首页> 外文期刊>European Journal of Medicinal Plants >Antioxidant Activity, Total Phenols, Flavonoids and LCMS Profile of Chamaecrista hildebrandtii (Vatke) Lock and Clerodendrum rotundifolium (Oliv.)
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Antioxidant Activity, Total Phenols, Flavonoids and LCMS Profile of Chamaecrista hildebrandtii (Vatke) Lock and Clerodendrum rotundifolium (Oliv.)

机译:Chamaecrista hildebrandtii(Vatke)Lock和圆形臭油菌(Oliv。)的抗氧化活性,总酚,类黄酮和LCMS谱

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Aims: The purpose of the study was to determine the antioxidant activity, quantify total phenols and total flavonoids and characterize the secondary metabolites present in methanolic extracts of Chamaecrista hildebrandtii and Clerodendrum rotundifolium using liquid chromatography coupled to mass spectrometry (LC-MS). Methodology: The total phenol and flavonoid contents were determined spectrophotometrically while the antioxidant activity was evaluated using the 2, 2-Diphenyl-1-Picrylhydrazyl (DPPH) free radical scavenging method. The secondary metabolites present in the methanolic leaves extracts were evaluated using LC-MS. Results: The extracts of C. hildebrandtii showed a significantly higher antioxidant activity (ICsub50/sub = 8.7 mg/mL) compared to C. rotundifolium (ICsub50/sub= 28.5 mg/mL). Both methanolic extracts of C. hildebrandtii and C. rotundifolium had common and different types of flavonoids such as quercetin, rutin, (+)-catechin 3-O-gallate and luteolin 6-C-glucoside among others that could be responsible for the observed antioxidant activity. The total phenolic content of C. hildebrandtii (1.33±0.07 mg/g tannic acid equivalents) was significantly higher than that of C. rotundifolium (0.25±0.00 mg/g tannic acid equivalents). However, there was no statistically significant difference ( p 0.05) in total flavonoid content of C. hildebrandtii (2.69±0.33 mg/g catechin equivalents) and C. rotundifolium (2.36±0.16 mg/g catechin equivalents). Conclusion: The results of the present study suggested that the good antioxidant activity exhibited by C. hildebrandtii may probably have been brought about by various secondary metabolites functioning in synergy.
机译:目的:本研究的目的是使用液相色谱-质谱联用技术(LC-MS)确定抗氧化活性,定量总酚和总黄酮,并表征Chamaecrista hildebrandtii和Clerodendrum rotundifolium甲醇提取物中存在的次级代谢产物。方法:用分光光度法测定总酚和类黄酮的含量,同时使用2,2-二苯基-1-吡啶基肼基(DPPH)自由基清除法评估抗氧化剂的活性。使用LC-MS对甲醇叶提取物中存在的次级代谢产物进行了评估。结果:希尔德布兰地提取物的抗氧化活性(IC 50 = 8.7 mg / mL)明显高于圆形假单胞菌(IC 50 = 28.5 mg / mL) )。 C. hildebrandtii和C. rotundifolium的甲醇提取物均具有常见和不同类型的类黄酮,例如槲皮素,芦丁,(+)-儿茶素3-O-没食子酸酯和木犀草素6-C-葡糖苷等可能是造成观察到的原因的原因。抗氧化活性。希尔德布兰地衣藻的总酚含量(1.33±0.07 mg / g单宁酸当量)显着高于圆头梭菌(0.25±0.00 mg / g单宁酸当量)。但是,希尔德布兰地衣藻(2.69±0.33 mg / g儿茶素当量)和圆形假单胞菌(2.36±0.16 mg / g儿茶素当量)的总黄酮含量无统计学意义(p> 0.05)。结论:本研究的结果表明,希尔德布兰氏菌表现出的良好的抗氧化活性可能是由多种协同作用的次生代谢产物引起的。

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