Avicennia alba Blume, (1826) Family avicenenaceae,叶片提取物抗氧化活性的DPPH测定

Felita C. Torero
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引用次数: 0

摘要

采用1,1-二苯基-2-苦味酰肼(DPPH)自由基清除活性法测定了白杨(Avicennia alba Blume, 1826)叶提取物的抗氧化活性。以石油醚和95%乙醇为溶剂,分别进行两次浸渍。只有无乙醇提取物(TSB)具有抗氧化活性;其颜色由紫色变为淡黄色,与阳性对照(抗坏血酸溶液)相似,吸光度相对于阴性对照(95%乙醇)降低。对DPPH自由基清除活性测定结果进行单因素方差分析,事后分析结果显示,TSB的抗氧化活性与阳性对照无显著差异,分别为68.24%±12.23和76.43%±9.22。经试管法筛选得到的无乙醇提取物(TSB)含有皂苷、单宁、黄酮类化合物和苷类化合物。然后用柱层析法对其化学成分进行部分纯化;根据其TLC特征,特别是Rf值,收集和汇总来自乳酸的分数。紫外光下斑点显著的部位为部位1、部位2、部位4、部位5。对两组馏分进行DPPH自由基清除试验。两组分的颜色变化与阳性对照相似,吸光度相对于阴性对照下降。组分1和组分2的抗氧化活性为69.97%±2.439 %,与阳性对照无显著差异,最高抗氧化活性为87.88%±3.357 %。得到的p值(<0.01)表明,各试验溶液的抗氧化活性差异显著。DPPH测定后,对活性最高的组分1和2进行FT-IR和GC-MS分析。红外光谱分析显示存在脂肪族C- h键、C=O键和-OH键,GC-MS分析显示有5个化合物基于m/z = 537.4的分子离子。FT-IR和GC-MS分析中化合物中的官能团以及植物化学筛选中存在的次级代谢物似乎是白杨叶提取物抗氧化活性的原因。
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Antioxidant Activity of Avicennia alba Blume, (1826) Family Avicenniaceae, Leaf Extracts Using DPPH Assay
The antioxidant activity of Avicennia alba Blume, (1826) leaf extract was determined using the 1,1-Diphenyl-2-picrylhydrazyl (DPPH) Free Radical Scavenging Activity Assay. Petroleum ether and 95 % ethanol were used as solvents in two separate macerations. Only the ethanol-free extract (TSB) exhibited antioxidant activity; it showed a color change from purple to light yellow similar to the positive control (ascorbic acid solution) and a decrease in absorbance relative to the negative control (95% ethanol). The results of the DPPH free radical scavenging activity assay were subjected to statistical analysis using one-way ANOVA then post hoc analysis results of TSB showed no significant difference vs positive control, with a percentage antioxidant activity of 68.24% ± 12.23 and 76.43% ± 9.22 respectively. The ethanol-free extract (TSB) underwent phytochemical screening by test tube method which revealed the presence of saponins, tannins, flavonoids, and glycosides. It was then subjected to column chromatography for partial purification of its chemical compounds; fractions from the eulates were collected and pooled according to their TLC profile specifically Rf values. The fractions that showed significant spots under UV light were fractions 1 and 2, and fractions 4 and 5. These two sets of fractions were tested to DPPH free radical scavenging assay. Both fractions showed a similar color change to the positive control and a decrease in absorbance relative to the negative control. Fractions 1&2 showed 69.97% ± 2.439 percentage antioxidant activity which had no significant difference from the positive control with the highest antioxidant activity of 87.88% ± 3.357. The p-value (<0.01) obtained manifested that there was a significant difference between the test solutions with their antioxidant activity. After the DPPH assay, the most active fractions 1 & 2, were subjected to FT-IR and GC-MS. The infrared spectrum showed the presence of aliphatic C-H bonds, C=O bonds, and –OH bonds while the GC-MS analysis revealed five compounds that were based on the molecular ion showed at m/z = 537.4. The functional groups present in the compounds from FT-IR and GC-MS analyses and the secondary metabolites present in phytochemical screening seemed to be responsible for the antioxidant activity of Avicennia alba leaf extracts.
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