Hitachi High-Tech Corp., Shinko-cho, Hitachinaka 312-8504, Japan.
Department of Chemistry, Syracuse University, Syracuse, New York 13244, United States.
J Phys Chem A. 2022 May 19;126(19):2879-2888. doi: 10.1021/acs.jpca.2c00301. Epub 2022 May 6.
Understanding the solid-state transitions of active pharmaceutical ingredients (APIs) is essential for quality control since differences in their forms affect the bioavailability of APIs. Terahertz (THz) frequency-domain spectroscopy is suitable for such an application since it can sensitively probe the lattice phonon modes originating in the crystal structures. THz absorption spectra were obtained for ezetimibe (EZT) and ezetimibe monohydrate (EZT-MH), which have similar crystalline structures and belong to the same space group. The observed absorption spectrum of EZT matched well with the solid-state density functional theory (ss-DFT)-simulated spectrum for the structures at 0 K and room temperature (modeled using constrained unit cell volumes). However for EZT-MH, the ss-DFT spectrum of the room-temperature structure showed better correlation with the experimental THz spectrum than that of the simulated spectrum of the 0 K structures, suggesting that the EZT-MH crystal has greater anharmonic character. Gibbs free-energy curves were calculated, and EZT-MH was found to be more stable than pure EZT and water in a broad temperature range. The hydrate stability may be influenced by the existence of more hydrogen bonds in EZT-MH. The hydration and dehydration of EZT in a pure API tablet and formulation tablets were monitored using a THz spectrometer with a humidity-controlled sample chamber. The effect of the excipient in the formulation tablet on hydration was successfully confirmed by showing that the solid-state transition of the API with excipients is significantly slower than that without it. Under a relative humidity of 60%, hydration of EZT in a pure EZT tablet occurred in 200 min, while the hydration of EZT in a formulation tablet was 50 times slower.
了解活性药物成分(API)的固态转变对于质量控制至关重要,因为它们的形式差异会影响 API 的生物利用度。太赫兹(THz)频域光谱非常适合这种应用,因为它可以敏感地探测源于晶体结构的晶格声子模式。获得了依泽替米贝(EZT)和依泽替米贝一水合物(EZT-MH)的太赫兹吸收光谱,它们具有相似的晶体结构,属于相同的空间群。EZT 的观察到的吸收光谱与 0 K 和室温下的晶体结构的固态密度泛函理论(ss-DFT)模拟光谱吻合得很好(使用约束晶胞体积建模)。然而,对于 EZT-MH,室温结构的 ss-DFT 光谱与实验 THz 光谱的相关性优于 0 K 结构的模拟光谱,这表明 EZT-MH 晶体具有更大的非谐性。计算了吉布斯自由能曲线,发现 EZT-MH 在较宽的温度范围内比纯 EZT 和水更稳定。水合物的稳定性可能受到 EZT-MH 中更多氢键的存在的影响。使用带有湿度控制样品室的太赫兹光谱仪监测了纯 API 片剂和制剂片剂中 EZT 的水合和脱水过程。通过证明制剂片剂中赋形剂对水合的影响,可以成功确认赋形剂对 API 水合的影响,即 API 与赋形剂的固态转变明显较慢。在相对湿度为 60%的条件下,纯 EZT 片剂中 EZT 的水合作用在 200 分钟内发生,而制剂片剂中 EZT 的水合作用则慢了 50 倍。