Evaluation of the Organ Microscopy, Chemical Composition and Anti-inflammatory Potentials of Methanolic Leaf Extract and Fractions of Diaphananthe bidens

I. C. Umeyor, C. Umeyor, Cyril O. Ogbue, F. Onyegbule, F. Okoye
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Abstract

Aim: The study aims to investigate high-pressure liquid chromatographic (HPLC)-based chemical composition and anti-inflammatory activity of methanolic leaf extract and fractions of D. bidens. Study Design: The study is a laboratory-based research involving collection, identification and preparation, of plants, extraction, characterization and evaluation of the anti-inflammatory potential of D. bidens. Place and Duration of Study: Department of Pharmacognosy and Traditional Medicine, Faculty of Pharmaceutical Sciences, Nnamdi Azikiwe University, Awka, Nigeria between January 2016 and June 2019. Methodology: Powdered leaves of D. bidens was macerated in methanol and the obtained crude extract was fractionated using n-hexane, ethylacetate, butanol, and water respectively. The acute toxicity profile of the extract was determined. Spectroscopic factors of the plant were assayed using HPLC-DAD and the anti-inflammatory activity of the extract and its fractions were evaluated. Results: Acute toxicity study showed that the crude extract has an LD50 > 5,000 mg/kg. HPLC-DAD analysis revealed the presence of compounds including apigenin monoglycoside, quercetin 3-O-(6''O-acetyl) galactopyranoside, kaempferol 3-O-(6" O-malonyl) glucoside, genistein 8-C-glucoside, while anti-inflammatory study showed that the extract and fractions inhibited cellular activities of inflammatory mediators (86 – 97 %) in comparison with the diclofenac (53 %); thus, supporting its ethnomedicinal use in the treatment of inflammation. Conclusions: Methanolic extract of D. bidens has wide margin of safety. It has sufficient deposit of flavonoids which might be responsible for its strong anti-inflammatory activity that is comparable with diclofenac.
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苦参叶甲醇提取物及部位的器官显微镜、化学成分及抗炎活性评价
目的:利用高压液相色谱法研究拜登叶甲醇提取物及其部位的化学成分和抗炎活性。研究设计:本研究是一项基于实验室的研究,涉及植物的收集、鉴定和制备、提取、表征和抗炎潜力的评估。学习地点和时间:2016年1月至2019年6月,尼日利亚阿夫卡Nnamdi Azikiwe大学药学院生药学和传统医学系。方法:用甲醇浸渍大黄叶粉,粗提物分别用正己烷、乙酸乙酯、丁醇和水进行分馏。测定了该提取物的急性毒性。采用高效液相色谱- dad法测定了该植物的光谱因子,并评价了提取物及其组分的抗炎活性。结果:急性毒性研究表明,粗提物的LD50 > 5000 mg/kg。HPLC-DAD分析显示,其中含有芹菜素单糖苷、槲皮素3-O-(6′o -乙酰基)半乳糖苷、山奈酚3-O-(6′o -丙二醇基)葡萄糖苷、染料木素8- c -葡萄糖苷等化合物,抗炎研究表明,与双氯芬酸相比,其提取物和组分对炎症介质细胞活性的抑制作用(86% - 97%)高于双氯芬酸(53%);从而支持其在治疗炎症方面的民族医学应用。结论:黄芩醇提物具有较大的安全裕度。它含有足够的黄酮类化合物,这可能是它具有与双氯芬酸相当的强抗炎活性的原因。
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