生物相容性
药物输送
吸附
朗缪尔吸附模型
化学工程
材料科学
热液循环
重量分析
热重分析
吸附
动力学
核化学
纳米技术
化学
有机化学
冶金
工程类
量子力学
物理
作者
Meta Angeline Simon,Erlina Anggraeni,Felycia Edi Soetaredjo,Shella Permatasari Santoso,Wenny Irawaty,Truong Chi Thanh,Sandy Budi Hartono,Maria Yuliana,Suryadi Ismadji
标识
DOI:10.1038/s41598-019-53436-3
摘要
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 m2/g) and pore volume (1.25 cm3/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.
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