CQE- Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal; CQFM - Centro de Química-Física Molecular and IN - Institute of Nanoscience and Nanotechnology, Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal.
CQFM - Centro de Química-Física Molecular and IN - Institute of Nanoscience and Nanotechnology, Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal; CQB - Centro de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, 1649-016 Lisboa, Portugal.
J Pharm Sci. 2019 Mar;108(3):1254-1263. doi: 10.1016/j.xphs.2018.10.050. Epub 2018 Nov 2.
The analysis of the thermal behavior of efavirenz showed a high glass-forming ability and good glass stability of this glass-forming liquid at room temperature. No polymorphic forms were formed either by cold crystallization or by recrystallization from solvent acetone. The determination of the dynamic fragility by the differential scanning calorimetry, thermally stimulated depolarization currents (TSDC), and dielectric relaxation spectroscopy (DRS) techniques is unanimous in suggesting efavirenz as a moderately fragile liquid. With DRS, secondary relaxations were detected, however, with weak intensities that did not allow the respective kinetic analysis; in contrast, TSDC allows clearly resolving the components of the secondary β-relaxation below T, with activation energies distributed between about 75 and 90 kJ mol and Arrhenius prefactors of the order of 10 s. In this regard, the TSDC technique proved to be more effective compared to DRS in characterizing the secondary relaxation. The glass forming ability and glass stability found for efavirenz have been discussed in terms of various thermodynamic and kinetic parameters such as the reduced glass transition temperature, T, the dynamic fragility, m, the stretching exponent, β, the melting entropy, ΔS, and the molecular stiffness. The exceptionally low value of efavirenz fusion entropy was highlighted as a key feature of the thermal behavior of this glass-forming liquid.
对依非韦伦的热行为分析表明,该玻璃形成液体在室温下具有高的玻璃形成能力和良好的玻璃稳定性。无论是通过冷结晶还是从溶剂丙酮重结晶都没有形成多晶型形式。通过差示扫描量热法、热刺激去极化电流(TSDC)和介电松弛谱(DRS)技术测定的动态脆性一致表明依非韦伦是一种中等脆性液体。通过 DRS 检测到了次级松弛,但是强度较弱,无法进行相应的动力学分析;相比之下,TSDC 允许在 T 以下清晰地分辨次级 β-松弛的成分,其活化能分布在约 75 至 90 kJ/mol 之间,Arrhenius 前因子约为 10 s。在这方面,与 DRS 相比,TSDC 技术在表征次级松弛方面更有效。依非韦伦的成玻璃能力和玻璃稳定性已根据各种热力学和动力学参数进行了讨论,如降低的玻璃化转变温度 T、动态脆性 m、拉伸指数β、熔融熵ΔS 和分子刚性。依非韦伦的熔融熵值异常低,这是该玻璃形成液体热行为的一个关键特征。