In-vitro α-Amylase Inhibitory Activity of Evolvulus alsinoides (L.) L. Extracts

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dc.contributor.author Ruberu, T.I.S.
dc.contributor.author Jayasuriya, W.J.A.B.N.
dc.contributor.author Arawwawala, L.D.A.M.
dc.contributor.author Liyanaarachchi, G.D.
dc.contributor.author Suresh, T.S.
dc.contributor.author Palliyagur, L.
dc.contributor.author Jayaweera, P.M.
dc.date.accessioned 2024-04-03T06:00:24Z
dc.date.available 2024-04-03T06:00:24Z
dc.date.issued 2023-11-10
dc.identifier.citation Ruberu, T.I.S. , Jayasuriya, W.J.A.B.N. , Arawwawala, L.D.A.M. , Liyanaarachchi, G.D. , Suresh, T.S. , Palliyaguru, L. , Jayaweera, P.M. (2023). In-vitro α-Amylase Inhibitory Activity of Evolvulus alsinoides (L.) L. Extracts. The International Research Symposium of the Faculty of Allied Health Sciences University of Ruhuna, Galle, Sri Lanka, 125. en_US
dc.identifier.issn 2659-2029
dc.identifier.uri http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/16728
dc.description.abstract Background: Evolvulus alsinoides (L.) L. commonly known as ‘Nil Vishnukranthi’ is known for its dietary enzyme inhibitory activity. It is a widely used medicinal herb in ayurvedic preparations, and reported to be effective against neurodegeneration, gastroprotection and diabetes. The quantitative analysis of the plant phytoconstituents has reported the presence of alkaloids, polyphenols, saponins, tannins and flavonoids and aqueous extract possessed significant antacid potential. Objectives: To evaluate α-amylase enzyme inhibition of aqueous (AqE), ethanolic (EE) and hexane (HE) extracts of E. alsinoides Methods: AqE, EE and HE were obtained by reflux method using dried whole plant powder. Solutions of 100 mg/mL preliminary screening concentrations were prepared by dissolving concentrated E. alsinoides extracts in sodium acetate buffer separately. In a microplate, samples with 40μL of the 0.1% starch solution and 120μL of E. alsinoides extract (n=3) were pre incubated at 37°C for 10 minutes. To each well, 40μL of 500µg/mL α-amylase enzyme (from bacterial source) was added and incubated at 37°C for 10 minutes. A volume of 100μL di nitrosalysilic acid (DNS) reagent was added to the reaction mixture and heated in a water bath at 90°C. The absorbance was measured at 540nm. A blank with starch replaced by buffer and a control with plant extract replaced by buffer were carried out. Acarbose was used as the standard. Statistical analysis was carried out with one-way ANOVA using SPSS. Results: AqE, EE and HE extracts of E. alsinoides exhibited percentage inhibitions of 62.35(±6.1)%, 17.66(±8.7)%, 76.71(±1.8)%, respectively. The standard (Acarbose) exhibited 50% inhibition at 140.62(±2.4)µg/mL concentration. Conclusions: Aqueous and hexane extracts of E. alsinoides possessed significant (p<0.001) amylase enzyme inhibitory activity compared to deionized water. However, ethanolic extract did not exhibit significant activity (p<0.05). en_US
dc.language.iso en en_US
dc.publisher FAHS en_US
dc.subject α-Aamylase inhibitory activity en_US
dc.subject Antidiabetic en_US
dc.subject Evolvulus alsinoide en_US
dc.title In-vitro α-Amylase Inhibitory Activity of Evolvulus alsinoides (L.) L. Extracts en_US
dc.type Article en_US


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