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摘要:
The interaction between ibuprofen and maltodextrins with different dextrose equivalent was studied in solution and solid state in order to investigate the effect on the solubility of ibuprofen and to determine their usefulness in terms of chiral recognition. Apparent binding constants were calculated using nuclear magnetic resonance spectroscopy experiments and solubility studies. The results showed an increase in the apparent solubility of ibuprofen in the presence of maltodextrins that depended on their ionization state. The freeze-drying method was used to prepare solid complexes, while physical mixtures were obtained by simple blending. These solid systems were characterized in the solid state using differential scanning calorimetry, thermogravimetric analysis, Fourier Transform-Infrared spectroscopy, scanning electron microscopy and X-ray diffractometry. Detailed nuclear magnetic resonance studies provided evidence of the influence of the type and concentration of the maltodextrin host on the chiral recognition of racemic ibuprofen, indicating that these linear ligands act as chiral selectors.
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篇名 Ibuprofen-Maltodextrin Interaction: Study of Enantiomeric Recognition and Complex Characterization
来源期刊 药理与制药(英文) 学科 化学
关键词 IBUPROFEN MALTODEXTRIN Chiral Recognition Complex Characterization Nuclear Magnetic Resonance Spectroscopy SOLUBILITY Studies
年,卷(期) 2013,(1) 所属期刊栏目
研究方向 页码范围 18-30
页数 13页 分类号 O6
字数 语种
DOI
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研究主题发展历程
节点文献
IBUPROFEN
MALTODEXTRIN
Chiral
Recognition
Complex
Characterization
Nuclear
Magnetic
Resonance
Spectroscopy
SOLUBILITY
Studies
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
药理与制药(英文)
月刊
2157-9423
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
444
总下载数(次)
0
总被引数(次)
0
期刊文献
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