Structural Characterization of Febuxostat/L-Pyroglutamic Acid Cocrystal Using Solid-State 13C-NMR and Investigational Study of Its Water Solubility

被引:16
|
作者
An, Ji-Hun [1 ]
Lim, Changjin [1 ]
Ryu, Hyung Chul [2 ]
Kim, Jae Sun [2 ]
Kim, Hyuk Min [2 ]
Kiyonga, Alice Nguvoko [1 ]
Park, Minho [1 ]
Suh, Young-Ger [1 ]
Park, Gyu Hwan [3 ]
Jung, Kiwon [1 ]
机构
[1] CHA Univ, Coll Pharm, Sungnam 13844, South Korea
[2] R&D Ctr, J2H Biotech, Ansan 15426, South Korea
[3] Kyungpook Natl Univ, Coll Pharm, Daegu 41566, South Korea
来源
CRYSTALS | 2017年 / 7卷 / 12期
基金
新加坡国家研究基金会;
关键词
Febuxostat; cocrystal; solid-state NMR; solubility; active pharmaceutical ingredient; PHARMACEUTICAL COCRYSTALS; NMR;
D O I
10.3390/cryst7120365
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Febuxostat (FB) is a poorly water-soluble drug that belongs to BCS class II. The drug is employed for the treatment of inflammatory disease arthritis urica (gout), and the free base, FB form-A, is most preferred for drug formulation. In order to achieve a goal of improving the water solubility of FB form-A, this study was carried out using the cocrystallization technique called the liquid-assisted grinding method to produce FB cocrystals. Here, five amino acids containing amine (NH), oxygen (O), and hydroxyl (OH) functional groups, and possessing difference of pKa less than 3 with FB, were selected as coformers. Then, solvents including methanol, ethanol, isopropyl alcohol, n-hexane, dichloromethane, and acetone were used for the cocrystal screening. As a result, a cocrystal was obtained when acetone and l-pyroglutamic acid (PG) of 0.5 eq. were employed as solvent and coformer, respectively. The ratio of 2:1, which is the ratio of FB to PG within FB-PG cocrystal, was predicted by means of solid-state CP/MAS C-13-NMR, solution-state NMR (H-1, C-13, and 2D) and FT-IR. Moreover, Powder X-ray Diffraction (PXRD), Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA) were used to investigate the characteristics of FB-PG cocrystal. In addition, comparative solubility tests between FB-PG cocrystal and FB form-A were conducted in deionized water and under simulated gastrointestinal pH (1.2, 4, and 6.8) conditions. The result revealed that FB-PG cocrystal has a solubility of four-fold higher than FB form-A in deionized water and two-fold and five-fold greater than FB form-A at simulated gastrointestinal pH 1.2 and pH 4, respectively. Besides, solubilities of FB-PG cocrystal and FB form-A at pH 6.8 were similar to the results measured in deionized water. Therefore, it is postulated that FB-PG cocrystal has a potential overcoming the limitations related to the low aqueous solubility of FB form-A. Accordingly, FB-PG cocrystal is suggested as an alternative active pharmaceutical ingredient of the currently used FB form-A.
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页数:11
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