Real-time Monitoring of Hydration Reaction of Theophylline Anhydrous via Terahertz Attenuated Total Reflection Time Domain Spectroscopy

被引:0
|
作者
Takahashi, Kazuhiro [1 ]
Akiyama, Koichiro [1 ]
Horita, Kazuki [1 ]
Sakamoto, Tomoaki [2 ]
Satozono, Hiroshi [1 ]
机构
[1] Hamamatsu Photon KK, Cent Res Lab, 5000 Hirakuchi,Hamana Ku, Hamamatsu, Shizuoka, Japan
[2] Natl Inst Hlth Sci, Div Drugs, 3-25-26 Tonomachi,Kawasaki Ku, Kawasaki, Kanagawa, Japan
关键词
Terahertz spectroscopy; Attenuated total reflection; Pseudo-polymorphism; Hydration monitoring; Theophylline; Pharmaceutical; WET GRANULATION; DEHYDRATION; TEMPERATURES;
D O I
10.1007/s10762-024-00986-x
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
In pharmaceuticals, pseudo-polymorphism, e.g., the existence of hydrate and anhydrous forms, affects their physicochemical characteristics. Therefore, the evaluation of pseudo-polymorphism is one of the most important quality analyses. In this research, we investigate the real-time monitoring of the hydration reaction of theophylline using terahertz attenuated total reflection time domain spectroscopy (THz-attenuated total reflection (ATR)-TDS). We continuously measured a mixture of hydroxypropyl cellulose solution and theophylline anhydrous (TPA) while keeping it pressed to the ATR surface. We observed that the absorption peaks derived from TPA decreased and those derived from theophylline monohydrate (TPM) increased with time, demonstrating that the hydrate reaction of TPA can be monitored. Subsequently, we performed an accurate and quantitative evaluation of the hydration reaction by calculating the temporal changes in the crystal form ratio of TPM based on the changes in its second derivative peak intensity followed by a curve fitting. In addition, we performed real-time monitoring of the reaction using two different pressure mechanisms, finding that using a weight to apply pressure provided better reproducibility than using a screw. This study demonstrates that THz spectroscopy is a useful method for the evaluation of pseudo-polymorphism in pharmaceuticals.
引用
收藏
页码:444 / 453
页数:10
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