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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Fe3O4-alginate nanocomposite hydrogel beads material: One-pot preparation, release kinetics and antibacterial activity
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Fe3O4-alginate nanocomposite hydrogel beads material: One-pot preparation, release kinetics and antibacterial activity

机译:Fe3O4-海藻酸钠纳米复合水凝胶珠材料:单罐制剂,释放动力学和抗菌活性

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In this work, a new and easy process was developed to fabricate a Fe3O4-alginate (Fe(3)O(4)NPs-ALG) hydrogel nano composite magnetic beads material. This preparation way consists in crosslinking sodium alginate solution in a mixed iron chloride solution containing FeCl3 and FeCl2. All characterization techniques confirmed the formation of small Fe3O4 nanoparticles with an average size of 9 nm in the alginate biopolymer matrix, in which iron atoms were linked to carbonyl acetyl groups through a bidentate bridging coordination. Furthermore, the magnetic nanocomposite beads have negatively charged surface. The obtained material was loaded with amoxicillin (AMOX) and tested as drug delivery system in the biolysis serum (NaCl 0.9% of pH 7) and in the simulated gastric medium (pH 2.1). The results showed that a cumulative release rate of 81.49% was obtained after three days in the biolysis serum, while this release rate was about 11.65% only, after four days, in the simulated gastric medium. The kinetic release data fulfilled Korsmeyer-Peppas model and the Hixson-Crowell, respectively. Antibacterial test on drug-loaded nanocomposite beads showed high activity against three of pathogenic bacteria strains. (C) 2019 Elsevier B.V. All rights reserved.
机译:在这项工作中,开发了一种新的和易于的方法来制造Fe3O4-藻酸盐(Fe(3)O(4)NPS-ALG)水凝胶纳米复合磁珠材料。该制备方式包括在含有FECL3和FECL2的混合氯化铁溶液中交联藻酸钠溶液。所有表征技术证实了藻酸盐生物聚合物基质中平均尺寸为9nm的小Fe3O4纳米颗粒的形成,其中铁原子通过二齿桥接配位与羰基乙酰基连接。此外,磁性纳米复合材料珠子具有带负电的表面。将所得材料用阿莫西林(Amox)加载并在生物分解血清中(NaCl 0.9%pH 7)和模拟胃介质(pH2.1)中测试为药物递送系统。结果表明,在模拟胃介质中,在生物分解血清中三天后,在三天后获得了81.49%的累积释放速率为81.49%,而在模拟胃介质中,该释放速率仅为11.65%。动力学释放数据分别实现了Korsmeyer-Peppas模型和Hixson-Crowell。药物负载纳米复合材料珠粒的抗菌试验表现出抗致病性细菌菌株的高活性。 (c)2019 Elsevier B.v.保留所有权利。

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