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

被引:109
|
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
相关论文
共 50 条
  • [41] A Novel Cocrystal of Daidzein with Piperazine to Optimize the Solubility, Permeability and Bioavailability of Daidzein
    Wang, Zhipeng
    Li, Shuang
    Li, Qi
    Wang, Wenwen
    Liu, Meiru
    Yang, Shiying
    Zhang, Li
    Yang, Dezhi
    Du, Guanhua
    Lu, Yang
    MOLECULES, 2024, 29 (08):
  • [42] Effect of magnesium carbonate on the solubility, dissolution and oral bioavailability of fenofibric acid powder as an alkalising solubilizer
    Kim, Kyeong Soo
    Kim, Jeong Hyun
    Jin, Sung Giu
    Kim, Dong Wuk
    Kim, Dong Shik
    Kim, Jong Oh
    Yong, Chul Soon
    Cho, Kwan Hyung
    Li, Dong Xun
    Woo, Jong Soo
    Choi, Han-Gon
    ARCHIVES OF PHARMACAL RESEARCH, 2016, 39 (04) : 531 - 538
  • [43] Effect of magnesium carbonate on the solubility, dissolution and oral bioavailability of fenofibric acid powder as an alkalising solubilizer
    Kyeong Soo Kim
    Jeong Hyun Kim
    Sung Giu Jin
    Dong Wuk Kim
    Dong Shik Kim
    Jong Oh Kim
    Chul Soon Yong
    Kwan Hyung Cho
    Dong Xun Li
    Jong Soo Woo
    Han-Gon Choi
    Archives of Pharmacal Research, 2016, 39 : 531 - 538
  • [44] Solid dispersion formulations of megestrol acetate with copovidone for enhanced dissolution and oral bioavailability
    Soon Wook Hong
    Bong Sang Lee
    Su Jun Park
    Hong Ryeol Jeon
    Ki Young Moon
    Mean Hyung Kang
    Sang Han Park
    Sung-Up Choi
    Woo Heon Song
    Jaehwi Lee
    Young Wook Choi
    Archives of Pharmacal Research, 2011, 34
  • [45] Piperine-loaded nanoparticles with enhanced dissolution and oral bioavailability for epilepsy control
    Ren, Tianjing
    Hu, Mengyun
    Cheng, Yan
    Shek, Tsum Lam
    Xiao, Min
    Ho, Nicolas James
    Zhang, Chunbo
    Leung, Sharon Shui Yee
    Zuo, Zhong
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 137
  • [46] Alternative Methotrexate Oral Formulation: Enhanced Aqueous Solubility, Bioavailability, Photostability, and Permeability
    Giri, Bhupendra Raj
    Yang, Hyun Seok
    Song, Im-Sook
    Choi, Han-Gon
    Cho, Jung Hyun
    Kim, Dong Wuk
    PHARMACEUTICS, 2022, 14 (10)
  • [47] Solid Dispersion Formulations of Megestrol Acetate with Copovidone for Enhanced Dissolution and Oral Bioavailability
    Hong, Soon Wook
    Lee, Bong Sang
    Park, Su Jun
    Jeon, Hong Ryeol
    Moon, Ki Young
    Kang, Mean Hyung
    Park, Sang Han
    Choi, Sung-Up
    Song, Woo Heon
    Lee, Jaehwi
    Choi, Young Wook
    ARCHIVES OF PHARMACAL RESEARCH, 2011, 34 (01) : 127 - 135
  • [48] A potential cocrystal strategy to tailor in-vitro dissolution and improve Caco-2 permeability and oral bioavailability of berberine
    Chen, Hui
    Ma, Jiangpo
    Zhou, Feng
    Yang, Junhui
    Jiang, Lei
    Chen, Quanbing
    Zhou, Yang
    Zhang, Jiantao
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2024, 666
  • [49] Solubility and Dissolution Enhancement of Luliconazole by a Cocrystal Engineering Technique with Different Coformers
    Aghara, Meet
    Dudhat, Kiran
    JOURNAL OF PHARMACEUTICAL INNOVATION, 2023, 18 (04) : 1701 - 1712
  • [50] Characterisation, solubility and intrinsic dissolution behaviour of benzamide: dibenzyl sulfoxide cocrystal
    Grossjohann, Christine
    Eccles, Kevin S.
    Maguire, Anita R.
    Lawrence, Simon E.
    Tajber, Lidia
    Corrigan, Owen I.
    Healy, Anne Marie
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2012, 422 (1-2) : 24 - 32