Anti-aging potential of extracts from Sclerocarya birrea (A. Rich.) Hochst and its chemical profiling by UPLC-Q-TOF-MS

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dc.contributor.author Shoko, Tinotenda
dc.contributor.author Maharaj, Vinesh J.
dc.contributor.author Naidoo, Dashnie
dc.contributor.author Tselanyane, Malefa
dc.contributor.author Nthambeleni, Rudzani
dc.contributor.author Khorombi, Eric
dc.contributor.author Apostolides, Zeno
dc.date.accessioned 2018-03-12T07:09:43Z
dc.date.available 2018-03-12T07:09:43Z
dc.date.issued 2018-02-07
dc.description Additional file 1: Positive mode Base Peak Ion (BPI) chromatogram of Marula stem extract. ESI positive mode BPI chromatogram of Marula stems extracted with ethanol. en_ZA
dc.description Additional file 2: Negative mode BPI chromatogram of Marula stem ethanol extract. Full chromatogram of the ESI negative mode BPI chromatogram of Marula stems extracted with ethanol overlaid with the solvent blank. en_ZA
dc.description Additional file 3: MS/MS fragmentation pattern of quinic acid pure standard overlaid with MS/MS fragmentation of peak 1. A comparison of MS/MS fragmentation pattern of quinic acid pure standard and MS/MS fragmentation pattern of peak 1 identified as quinic acid. en_ZA
dc.description Additional file 4: Negative mode BPI chromatogram of quinic acid pure standard overlaid with that of Marula stem ethanol extract. A comparison of the retention time of quinic acid pure standard with that of peak 1 identified a quinic acid in Marula stem ethanol extract. en_ZA
dc.description Additional file 5: MS/MS fragmentation pattern of catechin pure standard overlaid with MS/MS fragmentation of peak 2. A comparison of the MS/MS fragmentation pattern of catechin pure standard with the MS/MS fragmentation pattern of peak 2 identified as catechin. en_ZA
dc.description Additional file 6: Negative mode BPI chromatogram of catechin pure standard overlaid with that of Marula stem ethanol extract. A comparison of the retention time of catechin pure standard with that of peak 2 identified as catechin in Marula stem ethanol extract. en_ZA
dc.description Additional file 7: MS/MS fragmentation pattern of epigallocatechin gallate pure standard overlaid with MS/MS fragmentation of peak 4. A comparison of MS/MS fragmentation pattern of epigallocatechin gallate pure standard with that of peak 4 identified as epigallocatechin gallate in Marula stem ethanol extract. en_ZA
dc.description Additional file 8: Negative mode BPI chromatogram of epigallocatechin gallate pure standard overlaid with that of Marula stem ethanol extract. A comparison of the retention time of epigallocatechin gallate pure standard with that of peak 4 identified as epigallocatechin gallate in Marula stem ethanol extract. en_ZA
dc.description Additional file 9: MS and MS/MS fragmentation pattern of peak 5. An overlay of MS and MS/MS fragmentation pattern of peak 5 tentatively identified as epicatechin-3-O-gallate-epicatechin. en_ZA
dc.description Additional file 10: MS and MS MS fragmentation pattern of peak 6. An overlay of MS and MS/MS fragmentation pattern of peak 6 tentatively identified as procyanidin B2-3,3′ di-O-gallate. en_ZA
dc.description Additional file 11: MS/MS fragmentation pattern of epicatechin gallate pure standard overlaid with MS/MS fragmentation of peak 7. A comparison of the MS/MS fragmentation pattern of epicatechin gallate pure standard to that of peak 7 identified as epicatechin gallate in Marula stem ethanol extract. en_ZA
dc.description Additional file 12: Negative mode BPI chromatogram of epicatechin gallate pure standard overlaid with that of Marula stem ethanol extract. A comparison of the retention time of epicatechin gallate pure standard with that of peak 7 identified as epicatechin gallate in Marula stem ethanol extract. en_ZA
dc.description.abstract BACKGROUND : Degradation of components of the extracellular matrix such as elastin and collagen by elastase and collagenase accelerates skin aging. Phytochemicals that inhibit the activity of these enzymes can be developed as anti-aging ingredients. In this study, an investigation of the anti-aging properties of Sclerocarya birrea (A. Rich.) Hochst (Marula) extracts was conducted in vitro with the aim of developing chemically characterized anti-aging ingredients. METHODS : Marula stems, leaves and fruits were extracted using methanol:dichloromethane (DCM) (1:1). The stems were later extracted using acetone, ethanol, methanol:DCM (1:1) and sequentially using hexane, DCM, ethyl acetate and methanol. The stem ethanol extract was defatted and concentrated. Elastase and collagenase inhibition activities of these extracts and Marula oil were determined using spectrophotometric methods. The chemical profile of the ethanolic stem extract was developed using Ultra-performance-liquid chromatography quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF-MS) with MassLynx software. Pure standards were used to confirm the identity of major compounds and were screened for anti-elastase and anti-collagenase activity. RESULTS : Marula stems extracts were the most active as they exhibited anti-elastase activity comparable to that of elafin (> 88%) and anti-collagenase activity as potent as EDTA (> 76%). The leaf extract had moderate anti-elastase activity (54%) but was inactive agains collagenase. Marula fruits and oil exhibited limited activity in both assays. The ethanolic extract of Marula stems was the most suitable based on its acceptability to the cosmetic industry and its anti-collagenase activity (99%). Defatting and concentration improved its antiaging activity and lowered the colour intensity. Six compounds have been tentatively identified in the chemical profile of the ethanolic extract of Marula stems of which four; quinic acid, catechin, epigallocatechin gallate and epicatechin gallate have been confirmed using pure standards. Epigallocatechin gallate and epicatechin gallate were as potent (p < 0.05) as EDTA at 5 μg/ml in the anti-collagenase assay. CONCLUSIONS : The ethanolic extract of Marula stems can be developed into an anti-aging ingredient as it exhibited very good in vitro anti-aging activity and its chemical profile has been developed. Epicatechin gallate and epigallocatechin gallate contribute to the anti-aging activity of Marula stem ethanol extract. en_ZA
dc.description.department Biochemistry en_ZA
dc.description.department Chemistry en_ZA
dc.description.librarian am2018 en_ZA
dc.description.sponsorship The Regional Initiative for Science Education (RISE) through the Southern Africa Biochemistry and Informatics Network (SABINA) for Tinotenda Shoko’s PhD studies. Further, the Department of Science and Technology (South Africa) is acknowledged for funding the project under which this work was done at the Council for Scientific and Industrial Research (CSIR). en_ZA
dc.description.uri https://bmccomplementalternmed.biomedcentral.com en_ZA
dc.identifier.citation Shoko, T., Maharaj, V.J., Naidoo, D. et al. 2018, 'Anti-aging potential of extracts from Sclerocarya birrea (A. Rich.) Hochst and its chemical profiling by UPLC-Q-TOF-MS', BMC Complementary and Alternative Medicine, vol. 18, art. no. 54, pp. 1-14. en_ZA
dc.identifier.issn 1472-6882 (online)
dc.identifier.other 10.1186/s12906-018-2112-1
dc.identifier.uri http://hdl.handle.net/2263/64191
dc.language.iso en en_ZA
dc.publisher BioMed Central en_ZA
dc.rights © The Author(s). 2018. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/). en_ZA
dc.subject Marula en_ZA
dc.subject Sclerocarya birrea en_ZA
dc.subject Anti-collagenase en_ZA
dc.subject Anti-elastase en_ZA
dc.subject Chemical profile en_ZA
dc.subject Anti-aging en_ZA
dc.title Anti-aging potential of extracts from Sclerocarya birrea (A. Rich.) Hochst and its chemical profiling by UPLC-Q-TOF-MS en_ZA
dc.type Article en_ZA


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