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The Impact of Magnesium–Aluminum-Layered Double Hydroxide-Based Polyvinyl Alcohol Coated on Magnetite on the Preparation of Core-Shell Nanoparticles as a Drug Delivery Agent

机译:磁铁矿涂布镁 - 铝层双氢氧化镁基聚乙烯醇的影响核心壳纳米粒子作为药物递送剂的制备

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摘要

One of the current developments in drug research is the controlled release formulation of drugs, which can be released in a controlled manner at a specific target in the body. Due to the diverse physical and chemical properties of various drugs, a smart drug delivery system is highly sought after. The present study aimed to develop a novel drug delivery system using magnetite nanoparticles as the core and coated with polyvinyl alcohol (PVA), a drug 5-fluorouracil (5FU) and Mg−Al-layered double hydroxide (MLDH) for the formation of FPVA-FU-MLDH nanoparticles. The existence of the coated nanoparticles was supported by various physico-chemical analyses. In addition, the drug content, kinetics, and mechanism of drug release also were studied. 5-fluorouracil (5FU) was found to be released in a controlled manner from the nanoparticles at pH = 4.8 (representing the cancerous cellular environment) and pH = 7.4 (representing the blood environment), governed by pseudo-second-order kinetics. The cytotoxicity study revealed that the anticancer delivery system of FPVA-FU-MLDH nanoparticles showed much better anticancer activity than the free drug, 5FU, against liver cancer and HepG2 cells, and at the same time, it was found to be less toxic to the normal fibroblast 3T3 cells.
机译:药物研究的目前发展之一是药物的受控释放制剂,其可以在体内的特定靶标以受控方式释放。由于各种药物的各种物理和化学性质,高度追捧了智能药物输送系统。本研究旨在使用磁铁矿纳米颗粒作为芯的新型药物递送系统,并涂有聚乙烯醇(PVA),药物5-氟尿嘧啶(5Fu)和Mg-Al层双氢氧化物(MLDH),用于形成FPVA -Fu-MLDH纳米粒子。通过各种物理化学分析来支持涂覆的纳米颗粒的存在。此外,还研究了药物含量,动力学和药物释放机制。发现5-氟尿嘧啶(5Fu)以受控方式从pH = 4.8的纳米颗粒(代表癌细胞环境)和pH = 7.4(代表血液环境)以受控的方式释放,由伪二阶动力学治理。细胞毒性研究表明,FPVA-FU-MLDH纳米粒子的抗癌递送系统显示出比游离药物,5FU,对抗肝癌和HepG2细胞的更好的抗癌活性,并同时发现它对毒性较小正常成纤维细胞3T3细胞。

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