Bioactivity studies, potential uses and LC-MS/MS analysis of Flacourtiainermis fruits extracts

dc.contributor.authorAlakolanga, A. G. A. W.
dc.contributor.authorJayasinghe, U. L. B.
dc.contributor.authorKumar, N. S.
dc.date.accessioned2024-04-25T12:09:17Z
dc.date.available2024-04-25T12:09:17Z
dc.date.issued2013-07-04
dc.description.abstractFlacourtiainermis is a small, evergreen tree, native to Malaysia and grown in South Asian and African regions as well. Fruits are edible, red pulpy berries with an acidic taste and have some economic value. The current study was carried out to determine the bioactivity exhibited by chemical constituents present in extracts of the fruits of F. inermis and potential health benefits of consuming these fruits. Fruits of F. inermis have not been studied extensively for their biochemical properties. However, there are a few previous reports about their antioxidant, antifungal activity and antiprotozoal activities. The presence of caffeoylquinic acid derivatives, quinic acid, malic acid, phenolic glucoside derivatives, flavanoids, and phenolic acids has been reported. During the current study the cytotoxic activity, phytotoxic activity, antioxidant activity and amylase inhibition activity of the ethyl acetate (EtOAc) extract, methanol (MeOH) extract and n-butanol (n-BuOH) extract of fresh fruits of F. inermiswere determined. All three extracts showed significant cytotoxic activity against second instar nauplii of Artemiasalina. <Formula> values of EtOAc, MeOH and n-BuOH extracts were 289 ppm, 315 ppm and 260 ppm respectively. The EtOAc extract showed significant phytotoxic activity against seed germination of Lactuca sativa and100% inhibition was exhibited at 2000 ppm. The n-BuOH extract was moderately active and 100% inhibition was shown at 3000 ppm. The MeOH extract was least active and showed 100% inhibition at 5000 ppm. All three extracts showed amylase inhibition activity against porcine pancreatic α-amylase enzyme in phosphate buffer (pH 6.8) at room temperature. <Formula> values were; EtOAc extract- 1120 ppm, MeOH extract – 1855 ppm, n-BuOH extract- 2350 ppm and Acarbose (standard) – 20 ppm. All extracts showed significant antioxidant activity against DPPH free radical in methanol. <Formula> values observed were: EtOAc extract-115ppm; MeOH extract- 250 ppm; n-BuOH extract-175 ppm; Butylated hydroxyl anisole (standard) – 28 ppm. Preliminary results indicate that the fruits of F. inermisdisplay useful bioactivities. The high antioxidant activity of the MeOH and EtOAc extracts may be attributed to the presence of caffeoylquinic acid derivatives. Several isomeric 3-caffeoyl quinic acids m/z [M-H]- 353; 5-caffeoyl quinic acids m/z <Formula> 353; and dicaffeoylquinic acids m/z <Formula> 515, have been detected in the 90% MeOH extract using LC-MS/MS.
dc.identifier.citationPeradeniya University Research Sessions PURSE - 2012, Book of Abstracts, University of Peradeniya, Sri Lanka, Vol. 17, July. 4. 2012 pp.173
dc.identifier.isbn9789555891646
dc.identifier.issn13914111
dc.identifier.urihttps://ir.lib.pdn.ac.lk/handle/20.500.14444/382
dc.language.isoen_US
dc.publisherThe University of Peradeniya
dc.subjectFlacourtiainermis
dc.subjectBioactivity
dc.titleBioactivity studies, potential uses and LC-MS/MS analysis of Flacourtiainermis fruits extracts
dc.typeArticle

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