Colorimetric film sensor for monitoring rancidity reaction of intermediate-moisture (Cake)

Omer A. Abdalla, M. W. Saeed
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Abstract

Colorimetric films sensor based on wheat gliadin with natural dyes (including anthocyanin, chlorophyll, and beta carotene), glucose oxidase, alpha amylase /starch / were created and for real-time monitoring cake formula rancidity reaction is described in this study. The addition Glucose oxidase enzyme 0.9% (activity270U/0.09g), 0.9% (117U/0.09g) of α-Amylase, and 5% of natural extracted pigments   and concentration 1:0.1 of Gliadin/ glycerol composition films and starch greatly raised sensitivity the reaction of films to rancidity. The mixture of enzymes and substrate has a great impact on changing the intensity of color films. In addition, when the color attributes of the active film are examined, it is discovered that the color of the chlorophyll film changes (from green to yellow) whereas, beta –carotene film from (yellow to pale yellow) and Anthocyanin film (alterated from red to brown) with increasing storage duration and oxidant percent, which can be utilized to detect the rancidity reaction of cake's fat. The absorbance at 494, 450, and 666 nm, respectively, demonstrated that the intensity of anthocyanin, beta-carotene, and chlorophyll color films was greatly reduced as a result of rancidity reaction in cake samples after 3 weeks of storage at room temperature 30-35˚C and 25-30% of relative humidity. Moreover, all treated samples showed a decrease in color pigment intensity compared to the control after 15 minutes of exposure to peroxide hydrogen addition (1 ppm), the lowest concentration at which films are susceptible to oxidation. Furthermore, after 4 weeks of storage, samples of cakes, odor turned rancid under the same ambient conditions, and the cake's fat's peroxide value increased dramatically, from 1.3 to 8 mEqO2/kg were approximately close to the maximum permissible limit in Codex regulations therefore color of film sensor was changed fully as a result of increasing peroxide value and rancidity.
用于监测中间水分(蛋糕)酸败反应的比色薄膜传感器
本研究介绍了基于天然染料(包括花青素、叶绿素和β-胡萝卜素)、葡萄糖氧化酶、α-淀粉酶/淀粉/小麦胶蛋白的比色薄膜传感器,用于实时监测蛋糕配方酸败反应。添加葡萄糖氧化酶 0.9%(活性 270U/0.09g)、α-淀粉酶 0.9%(117U/0.09g)和天然提取色素 5%,以及胶蛋白/甘油成分薄膜和淀粉的浓度 1:0.1,大大提高了薄膜酸败反应的灵敏度。酶和底物的混合对改变薄膜的颜色强度有很大影响。此外,在检测活性膜的颜色属性时,发现叶绿素膜的颜色会发生变化(从绿色变为黄色),而β-胡萝卜素膜则由(黄色变为淡黄色)和花青素膜(从红色变为棕色)随着贮藏时间和氧化剂百分比的增加而变化,这可以用来检测蛋糕脂肪的酸败反应。在 494、450 和 666 纳米波长下的吸光度分别表明,蛋糕样品在室温 30-35 摄氏度和相对湿度 25-30% 的条件下储存 3 周后,由于酸败反应,花青素、β-胡萝卜素和叶绿素色膜的强度大大降低。此外,与对照组相比,所有经过处理的样品在过氧化氢添加剂(百万分之 1)(薄膜易氧化的最低浓度)中暴露 15 分钟后,色素强度都有所下降。此外,在相同的环境条件下,经过 4 周的储存,蛋糕样品的气味变得酸败,蛋糕脂肪的过氧化值急剧上升,从 1.3 到 8 mEqO2/kg,大约接近食品法典规定的最大允许限值,因此,由于过氧化值的增加和酸败,薄膜传感器的颜色完全改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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