Evaluation of antioxidant activity of parsley (Petroselinum crispum) essential oil and identification of its antioxidant constituents

Antioxidant capacities of the essential oil extracted from parsley (Petroselinum crispum) were evaluated by three different in vitro assays: β-carotene bleaching assay, DPPH free radical scavenging assay and Fe²⁺-metal chelating assay. Results showed that the parsley oil (PO) possessed a certain degree of antioxidant activities in terms of β-carotene bleaching capacity and free radical scavenging activity, but its metal chelating capacity was negligible. The antioxidant EC₅₀ values of the β-carotene bleaching assay and DPPH free radical scavenging assay of the crude PO dissolved in methanol were measured in about 5.12 and 80.21 mg/mL, respectively. However, these values were much weaker than those of BHT in 0.01 and 0.58 mg/mL, and of α-tocopherol in 0.01 and 0.10 mg/mL. Isolation and identification of the inherent antioxidants in PO involved using various chromatographic techniques including silica gel open column chromatography, normal phase-HPLC and GC–MS. Myristicin in PO was found as a dominant compound (32.75%) that exhibited a moderate antioxidant activity. Apiol was the second dominant compound (17.54%), but it might be the major contributor to the antioxidant activity of PO. These results suggest that the PO and its two major components can be potential alternative natural antioxidants.     

Carotenoid content,its stability during drying and the antioxidant activity of commercial coriander (Coriandrum sativum L.) varieties

Although populations of several tropical countries are under severe vitamin-A deficiency, traditional sources of pro-vitamin-A carotenoids have not been exploited due to the lack of relevant research data. In this study, ten commercial varieties of coriander (Coriandrum sativum L.), grown at identical conditions, were evaluated for carotenoids, their bio-efficacy and stability during drying, with the main emphasis on β-carotene (vitamin-A precursor) analysis by HPLC-MS. In all varieties, β-carotene content was higher in foliage at mature stage, than in seedlings and seeds. Variety GS4 Multicut produced highest biomass (6.18 ± 0.73 g/plant), total carotenoids (217.50 ± 5.6 mg/100 g DW) and β-carotene (73.64 ± 0.3 mg/100 g DW) at pre-flowering stage. Carotenoids extract showed a high antioxidant activity with IC₅₀ value of 14.29 ± 1.68 μg/ml, scavenging hydroxyl radicals and rendering higher protection to DNA than by standard gallic acid (IC₅₀ = 357.21 ± 4.29). Microwave drying of foliage was rapid with better retention of pigments, high intactness of trans-β-carotene and higher extractability of pigments when compared with oven drying.     

Antioxidant activity of palm oil carotenes in organic solution: effects of structure and chemical reactivity

The antioxidant effectiveness of palm oil α-carotene and comparison with β-carotene in organic solution containing egg-yolk phosphatidycholine (EYPC) in the presence of lipid soluble 2,2¹-azobis (2,4-dimethyl valeronitrile) (AMVN)-generated peroxyl radicals was investigated by measuring the formation of phosphatidyl choline hydroperoxide (PCOOH) and thiobarbituricacid reacting substances (TBARS). Lutein and zeaxanthin (xanthophylls), similar to α and β carotenes, respectively, but differing in containing hydroxyl groups on the two rings (3,3¹-diol), were also included in the investigation. The carotenes were more rapidly oxidised than the xanthophylls in the solution. The initial rates of oxidation of the carotenoid tested were 0.39 μM min⁻¹ (α-carotene), 0.44 μM min⁻¹ (β-carotene), 0.30 μM min⁻¹ (lutein) and 0.33 μM min⁻¹ (zeaxanthin). Incubation of EYPC with AMVN at 37°C induced the accumulation of PCOOH at the linear rate of 1.8 μM min⁻¹. Although, all the carotenoids tested at 1 mol % relative to EYPC retarded (p < 0.05) the chain propagation reaction of PCOOH formation α-carotene had the highest activity but this was less than α-tocopherol. α-Tocopherol, α-carotene, β-carotene, lutein and zeaxanthin reduced PCOOH accumulation by 78, 65, 40, 60 and 43%, respectively. AMVN incubated with EYPC for 2 h induced the formation of TBARS compared to the control (p < 0.001). α-Carotene significantly suppressed the TBARS formation by 68% whilst β-carotene, lutein and zeaxanthin elicited 50, 64 and 53% reductions, respectively. α-Tocopherol retarded the TBARS formation by 80%. These results suggest that α-carotene, a carotenoid abundantly present in human diets, especially red palm oil, may better attenuate peroxyl radical-dependent lipid peroxidation than β-carotene in organic solution.     

The phenolic compounds and the antioxidant potential of infusion of herbs from the Brazilian Amazonian region

The consumption of tea increased significantly in the past few years as a result of its health benefits as potent antioxidants in the diet. However, studies on the antioxidant compounds from Brazilian tea are scarce. Thus, the aim of this work was to evaluate the total phenolic compounds (TPC) and total flavonoids (TF) contents and the antioxidant capacity (DPPH and β-carotene/linoleic acid system) of nine herb infusions from the Amazonian region, namely agirú (Chrysobalanus icaco), açoita-cavalo (Luehea speciosa), capim-santo (Cymbopogon citratus), erva-cidreira (Lippia alba), graviola (Annona muricata L.), jucá (Libidibia ferrea), pata-de-vaca (Bauhinia ungulata), parirí (Fridericia chica) and sacaca comum (Croton spp.). These herbs were chosen based on popular knowledge and consumption. C. ferrea (68.13 mg GAE/g), L. speciosa (47.54 mg GAE/g) and C. icaco (51.30 mg GAE/g) presented the highest TPC contents, while L. speciosa (12.85 mg CE/g) and L. alba (15.42 mg CE/g) showed the highest TF contents. The highest antioxidant capacity, using both assays, was shown by L. ferrea. The three herbs with the highest TPC contents were selected to be analyzed by high performance liquid chromatography (HPLC) coupled to a diode array detector (DAD). A commercial green tea (Camellia sinensis) was also analyzed as a reference. The main compounds tentatively identified were gallic acid (0.45 mg/g), myricetin (0.78 mg/g) and quercetin (0.14 mg/g) in C. icaco; (+)-catechin (1.20 mg/g) and quercetin (0.14 mg/g) in L. speciosa; gallic acid (0.59 mg/g) and quercetin (0.13 mg/g) in C. ferrea; and gallic acid (0.24 mg/g), (−)-epicatechin (2.44 mg/g), (+)-catechin (0.68 mg/g) and quercetin (0.66 mg/g) in green tea. Among the nine studied herbs, the importance of L. ferrea should be pointed out since it presented the highest TPC content and antioxidant capacity and its gallic acid content was much higher than that of green tea.     

Antioxidant properties and polyphenolics composition of common hedge hyssop (Gratiola officinalis L.)

The antioxidant potential of Gratiola officinalis was evaluated by the off-line and on-line HPLC/UV/DPPH radical scavenging assays, phytochemical composition was analyzed by LC/MS. On-line method was validated by using reference antioxidants and linear dependence was found between their concentration and radical scavenging peak area. Radical scavenging capacity (RSC) of methanol and acetone extracts expressed in their concentration required to scavenge 50% of DPPH^? was 0.10% and 0.13%, respectively; the RSC in ABTS^?+ assay was 1093 ± 104 and 746 ± 18 μM of trolox equivalents in 1 g, respectively. Good correlation was observed between total amount of phenolic compounds and RSC. Preliminary HPLC/UV/MS analysis revealed that the main compounds possessing antioxidant activity in the extracts might be phenylpropanoid glycosides; UPLC/UV/ESI-QTOF-MS analysis suggested 15 structures: 2,5-dihydroxy-p-benzenediacetic and caffeic acids, apigenin 6,8-di-C-β-d-glucopyranoside (vicenin-2), apigenin 8-C-α-l-arabinoside 6-C-β-d-glucoside, (shaftoside), forsythoside B, arenarioside, verbascoside (acteoside), amioside, quercetin-6-O-(2-O-acetyl-glucopyranosyl)-glucopyranoside, isoverbascoside, quercetin glucuronide, linariifolioside, methoxy luteolin-7-O-(6-O-acetyl-glucopyranosyl)-glucopyranoside, methoxy luteolin-glucuronide and luteolin glucuronide.     

Carotenoid composition of two Brazilian genotypes of acerola (Malpighia punicifolia L.) from two harvests

Acerola fruit is native to Central America and adapted very well to Brazil, which in turn became the major worldwide acerola producer, consumer and exporter. Two acerola genotypes were harvested from a Brazilian plantation during the 2003 and 2004 summer harvests. Both genotypes presented β-carotene (265.5–1669.4 μg/100 g), lutein (37.6–100.7 μg/100 g), β-cryptoxanthin (16.3–56.5 μg/100 g) and α-carotene (7.8–59.3 μg/100 g) as the major carotenoids. In both harvests, the β-carotene, β-cryptoxanthin and α-carotene levels were higher in the Olivier genotype, whereas the lutein content was higher in the Waldy Cati 30 genotype. Due to higher sunlight exposure, the fruits harvested in 2004 showed higher total carotenoid contents than those from the 2003 harvest. Acerola, especially the Olivier genotype, with 148–283 RE/100 g, can be considered as a good source of provitamin A.     

Phytosterols and tocopherols content of pulps and nuts of Brazilian fruits

Fruits and nuts from the North and Northeast regions of Brazil were collected to determine their phytosterol and tocopherol content. The species studied were Cotia nut (Aptandra spruceana M.), Brazil nut (Bertholletia excelsa H.B.K.), Mucajá (Couma rigida M.), Red Açaí (Euterpe oleracea M.), Inajá (Maximiliana maripa D.), Jenipapo (Genipa Americana L.), Buriti (Mauritia flexuosa L.) and Uxi (Endopleura uchi C.). Phytosterols were analyzed by GC–FID using β-cholestanol as an internal standard, while tocopherols were determined by RP-HPLC-DAD. The pulps of Mucajá (26–236 mg 100 g^–1), Inajá (119–285 mg 100 g^–1) and Jenipapo (216 mg 100 g^–1) showed the highest total phytosterol contents. Considering α-tocopherol equivalents, the pulps of Buriti (346.72 μg g^–1) and Uxi (200.92 μg g^–1) contained the highest vitamin E activity. Therefore, the results indicate that these fruits and nuts have great potential to be cultivated and marketed as alternative dietary sources for these bioactive compounds.     

Thermal and light stabilities and antioxidant activity of carotenoids from tomatoes extracted using an ultrasound-assisted completely solvent-free method

The use of petroleum-derived solvents, particularly volatile organic compounds (VOCs), in the chemical industry has increased the contamination and residual effects of these solvents. Ionic liquids (ILs) can potentially replace VOCs, thereby reducing the risks of environmental contamination and toxicity. In this context, the objectives of this study were as follows: 1 — to obtain an ionic liquid for use in extracting carotenoids from tomatoes with ultrasound assistance; and 2 — to determine the stability and antioxidant activity of tomato carotenoid extracts. Ultrasound can also efficiently extract carotenoid compounds with ionic liquids in comparison with conventional VOC solvents (obtained from an all-trans-lycopene 7.5–8.0 μg·g^− 1 tomato sample by IL and 6.2–7.7 μg·g^− 1 by acetone). Similarly, the activation energies (E_a) in aqueous medium were obtained for the IL carotenoid extract (10.8 kJ·mol^− 1) and acetone carotenoid extract (9.4 kJ·mol^− 1). The antioxidant activities of the tomato carotenoid extract were 7.4 and 12.4 relative to α-tocopherol for the ionic liquid extract and acetone extract, respectively. The combination of chromatographic analysis and degradation kinetics provided data for positive assessment similarity of thermal and light stabilities of tomato carotenoids extracted by IL and extracted by acetone.     

Phenolic profile and antioxidant properties of a crude extract obtained from a brewery waste stream

The main aims of this study were to determine the phenolic profile of a crude extract obtained (at pilot scale) from a brewery waste stream and to evaluate the antioxidant activity of the extract. The total phenolic content was determined by the Folin–Ciocalteu assay, which revealed that 50% of the extract comprised phenolic compounds. The polyphenols, identified and quantified by RP-HPLC–DAD and HPLC-ESI–TOF-MS, were mainly flavonoids (catechin, epicatechin, gallocatechin, epigallocatechin, quercetin) and phenolic acids (ferulic acid, p-coumaric acid, caffeic acid, protocatechuic acid). The crude extract displayed a high DPPH radical scavenging activity (0.18 g/L), similar to that of BHA (0.248 g/L) and higher than that of BHT (2.54 g/L). All three tested products displayed a similar ability to decrease oxidative bleaching of β-carotene (antioxidant activity coefficient of 623.8 for the crude extract, 653.3 for BHA, 559.6 for BHT). This type of brewery waste stream may be a promising source of natural antioxidants to replace the synthetic antioxidants currently used in the food industry.     

Antimicrobial agent detection in ewes’ milk by the microbial inhibitor test brilliant black reduction test—BRT AiM®

The detection limits of 24 antimicrobial agents were determined in ewes’ milk by one commercially available version of brilliant black reduction test, BRT Inhibitor Test with prediffusion AiM^® (BRT AiM^®). For each drug, eight concentrations were tested on 20 milk samples from individual ewes. The detection limits of the BRT AIM^® method were determined by means of logistic regression models: 6 μg kg⁻¹ amoxycillin, 6 μg kg⁻¹ ampicillin, 51 μg kg⁻¹ cloxacillin, 2 μg kg⁻¹ penicillin “G”, 230 μg kg⁻¹ cefadroxil, 1330 μg kg⁻¹ cephalosporin “C”; 270 μg kg⁻¹ cephalexin, 92 μg kg⁻¹ cefoperazone, 120 μg kg⁻¹ ceftiofur, 69 μg kg⁻¹ cefuroxime, 6000 μg kg⁻¹ streptomycin, 1200 μg kg⁻¹ gentamycin, 3700 μg kg⁻¹ neomycin, 630 μg kg⁻¹ erythromycin, 120 μg kg⁻¹ tylosin, 390 μg kg⁻¹ doxycycline, 5500 μg kg⁻¹ oxytetracycline, 6200 μg kg⁻¹ tetracycline, 5400 μg kg⁻¹ sulfadiazine, 3200 μg kg⁻¹ sulfamethoxazole, 6500 μg kg⁻¹ sulfamethoxypyridazine, 6200 μg kg⁻¹ sulfaquinoxaline, 22000 μg kg⁻¹ chloramphenicol and 4100 μg kg⁻¹ trimethoprim. The BRT AiM^® method presents detection limits for β-lactam antibiotics that are similar to those obtained as Maximum Residue Limits (MRLs) according to Regulation 2377/90 EEC as set out by the European Union. However, for other antimicrobial agents the estimated limits were higher than those of the EU-MRLs. It is therefore advisable to enhance the sensitivity of the method for the detection of the different antimicrobial groups or to develop a combined system of different microbiological inhibitor tests that would enable the detection of a greater number of antimicrobial agents.     

Cyanidin-3-glucoside,nutritionally important constituents and in vitro antioxidant activities of Santalum album L. berries

Anthocyanins are ubiquitous plant pigments. They are hydrophilic, and have high tinctorial value hence, used as natural food colorant. The main aim of this study was characterization of Santalum album L. berries for its pigment content, nutritionally important phytoconstituents and functional attributes. Major pigment identified was cyanidin-3-glucoside (0.21% FW) as confirmed by spectral characteristics including LC–MS. Nutrients such as total carbohydrates (8.5), proteins (5.8), free amino acids (0.8 g), oil (1.5 g), ascorbic acid (1.5 μg), tocopherols (0.3 mg) and niacin (5.2 mg) per 100 g berries were determined along with total soluble solids (13.4°Brix) and phenols (3.1 mg GAE/g). Reducing power and DPPH· scavenging assays showed highest activity in methanol extract, which also efficiently protected bleaching of β-carotene (EC₅₀ 285 μg/mL) in β-carotene–linoleate model. Pigment rich crude extract was not toxic to HepG2 cells during 24 h exposure, whereas cyanidin-3-glucoside was cytotoxic (IC₅₀ 0.1 μg/mL).     

Quinone reductase inducing and antioxidant activities of aqueous isolates of green bean (Phaseolus vulgaris L.)

Aqueous extracts of green bean (Phaseolus vulgaris L.) were examined for antioxidant functions in terms of total reducing power (TRP), peroxyl radical quenching (PRAC), total antioxidant activity (TAA), and the ability to induce quinone reductase (QR) as a biomarker for phase II detoxification enzymes in Murine hepatoma (Hepa) cells. In terms of Trolox equivalents (TE), crude aqueous extracts exhibited 71 μmol TE/g dry weight (gdw) for TRP, 29 μmol TE/gdw for PRAC, and 8.5 μmol TE/gdw for TAA. Aqueous extractable QR-inducing activity was fractionated by Sephadex LH-20 chromatography with several resulting fractions capable of doubling QR specific activity in the Hepa bioassay. Of 10 recovered fractions, the first and most polar fraction doubled QR at a level of 39 μg/ml (CD value), while the ninth fraction exhibited a similar CD value of 35 μg/ml. Semi-preparative LC and UV spectral analysis of fraction 9 indicated the presence of quercetin and kaempferol glycosides, and simple phenolics among the enriched QR-inducing isolates.     

Determination of antioxidant activity and antioxidant content in tomato varieties and evaluation of mutual interactions between antioxidants

Major antioxidants and antioxidant activity in eight varieties of tomatoes were determined. Hydrophilic and lipophilic antioxidant activity (HAA and LAA) was determined by the ABTS assay and ascorbic acid and carotenoid contents were determined by HPLC-DAD. The HAA has far more significant impact on total antioxidant activity (83%) as compared with LAA. HAA was increasing during all ripening stages and was strongly correlated with ascorbic acid content (r = 0.83). During the ripening the LAA was increasing till the III. stage of maturity and then decreased. The main carotenoids determined in the red-fruit tomatoes were lycopene, β-carotene and lutein. The content of lycopene has been increasing equally during the ripening. β-Carotene and lutein were intensively synthesized between the I. and II. stage of maturity. Among ascorbic acid, α-tocopherol, lycopene, β-carotene and lutein standards ascorbic acid was determined as the most efficient antioxidant followed by α-tocopherol and β-carotene. Antioxidant activity of ascorbic acid, α-tocopherol, β-carotene and lutein grew equally with increasing concentration, however lycopene was the most effective in its lowest concentration. The analysis of two-component mixtures showed significant synergism between lycopene-lutein, lycopene-β-carotene and α-tocopherol-β-carotene.     

Determination of thermal oxidation and oxidation products of β-carotene in corn oil triacylglycerols

A reversed phase HPLC-DAD coupled to APCI-MS method is reported for the determination of the degradation of β-carotene and characterization of the oxidation products in corn oil. Corn oil containing β-carotene was oxidized in the Rancimat at 110 °C from 1 to 14 h. A significant degradation of β-carotene was observed in corn oil during accelerated thermal oxidation. A total of eight different oxidized products of β-carotene were identified, which includes 8′-apo-β-carotenal, 6′-apo-β-carotenal, 5,6-epoxy-8′-apo-β-carotenal, β-carotene-2,2′-dione, 13-Z-5,6,5′,6′-diepoxy-β-carotene, all-E-5,8-epoxy-β-carotene, all-E-5,6-epoxy-β-carotene, and 15-Z-5,6-epoxy-β-carotene. Corn oil triacylglycerols (TAGs) oxidation products were also identified using isocratic HPLC–ESI-MS. It was found that β-carotene promoted oxidation of TAGs especially at longer exposure times. For the first time two new classes of oxidized TAGs have been identified in corn oil, which were epidioxy bis-hydroperoxides and hydroxy bis-hydroperoxides. Other oxidation products of TAGs were mono-epoxides, mono-hydroperoxides, and epoxy hydroperoxides. It was found that complementing the HPLC-DAD method for β-carotene with ESI-MS method for TAGs oxidation provides a comprehensive set of analytical tools to characterize carotenoids and triacylglycerols oxidation and degradation in edible oils.     

Simultaneous determination of anthocyanins,coumarins and phenolic acids in fruits,kernels and liqueur of Prunus mahaleb L

In the fresh tissues of Prunus mahaleb L., three classes of phenolics were characterised: phenolic acid derivatives (main compound being o-coumaric acid glucoside), quercetin glycosides, and anthocyanins (cyanidin 3,5-diglucoside, cyanidin 3-sambubioside, cyanidin 3-xylosyl-rutinoside and cyanidin 3-rutinoside). Coumarin was also identified. The kernels showed a high content of coumarin (0.87 mg g^?1) which is the main class of metabolites in this sample, but present in pitted berries as well (0.63 mg g^?1). Flavonoids are mainly concentrated in the skin and pulp (0.55 mg g^?1). In ‘Mirinello di Torremaggiore’ liqueur, produced from P. mahaleb L. in accordance with traditional procedures, anthocyanins make up 16.5%, phenolic acids 43.3%, coumarin 36.2% and flavonoids 4% of total compounds. Anthocyanins are the main class in solid residues from liqueur production (70%). These findings point out that solid residues of P. mahaleb can be considered an interesting and innovative source of appreciable amounts of cyanidin glycosides (3.3 mg g^?1).     

Optimization of the associative growth of novel yoghurt cultures in the production of biomass, β-galactosidase and lactic acid using response surface methodology

The associative growth of Streptococcus thermophilus 95/2 (St 95/2) and Lactobacillus delbrueckii ssp. bulgaricus 77 (Lb 77) isolated from the Toros mountain region of Turkey was investigated with respect to lactic acid, biomass and β-galactosidase enzyme production using response surface methodology (RSM). The ratio (St 95/2:Lb 77) of the strains and media formulation had significant effect on all responses (p < 0.001). The predicted enzyme activity (2.14 U mL^?1), lactic acid (22.50 g L^?1) and biomass (7.11 g L^?1) production at optimum conditions were very close to the actual experimental values (2.14 U mL^?1, 22.94 g L^?1 and 7.86 g L^?1, respectively). The optimum conditions were to use these cultures in a ratio of 1.66:1.62 (St 95/2:Lb 77) in a medium containing whey (5%), corn steep liquor (4%), potassium phosphate (2%) and peptone (2%) at 43 °C for 8 h. The associative growth provided 6.4% and 39% more β-galactosidase activity and 8.73% and 44% more lactic acid compared with the results obtained using pure St 95/2 and Lb 77 strains, respectively.     

Bioactive substance contents and antioxidant capacity of raw and blanched vegetables

Five commonly consumed vegetables in Malaysia namely, four-angled bean (Psophocarpus tetragonolobus D.C.), French bean (Phaseolus vulgaris L.), long bean (Vigna sesquipedalis L.), snow pea (Pisum sativum var. macrocarpon L.) and snap pea (Pisum sativum) were blanched in boiling water for 10 min. The contents of total phenolics, ascorbic acid and β-carotene, and the antioxidant capacity as typified by β-carotene and free radical scavenging activity (DPPH) assays were determined for the raw and blanched vegetables. The study revealed that blanching caused a significant (p < 0.05) increase in β-carotene content [fresh (389–539 µg/100 g), blanched (510–818 µg/100 g)], except in snow pea. Conversely, there was a significant (p < 0.05) decrease in ascorbic acid content [fresh (1.2–7.8 mg/100 g), blanched (0.67–3.8 mg/100 g)]. After blanching, the total phenolic content and antioxidant activity either decreased or increased depending on the type of vegetables. The total phenolic content was positively correlated with the antioxidant activity of the studied vegetables to some extent, but not with ascorbic acid or β-carotene.Industrial relevanceBeans (four-angled bean, French bean and long bean), and peas (snow and snap pea) are commonly consumed vegetables in Malaysia. However, the scientific information regarding blanching and its effect on the total phenolic content and antioxidant activities is very limited. This work showed that blanching caused an increase in the carotene, total phenolic content and antioxidant activities in some of the selected vegetables. This work is important since, consumption of raw vegetables does not have high nutritional qualities and antioxidant activities as shown in this work.     

Ultrasonic cutting of cheese: Composition affects cutting work reduction and energy demand

Eight cheese varieties with different moisture (357–488 g kg^?1), fat (183–335 g kg^?1) and protein content (202–292 g kg^?1) were subjected to ultrasonic cutting using a 40 kHz guillotine sonotrode. Cutting force curves were evaluated with respect to ultrasound-induced cutting work reduction and energy demand of the sonotrode. With cutting velocity and ultrasonic amplitude set to 2500 mm min^?1 and 12 μm, respectively, composition had a significant effect on the response of the cheeses. Whereas cutting work reduction was mainly determined by fat-in-dry matter, the energy demanded by the sonotrode to maintain vibration was inversely interrelated to the ratio of moisture to solids-non-fat. Three selected cheeses were subjected to cutting experiments with systematically varied cutting velocity and amplitude. The results indicate that the cheeses respond differently to the cutting parameters, and that their careful adjustment is helpful for a target-orientated design of the process.     

Effects of Osmotic Dewatering and Oven Drying on β-Carotene Content of Sliced Light Yellow-Fleshed Sweet Potato (Ipomea batatas L.)

The effects of pre-treatment in osmotic salt solution followed by oven-drying on the moisture removal, and β-carotene content of yellow-fleshed sweet potato were investigated. Potato rings of 3 cm diameter and thicknesses of 2 mm, 3 mm and 4 mm were soaked in NaCI solutions of 10, 15, 20, 25 and 30% w/v, for varying time of 20, 40, 60, 80 and 100 minutes. The pre-treated slices were then oven-dried in a convective oven at 60 °C. Moisture diffusivity was determined by the method of slopes, while β-carotene was measured by UV/VIS- spectrophotometer. Moisture diffusivity values during drying were between 3.648 × 10^− 7 m²/s and 1.459 × 10^− 6 m²/s, while losses in β- carotene ranged from 47 to 86%. The amount of water removed by pre-treatment with NaCl solution decreased significantly as the concentration and the time soaking increased, however, the water out flow was found to increase significantly with increase in thickness of the samples, where the 4 mm size had the highest (1.535 g H₂O/g sample) and 2 mm the least (1.434 g H₂O/g sample) Osmotic pre-treatment in salt solution had no effect on β-carotene, but subsequent oven-drying however degraded the β-carotene.     

Elimination of aggregates of (1→3) (1→4)-β-D-glucan in dilute solutions for light scattering and size exclusion chromatography study

Methods for eliminating aggregates of cereal (1→3) (1→4)-β-D-glucan in dilute solutions were investigated using dynamic light scattering and size exclusion chromatography. Wheat β-D-glucan samples were selected and dissolved in various solvents under different preparation conditions. The molecular size distribution was monitored by dynamic light scattering measurement. In most of the solutions, there were two well separated species of different average sizes. It appeared that the specie with smaller average size represented the un-aggregated molecules (unimers) and the specie with larger particle size corresponded to the aggregates. The results showed that heat treatment, filtration, ultrasonication, and the use of urea solution (up to 6 M) could not eliminate aggregates completely. However, the percentage of aggregates in aqueous NaOH solution decreased significantly with the increase of NaOH concentration. In 0.5 M NaOH solution, no aggregation was detectable by dynamic light scattering measurement. Both dynamic light scattering and HPSEC data showed that wheat β-D-glucan was stable in 0.5 M NaOH solution without any noticeable degradation when stored at 25 °C for 12 h. The results of present study suggested that 0.5 M NaOH solution is a suitable solvent for cereal β-D-glucans. Using this solvent, the molecular characteristics of wheat β-D-glucan was studied by both dynamic and static light scattering. The weight average molecular weight (M_w), radius of gyration (R_g), hydrodynamic radius (R_h), and the second virial coefficient (A₂) were obtained with the values of 3.29×10⁵ g/mol, 45.6 nm, 26.2 nm, and 1.04×10⁻³ cm³ mol/g² respectively. This study also confirmed that wheat β-glucan in solution exhibited a random coil conformation.