Identification and investigation of the vibrational properties of crystalline and co-amorphous drugs with Raman and terahertz spectroscopy

被引:16
作者
Liu, Wei [1 ,2 ]
Liu, Yu [2 ]
Huang, Jiaoqi [2 ]
Lin, Zhongquan [2 ]
Pan, Xuancheng [3 ]
Zeng, Xiaojun [2 ]
de la Chapelle, Marc Lamy [4 ]
Zhang, Yang [2 ]
Fu, Weiling [2 ]
机构
[1] Southwest Univ, Fac Mat & Energy, Chongqing 400715, Peoples R China
[2] Army Mil Med Univ, Southwest Hosp, Dept Lab Med, Chongqing 400038, Peoples R China
[3] Wuhan Life Origin Biotech Joint Stock, Wuhan 430206, Hubei, Peoples R China
[4] Univ Mans, CNRS, UMR 6283, IMMM, Ave Olivier Messiaen, F-72085 Le Mans, France
关键词
ACTIVE PHARMACEUTICAL INGREDIENTS; SOLID DISPERSIONS; DISSOLUTION RATE; PHYSICOCHEMICAL PROPERTIES; CIMETIDINE; SYSTEMS; BIOAVAILABILITY; STABILIZATION; INDOMETHACIN; SOLUBILITY;
D O I
10.1364/BOE.10.004290
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Co-amorphous drugs have shown significant potential in improving the stability and bioavailability compared with single neat amorphous drugs. Here, we explored the molecular interactions of cimetidine, naproxen, indomethacin and their binary co-amorphous mixtures via Raman and terahertz (THz) spectroscopy. We used quench-cooled method to prepare the neat amorphous drugs and their binary co-amorphous mixtures and tested their thermodynamic properties through differential scanning calorimetry (DSC). Then, we found that the stability of co-amorphous drugs was stronger than their neat amorphous components. Furthermore, Raman spectroscopy was used to characterize the vibrational modes between different co-amorphous drugs. Generally, we found that the stability of co-amorphous drugs was better than their neat amorphous components for these samples we tested. Meanwhile, we complemented the detection of THz spectroscopy and found that crystalline and amorphous drugs could be better distinguished. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:4290 / 4304
页数:15
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