Anti-aging potential of extracts from Sclerocarya birrea (A. Rich.) Hochst and its chemical profiling by UPLC-Q-TOF-MS
Loading...
Date
Authors
Shoko, Tinotenda
Maharaj, Vinesh J.
Naidoo, Dashnie
Tselanyane, Malefa
Nthambeleni, Rudzani
Khorombi, Eric
Apostolides, Zeno
Journal Title
Journal ISSN
Volume Title
Publisher
BioMed Central
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Keywords
Marula, Sclerocarya birrea, Anti-collagenase, Anti-elastase, Chemical profile, Anti-aging
Sustainable Development Goals
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.