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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >UiO-66 metal organic framework nanoparticles loaded carboxymethyl chitosan/poly ethylene oxide/polyurethane core-shell nanofibers for controlled release of doxorubicin and folic acid
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UiO-66 metal organic framework nanoparticles loaded carboxymethyl chitosan/poly ethylene oxide/polyurethane core-shell nanofibers for controlled release of doxorubicin and folic acid

机译:UIO-66金属有机框架纳米粒子负载羧甲基壳聚糖/聚环氧/聚氨酯核心 - 壳纳米纤维,用于对多柔比星和叶酸的控释

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摘要

Doxorubicin (DOX) and folic acid (FA) were incorporated into the UiO-66 metal organic framework (MOF) and following were loaded into the carboxymethyl chitosan/poly ethylene oxide (PEO)/polyurethane core-shell nanofibers for controlled release of DOX and FA toward MCF-7 cells death. The synthesized nanocarriers were characterized using TEM, XRD, and SEM analysis. The drug loading efficiency and release profiles of DOX/MOF and FA/MOF from synthesized nanofibers have been investigated. The fitting of kinetic data by the pharmacokinetic models demonstrated the non-Fickian diffusion from nanofibers and Fickian diffusion from core-shell fibers. The cytotoxicity of synthesized nanofibers toward MCF-7 cancer cells was evaluated using DAPI staining, MTT assay and flow cytometry tests to investigate the simultaneous use of DOX and FA in the nanofibrous matrix for MCF-7 cells death in vitro. The maximum cell death using DOX-FA loaded-core-shell fibers produced by coaxial electrospinning method under 0.3, 0.5 and 0.8 mLh(-1) shell flow rates were found to be 82 +/- 0.7, 83 +/- 0.5 and 87 +/- 0.5% after 168, 240 and 240 h, respectively. The cytotoxicity results indicated that the co-delivery of DOX and FA into the core-shell fibers could be widely used for various cancers treatment. (c) 2020 Elsevier B.V. All rights reserved.
机译:将多柔比蛋白(DOX)和叶酸(FA)掺入UIO-66金属有机骨架(MOF)中,并将其负载到羧甲基壳聚糖/聚环氧乙烷(PEO)/聚氨酯核心 - 壳纳米纤维上,用于控制DOX和FA对MCF-7细胞死亡。使用TEM,XRD和SEM分析表征合成的纳米载体。研究了DOX / MOF和来自合成纳米纤维的FA / MOF的药物负载效率和释放型材。通过药代动力学模型的动力学数据的拟合证明了来自纳米纤维的非Fickian扩散和来自核心壳纤维的Fickian扩散。使用DAPI染色,MTT测定和流式细胞术试验评估合成纳米纤维的细胞毒性,以研究MCF-7细胞死亡中的DOX和FA的同时使用DOX和FA。使用由0.3,0.5和0.8mLh(-1)壳流速的同轴电纺丝方法产生的DOX-FA负载核 - 壳纤维的最大细胞死亡是82 +/- 0.7,83 +/- 0.5和87分别在168,240和240小时后+/- 0.5%。细胞毒性结果表明,DOX和Fa进入核心壳纤维的共递送可广泛用于各种癌症处理。 (c)2020 Elsevier B.v.保留所有权利。

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