‘Best before period once opened’ for honey samples from oceanic climates on the basis of their acidity types

Stability of food is of particular interest, as we should know the period for which a given food maintains its original quality. Acidity is a very important parameter as regards honey quality control. In this study we analysed a possible ‘best before period once opened’, regarding the evolution of acidity in honey throughout 30 months in samples from regions with oceanic climates. The study was carried out at room temperature (between 15 and 25 °C) by analysing all samples in duplicate each 5 months. We also researched the possible influence of induced granulation on the acidity evolution of honey samples, observing that as the analysis of variance showed significant differences at P‐value <0.05, this process had a significant influence on free acid and total acidity. All samples fulfilled the European Regulations regarding free acid, because no honey sample showed a free acid value higher than the limit of 50 meq kg^?1. Nevertheless, all honey samples suffered a continuous decrease of pH from 20 months on (averages: from 4.1 ± 0.25 at 20 months to 4.0 ± 0.23 at 30 months), and a continuous increase of both free acid (averages: from 27.6 ± 6.22 meq kg^?1 at 20 months to 33.5 ± 6.44 meq kg^?1 at 30 months) and total acidity (averages: from 42.5 ± 7.60 meq kg^?1 at 20 months to 44.7 ± 7.60 meq kg^?1 at 30 months). On the basis of acidity types, 20 months should be considered the ‘best before period once opened’ for honey from regions with oceanic climates.     

Characterisation of avocado (Persea americana Mill) honeys by their physicochemical characteristics

The quality of 12 avocado (Persea americana Mill) honeys from Spain was evaluated. Eight common physicochemical parameters were analysed, namely water content, pH, acidity (free, lactonic and total), sugar content, ash content and electrical conductivity. In addition, the honey samples were analysed using inductively coupled plasma optical emission spectrometry (ICP‐OES), and six minerals were quantified for each honey, namely potassium (K), calcium (Ca), magnesium (Mg), sodium (Na), phosphorus (P) and sulphur (S). Most samples showed proper maturity considering the medium water content (mean 17.7%). The total acidity (below 50 meq kg^?1 except for one sample) indicated absence of undesirable fermentation; also, the mean pH of around 4.77 is usual in this kind of honey. The values for ash content and electrical conductivity were high (0.77% and 798 µS cm^?1 respectively) and typical of dark honeys. K was the predominant mineral (accounting for 73% of the total minerals quantified), followed by Na (10%). Copyright © 2004 Society of Chemical Industry     

Effect of pre‐treatment and smoking process (cold and hot) on chemical,microbiological and sensory quality of mackerel (Scomber scombrus)

The sensory, hygienic, toxicological and nutritional profiles of hot‐ and cold‐smoked mackerel samples were studied with various pre‐treatments. The panellists assessed all smoked samples as barely to quite acceptable products whilst the product immersed in 120 g kg^?1 sodium chloride and 60 g kg^?1 fructose prior to smoking was assessed as very acceptable regarding its sensory characteristics. The available lysine in all hot smoked samples was reduced to the same extent (32%) whilst a very good correlation (r = 0.912) was observed between loss of available lysine and colour formation of the cold‐smoked products, indicating the high contribution of lysine in the interactions with carbonyls. Histamine was found in highly unacceptable levels even in the unprocessed samples (600 mg kg^?1) and strongly increased (2220 and 2250 mg kg^?1) in the cold‐ and hot‐smoked samples, respectively, due to all treatments. These are levels which would be expected to cause symptoms of scombrotoxin poisoning. Benzo(a)pyrene, fluoranthene and perylene were at high levels both in cold‐ (2.1, 4.3 ± 0.04 and 7.2 ± 0.05 µg kg^?1) and hot‐smoked samples (9.2, 7.8 ± 0.03 and 9.4 ± 0.14 µg kg^?1, respectively) and were, as expected, influenced by the temperature. The aerobic bacteria remained at acceptable levels, since salt and high temperature prevent bacterial growth. Copyright © 2004 Society of Chemical Industry     

Mercury in fruiting bodies of dark honey fungus (Armillaria solidipes) and beneath substratum soils collected from spatially distant areas

BACKGROUND: This paper reports data on bioconcentration potential and baseline mercury concentrations of fruiting bodies of dark honey fungus (Armillaria solidipes) Peck and soil substrate layer (0–10 cm) from 12 spatially distant sites across Poland. Mercury content of caps, stipes and soil samples were determined using validated analytical procedure including cold‐vapor atomic absorption spectroscopy after thermal decomposition of the sample matrix and further amalgamation and desorption of mercury from gold wool. RESULTS: Mean mercury concentrations ranged from 20 ± 8 to 300 ± 70 ng g^?1 dry weight (dw) in caps, from 20 ± 6 to 160 ± 40 ng g^?1 dw in stipes, and in underlying soil were from 20 ± 2 to 100 ± 130 ng g^?1 dw. The results showed that stipes mercury concentrations were 1.1‐ to 1.7‐fold lower than those of caps. All caps and the majority of stipes were characterized by bioconcentration factor values > 1, indicating that dark honey fungus can be characterized as a moderate mercury accumulator. CONCLUSION: Occasional or relatively frequent eating of meals including caps of dark honey fungus is considered safe in view of the low total mercury content, and the mercury intake rates are below the current reference dose and provisionally tolerable weekly intake limits for this hazardous metal. © 2012 Society of Chemical Industry     

Determination and surveillance of nine acaricides and one metabolite in honey by liquid chromatography-tandem mass spectrometry

A simple and accurate analytical method for the determination of acaricides in honey was developed and validated in accordance with Japanese validation guidelines. Analytes – amitraz, N-2,4-dimethylphenyl-N-methylformamidine (DMPF), etoxazole, fenpyroximate, fipronil, hexythiazox, propargite, pyridaben and spirodiclofen – were extracted with ethyl acetate under basic conditions and subsequently cleaned up using an InertSep^® MA-1 polymer-based anion-exchange column. The method was validated by fortified recovery tests at three different concentrations (1, 5 and 10 µg kg^?1) performed with three samples daily on five different days. The method exhibited recoveries of 77–116% and precision (relative standard deviations – RSDs) of repeatability and within-laboratory reproducibility ranged from 2% to 22% and from 3% to 23%, respectively. The sample solution was successfully cleaned up to enable quantification using external solvent calibration curves. The limits of quantification (LOQs) were estimated to be 1 µg kg^?1 for all analytes. The method was applied to honey samples commercially available in Tokyo, Japan. Analysis of 250 honey samples indicated that amitraz was present in 127 samples, and that its residual concentration was less than 20 µg kg^?1. Propargite was detected in 23 samples at concentrations less than 1 µg kg^?1.     

Chemical composition of two muscles of the common duiker (Sylvicapra grimmia)

Ten mature male common duikers (Sylvicapra grimmia) were cropped and their M longissimus dorsi (LD) and M biceps femoris (BF) dissected in order to determine the chemical composition of the meat of this species. There was no significant difference in proximate chemical composition between the LD and the BF. The duiker muscle had a moisture content of 713.1 g kg^?1, a high protein content (257.7 g kg^?1) and a low fat content (20.6 g kg^?1). Potassium and phosphorus were the minerals and lysine and leucine the amino acids present in highest concentrations in the meat. The LD contained higher levels of sodium and zinc than the BF but lower levels of alanine, leucine and lysine. Stearic acid, palmitoleic acid, oleic acid and linoleic acid constituted the greatest proportion of fatty acids in the meat. The common duiker's meat also had a high polyunsaturated fatty acid content (414.2 g kg^?1 total fatty acids), allowing it to be considered a healthy food commodity. Copyright © 2004 Society of Chemical Industry     

Characterization and prediction by near-infrared reflectance of mineral composition of rocket (Eruca vesicaria subsp. sativa and Eruca vesicaria subsp. vesicaria)

BACKGROUND: Minerals are essential for human nutrition and must be obtained from our diet. Crucifer vegetables are a good source of these nutrients. Our objectives were to determine the genetic variability for mineral content and to evaluate the use of near‐infrared reflectance spectroscopy (NIRS) for prediction of ashes and minerals among and within the rocket species Eruca vesicaria subsp. sativa and vesicaria. The minerals studied were iron (Fe), copper (Cu), sodium (Na), potassium (K), calcium (Ca), magnesium (Mg), manganese (Mn) and zinc (Zn). RESULTS: The maximum mean values obtained for all the accessions (mean ± SE) were 235.5 ± 1.5 mg ashes kg^?1, 273.3 ± 4.2 mg Fe kg^?1, 18.1 ± 0.4 mg Cu kg^?1, 2.8 ± 0.1 g Na kg^?1, 71.6 ± 1.0 g K kg^?1, 64.6 ± 1.2 g Ca kg^?1, 6.8 ± 0.1 g mg kg^?1, 101.6 ± 1.2 mg Mn kg^?1, and 67.1 ± 0.4 mg Zn kg^?1 of dry weight. CONCLUSION: The statistical analysis showed significant differences for all the minerals, except Ca, for each accession studied individually and for accessions grouped within countries. The results indicate that NIRS can be used as a rapid screening method for determining total mineral, Fe, Na, K, and Zn in rocket. Copyright © 2011 Society of Chemical Industry     

Residues of antibiotics and sulfonamides in honeys from Basque Country (NE Spain)

BACKGROUND: The aim of this work was to ensure that Label Basque market honey is free of veterinary residues. RESULTS: A total of 567 Basque honey samples were previously analyzed with the respective Charm II system—68 samples were presumptive positive for sulfonamides (SA‐s), 24 samples for tetracyclines (TC‐s), and no positive samples for chloramphenicol (CAP) (<0.3 µg kg^?1) residues. The residues were mostly confirmed by liquid chromatography fluorescence detection (LC‐FD) and tandem mass spectrometry (LC‐MS/MS), according to the latest European Union criteria for the analyses of veterinary drug residues (2002/657/EC). These techniques confirmed that 19 of the 68 samples, presumptive contaminated with SA‐s, contained sulfathiazole (STZ) residues at levels from 20 to 210 µg kg^?1, and the 24 samples presumptive contaminated with TC‐s, were also confirmed, showing tetracycline (TC) levels from 15 to 920 µg kg^?1. Linearity range, decision limit (CCα), detection capability (CCβ), precision and reproducibility were also determined. CONCLUSION: Residues of veterinary drugs were confirmed in a very limited number of honey samples: sulfathiazole (3.40%) and tetracycline (4.22%). This work reports the advantages of the Charm II assay, but also its limitations, detecting SA‐s in most (87.7%) of the heather (Erica vagans) honey samples. The false positives detected in this honey were assumed to be of an unknown compound that has not been confirmed as a drug residue. Until now, no studies have been performed to find out if other heather honeys of different geographical origins give similar false positives for SA‐s. Copyright © 2008 Society of Chemical Industry     

Pyrrolizidine alkaloids: their occurrence in Spanish honey collected from purple viper’s bugloss (Echium spp.)

The incidence and concentration of pyrrolizidine alkaloids (PAs) from Echium spp. plant have been defined in 103 Spanish honey samples. Each sample was examined to determine total pollen content, the percentage of Echium spp. pollen, and simultaneous measurements of PAs and their N-oxides concentrations by the HPLC-ESI/MS method to identify the potential origin of PAs in honey. PAs were found in 94.2% of the raw honey samples analysed, in the range of 1–237 µg kg^?1 (average concentration = 48 µg kg^?1). The PA pattern was clearly dominated by echimidine, lycopsamine and their N-oxides, representing the 97.8% of total ∑PAs, and only echimidine and echimidine-N-oxide surpassed the 87% of total ∑PA content. Others PAs, seneciphylline and heliotrine-N-oxide, appear to be reported in a lower incidence and concentration (average of 3 and 1 µg kg^?1, respectively). The Pearson Chi-squared test (p ≤ 0.01) confirms the non-correspondence between pollen plants and PA content. This study was also realised to generate a dataset in order to evaluate the potential risk of Spanish honeys containing PA plants belonging to the genera Echium.     

Rapid multi-class multi-residue method for the confirmation of chloramphenicol and eleven nitroimidazoles in milk and honey by liquid chromatography-tandem mass spectrometry (LC-MS)

A confirmatory method was developed to allow for the analysis of eleven nitroimidazoles and also chloramphenicol in milk and honey samples. These compounds are classified as A6 compounds in Annex IV of Council Regulation 2377/90 (European Commission 1990) and therefore prohibited for use in animal husbandry. Milk samples were extracted by acetonitrile with the addition of NaCl; honey samples were first dissolved in water before a similar extraction. Honey extracts underwent a hexane wash to remove impurities. Both milk and honey extracts were evaporated to dryness and reconstituted in initial mobile phase. These were then injected onto a liquid chromatography-tandem mass spectrometry (LC-MS/MS) system and analysed in less than 9 min. The MS/MS was operated in multiple reaction monitoring (MRM) mode with positive and negative electrospray ionization. The method was validated in accordance with Commission Decision 2002/657/EC and is capable of analysing metronidazole, dimetridazole, ronidazole, ipronidazole and there hydroxy metabolites hydroxymetronidazole, 2-hydroxymethyl-1-methyl-5-nitroimidazole, and hydroxyipronidazole. The method can also analyse for carnidazole, ornidazole, ternidazole, tinidazole, and chloramphenicol. A recommended level of 3 µg l^?1/µg kg^?1 for methods for metronidazole, dimetridazole, and ronidazole has been recommended by the Community Reference Laboratory (CRL) responsible for this substance group, and this method can easily detect all nitroimidazoles at this level. A minimum required performance level of 0.3 µg l^?1/µg kg^?1 is in place for chloramphenicol which the method can also easily detect. For nitroimidazoles, the decision limits (CCα) and detection capabilities (CCβ) ranged from 0.41 to 1.55 µg l^?1 and from 0.70 to 2.64 µg l^?1, respectively, in milk; and from 0.38 to 1.16 µg kg^?1 and from 0.66 to 1.98 µg kg^?1, respectively, in honey. For chloramphenicol, the values are 0.07 and 0.11 µg l^?1 in milk and 0.08 and 0.13 µg kg^?1 in honey. Validation criteria of accuracy, precision, repeatability, and reproducibility along with measurement uncertainty were calculated for all analytes in both matrices.     

Chemical composition,protein fractionation,essential amino acid potential and antimetabolic constituents of an unconventional legume,Gila bean (Entada phaseoloides Merrill) seed kernel

Physical characteristics of pods and seeds, proximate composition, different protein fractionation, SDS‐PAGE analysis of proteins, amino acid composition, starch content, fatty acid profiles and various antimetabolic substances of Gila bean (Entada phaseoloides Merrill) were studied. The pod length and the number of seeds per pod ranged from 55 to 90 cm and from 5 to 11 respectively. The kernel comprised 66.1% of the seed weight (18.41 ± 1.14 g). The seed kernels contained 256.7 g kg^?1 crude protein, 108.1 g kg^?1 lipid, 27.3 g kg^?1 ash and a high content of carbohydrate (585.7 g kg^?1). The levels of potassium, phosphorus, zinc and iron were similar to those in conventional pulses. Among the different protein fractions of seed kernels, albumins constituted the major storage proteins (69.7%). The kernel proteins were rich in essential amino acids, particularly sulphur‐containing amino acids, and their values appeared to be higher than the FAO/WHO (1990) reference protein for a 2–5‐year‐old growing child and soybean, and comparable to hen egg. Seed kernel lipids contained high levels of unsaturated fatty acids, oleic and linoleic acids, which accounted for 83% of the total fatty acid recovered. The kernel exhibited high trypsin and chymotrypsin inhibitor activities (96.65 mg TI g^?1 and 30.02 CIU mg^?1 sample respectively) in addition to containing phenolics, phytic acid, lectins and oligosaccharides. Another major toxic constituent was identified as a group of triterpenoid saponins (3.21%), which had high haemolytic activity (HeU) against cattle erythrocytes and caused high mortality in fish. The in vitro digestibility of the kernel protein was low (67%). © 2001 Society of Chemical Industry     

Chemical characterisation of Tylosema fassoglensis (Kotschy) Torre & Hillc oilseed

Tylosema fassoglensis seeds contain high levels of lipids (240–300 g kg^?1) and proteins (446 g kg^?1 dry weight). Major fatty acids contained in the oil are linoleic (36–42% of the total fatty acids) oleic (32–35%) and palmitic (11.5–15.7%) acids. The proteins are characteristic with their high levels of lysine, proline and tyrosine. Due to their very low content, both methionine and cystine appear to be the limiting amino acids. Tylosema fassoglensis defatted meal contains substantial amounts of trypsin inhibitors and phytates 295 TUI mg^?1 and 35 g kg^?1 dry weight, respectively.     

Effect of cellulase/glucanase/xylanase (Roxazyme G2) enzymes combination on nutrients utilisation of vegetable meal (Amaranthus cruentus) fed as sole dietary protein source in rat assay

Amaranthus cruentus vegetable meal (ACVM) had 23% crude protein. Ca, Na, K, Mg and Fe were abundant at 2.0 g kg^?1, 7.1 g kg^?1, 4.8 g kg^?1, 2.5 g kg^?1, 1109 mg kg^?1, respectively. P‐phosporous, oxalates and tannins were noticeable. Lysine, methionine and cystine were limiting. Weight gain for rats on the reference (casein) diet 2 at 6.30 g ±2.87 was highest (P < 0.05) followed by diet 6 (12% ACVM with enzyme supplementation) at 5.01 g ±2.42. Feed intakes were similar (P > 0.05) for rats on the reference diet and for rats on 10% and 12% with/without enzyme supplementation ranging from 42.90 g ± 4.52 in reference diet to 45.12 g ± 3.64. Nitrogen retention was highest for rats on reference diet but similar (P > 0.05) to rats on 12% enzyme supplemented diet at 0.53 ± 1.12 and 0.53 ± 2.10, respectively. Other investigated protein evaluation parameters revealed similar results among rats kept on reference diet and the rats on ACVM based diets with enzyme supplementations. Enzyme supplementation had a complimentary role in ACVM nutrition in rat trial.     

Characterisation of musk lime (Citrusmicrocarpa) seed oil

BACKGROUND: The seeds of musk lime (Citrus microcarpa) represent a substantial waste product of small‐scale citrus‐processing factories, as they constitute about 100.0 ± 3.2 g kg^?1 of the whole fruit and contain a considerable amount of crude fat (338.0 ± 11.3 g kg^?1). Thus the aim of the present study was to determine the physicochemical properties of this fat with a view to potential applications. RESULTS: The iodine and saponification values and unsaponifiable matter and free fatty acid contents of the freshly extracted oil were 118.0 g I₂ per 100 g oil, 192.6 mg KOH g^?1 oil, 22 mg g^?1 oil and 18 mg oleic acid g^?1 oil respectively. The oil had a Lovibond colour index of 33.1 Y + 1.1 B. Its fatty acid profile indicated that 73.6% of the fatty acids present were unsaturated. Linoleic (L, 31.8%), oleic (O, 29.6%) and palmitic (P, 21.4%) acids were the predominant fatty acids, existing mainly as the triacylglycerols POL (18.9%), PLL (13.7%) and OLL (11.9%). The melting and cooling points of the oil were 10.7 and ? 45.2 °C respectively. Electronic nose qualitative analysis of the oil showed the presence of volatile (aroma) compounds, although the concentrations of the more volatile compounds were lower than those present in the seeds. CONCLUSION: Musk lime seeds are a rich source of oil, which is unusual in having linoleic, oleic and palmitic acids dominating the fatty acid composition. This property should make the oil both relatively stable to thermal oxidation owing to the combined presence of oleic and palmitic acids (61.0%) and highly nutritive owing to its high concentration of unsaturated fatty acids (73.6%). Copyright © 2007 Society of Chemical Industry     

Compositional analysis and antimicrobial activity of various honey types of Pakistan

Antibacterial activities of various honey samples were assessed by using clinical isolates like S. aureus (Gram‐positive), E. coli, P. aeruginosa and K. pneumonia (Gram‐negative). It was observed that acacia and citrus honey has inhibited growth of all bacterial strains as compared to standard antibiotics (Gentamicine). Inhibition zones for S. aureus (27.4 ± 0.5 mm), E. coli (26.5 ± 0.7 mm), K. pneumonia (24.4 ± 0.5 mm) and P. aeruginosa (22.4 ± 0.2 were observed. Minimum inhibitory concentration of S. aureu (0.068 mg mL^?1), E. coli (0.072 mg mL^?1), P. aeruginosa (0.084 mg mL^?1) and K. pneumonia (0.085 mg mL^?1) was obtained for various types of honey samples. Pronounced antibacterial activities as well as standard values of various quality parameters of honey samples are scientifically proven for its use in traditional medicine since ancient time throughout the world.     

CHARACTERIZATION OF SURFACE AUXIN RESIDUE IN GREENHOUSE TOMATOES (LYCOPERSICON ESCULENTUM)

Greenhouse tomato samples (n = 20) was analyzed before and after peel removal in order to determine surface auxin residue. Mean 4‐CPA residue levels of greenhouse tomatoes with and without peels were 0.383 ± 0.123 mg kg^?1 and 0.241 ±0.085 mg kg^?1, respectively. This difference (36 ±13%) was statistically significant. The frequency distribution curve of tomatoes with peel had a peak point at 4‐CPA reside interval of 0.4‐ < 0.5 mg kg^?1 tomato, and shifted back to 4‐CPA residue interval of 0.2‐ < 0.3 mg kg^?1 for tomatoes without peel. Percentage of samples having 4‐CPA level lower than the critical concentration of 0.5 mg kg^?1 was 80% before peel removal, but increased to 100% upon being peeled. The mean 4‐CPA residue of peels was roughly estimated to be 3.449 mg kg^?1 peel based on peeled versus nonpeeled fruit residue.     

Energy and nutrient digestibilities in wheat dried distillers' grains with solubles fed to growing pigs

The aim of this study was to characterize the nutritional profile and to determine the digestibilities of nutrients in wheat‐based dried distillers' grains with solubles (DDGS) fed to growing pigs. Six ileal cannulated barrows individually housed in metabolism crates were fed experimental diets which consisted of a basal wheat‐based diet or the basal diet with wheat replaced by 400 g kg^?1 mixed wheat or winter wheat DDGS in a replicated 3 × 3 Latin square design. Ileal digesta and fecal samples were collected for determining apparent ileal (AID) and apparent total tract digestibilities (ATTD), respectively. The contents of proximate components and amino acids in DDGS were about three times higher than in wheat. The AID and ATTD of dry matter, nitrogen and energy were lower (P < 0.05) in DDGS compared with wheat. The DDGS samples had lower (P < 0.05) AID of amino acids compared with wheat; average values for lysine, threonine and isoleucine in DDGS were 43.8, 62.9 and 68.0%, respectively. The ileal and fecal digestible energy content in DDGS averaged 9.7 ± 1.18 and 13.5 ± 0.61 MJ kg^?1, respectively. Respective values for wheat were 13.3 ± 0.52 and 14.6 ± 0.22 MJ kg^?1 and both were higher (P < 0.05) than in DDGS. Copyright © 2005 Society of Chemical Industry     

Identification of Acacia Honey Adulteration with Rape Honey Using Liquid Chromatography–Electrochemical Detection and Chemometrics

The adulteration of honey is generally a concern of consumers and management departments of safety and quality. Adding low-price honey to high-price honey is often seen in the market. In this study, a reliable and simple method of liquid chromatography–electrochemical detection (LC-ECD) was presented to detect the adulteration of acacia honey which was added with rape honey at different levels (5–50 %, w/w). Chromatographic separation was carried out with a reversed phase column, and the mobile phase was methanol/2 % (v/v) aqueous acetic acid. Fingerprints of authentic honeys showed that the contents of chlorogenic acid were higher in acacia honey (1.738 mg kg^?1), while those of ellagic acid were much lower (0.274 mg kg^?1) in rape honey, so the chlorogenic acid and ellagic acid could be considered as possible markers of acacia and rape honeys, respectively. Samples were classified by cluster analysis and principal component analysis (PCA) according to the contents of phenolic acids. The results of PCA showed that chlorogenic acid and ellagic acid were the major variables, and no adulterated sample was identified as authentic honey. The results of cluster analysis (CA) indicated that the samples were appropriately divided into three main clusters, and adulterated samples were identified. Therefore, acacia honey adulteration with rape honey could be undoubtedly detected by LC-ECD combined with chemometric methods down to the level of 5 %.     

Influence of different crop management practices on the nutritional properties and benefits of tomato ‐Lycopersicon esculentum cv Perfectpeel‐

In this study, we have explored the relationship between the cultivation method and the concentration of major flavonoid aglycones, hydroxycinnamic acids, carotenoids and the total antioxidant activity of tomato (Lycopersicon esculentum cv Perfectpeel); in addition, we have investigated the bioactivity of polyphenol extracts from tomato. The main polyphenols in extracts were quercetin (33.90 ± 6.31 mg kg^?1 and 17.92 ± 1.09 mg kg^?1 in conventional and organic extracts), chlorogenic acid (3.52 ± 0.74 mg kg^?1 and 2.82 ± 0.92 mg kg^?1 in conventional and organic extracts) and caffeic acid (3.61 ± 0.71 mg kg^?1 and 3.29 ± 0.33 mg kg^?1 in conventional and organic extracts). Although statistical differences were found between organic and conventional extracts in several target compounds, no difference in biological effect was observed using cell models. The observed Trans Epithelial Electrical Resistance values were not significantly different between organic and conventional tomato extracts, but we have observed, in both samples, a decrease in tight‐junction permeability at 17 μm of polyphenol concentrations. Antioxidant compounds entering within the cell could exert an antioxidant action, nevertheless at concentrations >17 μm could have a pro‐oxidant effect.     

Phenolic compounds,lycopene and antioxidant activity in commercial varieties of tomato (Lycopersicum esculentum)

Nine commercial varieties of tomato (Rambo, Senior, Ramillete, Liso, Pera, Canario, Durina, Daniella and Remate) produced in Spain were analysed for their lycopene content, content of phenolic compounds and antioxidant capacity. The phenolic compounds were characterised as flavonoids (quercetin, kaempferol and naringenin) and hydroxycinnamic acids (caffeic, chlorogenic, ferulic and p‐coumaric acids). Antioxidant activity was measured using the DPPH and ABTS assays. The concentrations of lycopene and the various phenolic compounds as well as the antioxidant activity were significantly influenced by the tomato variety. Quercetin, the most abundant flavonoid, was found in concentrations ranging between 7.19 and 43.59 mg kg^?1 fresh weight, while naringenin levels were lower than 12.55 mg kg^?1. The most abundant hydroxycinnamic acid was chlorogenic acid, with values ranging from 14 to 32 mg kg^?1 fresh weight, followed by caffeic acid, while p‐coumaric and ferulic acids showed similar concentrations lower than 5 mg kg^?1. The highest content of lycopene was found in Ramillete, Pera and Durina (>50 mg kg^?1 fresh weight), while the concentration in the other varieties was between 50 and 30 mg kg^?1, with the exception of Liso (less than 20 mg kg^?1). The antioxidant activity of tomato extracts varied with the tomato variety and the assay method used. Individual compounds found to be significantly related to antioxidant capacity were lycopene and ferulic and caffeic acids, but not quercetin and chlorogenic acid. © 2002 Society of Chemical Industry