦合剂的热稳定性和焓。这项研究为磁性药物载体的工业化提供了潜力,以增加其成本效益和利用磁性药物载体进行药物输送和其他应用的手段。

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