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Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery

机译:HF-Free MIL-100(Fe)的水热合成用于异烟肼 - 药物递送

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Sustainable development of drug delivery materials with good biocompatibility and controlled-release is a popular topic among researchers. In this research study, we demonstrated the potential of the metal-organic framework, that is MIL-100(Fe), as a drug delivery platform for isoniazid (INH). The MIL-100(Fe) was prepared by using the hydrofluoric acid-free hydrothermal method. Several physical measurements were conducted to characterize the MIL-100(Fe), including x-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen sorption, and thermal-gravimetric (TG). The synthesized MIL-100(Fe) has octahedron-shaped particles with superior properties, that is large surface area (1456.10?msup2/sup/g) and pore volume (1.25?cmsup3/sup/g). The drug loading rate and capacity were determined by means of adsorption kinetic and isotherm. The studied INH@MIL-100(Fe) adsorption system kinetics follow the pseudo-first-order model, while the isotherm system follows the Langmuir model with the maximum adsorption capacity of 128.5?mg/g at 30?°C. MIL-100(Fe) shows adequate biocompatibility, also exhibits a reasonable and controlled drug release kinetics. The results obtained show that MIL-100 (Fe) can be a good choice of drug delivery platform among other available platforms.
机译:具有良好生物相容性和控制释放的药物递送材料的可持续发展是研究人员中的流行课题。在这项研究中,我们证明了金属有机框架的潜力,即MIL-100(Fe),作为异烟肼的药物递送平台(INH)。通过使用无氢氟酸的水热法制备MIL-100(Fe)。进行了几种物理测量以表征MIL-100(Fe),包括X射线衍射(XRD),扫描电子显微镜(SEM),氮吸附和热重量(Tg)。合成的MIL-100(Fe)具有具有优异性能的八面体形颗粒,表面积大(1456.10μm 2 / g)和孔体积(1.25Ωcm 3 / g)。通过吸附动力学和等温线测定药物载量和容量。研究的Inh @ MIL-100(FE)吸附系统动力学遵循伪第一阶模型,而等温系统遵循Langmuir模型,最大吸附容量为128.5Ω·mg / g。 MIL-100(FE)显示了足够的生物相容性,也表现出合理和控制的药物释放动力学。得到的结果表明,MIL-100(FE)可以是其他可用平台中的药物送货平台的良好选择。

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