FTIR, Raman spectroscopy and HT-XRD in compatibility study between naproxen and excipients

被引:7
|
作者
Rojek, Barbara [1 ]
Gazda, Maria [2 ]
Plenis, Alina [1 ]
机构
[1] Med Univ Gdansk, Fac Pharm, Dept Analyt Chem, Al Gen Hallera 107, PL-80416 Gdansk, Poland
[2] Gdansk Univ Technol, Fac Appl Phys & Math, Narutowicza 11-12, PL-80233 Gdansk, Poland
关键词
FTIR; Raman spectroscopy; HT-XRD; DSC; Compatibility; incompatibility; Naproxen; IR SPECTROSCOPY; DRUG;
D O I
10.1016/j.saa.2023.123048
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Detection of incompatibility between an active pharmaceutical ingredient (API) and excipients, including the selection of the most biopharmaceutical advantageous excipients is extremely important in the pre-formulation process of developing a solid dosage form technology. Therefore, having fast and reliable methods for identifying incompatibility is fundamental in pharmaceutical technology. For this purpose, combined Fourier transform infrared (FTIR) and Raman spectroscopy as well as high-temperature X-ray diffraction (HT-XRD) were used as a new approach for incompatibility detection, whereas differential scanning calorimetry (DSC) was applied as a reference method. In addition, to facilitate the interpretation of FTIR and Raman data, a multivariate analysis was used - hierarchical cluster analysis (HCA). The tests were carried out in mixtures of naproxen (NPX) with eight selected polymer excipients, mixed at a 1:1 ratio. The results of spectroscopic analyses have shown the physical incompatibility of NPX with methylcellulose (MC), hydroxypropylmethylcellulose (HPMC), hydroxyethylcellulose (HEC), sodium starch glycolate (SSG) and sodium carboxymethylcellulose (CMC). HT-XRD studies performed when these mixtures were heated to 156 degrees C and then cooled to 25 degrees C showed a decrease in naproxen crystallinity in these mixtures. Furthermore, the results obtained with spectroscopic methods were confirmed by DSC tests and an intrinsic dissolution rate study.
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页数:11
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