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RELEASE MECHANISM OF ESSENTIAL FATTY ACIDS IN POLYSACCHARIDE MATRICES UNDERGOING GLASS TRANSITION

机译:玻璃化转变多糖基质中必需脂肪酸的释放机制

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Identification of theoretical mechanisms governing molecular diffusion of essential fatty acids (oleic and α-linolenic acid) in high solid matrices was carried out on two polysaccharide matrices of high-methoxy pectin and κ-carrageenan in the presence of co-solute glucose syrup and polydextrose, respectively. Physicochemical analysis of this system utilised modulated DSC, dynamic oscillation in shear, ESEM, FTIR and WAX diffraction. The carbohydrate matrices were conditioned through an extensive temperature range to induce changes in molecular morphology and identify the network glass transition temperature. Thermally induced variation in phase morphology was employed to rationalise transportation patterns of the bioactive compound within the high-solid preparation. Thus, experimental observations using UV-vis spectroscopy modelled diffusion kinetics to document the mobility arresting effect of the vitrifying matrix on the micro-constituent. Within the glass transition region, results argue that free volume theory is the molecular process governing structural relaxation. Further, Less Fickian diffusion follows well the rate of molecular transport of the fatty acids as a function of time and temperature of observation in the condensed matrices.
机译:在共溶葡萄糖糖浆和聚籽籽糖浆存在下,对高固体基质中必需脂肪酸(油酸和α-亚麻酸)分子扩散的理论机制的鉴定在高甲氧基果胶和κ树蛋白南甘蔗和聚籽籽, 分别。该系统的物理化学分析利用调制的DSC,剪切,ESEM,FTIR和蜡衍射中的动态振荡。通过广泛的温度范围调节碳水化合物基质,以诱导分子形态的变化并确定网络玻璃化转变温度。采用热诱导的相位形态的变化,以在高固体制剂中合理化生物活性化合物的运输模式。因此,使用UV-VIS光谱建模扩散动力学的实验观察记录玻璃化基质对微量成分的迁移率滞留作用。在玻璃过渡区域内,结果争论自由体积理论是控制结构松弛的分子过程。此外,较少的Fichian扩散遵循脂肪酸的分子传输速率作为在冷凝基质中观察的时间和温度的函数。

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