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首页> 外文期刊>Journal of Bioactive and Compatible Polymers >Transferrin-targeted poly(butylene adipate)/terephthalate nanoparticles for targeted delivery of 5-fluorouracil in HT29 colorectal cancer cell line
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Transferrin-targeted poly(butylene adipate)/terephthalate nanoparticles for targeted delivery of 5-fluorouracil in HT29 colorectal cancer cell line

机译:转铁蛋白靶向聚(丁烯己二酸丁酯)/对苯二甲酸酯纳米颗粒用于HT29结直肠癌细胞系中的5-氟尿嘧啶靶向递送

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摘要

The purpose of this study was to design 5-fluorouracil-loaded poly(butylene adipate)/terephthalate (Ecoflex((R))) nanoparticles for targeting colorectal cancer. The nanoparticles were prepared by emulsification-solvent evaporation method and optimized by a full factorial design. The effects of polymer and surfactant concentration, surfactant type, and stirrer rate were studied on the particle size, zeta potential, loading efficiency, and release efficiency of nanoparticles. For production of targeted nanoparticles, chitosan was conjugated to transferrin which was then coated on the surface of Ecoflex nanoparticles via electrostatic interactions. The conjugation of transferrin/chitosan was verified by Fourier transform infrared spectroscopy, ultraviolet spectroscopy, and SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) methods and quantified by ultraviolet spectroscopy assay. The cytotoxicity of 5-fluorouracil loaded in targeted and non-targeted nanoparticles was studied on human colon adenocarcinomacellline (HT29), Michigan Cancer Foundation-7 (MCF-7), and human umbilical vein endothelial cells using MTT (thiazolyl blue tetrazolium bromide) assay. The best results were obtained from nanoparticles prepared by 0.2% of the polymer, 2% of Tween 20, and stirrer speed of 17,500r/min. The successful conjugation of transferrin/chitosan was confirmed by Fourier transform infrared spectrum and SDS-PAGE results and was about 80%. The targeted nanoparticles showed significantly more cytotoxic effects on HT29 cells compared to free 5-fluorouracil and non-targeted nanoparticles. Blocking transferrin receptors resulted in a significantly higher cell survival for targeted nanoparticles which confirmed receptor-mediated cellular uptake of targeted nanoparticles.
机译:本研究的目的是设计5-氟尿嘧啶的聚(丁烯己二酸)/对苯二甲酸酯(EcoFlex((R)))纳米颗粒用于靶向结直肠癌。通过乳化溶剂蒸发方法制备纳米颗粒,并通过完整的因子设计进行优化。研究了聚合物和表面活性剂浓度,表面活性剂型和搅拌率的效果对纳米颗粒的粒度,Zeta电位,加载效率和释放效率研究。对于靶向纳米颗粒的生产,壳聚糖与转移素缀合,然后通过静电相互作用涂覆在EcoFlex纳米颗粒的表面上。通过傅里叶变换红外光谱,紫外光谱和SDS-PACE(十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳)验证转铁蛋白/壳聚糖的缀合物,并通过紫外光谱测定量化。在人结肠腺癌(HT29),密歇根癌基础-7(MCF-7)和人脐静脉内皮细胞中研究了5-氟尿嘧啶的细胞毒性,使用MTT(噻唑基蓝四溴化沸石)测定。从0.2%聚合物制备的纳米颗粒,2%吐温20的纳米颗粒获得最佳结果,搅拌速度为17,500r / min。通过傅里叶变换红外光谱和SDS-PAGE结果证实了转铁蛋白/壳聚糖的成功缀合,约为80%。与游离5-氟尿嘧啶和非靶向纳米颗粒相比,靶向纳米颗粒对HT29细胞显着更具细胞毒性作用。阻断转化素受体导致靶向纳米颗粒的细胞存活率显着更高,该纳米颗粒确认了受体介导的靶向纳米颗粒的细胞吸收。

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