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.
引用
收藏
页数:11
相关论文
共 37 条
  • [21] Characterization of Melanin-TiO2 Complexes Using FT-IR and 13C Solid-state NMR Spectroscopy
    Park, Tae-Joon
    Kim, Jinsoo
    Kim, Tae-Kyung
    Park, Hee-Moon
    Choi, Sung-Sup
    Kim, Yongae
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2008, 29 (12): : 2459 - 2464
  • [22] SOLID-STATE C-13 AND H-1-NMR STUDY OF ANOMALOUS ACID SALTS OF DIBASIC CARBOXYLIC-ACIDS
    MERWIN, LH
    ROSS, SD
    MAGNETIC RESONANCE IN CHEMISTRY, 1992, 30 (05) : 440 - 448
  • [23] Structure determination of uniformly 13C, 15N labeled protein using qualitative distance restraints from MAS solid-state 13C-NMR observed paramagnetic relaxation enhancement
    Hajime Tamaki
    Ayako Egawa
    Kouki Kido
    Tomoshi Kameda
    Masakatsu Kamiya
    Takashi Kikukawa
    Tomoyasu Aizawa
    Toshimichi Fujiwara
    Makoto Demura
    Journal of Biomolecular NMR, 2016, 64 : 87 - 101
  • [24] Structure determination of uniformly 13C, 15N labeled protein using qualitative distance restraints from MAS solid-state 13C-NMR observed paramagnetic relaxation enhancement
    Tamaki, Hajime
    Egawa, Ayako
    Kido, Kouki
    Kameda, Tomoshi
    Kamiya, Masakatsu
    Kikukawa, Takashi
    Aizawa, Tomoyasu
    Fujiwara, Toshimichi
    Demura, Makoto
    JOURNAL OF BIOMOLECULAR NMR, 2016, 64 (01) : 87 - 101
  • [25] A 13C and 15N Solid-State NMR Study of Structural Disorder and Aurophilic Bonding in AuI and AuIII Cyanide Complexes
    Harris, Kristopher J.
    Wasylishen, Roderick E.
    INORGANIC CHEMISTRY, 2009, 48 (05) : 2316 - 2332
  • [26] Solid-state 13C NMR study of annealing effect on the crystalline phase of poly(ethylene-co-methacrylic acid) ionomers
    Mikage, Shohei
    Matsukawa, Takayuki
    Nakazawa, Chikako T.
    Asano, Atsushi
    POLYMER, 2022, 261
  • [27] Structural analysis of microbial poly(ɛ-L-lysine)/poly(acrylic acid) complex by FT-IR, DSC, and solid-state 13C and 15N NMR
    Shiro Maeda
    Yasuhiro Fujiwara
    Chizuru Sasaki
    Ko-Ki Kunimoto
    Polymer Journal, 2012, 44 : 200 - 203
  • [28] Structural analysis of microbial poly(ε-L-lysine)/poly(acrylic acid) complex by FT-IR, DSC, and solid-state 13C and 15N NMR
    Maeda, Shiro
    Fujiwara, Yasuhiro
    Sasaki, Chizuru
    Kunimoto, Ko-Ki
    POLYMER JOURNAL, 2012, 44 (02) : 200 - 203
  • [29] A study on molecular structural evolution of type II kerogen in a gold tube thermal system: Insights from solid-state 13C NMR
    Zhang, Deping
    Cao, Huairen
    Lei, Yan
    Wu, Hao
    Wang, Xiaoyu
    Guo, Xuelian
    Yan, Jianping
    Wang, Shuhua
    Shi, Tianchi
    Li, Haolin
    Zou, Yan-rong
    Peng, Ping'an
    FUEL, 2023, 331
  • [30] What Is Wrong with Hyaluronic Acid Chemistry? A 15N/13C Solid-State NMR Re-Evaluation of Its Dopamine Conjugates
    Grosu, Ioana-Georgeta
    Mot, Augustin
    Filip, Xenia
    Filip, Claudiu
    POLYMERS, 2023, 15 (13)