首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >ALPHA AMYLASE INHIBITORY ACTIVITY OF DIFFERENT EXTRACT OF BARK OF ALBIZIA LEBBECK (L.) BENTH
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ALPHA AMYLASE INHIBITORY ACTIVITY OF DIFFERENT EXTRACT OF BARK OF ALBIZIA LEBBECK (L.) BENTH

机译:紫花苜蓿(L.)的不同树皮提取物的淀粉酶抑制作用。

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Objective: To evaluate the alpha amylase inhibitory activity of different extract of bark of Albizia lebbeck (L.) Benth. Methods: Bark of A. lebbeck was collected and air dried. Extraction of flavonoid, alkaloid and steroid carried out using standard methods. Extracts in different polar and non polar solvents were extracted using soxhlet method. Filtered extracts were subsequently tested for alpha amylase inhibitory activity using the chromogenic dinitrosalicylic acid (DNSA) method and starch iodine method. Experiments were performed in triplicates for three different sets and mean±standard error of the mean was used for calculation. Graphpad prism 5 software was used for one way analysis of variance (ANOVA), linear regression and statistical difference analysis. IC 50 values were also calculated. Results: We found that the free flavonoid extract had higher 43.50±0.17% to 73.43±0.08% inhibition (at a concentration 0.5-1.5 mg/ml) with an IC 50 value of 0.6653 mg/ml. At the same concentration methanol, water and bound flavonoid extracts also showed good inhibitory activity i.e. 28.63±0.15% to 37.50±0.20%, 26.67±0.12% to 32.07±0.17% and 26.70±0.15 to 32.67±0.12% with an IC 50 value of 7.3621 mg/ml, 22.2844 mg/ml and 41.6869 mg/ml respectively. Conclusion: The prepared free flavonoid, bound flavonoid, water and methanol bark extracts of Albizia lebbeck showed the significant alpha amylase inhibitory activity. Further works is required to identify the bioactive compound responsible for inhibition of alpha amylse enzyme.
机译:目的:评价不同的Albizia lebbeck(L.)Benth树皮提取物的α淀粉酶抑制活性。方法:收集A. lebbeck的树皮并风干。类黄酮,生物碱和类固醇的提取采用标准方法进行。使用索氏萃取法提取不同极性和非极性溶剂中的提取物。随后使用发色二硝基水杨酸(DNSA)方法和淀粉碘法测试过滤后的提取物的α淀粉酶抑制活性。一式三份地针对三个不同的组进行实验,并且使用平均值的平均值±标准误差进行计算。使用Graphpad Prism 5软件进行单向方差分析(ANOVA),线性回归和统计差异分析。还计算了IC 50值。结果:我们发现游离类黄酮提取物具有较高的抑制作用(浓度为0.5-1.5 mg / ml时,抑制率为43.50±0.17%至73.43±0.08%),IC 50值为0.6653 mg / ml。在相同浓度下,甲醇,水和结合的类黄酮提取物也表现出良好的抑制活性,即28.63±0.15%至37.50±0.20%,26.67±0.12%至32.07±0.17%和26.70±0.15至32.67±0.12%,IC 50值分别为7.3621 mg / ml,22.2844 mg / ml和41.6869 mg / ml。结论:制得的Albizia lebbeck的游离类黄酮,结合类黄酮,水和甲醇树皮提取物均具有明显的α淀粉酶抑制活性。需要进一步的工作来鉴定负责抑制α-淀粉酶的生物活性化合物。

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