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Magnetic Nanoparticles Grafted with Cyclodextrin for Hydrophobic Drug Delivery

机译:磁性纳米粒子与环糊精接枝的疏水性药物递送。

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摘要

A novel magnetic nanocarrier,cyclodextrin(CD)-citrate-gum arabic modified magnetic nanoparticles(GAMNPs),for hydrophobic drug delivery was fabricated by grafting the citrate-modified CD onto the GAMNPs via carbodiimide activation.The analyses of the transmission electron microscopy and the dynamic light scattering revealed that the product had a mean diameter of 14.6 nm and a mean hydrodynamic diameter of 26.2 nm.The CD grafting was confirmed by Fourier transform infrared spectroscopy,and the amount of CD grafted on the GAMNPs was determined to be 28.7 mg/g by the thermpgravimetric analysis.The feasibility of using CD-citrate-GAMNPs as a carrier for hydrophobic drug delivery was demonstrated by investigating the formation of the inclusion complex and the in vitro release profile using ketoprofen as a model hydrophobic drug.It was found that CD-citrate-GAMNPs exhibited a considerable adsorption capability for ketoprofen as compared to GAMNPs.The complexation of CD-citrate-GAMNPs with ketoprofen was found to be exothermic and follow the Langmuir adsorption isotherm.Also,the presence of surfactant(sodium dodecyl sulfate,SDS)led to a decrease in the,inclusion of ketoprofen because the linear structure of SDS made it easier to enter the cavity of CD as compared with the less linear ketoprofen.The results of the ketoprofen inclusion and the release experiments indicate that this system seems to be a very promising vehicle for the administration of hydrophobic drugs.
机译:通过碳二亚胺活化将柠檬酸盐修饰的CD接枝到GAMNPs上,制备了疏水性递药的新型磁性纳米载体环糊精(CD)-柠檬酸-阿拉伯胶修饰的磁性纳米颗粒(GAMNPs)。动态光散射显示产物的平均直径为14.6 nm,平均流体动力学直径为26.2 nm。通过傅里叶变换红外光谱法确认了CD接枝,GAMNPs上的CD接枝量为28.7 mg /通过热重分析,通过研究酮洛芬作为模型疏水性药物的包合物的形成和体外释放情况,证明了将CD-柠檬酸盐-GAMNPs用作疏水性药物递送的载体的可行性。与GAMNPs相比,CD-柠檬酸盐-GAMNPs对酮洛芬的吸附能力强.CD-柠檬酸盐-GAMNPs与ke的络合此外,表面活性剂(十二烷基硫酸钠,SDS)的存在导致酮洛芬的含量减少,因为SDS的线性结构使其更易于进入腔内。 CD与线性度较低的酮洛芬相比。酮洛芬的包合和释放实验结果表明,该系统似乎是疏水药物给药的非常有前景的载体。

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