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Poly (methacrylic acid-co-acrylic acid)-grafted polyvinylpyrrolidone coated Magnetic nanoparticles as a pH-responsive magnetic Nano-carrier for controlled delivery of antibiotics

机译:聚(甲基丙烯酸-丙烯酸共聚物)接枝的聚乙烯吡咯烷酮涂层磁性纳米粒子,作为pH响应磁性纳米载体,可控制抗生素的输送

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Objective(s): Pharmaceutical industries are leading to improved medications that can target diseases more effectively and precisely. Researchers have intended to reformulate drugs so that they may be more safely used in human body. The more targeted a drug is, the lower its chance of triggering drug resistance, a cautionary concern surrounding the use of broad-spectrum antibiotics. The aim of this paper is to introduce efficient drug delivery vehicles which can perform both targeted and controlled antibiotic release by synthesis of magnetic pH-responsive polymer. Materials and Methods: Iron oxide nanoparticles were synthesized by chemical co-precipitation technique and primary coated with 3-trimethoxysilylpropylamine (APTS). APTS coated MNPs was used in the reaction medium for synthesis of a pH-responsive poly (MAA-co-AAc)-grafted PVP. The prepared vehicle was characterized by TEM, XRD, FT-IR, TGA, DSC and elemental analysis. Drug loading, release, kinetics and mechanism of the system were evaluated.Results: The results for drug release showed that the release of antibiotics in pH 5.5 and 7.2 could be effectively sustained, while about 92 % of the drugs were released at pH 1.2. Considerations demonstrate the tendency of drug release by Fickian mechanism and diffusion controlled release.Conclusion: The results indicate that the prepared magnetic nano-carrier could be suitable for site-specific antibiotic delivery through oral administration.
机译:目标:制药行业正在导致改进的药物,这些药物可以更有效,更准确地针对疾病。研究人员打算重新配制药物,以便可以更安全地在人体中使用它们。药物的靶向性越强,触发耐药性的机会就越低,这是广谱抗生素使用的一个警惕性问题。本文的目的是介绍可以通过磁性pH响应聚合物的合成实现靶向和受控抗生素释放的高效药物输送载体。材料和方法:通过化学共沉淀技术合成氧化铁纳米粒子,并初步涂覆3-三甲氧基甲硅烷基丙胺(APTS)。将APTS包被的MNP用于反应介质中,以合成pH响应型聚(MAA-co-AAc)接枝的PVP。通过TEM,XRD,FT-IR,TGA,DSC和元素分析对制得的载体进行表征。结果:药物释放的结果表明,在pH 5.5和7.2下,抗生素的释放可以被有效地维持,而在pH 1.2下,约有92%的药物被释放。结论表明,所制备的磁性纳米载体可通过口服给药,适合于特定部位的抗生素给药。

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