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Degradation of L-Ascorbic Acid in the Amorphous Solid State

机译:非晶态L-抗坏血酸的降解

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Ascorbic acid degradation in amorphous solid dispersions was compared to its degradation in the crystalline state. Physical blends and lyophiles of ascorbic acid and polymers (pectins and polyvinylpyrrolidone [PVP]) were prepared initially at 50:50 (w/w), with further studies using the polymer that best inhibited ascorbic acid crystallization in the lyophiles in 14 vitamin : PVP ratios. Samples were stored in controlled environments (25 to 60 ℃, 0% to 23% RH) for 1 mo and analyzed periodically to track the physical appearance, change in moisture content, physical state (powder x-ray diffraction and polarized light microscopy), and vitamin loss (high performance liquid chromatography) over time. The glass transition temperatures of select samples were determined using differential scanning calorimetry, and moisture sorption profiles were generated. Ascorbic acid in the amorphous form, even in the glassy amorphous state, was more labile than in the crystalline form in some formulations at the highest storage temperature. Lyophiles stored at 25 and 40 ℃ and those in which ascorbic acid had crystallized at 60 ℃ (≥70% ascorbic acid : PVP) had no significant difference in vitamin loss (P > 0.05) relative to physical blend controls, and the length of storage had little effect. At 60 ℃, amorphous ascorbic acid lyophiles (≤60% ascorbic acid : PVP) lost significantly more vitamin (P < 0.05) relative to physical blend controls after 1 wk, and vitamin loss significantly increased over time. In these lyophiles, vitamin degradation also significantly increased (P < 0.05) at lower proportions of ascorbic acid, a scenario likely encountered in foods wherein vitamins are naturally present or added at low concentrations and production practices may promote amorphization of the vitamin.
机译:将抗坏血酸在非晶态固体分散体中的降解与其在结晶态的降解进行了比较。最初以50:50(w / w)的比例制备了抗坏血酸与聚合物(果胶和聚乙烯吡咯烷酮[PVP])的物理混合物和冻干物,并使用在14种维生素:PVP中能最好地抑制冻干物中抗坏血酸结晶的聚合物进行了进一步研究。比率。样品在受控环境(25至60℃,相对湿度0%至23%)中存储1个月,并定期进行分析以追踪物理外观,水分含量变化,物理状态(粉末X射线衍射和偏光显微镜),和维生素随时间流失(高效液相色谱)。使用差示扫描量热法测定了所选样品的玻璃化转变温度,并生成了吸湿曲线。在某些配方中,即使在玻璃态的无定形状态下,即使在玻璃态的无定形状态下,抗坏血酸也比晶体状的不稳定。相对于物理混合对照,在25和40℃储存的冻干液和在60℃抗坏血酸结晶的冻干液(≥70%的抗坏血酸:PVP)的维生素流失(P> 0.05)无显着差异。效果不大。在60℃下,无定形抗坏血酸冻干物(≤60%抗坏血酸:PVP)在1周后损失的维生素(P <0.05)相对于物理混合物对照显着增加,并且维生素损失随时间显着增加。在这些冻干物中,在较低比例的抗坏血酸下,维生素的降解也会显着增加(P <0.05),这种情况可能发生在天然存在或以低浓度添加维生素且生产实践可能促进维生素无定形的食品中。

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