Chemical composition and in vitro antioxidant studies on Syzygium cumini fruit

Syzygium cumini, widely known as Jamun, is a tropical tree that yields purple ovoid fleshy fruit. Its seed has traditionally been used in India for the treatment of diabetes. Based on the available ethno‐pharmacological knowledge, further studies were extended to understand the chemical composition and antioxidant activities of three anatomically distinct parts of fruit: the pulp, kernel and seed coat. Fruit parts, their corresponding ethanol extracts and residues were evaluated for chemical composition. The alcoholic extract was evaluated for its antioxidant potential against DPPH^?, OH^?, O₂^?? and lipid peroxidation. The whole fruit consisted of 666.0 ± 111.0 g kg^?1 pulp, 290.0 ± 40.0 g kg^?1 kernel and 50.0 ± 15.0 g kg^?1 seed coat. Fresh pulp was rich in carbohydrates, protein and minerals. Total fatty matter was not significant in all three parts of fruit. Detailed mineral analysis showed calcium was abundant in all fruit parts and extracts. Total phenolics, anthocyanins and flavonoid contents of pulp were 3.9 ± 0.5, 1.34 ± 0.2 and 0.07 ± 0.04 g kg^?1, respectively. Kernel and seed coat contained 9.0 ± 0.7 and 8.1 ± 0.8 g kg^?1 total phenolics respectively. Jamun pulp ethanol extract (PEE), kernel ethanol extract (KEE) and seed coat ethanol extract (SCEE) showed a high degree of phenolic enrichment. DPPH radical scavenging activity of the samples and standards in descending order was: gallic acid > quercetin > Trolox > KEE > BHT > SCEE > PEE. Superoxide radical scavenging activity (IC₅₀) of KEE was six times higher (85.0 ± 5.0 µg mL^?1) compared to Trolox (540.0 ± 5.0 µg mL^?1) and three times compared to catechin (296.0 ± 11.0 µg mL^?1). Hydroxyl radical scavenging activity (IC₅₀) of KEE was 151.0 ± 5.0 µg mL^?1 which was comparable with catechin (188.0 ± 6.0 µg mL^?1). Inhibition of lipid peroxidation of the extracts was also studied and their activity against peroxide radicals were lower than that of standard compounds (BHT, 79.0 ± 4.0 µg mL^?1; quercetin, 166.0 ± 13.0 µg mL^?1; Trolox, 175.0 ± 4.0 µg mL^?1; PEE, 342.0 ± 17.0 µg mL^?1; KEE, 202.0 ± 13.0 µg mL^?1 and SCEE, 268.0 ± 13.0 µg mL^?1. Copyright © 2007 Society of Chemical Industry     

Antioxidant/anti-inflammatory activities and total phenolic content of extracts obtained from plants grown in Vietnam

BACKGROUND: Medicinal plants have been used to treat various diseases since ancient times. Their specific activities, such as antioxidant, anti‐inflammatory and anti‐cancer, have been studied intensively. In particular, plants grown in Vietnam have attracted considerable attention among food chemists as ideal sources of natural medicinal chemicals. RESULTS: The methanol extracts from three edible Vietnamese‐grown plants, Tram, Voi and Gac, tested with the DPPH assay showed antioxidant activities of 91.7 ± 0.4, 63.4 ± 0.7 and 3.7 ± 0.1% respectively. The malonaldehyde/gas chromatography assay also revealed strong antioxidant activity in Tram and Voi at a level of 25 µg mL^?1 (95.5 ± 0.3 and 78.5 ± 1.4% respectively). These results were confirmed by the thiobarbituric acid assay. The antioxidant activities correlated positively with the level of total phenolics in all plants. Tram exhibited dose response‐related lipoxygenase‐inhibitory activity, with values of 74.2 ± 3.1% at 5 µg mL^?1, 62.0 ± 0% at 0.5 µg mL^?1 and 3.0 ± 1.5% at 0.05 µg mL^?1. Conversely, Voi and Gac showed negative anti‐lipoxygenase activity. CONCLUSION: The antioxidant/anti‐inflammatory activities and total phenolic contents of the three edible plants grown in Vietnam revealed that they are good sources of supplements for human health. Copyright © 2011 Society of Chemical Industry     

The in vitro antioxidant and antimicrobial activities of the essential oil and various extracts of Origanum syriacum L var bevanii

The present work examines the in vitro antioxidant and antimicrobial properties of the essential oil and various extracts from the herbal parts of Origanum syriacum L var bevanii. Polar subfractions of methanol extracts from both deodorised and non‐deodorised materials showed the highest DPPH (2,2‐diphenyl‐l‐picrylhydrazyl) radical‐scavenging activity, with IC₅₀ values of 21.40 and 26.98 µg ml^?1 respectively, whereas the IC₅₀ of the essential oil was 134.00 µg ml^?1. The antioxidant potential of the extracts appeared to be closely related to the presence of polar phenolics. However, the inhibitive effect on linoleic acid oxidation might be promoted by the presence of non‐polar phenolics, as both hexane and dichloromethane extracts showed high antioxidant activities. The antimicrobial activity of the essential oil was superior to those of the other extracts. Nineteen compounds representing 962 g kg^?1 of the essential oil were identified; carvacrol (669 g kg^?1) was the main component. Overall, the results suggest that the essential oil and extracts from the herbal parts of O syriacum could be used as natural preservative ingredients in the food industry. Copyright © 2004 Society of Chemical Industry     

Antioxidant and semicarbazide‐sensitive amine oxidase inhibitory activities of alginic acid hydroxamates

The commercial polysaccharides of alginic acid (medium (3500 cps, 2% solution) and low (250 cps, 2% solution) viscosities) were esterified with acidic methanol (1 mmol L^?1 HCl) at 4 °C with gentle stirring for 5 days to obtain methyl esters of medium‐viscosity alginic acid (ME‐MVA) and low‐viscosity alginic acid (ME‐LVA). These ME‐MVA and ME‐LVA were reacted with alkaline hydroxylamine to obtain medium‐viscosity alginic acid hydroxamates (MVA‐NHOH) and LVA‐NHOH. The percentages of hydroxamic acid content in MVA‐NHOH and LVA‐NHOH were calculated as 25% and 20%, respectively. The hydroxamate derivatives of alginic acid were used to test the antioxidant and semicarbazide‐sensitive amine oxidase (SSAO) inhibitory activities in comparison with original materials (MVA and LVA). The half‐inhibition concentrations, IC₅₀, of scavenging activity against 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) were 24.5 and 29.8 µg mL^?1 for MVA‐NHOH and LVA‐NHOH, respectively. However, few scavenging activities of the MVA and LVA were found at the same concentrations. The IC₅₀ of the positive control of butylated hydroxytoluene was 5 µg mL^?1. The scavenging activity of DPPH radical was pH‐dependent, and the optimal pH for both of MVA‐NHOH and LVA‐NHOH was the Tris‐HCl buffer (pH 7.9). Using electron spin resonance (ESR) to detect the activity of scavenging hydroxyl radicals, both alginic acid hydroxamates showed dose‐dependent scavenging activities, and the IC₅₀ was 90 and 92 µg mL^?1, respectively, for MVA‐NHOH and LVA‐NHOH. Both alginic acid hydroxamates also exhibited protection against hydroxyl radical‐mediated DNA damage. Both MVA‐NHOH and LVA‐NHOH showed dose‐dependent inhibitory activities against bovine SSAO (2.53 units); the IC₅₀ was 0.16 and 0.09 µg mL^?1, respectively, for MVA‐NHOH and LVA‐NHOH, compared with 3.81 µg mL^?1 of semicarbazide (positive controls). Amine oxidase activity staining also revealed that both MVA‐NHOH and LVA‐NHOH exhibited SSAO inhibitory activities. Both MVA‐NHOH and LVA‐NHOH showed mixed non‐competitive inhibition against bovine SSAO. It was found that the V′_max value was reduced and the K′_m value was either increased (added MVA‐NHOH, 0.05 µg mL^?1) or reduced (added LVA‐NHOH, 0.11 µg mL^?1) in the presence of alginic acid hydroxamate. Copyright © 2006 Society of Chemical Industry     

Solvent effects on antioxidant properties of persimmon (Diospyros kaki L. cv. Daebong) seeds

The aim of this study was to investigate the antioxidant activities of persimmon seed extracts (PSE) using different solvents such as ethanol, methanol, acetone, and their aqueous 80% solvents. The EC₅₀ values of the extracts from absolute ethanol (EE) and methanol (ME) in 2, 2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical–scavenging assay were 49.71 and 51.15 μg mL^?1, respectively, while the EC₅₀ of butylated hydroxyanisole (BHA) was 70.82 μg mL^?1. However, the EC₅₀ value of reducing power for the absolute acetone extract (AE) was higher (210.06 μg mL^?1) than that of BHA (212.67 μg mL^?1). Although the absolute ME had the highest antioxidant activity, it exhibited the lowest total phenolics and flavonoids. In contrast, the antioxidant activities of the aqueous solvent extracts showed a good correlation with total phenolics and flavonoids when compared to the absolute solvent extracts. The results showed that PSE could potentially be used as an inexpensive source of natural antioxidant in food and pharmaceutical industries.     

Antioxidant and melanogenesis‐inhibitory activities of collagen peptide from jellyfish (Rhopilema esculentum)

BACKGROUND: Jellyfish collagen was hydrolysed with trypsin and properase E, and jellyfish collagen peptide (JCP) was purified from the enzymatic hydrolysate using ion exchange chromatography and gel filtration. The antioxidant activity of JCP in a linoleic acid emulsion system, its superoxide anion‐ and hydroxyl radical‐scavenging activities and its copper‐chelating ability were evaluated in vitro. Initial investigations of JCP's ability to inhibit melanogenesis were carried out using cultured B16 melanoma cells. RESULTS: The molecular weight distribution of JCP was from 400 to 1200 Da. Amino acid analysis showed that JCP was rich in Gly, Pro, Ser, Ala, Glu and Asp and had a total hydrophobic amino acid content of 384.2 g kg^?1. JCP showed high antioxidant activity (IC₅₀147.8 µg mL^?1), superoxide anion‐scavenging activity (IC₅₀21.9 µg mL^?1), hydroxyl radical‐scavenging activity (IC₅₀16.7 µg mL^?1) and copper‐chelating ability (IC₅₀88.7 µg mL^?1) in vitro. It also significantly inhibited intracellular tyrosinase activity, decreased melanin content and enhanced glutathione synthesis (P < 0.05). Furthermore, JCP decreased intracellular cAMP levels and suppressed tyrosinase mRNA expression. CONCLUSION: Based on the results of this study, JCP exerts anti‐melanogenic actions via its antioxidant properties and copper‐chelating ability. JCP could be used as a natural skin‐lightening agent in the medicine and food industries. Copyright © 2009 Society of Chemical Industry     

Volatile compounds and antimicrobial and antioxidant activities of the essential oils of the needles of Pinus densiflora and Pinus thunbergii

BACKGROUND: To investigate the volatile compounds and the antibacterial and antioxidant effects of the essential oils of Pinus densiflora needles (EPDN) and Pinus thunbergii needles (EPTN), the volatile compounds of steam‐distilled essential oils were analysed by gas chromatography–mass spectrometry. Antibacterial activities were analysed by performing disc‐agar diffusion assay and determining the minimum inhibitory concentrations (MICs) of the essential oils. Antioxidant activities were analysed via radical‐ and nitrite‐scavenging activity assays. RESULTS: The yields of EPDN and EPTN were 0.304% (v/w) and 0.296% (v/w), respectively. In the antibacterial activity assay, the MICs of EPDN and EPTN for Klebsiella pneumoniae, Shigella flexneri and Proteus vulgaris were < 0.4 mg mL^?1. In the antioxidant activity assay, the 50% inhibitory concentrations (IC₅₀) of EPDN and EPTN were 120 and 30 µg mL^?1, respectively. At 1680 µg mL^?1, both EPDN and EPTN exhibited > 50% nitrite‐scavenging activity. CONCLUSION: EPDN can be used as a natural antimicrobial substance. Copyright © 2011 Society of Chemical Industry     

Antioxidant and antimicrobial activities of Polygonum cognatum Meissn extracts

The antioxidant activities, reducing powers, 2,2‐diphenyl‐l‐picrylhydrazyl (DPPH) radical‐scavenging activities, total phenolic compound contents and antimicrobial activities of ether, ethanol and hot water extracts of Polygonum cognatum Meissn were studied in vitro. The highest antioxidant activity was found in the water extract. However, there were no statistically significant differences among 15 µg ml^?1 extract‐containing samples in linoleic acid emulsion (0.02 M , pH 7.0) during 120 h of incubation (P > 0.05). The reducing power of the water extract was the highest, but its reducing power was markedly lower than that of ascorbic acid. The highest DPPH radical‐scavenging activity was found in the water extract, with 50% DPPH radical scavenging at a concentration of 100 µg ml^?1 dried water extract, while at the same concentration of dried ethanol extract the value was 12%. Surprisingly, no DPPH radical‐scavenging activity was observed in the ether extract. The concentrations of phenolic compounds found were 0.48, 0.50 and 0.01 µg ml^?1 gallic acid equivalent in 10 µg ml^?1 water, ethanol and ether extracts respectively. The ether and ethanol extracts showed antimicrobial activity against Staphylococcus aureus and Bacillus subtilis. The water extract did not show antimicrobial activity against the studied micro‐organisms. © 2002 Society of Chemical Industry     

Antioxidant and antiproliferative effects of methanol extracts from raw and fermented parts of mulberry plant (<Emphasis Type="Italic">Morus alba</Emphasis> L.)

Total phenolic content, phenolic acids, radical scavenging activity and antiproliferative properties of different parts of mulberry (Morus alba L.) were determined. The highest phenolic content was found in methanol extracts of mulberry root (117.7 ± 2.0), followed by leaves (71.4 ± 2.4), branches (49.0 ± 1.5) and fruit (11.2 ± 0.3) [mg ferulic acid equivalents (FAE) kg⁻¹ dry weight (DW)] (P < 0.05). The highest level of total phenolics in the fractions was in roots (166.2 ± 7.5 and 160.8 ± 7.2 mg kg⁻¹ DW for BuOH and EtOAC, respectively). Methanol extracts and their fractions dose dependently increased radical scavenging activity of mulberry branches, roots and leafs (more than 70%). Total phenolic content of the tested plant extracts was highly correlated with the radical scavenging activity. The antiproliferative effect of mulberry parts on human cell lines was different and connected to the concentrations of the investigated extracts. The fermentation of the mulberry leaves did increase their methanol extract antiproliferative effect only on human gastric carcinoma (SNU-601) cell line in concentration of 1,000 mg mL⁻¹. In conclusion, some plant parts of the Korean mulberry could be recommended as preventative and therapeutic agents, based on their antioxidant and antiproliferative properties.     

Antioxidant properties of Korean black raspberry wines and their apoptotic effects on cancer cells

BACKGROUND: The objective of the study was to determine the antioxidant activities of Korean black raspberry concentrate (KBR: Rubus coreanus Miq.) and Korean black raspberry wine concentrates (KBRW‐1 and KBRW‐2) using the DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) radical scavenging assay. The apoptotic effects of the KBRW concentrates on various cancer cells were also investigated. RESULTS: Both the KBR concentrate and KBRW concentrates showed dose‐related antioxidant activities in the DPPH assay. At concentrations of 500 µg mL^?1 and 1000 µg mL^?1, the KBR concentrate antioxidant activities were 59% and 79%, respectively. KBRW‐1 and KBRW‐2 inhibited radical formation at 500 µg mL^?1 by 19% and 48%, respectively. The antioxidant activity of KBRW‐2 was comparable to various red wines (RW‐1, RW‐2, RW‐3, and RW‐4). However, at 1000 µg mL^?1, the antioxidant activities of KBRW‐1 and KBRW‐2 were 53% and 83% that of α‐tocopherol, respectively. Both RW‐1 and KBRW‐2 showed marked antiproliferative effects on all cancer cell types, with decreases in cell viability greater than 50%. This was co‐related with apoptotic characteristics, including chromatin condensation and apoptotic body formation, as determined by cell morphological assessment. Cell cycle analysis showed that treating AGS cells with RW‐1 and KBRW‐2 resulted in 25% and 30% apoptotic cell accumulation, respectively. KBRW‐2 induced the cleavage of poly(ADP‐ribose) polymerase (PARP) and the activation of caspase‐3 within the AGS cells. Levels of PARP cleavage were increased five‐ and three‐fold by RW‐1 and KBRW‐2, respectively, and the level of caspase‐3 was significantly increased by the treatment with KBRW‐2. CONCLUSION: Overall, the results of this study suggest that Korean black raspberry wine displays antioxidant activity comparable to that of imported red wines, and has anticancer effects that may be attributed to induction of the apoptotic pathway. Copyright © 2009 Society of Chemical Industry     

Chemical composition,antioxidant and cytotoxicity activities of the essential oils of Myristica fragrans and Morinda citrifolia

BACKGROUND: In this study the chemical composition, antioxidant activities and cytotoxic effect of the essential oils of Myristica fragrans (nutmeg) and Morinda citrifolia (mengkudu) were determined. RESULTS: Thirty‐eight compounds in nutmeg oil and six compounds in mengkudu oil were identified by gas chromatography–mass spectrometry. The free radical scavenging activity of nutmeg oil was superior of that mengkudu oil. The MTT assay of nutmeg oil on human colorectal carcinoma (HCT‐116) and human breast carcinoma (MCF‐7) cell lines showed IC₅₀ values of 78.61 and 66.45 µg mL^?1, respectively. The mengkudu oil exhibited IC₅₀ values of 91.46 and 78.15 µg mL^?1 for HCT‐116 and MCF‐7, respectively. CONCLUSION: The results showed that nutmeg oil can be developed as potent anti‐cancer and antioxidant drugs. Copyright © 2011 Society of Chemical Industry     

Protective effects of solvent extracts from Taiwanese Agrocybe cylindracea strain B against DNA damage induced by environmental mutagens

Antioxidant activity of a water extract from Agrocybe cylindracea strain B (ACB) against iron‐mediated lipid peroxidation has been demonstrated. In addition, the protective effect of water extracts from ACB (WAC) on hydroxyl radical‐mediated DNA strand breaks was better than that of the shiitake mushroom (Lentinula edodes). Therefore, we decided to investigate whether different solvent extracts from ACB (ACES) protect DNA against oxidative stress induced by environmental mutagens, such as cooking oil fumes (COF) and benzo[a]pyrene (BaP). Oxidative DNA damage and intercellular DNA migration (tail length) were quantified by determining the decrease of extracellular supercoiled (SC) plasmid DNA and by using the ‘comet assay’ in the human adenocarcinoma CL‐3 cell line, respectively. IC₅₀ values of water, boiled water, methanol and acetone extracts from ACB were 108.97, 87.21, 970.52 and 1005.87 µg mL^?1, respectively, for the decrease in cupric/COF‐mediated SC plasmid DNA damage. The boiled water extract has the best protective effect. The ethyl acetate and ether extracts did not inhibit plasmid DNA damage. By using the comet assay, IC₅₀ values of the ether, methanol and acetone extracts from ACB were 672.95, 64.34, and 397.77 µg mL^?1, respectively, for the decrease in COF‐mediated DNA migration in CL‐3 cells. The methanol extract had the best protective effect. However, water, boiled water and ethyl acetate extracts from ACB showed no protective effect on COF‐mediated DNA migration. These results indicate that the protective capacity of ACES on DNA damage induced by environmental mutagens is different in pUC18 plasmid DNA and CL‐3 cell DNA. Copyright © 2006 Society of Chemical Industry     

Phenolic profile,antioxidant, anticholinesterase,and anti-tyrosinase activities of the various extracts of Ferula elaeochytris and Sideritis stricta

In this study, the antioxidant, anticholinesterase, and anti-tyrosinase properties of (hexane, acetone, methanol, and water) extracts of Ferula elaeochytris and Sideritis stricta were determined with the total phenolic and flavonoid contents. The phenolic profile of the methanol and water extracts was analysed using HPLC-DAD. Protocatechuic acid was found as the major phenolic compound in the methanol (116.3 ± 3.1 µg/g) and water extracts (69.4 ± 1.3 µg/g) of F. elaeochytris. Coumarins (253.9 ± 4.1 µg/g) and catechin hydrate (175.2 ± 2.9 µg/g) were the most abundant phenolic compounds in the methanol and water extracts of S. stricta. β-carotene–linoleic acid, DPPH^?, ABTS^?+, CUPRAC, and metal-chelating assays were used to evaluate antioxidant properties of the extracts. The methanol and water extracts of F. elaeochytris and the acetone and methanol extracts of S. stricta containing the highest amount of total phenolic and flavonoid contents showed the highest antioxidant activities in β-carotene–linoleic acid, DPPH^?, ABTS^?+, and CUPRAC assays. The enzyme inhibitory potential of extracts was investigated against key enzymes involved in neurodegenerative (acetylcholinesterase (AChE) and butyrylcholinesterase (BChE)) and skin (tyrosinase) disorders. In the cholinesterase inhibitory assays, the hexane extracts of two species exhibited the best activity against AChE, while the hexane extract of F. elaeochytris and the methanol extract of S. stricta observed to be the most active against BChE. As for anti-tyrosinase activity results of extracts, the only acetone and methanol extracts showed mild inhibitory activity for both species.     

Assessment of in vitro antioxidant, antibacterial and immune activation potentials of aqueous and ethanol extracts of Phyllanthus niruri

BACKGROUND: Recently much attention has been paid to biologically active plants because of their low production cost and fewer adverse effects compared with chemical drugs. In the present investigation the bioactivity of Phyllanthus niruri ethanol and aqueous extracts was evaluated in vitro. RESULTS: The ethanol extract of P. niruri showed a high level of flavonoid content (123.9 ± 0.002 mg g^?1), while the aqueous extract showed the highest 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH; IC₅₀6.85 ± 1.80 µmol L^?1) and 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid) (ABTS; 46.44 ± 0.53 µmol L^?1) free radical scavenging activities with high phenol content (376 ± 0.02 mg g^?1) and elevated levels of ferric reducing antioxidant power (FRAP; 23 883 ± 0.019 mmol g^?1) with excellent antibacterial activity against Staphylococcus aureus (20 mm inhibition zone) and Streptococcus agalactiae (12 mm inhibition zone), respectively, in addition to the best immune activation potential of human peripheral blood mononuclear cells (450.5%). CONCLUSIONS: It is clear from our results that both extracts of P. niruri has excellent bioactivity roles via elevated levels of antibacterial, antioxidant and percentage of peripheral blood mononuclear cell proliferation, which could lead to the development of medications for clinical use. Copyright © 2012 Society of Chemical Industry     

Chemical composition and in vitro control of agricultural plant pathogens by the essential oil and various extracts of Nandina domestica Thunb.

BACKGROUND: The aims of this study were to examine the chemical composition of the essential oil isolated from the floral parts of Nandina domestica Thunb. by hydrodistillation, and to test the efficacy of essential oil and various leaf extracts (n‐hexane, chloroform, ethyl acetate and methanol) as an antifungal potential against a panel of agricultural plant pathogens. RESULTS: The GC‐MS analysis determined that 79 compounds, which represented 87.06% of total oil, were present in the oil containing mainly 1‐indolizino carbazole (19.65%), 2‐pentanone (16.4%), mono phenol (12.1%), aziridine (9.01%), methylcarbinol (4.6%), ethanone (3.3%), furfural (2.96%), 3,5‐dimethylpyrazole (1.29%) and 2(5H)‐furanone (1.32%). The oil (1000 ppm disc^?1) and the leaf extracts (1500 ppm disc^?1) revealed remarkable antifungal effect against Fusarium oxysporum, Fusarium solani, Phytophthora capsici, Colletotrichum capsici, Sclerotinia sclerotiorum, Botrytis cinerea and Rhizoctonia solani in the growth inhibition range of 53.3–64.3% and 33.3–56.0%, respectively, along with their respective values for mimimum inhibitory concentration (MIC) ranging from 125 to 1000 µg mL^?1 and 500 to 2000 µg mL^?1. The values for minimal fungicidal concentration (MFC) of the oil and extracts were obtained in the range of 125 to 1000 µg mL^?1 and 500 to 2000 µg mL^?1, respectively. The essential oil also had a strong detrimental effect on spore germination of all the plant pathogens tested along with concentration as well as time‐dependent kinetic inhibition of B. cinerea. CONCLUSION: The results obtained in this study demonstrate that N. domestica mediated oil and extracts could become potential alternatives to synthetic fungicides for controlling certain important agricultural plant pathogenic fungi. Copyright © 2008 Society of Chemical Industry     

Antimicrobial activity of food-compatible plant extracts and chitosan against naturally occurring micro-organisms in tomato juice

BACKGROUND: Chitosan (AC) and five hydroalcoholic extracts from Lithospermum erythrorhizon (SE), Rheum palmatum (RE), Thymus vulgaris (AT), Lippia citriodora (PLX) and a mixture of Rosmarinus officinalis, Salvia lavandulifolia and Thymus mastichina (LA) were tested for antimicrobial activity against bacteria, yeasts and filamentous fungi using two broth dilution methods. The effects of adding single extracts on naturally occurring micro‐organisms and sensory qualities of raw tomato juice were also evaluated. RESULTS: SE extract exhibited the strongest activity, with minimum inhibitory concentrations (MICs) of 100–400 µg mL^?1 for Gram‐positive and 1600–3200 µg mL^?1 for Gram‐negative bacteria. Enterobacter aerogenes showed the greatest susceptibility to AC (MIC 1600 µg mL^?1). Lethal effects of extracts and AC were achieved at a minimum bactericidal concentration (MBC)/MIC ratio of 2 in 88% of assays. SE and RE extracts and AC also exhibited antifungal effect against yeasts, but they had no activity on filamentous fungi. Control and 100 mg L^?1 SE‐added tomato juices did not differ in acceptance, but this SE concentration was not effective in the control of microbial load throughout cold storage. CONCLUSION: Results confirm the antimicrobial potential of the plant extracts, but additional research is needed until the agents responsible for the activities have been determined in order to use them as natural constituents of multiple‐barrier food preservation systems. Copyright © 2012 Society of Chemical Industry     

Optimisation of hydrolysis of purple sea urchin (Strongylocentrotus nudus) gonad by response surface methodology and evaluation of in vitro antioxidant activity of the hydrolysate

BACKGROUND: Hydrolysates prepared from sea urchin (Strongylocentrotus nudus) gonad by enzymatic treatment showed strong 1,1‐diphenyl‐2‐picrylhydrazyl radical scavenging activity and reducing power. RESULTS: Hydrolysis of S. nudus gonad by the commercial protease papain was optimised for maximum degree of hydrolysis (DH) and trichloroacetic acid‐soluble peptide index (TCA‐SPI) using response surface methodology. Results showed that the optimal conditions were the following: temperature of 48.83 °C, pH of 6.92, enzyme‐to‐substrate ratio of 3143 U g^?1, and substrate concentration of 83.5 g L^?1. Under these conditions, a DH of 27.96 ± 0.54% and a TCA‐SPI of 57.32 ± 0.63% were obtained. The hydrolysate prepared in the optimal conditions was fractionated by an ultra‐filtration system and the resultant fraction below 10 kDa was found to effectively scavenge hydroxyl radical (EC₅₀ = 13.29 ± 0.33 mg mL^?1) and hydrogen peroxide (EC₅₀ = 16.40 ± 0.37 mg mL^?1), inhibit lipid peroxidation (EC₅₀ = 11.05 ± 0.62 mg mL^?1), chelate Fe²⁺ (EC₅₀ = 7.26 ± 0.44 mg mL^?1), and protect mice macrophages against death induced by tert‐butyl hydroperoxide. CONCLUSION: Hydrolysates prepared from S. nudus gonad have the potential to be applied as natural antioxidant agents. Copyright © 2012 Society of Chemical Industry     

Antioxidant and Antihemolytic Activities of Ethanolic Extract of Flowers,Leaves, and Stems of Hyssopus officinalis L. Var. angustifolius

In this study, antioxidant and antihemolytic activities of ethanolic extract of flowers, leaves, and stems of Hyssopus officinalis L. Var. angustifolius were investigated employing different in vitro assay systems. Extracts showed good antioxidant activity. IC₅₀ for 1,1-diphenyl-2-picryl hydrazyl radical-scavenging activity were 148.8 ± 4.31 μg mL^?1 for flowers, 79.9 ± 2.63 μg mL^?1 for stems, and 208.2 ± 6.45 μg mL^?1 for leaves. All extracts showed moderate iron (II) chelating ability. Extracts exhibited good antioxidant activity in the hemoglobin-induced linoleic acid model and also they were capable of scavenging hydrogen peroxide in a concentration dependent manner. Extracts showed good antihemolytic activity againts hydrogen peroxide-induced hemolysis (IC₅₀ were 48.51 ± 2.27 μg mL^?1 for flowers, 19.47 ± 0.73 μg mL^?1 for leaves, and 63.1 ± 2.65 μg mL^?1 for stems). The total amount of phenolic compounds in the extracts was determined as gallic acid equivalents and total flavonoid content was calculated as quercetin equivalents from a calibration curve.     

Characterisation of the phenolic and flavonoid fractions and antioxidant power of Italian honeys of different botanical origin

BACKGROUND: Twenty‐seven Italian honey samples of different floral origin were analysed for total phenolic and flavonoid contents by a spectrophotometric method and for antioxidant power and radical‐scavenging activity by the ferric‐reducing/antioxidant power (FRAP) and 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) assays respectively. In addition, the phenolic and flavonoid profiles were analysed using high‐performance liquid chromatography with UV detection (HPLC‐UV). RESULTS: The results of this study showed that honey contains copious amounts of phenolics and flavonoids. HPLC‐UV analysis showed a similar qualitative polyphenolic profile for all honey samples analysed. The main difference among samples was in the contribution of individual analytes, which was affected by floral origin. Total phenolic and flavonoid contents varied from 60.50 to 276.04 mg gallic acid equivalent kg^?1 and from 41.88 to 211.68 mg quercetin equivalent kg^?1 respectively. The antioxidant capacity was high and differed widely among samples. The FRAP value varied from 1.265 to 4.396 mmol Fe²⁺ kg^?1, while the radical‐scavenging activity expressed as DPPH‐IC₅₀ varied from 7.08 to 64.09 mg mL^?1. Correlations between the parameters analysed were found to be statistically significant (P < 0.05). CONCLUSION: The present study shows that honey contains high levels of phenolics and flavonoids and that the distribution of these compounds is influenced by the honey's floral origin. Copyright © 2009 Society of Chemical Industry     

Comparative characterisation of durian,mango and avocado

The aim of this investigation was to determine the nutritional and bioactive properties of relatively less investigated exotic fruit durian (Durio zibethinus Murr.) and to compare these indices with widely used mango (Mangifera indica L.) and avocado (Persea americana). For this purpose HPLC, three‐dimensional fluorescence (3D‐FL), several radical scavenging assays and multivariate factor analysis were used. It was found a similarity in acetone extracts between durian and mango in the contents of polyphenols (1.66 ± 0.08, 1.48 ± 0.05, mg GAE g^?1 DW, respectively), and in some antioxidant assays such as ABTS (11.98 ± 0.5, 12.24 ± 0.5, μm TE g^?1DW, respectively) and DPPH (5.61 ± 0.3, 5.22 ± 0.2, μm TE g^?1 DW, respectively). Durian and avocado were similar in the contents of polyphenols, and ABTS and DPPH values in water and in methanol extracts, respectively. Based on the obtained results the nutritional and bioactive properties of durian are comparable with those indices in mango and avocado. In conclusion, durian can be recommended as a part of disease prevented diets.