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Method Development and Validation for Spectrophotometric Determination of Ascorbic Acid in M. stenopetala Leaves Through Catalytic Titration with Hexavalent Chromium

机译:通过催化滴定与六价铬催化滴定分光光度法测定分光光度法测定的方法的开发和验证

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M. stenopetala has gained attention recently in Ethiopia due to its multiple uses. It is a drought tolerant fast growing indigenous tree mainly planted and maintained for its nutritional value. An ascorbic acid excess can lead to gastric irritation and the metabolic product of vitamin C (oxalic acid) can cause renal problems. Thus, its level in food stuffs should be monitored. Hence, in this project, it was aimed to develop a novel spectrophotometer method for determination of ascorbic acid content in M. Stenopetala through Catalytic titration with Hexavalent chromium. The developed method was validated against HPLC as standard technique. Cr (VI) was used as UV-active material and Mn (II) used as catalyst. Determination of AA was based on the decrease in absorbance of the Cr (VI) solution as a result of its reaction with AA. Factors influencing the reduction of Cr (VI), including incubation time, solution pH and background concentration ratio had been optimized. The theoretical detection limit and Limit of quantification were calculated to be 0.00154 and 0.005134 mg/ml, respectively. Out of the 3 different area of Ms Leave sample studied, FMs from Arbaminch contained highest concentration (237 0.001 mg/100g) of AA, Followed by FMs from Konso (233 0.48 mg/100g and FMs from Dilla (21 0.48 mg/100g), respectively. But it was reduced significantly after boiling for ten minute. The level of AA content in the analyzed Ms Leave samples was found to decrease with increasing cooking time. Cooked Ms Leave sample contained lower concentration of AA than Fresh M. stenopetala leave sample. All studied Ms Leave samples contained relatively acceptable range or moderate amounts of total AA (200-250 mg/100g) and the results obtained from the modified UV-vis Spectrophotometric and HPLC methods were statistically consistent.
机译:由于多种用途,M. Stenopetala最近在埃塞俄比亚获得了关注。它是一种耐旱性快速生长的土着树,主要种植和维持其营养价值。抗坏血酸过量会导致胃刺激,维生素C(草酸)的代谢产物会导致肾脏问题。因此,应监测其食物中的水平。因此,在该项目中,旨在通过用六价铬催化滴定来制定一种新的分光光度计方法,用于测定M. Stenopetala中的抗坏血酸含量。作为标准技术的HPLC验证了开发的方法。 Cr(VI)用作紫外线活性物质和用作催化剂的Mn(II)。 AA的测定基于其与AA反应的结果的吸光度降低。影响CR(VI)减少的因素,包括孵育时间,溶液pH和背景浓度比已得到优化。将理论检测限度和定量限制分别计算为0.00154和0.005134mg / ml。在研究的3个不同区域中,研究了来自Arbaminch的FMS含有最高浓度(237.001mg / 100g)的AA,其次是来自KONSO的FMS(233 0.48mg / 100g,来自DILLA的FMS(21.48 mg / 100g)分别。但沸腾后它显着减少了十分钟。发现分析的MS离开样品中的AA含量水平随着烹饪时间的增加而降低。煮熟的MS离开样品含有比新鲜的M. Stenopetala离开样品的浓度较低的AA浓度。所有研究的MS留下样品含有相对可接受的范围或中等量的总AA(200-250mg / 100g),并且从改性的UV-Vis分光光度法和HPLC方法获得的结果是统计学上一致的。

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