Baicalein-Nicotinamide Cocrystal with Enhanced Solubility, Dissolution, and Oral Bioavailability

被引:110
作者
Huang, Yanting [1 ]
Zhang, Bowen [2 ]
Gao, Yuan [2 ]
Zhang, Jianjun [1 ]
Shi, Limin [3 ]
机构
[1] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Sch Tradit Chinese Med, Nanjing 210009, Peoples R China
[3] Univ Minnesota, Dept Pharmaceut, Coll Pharm, Minneapolis, MN 55455 USA
关键词
baicalein; cocrystal; solid state; solubility; dissolution; bioavailability; PHARMACEUTICAL COCRYSTALS; SCUTELLARIAE RADIX; COFORMER SELECTION; ADEFOVIR DIPIVOXIL; ACID COCRYSTAL; MELTING-POINTS; PHARMACOKINETICS; CARBAMAZEPINE; PERFORMANCE; STABILITY;
D O I
10.1002/jps.24048
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purpose of this study was to investigate the effect of preparation methods on cocrystallization between baicalein (BE) and nicotinamide (NCT), their intermolecular interaction, and to demonstrate that BE-NCT cocrystal can achieve the simultaneous enhancement in solubility, dissolution, and oral bioavailability of BE. The cocrystals from three preparation methods have the similar differential scanning calorimetry thermograms and X-ray powder diffraction patterns. Compared with crystalline BE, BE-NCT cocrystal has significantly improved the solubility and dissolution of BE. In addition, the cocrystal exhibits a 2.49-fold higher peak plasma concentration (C-max) and 2.80-fold higher area under the curve (AUC) in rats. This prominent improvement in oral bioavailability is even greater than the previously reported BE nanocrystal. This investigation enriched the present understanding of cocrystals on their behavior in vitro and in vivo, and built the groundwork for future development of BE as a promising compound into efficacious drug products. (c) 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:2330-2337, 2014
引用
收藏
页码:2330 / 2337
页数:8
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