A comparative study on the polyphenolic content,antibacterial activity and antioxidant capacity of different solvent extracts of Brassica oleracea vegetables

Brassica vegetables are rich in polyphenols, flavonoids and glucosinolates. Investigation was undertaken to optimise the best solvents among 60% ethanol, acetone and methanol for the extraction of polyphenols from Brassica vegetables. Furthermore, different properties such as antibacterial activity and antioxidant capacity were also investigated. Results showed that a 60% methanolic extract showed the highest total phenolic content which was 23.6, 20.4 and 18.7 mg gallic acid equivalents (GAE) g^?1 extract for broccoli, Brussels sprouts and white cabbage, respectively. The hydroxybenzoic acid content of various solvent extracts ranged from 5.86 to 8.91 GAE g^?1 extract for broccoli, 2.70 to 5.44 GAE g^?1 extract for Brussels sprouts and 3.69 to 4.86 GAE g^?1 extract for white cabbage, while the hydroxycinnamic acid content ranged from 0.78 to 1.26 chlorogenic acid equivalents (CAE) g^?1 extract for broccoli, 1.41 to 3.45 CAE g^?1 extract for Brussels sprouts and 0.49 to 1.14 CAE g^?1 extract for white cabbage. A concentration‐dependent antioxidative capacity was confirmed for different reactive oxygen species, and moderate antibacterial activity was observed against a number of Gram‐negative and Gram‐positive food spoilage and food pathogenic bacteria. Solvents significantly affected polyphenolic content and its different properties, and the methanol was found to be the best solvent for the extraction of polyphenols from studied Brassica vegetables.     

Optimization of extraction of phenolic antioxidants from peanut skins

This work was conducted to optimize the extraction conditions for the best recovery of antioxidant compounds from peanut skins. The extracts from the peanut skins were obtained by different extraction methods. The extraction conditions were: different ethanol proportions as the solvent (0, 30, 50, 70 and 96% v/v in distilled water), different peanut skin particle sizes (0–1, 1–2 and 2–10 mm and non‐crushed skins), different proportions of solvent/skins (20, 30, 40, 50 and 60 ml g^?1), different extraction times (by maceration and shaking) and different numbers of extractions. The different extracts obtained under different extraction conditions were compared with special regard to yield, total phenolic compounds and radical scavenging activity. The results showed that the best delivery of phenolic compounds was reached using 70% ethanol, non‐crushed peanut skins, ratio of solvent/solid of 20 ml g^?1, at 10 min shaking and three extractions. The maximum yield of 0.118 g g^?1 was recorded for phenolic compounds when extracted at the optimum conditions. Copyright © 2004 Society of Chemical Industry     

Comparison of extraction conditions for phenolic,flavonoid content and determination of rosmarinic acid from Perilla frutescens var. acuta

Perilla frutescens var. acuta has traditionally been used to treat disease including, depression, inflammation and tumors. Especially, the presence of rosmarinic acid can induce beneficial and health promoting effects. According to, this work was conducted to comparison of various extraction conditions (extraction process, solvent and time) of total phenolic, floavonoid and rosmainic acid contents from the leaves of Perilla frutescens var. acuta. Also, rosmarinic acid was determined in leaves of Perilla frutescens var. acuta by high‐performance liquid chromatography (HPLC) and the described method was ideally suited for rapid routine analysis. The highest yield of total phenolic, flavonoid and rosmarinic acid was shown 12.15 mg gallic acid equivalents g^?1 dry weight (DW), 7.23 mg rutin equivalents g^?1 DW and 3.76 mg g^?1 DW, respectively. The best condition for extraction efficiency of total phenolic, flovonoid and rosmarinic were found to be: ethanol concentration of 70%, extraction time of 24 h and extraction process of refluxed extraction.     

Optimum aqueous extraction conditions for preparation of a phenolic‐enriched Davidson's plum (Davidsonia pruriens F. Muell) extract

This study aimed to optimise aqueous extraction conditions for total phenolic compounds (TPC) from Davidson's plum (Davidsonia pruriens F. Muell) and to assess the physicochemical and antioxidant properties of the phenolic‐enriched extract. The results showed that temperature, time and ratio significantly affected the extraction of TPC. Optimization of extraction conditions was performed using response surface methodology (RSM) utilising a Box–Behnken design. Optimal extraction conditions were determined to be temperature: 90 °C, extraction time: 30 min and solvent to mass ratio: 20:1 mL g^?1. The extracted solid obtained under these conditions had low‐moisture content, high water solubility and contained 45 mg GAE g^?1 of TPC, 22 mg RUE g^?1 of flavonoids, 3.2 mg CAE g^?1 of proanthocyanidins, 2 mg CGE g^?1 of anthocyanidins and 56 mg ACE g^?1 vitamin C. The extract possessed potent antioxidant capacity, but was comparatively lower than those of vitamin E and BHT. Thus, Davidson's plum should be further investigated for its potential health promoting benefits and utilisation in the nutraceutical and food industries.     

Optimization of phenolic compound recovery and antioxidant activity of light and dark dried fig (Ficus carica L.) varieties

The optimum conditions for extraction of total phenolic contents (TPC) and for enhancing the antioxidant activity from light and dark dried figs were determined. The effects of the solvent nature (acetone, ethanol, methanol, or water), solvent concentration (20–80%), acetic acid concentration (0–2%), extraction temperature (25–70°C), extraction time (0.5–4 h), sample to solvent ratio (1/25–1/100), and number of extractions (1, 2, and 3) were determined. The TPC was used to identify antioxidant compounds. 2,2-diphenyl-1-picrylhydrazyl (DPPH) was used to evaluate antioxidant activity. All extraction parameters had significant effects (p<0.05) on the TPC and the antioxidant activities. The best conditions were obtained with double extraction using 60% acetone without acidification, at 40°C for 120 min, and with a 1/75 solid to solvent ratio. These conditions resulted in TPC concentrations of 469.46 (light variety) and 399.79 mg of gallic acid (GAE)/100 g (dark variety), and antioxidant activities of 96.47 and 102.28 mg of GAE/100 g, respectively.     

Optimisation of pressurised liquid extraction for antioxidative polyphenolic compound from Momordica charantia using response surface methodology

Pressurised liquid extraction (PLE) of antioxidant compounds from bitter gourd fruits (Momordica charantia) in aqueous ethanolic solvent was investigated using response surface methodology at laboratory scale to understand key impact of extraction variables. Extraction efficiency was optimised by measuring the yield of extraction, total phenolic content (TPC), total flavonoid content (TFC), ferric reducing/antioxidant power assay (FRAP) and radical scavenging activity (RSA). The optimal extraction conditions were reached at 80% ethanol concentration, 10‐min extraction time and at 160 °C. Under these extraction conditions, values of TPC (5.40 ± 0.30 g GAE per 100 g), TFC (1.50 ± 0.10 g QE per 100 g), FRAP (778.55 ± 10 μmol eq Fe (II) g^?1), yield (178.50 ± 5.50 mg g^?1 dc) and RSA (75.50 ± 4.50%) were achieved. Furthermore, statistical analysis revealed that antioxidative attributes of bitter gourd extract were strongly and positively correlated with extraction temperature and ethanol concentration rather than processing time. This study illustrated that PLE has the potential to extract antioxidant compounds from tropical fruit vegetables in an accelerated manner. Furthermore, influential parameters affecting the process could be optimised for further industrial intake.     

Optimization of Microwave-Assisted Extraction of Phenolic Antioxidants from Grape Seeds (Vitis vinifera)

Grape seeds (Vitis vinifera) are rich in phytochemicals that have antioxidant properties. The influence of independent variables such as microwave power (100, 150, and 200 W), extraction time (2, 4, and 6 min), and solvent concentration (30%, 45%, and 60% ethanol) and their interactions on total phenols and the antioxidant activity (1,1-diphenyl-2-picrylhydrazyl (DPPH) and ferric ion reducing antioxidant power (FRAP)) were determined; and the microwave-assisted extraction (MAE) process was optimized using a central composite design. The total phenols that were expressed as gallic acid equivalents (GAE), catechin equivalents (CAT), and tannic acid equivalents (TAE) were significantly influenced by the solvent concentration and the time of extraction. A numerical optimization was carried out to obtain the overall conditions for MAE of phenolic antioxidants from grape seed. The response variables were maximized for 6 min of MAE of grape seed (GS) with 32.6% ethanol at 121 W with a desirability function of 0.947. The predicted extraction yields were 13?±?0.89, 21.6?±?1.59, and 15.9?±?1.32 mg GAE, CAT, and TAE, respectively per gram of GS. The predicted antioxidant activity per gram of dry weight GS was 80.9% for the inhibition of DPPH and 135 μM ascorbic acid equivalents for FRAP test. The predicted response values were significantly correlated with the observed ones as follows: GAE r?=?0.995, CAT r?=?0.990, TAE r?=?0.996, DPPH r?=?0.996, and FRAP r?=?0.996.     

Effect of solvent type on the extractability of bioactive compounds,antioxidant capacity and colour properties of natural annatto extracts

This study was conducted to obtain annatto extracts with both high antioxidant capacity and colour potential using solvents of different polarities (water, ethanol/water, ethanol, ethanol/ethyl acetate and ethyl acetate). The highest levels of total phenolic compounds were found in the water, ethanol/water and ethanol extracts (0.5 mg GAE mL^?1), and the highest level of bixin was found in the ethanol/ethyl acetate extract (5.2 mg mL^?1), which was characterised as the reddest and the most vivid one (a* = 40.5, h° = 46.1, C* = 58.4). The ethanol/ethyl acetate extract also showed the highest antioxidant activity (4.7 μm TEAC mL^?1) and the highest percentage of tryptophan protection against singlet oxygen (63.6%). On the other hand, ethyl acetate and ethanol/water were the least effective solvents for the extraction of phenolic compounds and bixin, respectively. According to the multivariate statistical analysis, ethanol/ethyl acetate and ethyl acetate were the most promising solvents to obtain annatto extracts with both antioxidant and colour properties.     

Microwave and ultrasound assisted extraction of phytocompounds from black jamun pulp: Kinetic and thermodynamics characteristics

The present study focuses on the extraction of phenolic compounds, anthocyanin and antioxidants from black jamun pulp by microwave and ultrasound assisted extraction process. The microwave-assisted extraction was carried out for 240 s at microwave power level of 100–400 W. The yield of total anthocyanin and total phenolic content in the microwave assisted extraction process at 400 W power level after an extraction period of 240 s was 8.197 mg of C3G g⁻¹ and 37.671 40.632 mg GAE g⁻¹, respectively. The ultrasound assisted extraction was performed at temperatures of 40, 50, 60, and 70 °C for 150 min. In the ultrasound assisted extraction at a sonication temperature of 70 °C, the yield of anthocyanin was 8.525 mg of C3G g⁻¹, while the yield of the phenolic compound was 47.331 mg GAE g⁻¹. The pseudo-second order model was found to be the most suitable model to represent the extraction kinetics of anthocyanin, phenolic compounds, and antioxidant activity of black jamun pulp. The effective diffusion coefficient for ultrasound assisted extraction of phenolic components, anthocyanin, and antioxidant activity in the temperature range of 40-70 °C was 5.704× 10⁻¹²–10.515 10⁻¹², 2.485× 10⁻¹² -8.507× 10⁻¹², and 2.061× 10⁻¹²–11.977 × 10⁻¹² m².s⁻¹ respectively. The negative Gibbs free energy change values for extraction of phenolic compounds and anthocyanin specified that the reaction was feasible and spontaneous. Thermodynamic parameters such as positive enthalpy change and positive entropy change indicated that the ultrasound assisted extraction process was endothermic and irreversible in nature.     

Antioxidant activity of the ethanolic extract from the bark of Chamaecyparis obtusa var. formosana

BACKGROUND: Chamaecyparis obtusa var. formosana (Taiwan hinoki) is an endemic conifer in Taiwan and the purpose of this study is to evaluate the antioxidant activity of various fractions obtained from the bark of this plant material. The ethanolic extract of the bark was sequentially separated into three fractions, including n‐hexane, ethyl acetate and ethanol soluble fractions, by liquid–liquid partition. Then the antioxidant activities of crude extract and three fractions along with 13 subfractions obtained from the ethyl acetate (EA) soluble fraction were tested for several antioxidant assays. RESULTS: The total phenolic content of the samples varied from 27.71 to 102.86 mg GAE g^?1 dry weight for fractions, and from 49.94 to 206.46 mg GAE g^?1 for subfractions (where GAE is milligrams of gallic acid per gram of extract). The Trolox equivalent antioxidant capacity (TEAC) ranged from 0.15 to 0.26 mmol L^?1 Trolox equivalents. The EA soluble fraction was found to be the best antioxidant‐rich fraction in terms of DPPH and reducing power assays. With further data analysis it was found that there was a positive correlation between the total phenolic content of extracts and TEAC is R² = 0.61. CONCLUSION: Results from various antioxidant assays showed that the EA fraction possessed strong antioxidant activity. This would provide additional information about the antioxidant activity of bark extract of this plant species. Copyright © 2008 Society of Chemical Industry     

Extraction of antioxidant and antimicrobial compounds from Inga marginata Willd bark and pulp using different extraction techniques and phytochemical characterization

This study aimed to identify the least aggressive and highest yield extraction method to obtain bioactive compounds from Inga marginata Willd fruits, determine the chemical components, and evaluate the extracts’' antimicrobial and cytotoxic activity. The extraction efficiency was expressed by the total phenolic and total flavonoid content and antioxidant activity (DPPH, IC₅₀, and ORAC) using conventional, ultrasound, and microwave-assisted extraction. The highest bioactive compound content was achieved using 5 min at 60 °C for total phenolic content (214.98 mg GAE g⁻¹), total flavonoid content (22.90 mg EQ g⁻¹), DPPH (45.98 μmol TEAC g⁻¹), inhibitory capacity (0.80 mg mL⁻¹), and ORAC (167.25 μmol Trolox g⁻¹) using ultrasonic extraction, and the extract inhibited the growth of all microorganisms tested. Thirteen chemical compounds were determined by ESI-ToF-MS, confirming the high phytochemical capacity of the extract. Lastly, the Inga extract showed no cytotoxicity at the concentrations used.     

Determination of bisphenol A in canned fatty foods by coacervative microextraction,liquid chromatography and fluorimetry

Decanoic acid reverse micelle-based coacervates were used to provide simple, rapid and almost solventless extraction of bisphenol A (BPA) from canned fatty foods. The procedure involved the extraction of 200–400 mg of homogenised food sample with an aqueous solution containing 20% THF and 200 mg of decanoic acid, conditions under which the coacervate (around 550 µl) formed in situ and instantaneously. The overall sample treatment took about 30 min and several samples could be simultaneously treated using conventional laboratory equipment. No clean-up or solvent evaporation were required before determination of BPA by liquid chromatography and fluorescence detection. Recoveries in samples were between 90 and 99%, with relative standard deviations in the range 2–7%. The limit of quantification ranged 29–15 ng g^?1 for 200–400 mg of sample, being far below the current specific migration limit (SML) set by the European Commission (600 ng g^?1). The method was successfully applied to the determination of BPA in the solid content of canned fish (from 20 to 129 ng g^?1) and meat (from undetected to 37 ng g^?1).     

Solvent extraction and in vitro simulated gastrointestinal digestion of phenolic compounds from purple sweet potato

The total content of phenolic compounds in purple sweet potato (PSP) was determined and the release of such compounds from PSP in gastrointestinal digestion was studied in vitro. The extraction conditions for the maximum recovery of free phenol (FP) and bound phenol (BP) from PSP were determined by response surface methodology (RSM). The maximum recovery of FPPSP was 14.16 ± 0.87 mg GAE per g short for dry weight (DW), which was obtained using 60% (v/v) ethanol maceration with a liquid–solid ratio of 57.21:1 (mL g⁻¹) at 51.93 °C for 2.12 h. The maximum recovery for BPPSP was 7.54 mg GAE per g DW, which was obtained upon hydrolysis with 1.87 mol L⁻¹ NaOH at a liquid–solid ratio of 35.93:1 (mL g⁻¹) for 4.74 h. The maximum phenolic content was released after 1 and 2 h for the in vitro gastric and intestinal digestion respectively. The release of the phenolics was promoted by pepsin and gastric acid during gastric digestion, while it was further promoted by trypsin during intestinal digestion.     

Determination of alkaloids and phenolic compounds in black tea processed by two different methods in different plucking seasons

The effects of two different rolling methods and three tea plucking seasons on alkaloids and phenolics, mainly flavan‐3‐ols and theaflavins, in black tea were studied using an improved high‐performance liquid chromatographic method. Better separation of all tea compounds analyzed—the most important factor for their identification and quantitation—was achieved only with long elution gradients, which overcame the limitations of previously reported methods. Precision of the assay method was very high since intra‐day and inter‐day variations were within 0.76% and 1.66%, respectively. All analytes exhibited good linearity over the range evaluated with a correlation coefficient of 0.9987–1.000. Among the four solvents evaluated, 80% methanol was the most solvent for extracting individual tea compounds. The extraction method applied exhibited good repeatability (CV: 0.39–3.29%). The content of tea compounds analyzed varied with processing method and plucking season. Teas processed using the Cay‐Kur method contained higher levels of identified phenolic compounds than orthodox teas, but their alkaloid content was similar to each other. The most abundant alkaloid in teas was caffeine, ranging from 17.84 mg g^?1 dry weight in September plucking to 23.79 mg g^?1 dry weight in May plucking. With respect to phenolic compounds, theaflavins were at the highest level, 14.27 mg g^?1 dry weight, in Cay‐Kur tea processed in May. Copyright © 2007 Society of Chemical Industry     

Selection of the Solvent and Extraction Conditions for Maximum Recovery of Antioxidant Phenolic Compounds from Coffee Silverskin

The extraction of antioxidant phenolic compounds from coffee silverskin (CS) was studied. Firstly, the effect of different solvents (methanol, ethanol, acetone, and distilled water) on the production of antioxidant extracts was evaluated. All the extracts showed antioxidant activity (FRAP and DPPH assays), but those obtained with methanol and ethanol had significantly higher (p?<?0.05) DPPH inhibition than the remaining ones. Due to the lower toxicity, ethanol was selected as extraction solvent, and further experiments were performed in order to define the solvent concentration, solvent/solid ratio, and time to maximize the extraction results. The best condition to produce an extract with high content of phenolic compounds (13 mg gallic acid equivalents/g CS) and antioxidant activity [DPPH?=?18.24 μmol Trolox equivalents/g CS and FRAP?=?0.83 mmol Fe(II)/g CS] was achieved when using 60 % ethanol in a ratio of 35 ml/g CS, during 30 min at 60–65 °C.     

Comparative analyses of total phenols,flavonoids, saponins and antioxidant activity in yellow soy beans and mung beans

Total phenol, flavonoid and saponin content of soy bean and mung bean were systemically compared in order to evaluate their contribution to overall antioxidant activity. Mung bean extract possessed significantly higher total phenol (2.03 GAE g^?1 vs. 1.13 GAE g^?1) and flavonoid contents (1.49 GAE g^?1 vs. 0.41 CAE g^?1) than soy bean extract, while the saponin content of the soy beans was 4.5 times greater than that of the mung beans. In several antioxidant assays including DPPH and ABTS radical scavenging, FRAP, SOD‐like activity, and a β‐carotene bleaching assay, mung bean extract consistently showed significantly greater antioxidant activity than soy bean extract. The specific antioxidant activity, which was evaluated at the same phenolic content suggested that the phenolic compounds present in the mung bean extract were not only of greater quantity but also had better quality to eliminate radicals. The radical scavenging activities of saponins were only marginal.     

Enhancement of antimicrobial and antimutagenic activities of Korean barberry (Berberis koreana Palib.) by the combined process of high‐pressure extraction with probiotic fermentation

BACKGROUND: To evaluate the combined effects of high pressure extraction (HPE) and probiotic fermentation on the antimicrobial and antimutagenic activities, Berberis koreana was subjected to 500 MPa for 30 min and then fermented with Bifidobacterium longum B6 (HPE‐BLF) and Lactobacillus paracasei (HPE‐LPF) at 37 °C for 6 days. RESULTS: The phenol content was significantly increased to 228 mg GAE g^?1 by the HPE compared to the conventional extraction (CE, 188 mg GAE g^?1). The HPE‐BLF and HPE‐LPF showed the highest antimicrobial activity (MIC < 4 mg mL^?1) against β‐lactam antibiotic sensitive and resistant Staphylococcus aureus. No significant mutagenic effect was observed for CE, HPE, HPE‐BLF, and HPE‐LPF extracts. The highest antimutagenic activities against frame‐shift mutant Salmonella typhimurium were observed at the HPE‐LPF (82%), followed by the HPE‐BLF (77%). CONCLUSION: The combined HPE and fermentation process could be used as an alternative extraction method for improving the extraction efficacy of medicinal plants. The results will provide pharmaceutically useful information and potential direction for finding new drug sources from medicinal plants. Copyright © 2010 Society of Chemical Industry     

Waste from peach (Prunus persica) processing used for optimisation of carotenoids ethanolic extraction

The processing of peaches to produce fruit pulp generates solid and liquid wastes rich in phytochemicals, such as carotenoids; thus, the objective of this work was to study the use of this waste for carotenoid extraction based on a complete experimental design and using response surface methodology. The parameters studied were the amount of solvent (20–50 mL), the number of extractions (1–5) and the extraction time (10–30 min). The extracts were analysed by spectrophotometry and the optimised conditions by HPLC. The optimised results were four extractions of 10 min using 38.5 mL of ethanol, which presented a yield of 168.59 μg g^?1 DW of total carotenoids of which 67.55 μg g^?1 corresponds to β‐carotene, 86.75 μg g^?1 to cryptoxanthin, 12.08 μg g^?1 to zeaxanthin and 2.2 μg g^?1 to lutein, which representing 66% of extraction pigments relative to the total content of carotenoids present in the peach waste.     

Purification and identification of rambutan (Nephelium lappaceum) peel phenolics with evaluation of antioxidant and antiglycation activities in vitro

The crude rambutan peel phenolic (RPP) extracts were purified by resin adsorption technology. NKA‐9 resin with the best adsorption capacity and desorption ratio was chosen to dynamically purify crude RPP. Adsorption capacity and desorption ratio of NKA‐9 resin were 91.85 mg gallic acid equivalent (GAE) g^?1 and 90.45%, respectively. Purification processes enriched total phenolic content, and the contents in crude and purified RPP were 579.72 and 877.11 mg GAE g^?1 extract powder, respectively. Phytochemical compounds of RPP were qualitatively and quantitatively indentified by mass spectrometry. Purification of the resin as expected elevated the concentrations of major phenolic compounds, especially geraniin and ellagic acid. Antioxidant and antiglycation activities of crude and purified fractions were evaluated in vitro. Crude and purified RPP had high inhibitory effects on oxidation and glycation, and purified RPP showed stronger bioactivity than crude RPP (P < 0.05), which might be due to their differences in phenolic profiles.