Enhanced Drug Delivery by Dissolution of Amorphous Drug Encapsulated in a Water Unstable Metal-Organic Framework (MOF)

被引:246
|
作者
Suresh, Kuthuru [1 ,2 ]
Matzger, Adam J. [1 ,2 ]
机构
[1] Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Macromol Sci & Engn Program, 930 North Univ Ave, Ann Arbor, MI 48109 USA
基金
美国能源部;
关键词
amorphous drug; drug delivery; immediate drug release; metal-organic framework; stability; PHYSICAL STABILITY; SOLID DISPERSIONS; PHARMACEUTICALS; SOLUBILIZATION; POLYMERS; MOLECULE; RELEASE; DESIGN;
D O I
10.1002/anie.201907652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Encapsulating a drug molecule into a water-reactive metal-organic framework (MOF) leads to amorphous drug confined within the nanoscale pores. Rapid release of drug occurs upon hydrolytic decomposition of MOF in dissolution media. Application to improve dissolution and solubility for the hydrophobic small drug molecules curcumin, sulindac, and triamterene is demonstrated. The drug@MOF composites exhibit significantly enhanced dissolution and achieves high supersaturation in simulated gastric and/or phosphate buffer saline media. This combination strategy where MOF inhibits crystallization of the amorphous phase and then releases drug upon MOF irreversible structural collapse represents a novel and generalizable approach for drug delivery of poorly soluble compounds while overcoming the traditional weakness of amorphous drug delivery: physical instability of the amorphous form.
引用
收藏
页码:16790 / 16794
页数:5
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