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Preparation and characterization of iminodiacetic acid: magnetite nano-particles as a novel famotidine carrier substrate for sustained drug release

机译:亚氨基二乙酸的制备和表征:磁铁矿纳米颗粒作为新型法莫替丁载体基质,可持续释放药物

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In this paper, a new method is reported for the surface immobilization of magnetic nano-particles modified by iminodiacetic acid. The immobilized nano-sorbent was characterized by Fourier transform infrared spectroscopy, elemental analysis, thermogravimetric analysis, and transmission electron microscopy. Agglomerated magnetic nano-particles were used for sorption of famotidine in simulated intestinal and gastric fluids. The profile of the famotidine uptake by nano-sorbent reflected the high accessibility of the active sites in the immobilized sorbent. The equilibrium adsorption data of famotidine by nano-sorbent were analyzed by Langmuir, Freundlich, Temkin, and Redlich-Peterson isotherm models. The sorption capacity was 15.2 mg g(-1) at optimum pH of 5. Nearly 86 % of famotidine was released in simulated gastric fluid, pH = 1.2, in 60 min and 60 % in simulated intestinal fluid, pH = 7.4, in 30 h. These results indicate the efficiency of the famotidine loaded onto immobilized magnetic nano-sorbent for targeted drug delivery.
机译:本文报道了一种新方法,用于表面固定亚氨基二乙酸修饰的磁性纳米粒子。通过傅立叶变换红外光谱,元素分析,热重分析和透射电子显微镜对固定化的纳米吸附剂进行了表征。团聚的磁性纳米粒子用于模拟肠和胃液中法莫替丁的吸附。纳米吸附剂对法莫替丁的吸收情况反映了固定化吸附剂中活性部位的高度可及性。用Langmuir,Freundlich,Temkin和Redlich-Peterson等温模型分析法莫替丁在纳米吸附剂上的平衡吸附数据。在最佳pH为5时,吸附容量为15.2 mg g(-1)。在60分钟内,模拟胃液pH = 1.2中有近86%的法莫替丁在30分钟内在pH = 7.4的模拟肠液中有近60%释放。 H。这些结果表明法莫替丁加载到固定的磁性纳米吸附剂上以进行靶向药物递送的效率。

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