首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Synthesis and characterization of silane coated magnetic nanoparticles/glycidylmethacrylate-grafted-maleated cyclodextrin composite hydrogel as a drug carrier for the controlled delivery of 5-fluorouracil
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Synthesis and characterization of silane coated magnetic nanoparticles/glycidylmethacrylate-grafted-maleated cyclodextrin composite hydrogel as a drug carrier for the controlled delivery of 5-fluorouracil

机译:硅烷包覆的磁性纳米粒子/甲基丙烯酸缩水甘油酯接枝的马来酸环糊精复合水凝胶的合成和表征作为药物载体控制5-氟尿嘧啶的传递

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摘要

A novel drug delivery system (DDS), 3-methacryloxypropyl trimethoxy silane coated magnetic nanoparticles polymerized with glycidylmethacrylate-grafted-maleated cyclodextrin (MPTMS-MNP-poly-(GMA-g-MACD)) was prepared in the presence of ethyleneglycoldimethacrylate as cross-linker and a,a'-azobisisobutyronitrile as initiator and characterized by means of SEM, FT-IR, XRD, DLS, VSM and TEM. The encapsulation efficiency (EE) and drug loading efficiency (DLE) of the DDS were tested using various formulations of DDS. The DDS showed activity against gram positive and negative bacteria. The cytotoxicity studies were also performed using MCF-7 (human breast carcinoma) cells and found that the drug carrier is biocompatible and it shows sustained and controlled release of drug to the targeted site. The drug release mechanism was found to obey non-Fickian diffusion (n = 0.709) method where polymer relaxation and drug diffusion played important roles in drug release. In this DDS, advantages of core magnetic nanoparticles and host-guest interactions of beta-CD were combined for the controlled delivery of 5-Fluorouracil (5-FU) to maintain the therapeutic index of the drug. (C) 2015 Elsevier B.V. All rights reserved.
机译:制备了一种新型的药物递送系统(DDS),在甲基丙烯酸缩水甘油酯存在下,将甲基丙烯酸缩水甘油酯接枝的马来酸环糊精聚合成3-甲基丙烯酰氧基丙基三甲氧基硅烷包覆的磁性纳米粒子(MPTMS-MNP-poly-(GMA-g-MACD))。接头和a,a'-偶氮二异丁腈作为引发剂,并通过SEM,FT-IR,XRD,DLS,VSM和TEM表征。使用各种DDS配方测试了DDS的包封效率(EE)和载药效率(DLE)。 DDS对革兰氏阳性和阴性细菌表现出活性。还使用MCF-7(人类乳腺癌)细胞进行了细胞毒性研究,发现药物载体具有生物相容性,并且显示出药物向靶部位的持续和受控释放。发现药物释放机制服从非菲克扩散(n = 0.709)方法,其中聚合物松弛和药物扩散在药物释放中起重要作用。在此DDS中,结合了核心磁性纳米颗粒和β-CD的宿主-客体相互作用的优势,可控制递送5-氟尿嘧啶(5-FU)以维持药物的治疗指数。 (C)2015 Elsevier B.V.保留所有权利。

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