305 research outputs found
Indigenous Salvia species : an investigation of their pharmacological activities and phytochemistry
The genus Salvia belongs to the family Lamiaceae and encompasses 900 species
worldwide of which 26 are found in southern Africa and many of them are used in local
traditional medicine. However, the phytochemistry and pharmacological activities of the
South African species have not been extensively investigated.
The leaf trichome morphology that may be used to distinguish species was investigated
with the scanning electron and light microscopy. Both glandular (capitate or peltate) and
non-glandular trichomes were identified in all species.
The essential oils were isolated by hydro-distillation and analysed by GC and GC-MS
methods. The oil yield was relatively low and ranged from 0.004 (S. radula) to 0.50% (S.
muirii) (w/w). Major components identified include α-pinene, 1,8-cineole, linalool,
limonene, myrcene, β-caryophyllene, spathulenol, β-caryophyllene oxide, viridiflorol, δ-3-
carene and α-bisabolol. High performance liquid chromatography analysis was used to
identify phenolic compounds in 17 solvent extracts. Betulafolientriol oxide was detected
in all species. Rosmarinic acid was only absent in S. verbenaca, while S. garipensis and S.
radula were the only species which lacked oleanolic acid/ursolic acid.
Various in vitro biological activities were investigated. Nearly all the solvent extracts
displayed anti-oxidant activity with IC50 values ranging from 1.61 to 74.50 μg/ml using the
DPPH· radical, while the IC50 values ranged from 11.88 to 69.26 μg/ml with the ABTS·+
radical. The solvent extract of S. schlechteri was three times more active than vitamin C.
Total phenolic content based on gallic acid equivalents (GAE) revealed the presence of
total soluble phenolics in the extract at 45 to 211 mg of GAE dry sample. Almost all the
essential oils exhibited promising anti-inflammatory activity (5-lipoxygenase assay) with
IC50 values ranging from 22.81 to 77.32 μg/ml. The antimalarial activity was determined
using [3H]-hypoxanthine method on the Plasmodium falciparum (FCR-3) strain. The IC50
values of the essential oils ranged from 1.20 to 13.50 μg/ml and were low compared to the
solvent extracts (IC50 values ranging from 3.91 to 26.01 μg/ml). Betulafolientriol oxide
and salvigenin isolated from S. radula inhibited the growth of malaria parasites with IC50
values of 4.95 and 24.60 μg/ml, respectively. With the exception of S. radula, all the
solvent extracts displayed moderate to good activity against Staphylococcus aureus,
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Bacillus cereus, Klebsiella pneumoniae, Escherichia coli and Mycobacterium tuberculosis
with the MIC values ranging from 0.03 to 8.00 mg/ml. Four compounds, namely carnosol,
7-O-methylepirosmanol, oleanolic acid and its isomer ursolic acid were isolated from S.
chamelaeagnea as the active principles against S. aureus. The solvent extracts of Salvia
species were tested for in vitro anticancer activity against human breast adenocarcinoma
(MCF-7), colon adenocarcinoma (HT-29) and glioblastoma (SF-268) using the
sulforhodamine B assay. The extracts inhibited cell proliferation of all three cell lines to
varying degrees, with the IC50 values ranging between 9.69 and 43.65 μg/ml and 8.72 and
59.12 μg/ml against the MCF-7 and SF-268 cell lines, respectively. The IC50 values
against the HT-29 cell line ranged from 17.05 to 57.00 μg/ml. The in vitro toxicity profile
of 28 samples (17 solvent extracts and 11 essential oils) was evaluated on human kidney
epithelial cells using the 3-(4,5-dimethylthiazol-2-yl)-2,5 dimethyl tetrazolium bromide
method. The samples displayed some degree of toxicity with IC50 values ranging from
1.79 to 22.9 μg/ml for the essential oils and from 12.12 to 53.34 μg/ml for the solvent
extracts. The essential oil composition of S. africana-caerulea, S. africana-lutea and S.
lanceolata, collected at the same locality throughout the 2004/2005 growing season, was
compared in terms of essential oil yields, chemical composition and biological activities.
Mostly quantitative, rather than qualitative variation was observed. Major seasonal
fluctuations of certain essential oil compounds were observed in all three species.
Variations in biological activities of the solvent extracts over seasons were noted. The
biological activities of the solvent extracts of three Salvia species (Salvia africanacaerulea,
S. africana-lutea and S. lanceolata) were evaluated in the presence and absence
of essential oils. The solvent extract of S. africana-caerulea without essential oil exhibited
the best activity against Gram-positive bacteria (MIC value: 0.1 mg/ml), while the solvent
extract containing essential oil of S. africana-lutea was the most active against Gramnegative
bacteria. The toxicity profile of all three species was significantly higher (P <
0.05) with the solvent extracts containing essential oils. The in vitro biological activities
add scientific support to the use of Salvia species in traditional medicine
An overview of the biological activities and essential-oil composition of three South African Salvia species
Essential oils produced by aromatic plants have been used to treat various ailments such as malaria and microbial infections for many years. In South Africa, there are 26 indigenous Salvia species and most of them have been reported for use in the treatment of malaria, tumors, microbial infections. Among those of ethnomedicinal value are S. repens, S. stenophylla and S. runcinata which form a species complex. The current study aimed to profile the essential-oil composition and investigate the bioactivities related to the traditional uses. The essential oil of the three species (S. repens, S. stenophylla and S. runcinata) was isolated by hydrodistillation and the antimalarial, anti-inflammatory, antimicrobial activities and the toxicity profiles were evaluated using the [3H]hypoxanthine incorporation assay, 5-lipoxygenase assay, minimum inhibitory concentration assay and the MTT colorimetric method, respectively. The essential-oil composition was analyzed using the GC-MS and GC-FID methods. The oil of S. repens was dominated by 1,8-cineole (12.8%), p-cymene (9.5%) and limonene (9.4%), while α-bisabolol (65.0%) and β-caryophyllene (10.5%) were the major constituents of S. runcinata. α-Bisabolol (26.1%) and δ-3-carene (22.6%) were the dominant constituents of S. stenophylla. The anti-inflammatory activity of the three oils (IC50 value) ranged from 22.8 to 49 µg/mL with S. runcinata exhibiting the best activity. The three oils also inhibited the growth of Plasmodium falciparum FCR-3 strain with IC50 values ranging from 1.2-4.1 µg/mL with the oil of S. runcinata showing the best antimalarial activity. The essential oils showed poor antimicrobial activity (MIC value > 32 mg/mL) and were also toxic to normal kidney epithelial cells (IC50 value < 6.6 µg/mL). The essential oils displayed some degree of activity, however, the toxicity exhibited against kidney cells indicated that the oils should be used with caution
Antibacterial and antimycobacterial activities of South African Salvia species and isolated compounds from S. chamelaeagnea
Extracts of 16 South African Salvia species commonly used in traditional medicine to treat various microbial infections were investigated for in vitro antibacterial and antimycobacterial activities using the micro-dilution and respiratory BACTEC method, respectively. The micro-organisms tested include two Gram-positive (Staphylococcus aureus and Bacillus cereus); two Gram-negative (Escherichia coli and Klebsiella pneumoniae) bacterial strains and the common pathogen responsible for tuberculosis, Mycobacterium tuberculosis. Extracts of the majority of species exhibited moderate to good antibacterial activity with minimum inhibitory concentration (MIC) values ranging from 0.03 to 8.00 mg/ml. Promising activity was observed against M. tuberculosis (MIC ≤ 0.50 mg/ml) with S. radula, S. verbenaca and S. dolomitica displaying the most favourable activity (MIC: 0.10 mg/ml). The antibacterial bioassay-guided fractionation of S. chamelaeagnea resulted in the isolation of four compounds: carnosol, 7-O-methylepirosmanol, oleanolic acid and its isomer ursolic acid as the active principles against S. aureus. The in vitro antibacterial and antimycobacterial activities may support the use of Salvia species in traditional medicine to treat microbial infections
The In Vitro
The antimicrobial activity of Lavandula angustifolia essential oil was assessed in combination with 45 other oils to establish possible interactive properties. The composition of the selected essential oils was confirmed using GC-MS with a flame ionization detector. The microdilution minimum inhibitory concentration (MIC) assay was undertaken, whereby the fractional inhibitory concentration (ΣFIC) was calculated for the oil combinations. When lavender oil was assayed in 1 : 1 ratios with other oils, synergistic (26.7%), additive (48.9%), non-interactive (23.7%), and antagonistic (0.7%) interactions were observed. When investigating different ratios of the two oils in combination, the most favourable interactions were when L. angustifolia was combined with Cinnamomum zeylanicum or with Citrus sinensis, against C. albicans and S. aureus, respectively. In 1 : 1 ratios, 75.6% of the essential oils investigated showed either synergistic or additive results, lending in vitro credibility to the use of essential oil blends in aroma-therapeutic practices. Within the field of aromatherapy, essential oils are commonly employed in mixtures for the treatment of infectious diseases; however, very little evidence exists to support the use in combination. This study lends some credence to the concomitant use of essential oils blended with lavender
Effect of thermal treatment and storage on bioactive compounds, organic acids and antioxidant activity of baobab fruit (Adansonia digitata) pulp from Malawi
Bioactive compounds of baobab (Adansonia digitata) pulp from Malawi were investigated. The effect of thermal treatment and storage on selected quality attributes of the juice was also evaluated. Organic compounds were analysed by HPLC; total phenol content (TPC) and total antioxidant activity (FRAP, ABTS and DPPH) were measured by spectrophotometry. Malawi baobab pulp contains high levels of procyanidin B2 (533 ± 22.6 mg/100 g FW), vitamin C (AA + DHA) (466 ± 2.5 mg/100 g FW), gallic acid (68.5 ± 12.4 mg/100 g FW) and (−)-epicatechin (43.0 ± 3.0 mg/100 g FW) and showed a maximum TPC of 1.89 × 103 ± 1.61 mg GAE/100 g FW. The maximum antioxidant activity was 2.81 × 103 ± 92.8 mg TEAC/100 g FW for FRAP, 1.52 × 103 ± 17.1 mg TEAC/100 g FW for ABTS and 50.9 ± 0.43% DPPH for DPPH. Thermal pasteurisation (72 °C, 15 s) retained vitamin C which further showed extended half-life under refrigeration temperature (6 °C). Procyanidin B2, (−)-epicatechin, TPC and antioxidant activity fluctuated during storage. Antioxidant activity was significantly correlated (p ≤ 0.05) with bioactive compounds and TPC
Antioxidant and Anti-Inflammatory Activities of Essential Oils: A Short Review
Essential oils are complex mixtures isolated from aromatic plants which may possess antioxidant and anti-inflammatory activities of interest in thye food and cosmetic industries as well as in the human health field. In this work, a review was done on the most recent publications concerning their antioxidant and anti-inflammatory activities. At the same time a survey of the methods generally used for the evaluation of antioxidant activity and some of the mechanisms involved in the anti-inflammatory activities of essential oils are also reported
Antioxidant starch-based films with encapsulated eugenol. Application to sunflower oil preservation
[EN] Starch films containing eugenol, which was added to the film-forming dispersion in free form or encapsulated with different wall materials (whey protein or lecithin), were obtained by casting. The physical and the antioxidant properties of the films, the release kinetics of eugenol in different food simulants and their performance at preventing sunflower oil oxidation during storage were evaluated. Encapsulated eugenol modified the film microstructure, yielding less stretchable films with reduced water affinity, transparency and oxygen permeability as compared to films formulated with non-encapsulated eugenol. The addition of eugenol microcapsules containing oleic acid promoted the eugenol retention in the starch matrix during film formation and thus, these films exhibited the greatest antioxidant activity. Films developed with encapsulated eugenol powder containing lecithin and oleic acid were highly effective at preventing sunflower oil oxidation even throughout 53 days of storage at 30¿°C, maintaining low and almost constant values of peroxide index, conjugated dienes and trienes in comparison with the control samples.The authors acknowledge the financial support provided by the Spanish Ministerio de Educacion y Ciencia (Projects AGL2013-42989-R and AGL2016-76699-R). Author Emma Talon thanks the Universitat Politecnica de Valencia for a FPI Grant (99/2011). The authors also thank the services rendered by the Electron Microscopy Service of the UPV.Talón-Argente, E.; Vargas, M.; Chiralt, A.; González Martínez, MC. (2019). Antioxidant starch-based films with encapsulated eugenol. Application to sunflower oil preservation. LWT - Food Science and Technology. 113:1-10. https://doi.org/10.1016/j.lwt.2019.108290S11011
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