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Molecular mobility of hydroxyethyl cellulose (HEC) films characterised by thermally stimulated currents (TSC) spectroscopy

机译:羟乙基纤维素(HEC)膜的分子迁移率以热刺激电流(TSC)光谱为特征

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摘要

Molecular mobility has long been established to relate to textural properties and stability of polymer films and is therefore an important property to characterise to better understand pharmaceutical film formulations. The molecular mobility of solvent cast hydroxyethyl cellulose (HEC) films has been investigated by means of thermally stimulated current (TSC) below the temperature at which the film was formed. Preliminary physical characterisation of the films was performed using XRPD, TGA, DSC and texture analysis (tensile properties). XRPD results showed the films to be completely amorphous with Tg determined by DSC to be 127 ± 1 °C. TGA analysis showed the films to contain 8 ± 1% water and film was dried to only 0.06 ± 0.01% water content when heated to 160 °C. Application of TSC detected molecular mobility in HEC films at sub-zero temperatures. Two motional transitions with average relaxation time of 50 ± 3 s were identified; a β-relaxation at −57 ± 2 °C, attributed to localised non-cooperative orientation of HEC polymer chain ends and the hydroxyethyl side groups and an α-relaxation, originating from cooperative segmental mobility, at −20 ± 2 °C. The tensile properties i.e., elongation, tensile strength and elastic modulus of the HEC film have been related to the molecular relaxation processes detected by TSC.
机译:早已建立了与聚合物膜的质地特性和稳定性有关的分子迁移率,因此,分子迁移率是表征以更好地理解药物膜制剂的重要特性。已经通过低于膜形成温度的热刺激电流(TSC)研究了溶剂流延羟乙基纤维素(HEC)膜的分子迁移率。使用XRPD,TGA,DSC和质构分析(拉伸性能)对薄膜进行了初步的物理表征。 XRPD结果显示膜是完全无定形的,由DSC测定的Tg为127±1℃。 TGA分析表明,膜含有8±1%的水,并且加热至160℃时,膜干燥至仅0.06±0.01%的水含量。 TSC的应用在低于零的温度下检测了HEC膜中的分子迁移率。确定了两个运动过渡,平均弛豫时间为50±3 s。在-57±2°C时发生β松弛,归因于HEC聚合物链端和羟乙基侧基的局部非合作取向,而在20±2°C时发生α松弛,其源于合作的链段迁移率。 HEC膜的拉伸性能,即伸长率,拉伸强度和弹性模量与TSC检测到的分子松弛过程有关。

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