Application of an ultrasound field in chemical cleaning of ceramic tubular membrane fouled with whey proteins

Chemical cleaning of a severe in-pore-fouling may be improved by applying an ultrasound (US) field in a cleaning-in-place (CIP) system, under both the batch and flow conditions. This study is concerned with the cleaning of a 200-nm ceramic membrane, fouled with whey proteins, in an US field of relatively low frequency of 35 kHz, without applying a transmembrane pressure (TMP) and cross-flow velocity. Two types of cleaning agent solutions of different concentrations were applied: alkali (NaOH) and a mixture of commercial detergents (P3-Ultrasil 67 and 69) at a sonication time of 30 min. It was found that the application of US was less effective in the combination with sodium hydroxide than with the mixture of commercial detergents. Using US in a mixture of 0.25% w/w P3-Ultrasil 67 and 0.4% w/w P3-Ultrasil 69 resulted in the highest flux recovery of 86.5 ± 2.9%, after 30 min of sonication, and produced an overall efficiency of 96.3 ± 0.4%, after the second sonication. It was concluded that the application of the US field in a batch mode, combined with the mentioned chemical agents, can significantly improve the cleaning efficiency.     

An experimental investigation into the pre-treatment of synthetic membranes using sodium hydroxide solutions

In this paper the effect of two pre-treatment methods are compared experimentally for the filtration of (i) a spent sulphite liquor (17.8 wt.% dry solids) using a 20 kg mol⁻¹ molar mass cut off (MMCO) fluoropolymer membrane and (ii) a molasses solution (45° Brix) using a polysulphone (Psf) membrane (1.5 μm pore size). Both feeds are industrially relevant, and subject to severe fouling issues when membranes are used in their subsequent processing. The pre-treatment methods evaluated were: (i) conditioning with water at 60 °C only [Protocol 1], and (ii) conditioning with water at 60 °C followed by cleaning with 0.5 wt.% NaOH [Protocol 2]. Results are presented that confirm the benefits of sodium hydroxide preconditioning upon performance, supporting the suggestion by some membrane manufacturers that this step be included as part of the pre-treatment protocol.     

Chicory juice clarification by membrane filtration using rotating disk module

Clarification is the first step of inulin production from chicory juice, and membrane filtration as an alternative can greatly simplify this process, increase juice yield, improve product quality, and reduce the cost and waste volume. In this study, a rotating disk module (RDM) was used to investigate the clarification of chicory juice by four micro- and ultrafiltration membranes. Compared with dead end filtration, the RDM had a much higher permeate flux and product quality. High rotating speeds produced high permeate fluxes and reduced flux decline, because of the strong back transport of foulant from fouling layer to feed solution. At high rotating speeds of 1500–2000 rpm, the permeate flux increased with membrane pore size and transmembrane pressure (TMP), while at low rotating speeds (<1000 rpm), permeate flux was independent of membrane type and TMP due to a thick deposited fouling layer as a dominant filtration resistance, while carbohydrate transmission decreased at higher TMP because of denser cake layer as an additional selective membrane. The highest carbohydrate transmission (∼98%) and desirable permeate turbidity (2.4 NTU) was obtained at a TMP of 75 kPa and a rotating speed of 2000 rpm for FSM0.45PP membrane. With the RDM, the Volume Reduction Ratio (VRR) could reach 10 with a high permeate flux (106 L m⁻² h⁻¹) in the concentration test, and permeate was still rich in carbohydrate and well clarified. Chemical cleaning with 0.5% P3-ultrasil 10 detergent solution was able to recover 90% water flux of fouled membrane.     

Effects of particle size and its distribution on specific cake resistance during rice wine microfiltration

The effects of particle size and its distribution on permeate flux and specific cake resistance (α) of rice wine suspensions were determined. Specific cake resistance decreased as the ratio of particles having size larger than 45 μm increased. For rice wine suspensions with particle sizes in the range of 1-20 μm (mean diameter of 5-6 μm), α increased linearly with total suspended solids concentration. The dependence of α on total suspended solids concentration was minimal when particles with size greater than 20 μm were present. Specific cake resistance was independent of total suspended solids concentration when rice wine suspensions contained greater than 50% by weight of particles having size larger than 45 μm.     

Effect of membrane property and operating conditions on phytochemical properties and permeate flux during clarification of pineapple juice

The effects of membrane property on the permeate flux, membrane fouling and quality of clarified pineapple juice were studied. Both microfiltration (membrane pore size of 0.1 and 0.2 μm) and ultrafiltration (membrane molecular weight cut-off (MWCO) of 30 and 100 kDa) membranes were employed. Membrane filtration did not have significant effects on the pH, reducing sugar and acidity of clarified juice whereas the suspended solids and microorganism were completely removed. The 0.2 μm membrane gave the highest permeate flux, total vitamin C content, total phenolic content and antioxidant capacity as well as the highest value of irreversible fouling. Based on these results, the membrane with pore size of 0.2 μm was considered to be the most suitable membrane for the clarification of pineapple juice. The optimum operating conditions for the clarification pineapple juice by membrane filtration was a cross-flow velocity of 3.4 ms⁻¹ and transmembrane pressure (TMP) of 0.7 bar. An average flux of about 37 lm⁻² h⁻¹ was obtained during the microfiltration of pineapple juice under the optimum conditions using batch concentration mode.     

Antioxidant activity of sugarcane molasses against 2,2′-azobis(2-amidinopropane) dihydrochloride-induced peroxyl radicals

Sugarcane molasses is a rich source of antioxidant materials with peroxyl radical scavenging effects. To explore the potent antioxidant activity of sugarcane molasses against 2,2′-azobis(2-amidinopropane) dihydrochloride (AAPH)-induced peroxyl radicals, 7 methanolic fractions of sugarcane molasses (F1–F7) were separated via bioassay-guided fractionation and evaluated by oxygen radical absorbance capacity (ORAC), cellular antioxidant activity (CAA), and oxidative DNA damage protective activity assays. The ORAC values of sugarcane molasses fractions ranged from 4399 to 6266 μmol TE/g, whilst the EC₅₀ values for CAA ranged from 3.7 to 5.9 μg/ml. Moreover, it was found that sugarcane molasses fractions, particularly F6 and F7, could protect against oxidative DNA damage caused by peroxyl radicals at an effective concentration of 100 μg/ml. Ten phenolic constituents were identified in the fractions, including known antioxidative compounds, viz., schaftoside, isoschaftoside, ferulic acid, p-coumaric acid, and p-hydroxybenzaldehyde.     

Efficiency of serum protein removal from skim milk with ceramic and polymeric membranes at 50°C

Raw milk (2,710 kg) was separated at 4°C, the skim milk was pasteurized (72°C, 16 s), split into 3 batches, and microfiltered using pilot-scale ceramic uniform transmembrane pressure (UTP; Membralox model EP1940GL0.1μA, 0.1 μm alumina, Pall Corp., East Hills, NY), ceramic graded permeability (GP; Membralox model EP1940GL0.1μAGP1020, 0.1 μm alumina, Pall Corp.), and polymeric spiral-wound (SW; model FG7838-OS0x-S, 0.3 μm polyvinylidene fluoride, Parker-Hannifin, Process Advanced Filtration Division, Tell City, IN) membranes. There were differences in flux among ceramic UTP, ceramic GP, and polymeric SW microfiltration membranes (54.08, 71.79, and 16.21 kg/m² per hour, respectively) when processing skim milk at 50°C in a continuous bleed-and-feed 3× process. These differences in flux among the membranes would influence the amount of membrane surface area required to process a given volume of milk in a given time. Further work is needed to determine if these differences in flux are maintained over longer processing times. The true protein contents of the microfiltration permeates from UTP and GP membranes were higher than from SW membranes (0.57, 0.56, and 0.38%, respectively). Sodium-dodecyl-sulfate-PAGE gels for permeates revealed a higher casein proportion in GP and SW permeate than in UTP permeate, with the highest passage of casein through the GP membrane under the operational conditions used in this study. The slight cloudiness of the permeates produced using the GP and SW systems may have been due to the presence of a small amount of casein, which may present an obstacle in their use in applications when clarity is an important functional characteristic. More β-lactoglobulin passed through the ceramic membranes than through the polymeric membrane. The efficiency of removal of serum proteins in a continuous bleed-and-feed 3× process at 50°C was 64.40% for UTP, 61.04% for GP, and 38.62% for SW microfiltration membranes. The SW polymeric membranes had a much higher rejection of serum proteins than did the ceramic membranes, consistent with the sodium-dodecyl-sulfate PAGE data. Multiple stages and diafiltration would be required to produce a 60 to 65% serum protein reduced micellar casein concentrate with SW membranes, whereas only one stage would be needed for the ceramic membranes used in this study.     

A physicochemical investigation of membrane fouling in cold microfiltration of skim milk

The main challenge in microfiltration (MF) is membrane fouling, which leads to a significant decline in permeate flux and a change in membrane selectivity over time. This work aims to elucidate the mechanisms of membrane fouling in cold MF of skim milk by identifying and quantifying the proteins and minerals involved in external and internal membrane fouling. Microfiltration was conducted using a 1.4-μm ceramic membrane, at a temperature of 6 ± 1°C, cross-flow velocity of 6 m/s, and transmembrane pressure of 159 kPa, for 90 min. Internal and external foulants were extracted from a ceramic membrane both after a brief contact between the membrane and skim milk, to evaluate instantaneous adsorption of foulants, and after MF. Four foulant streams were collected: weakly attached external foulants, weakly attached internal foulants, strongly attached external foulants, and strongly attached internal foulants. Liquid chromatography coupled with tandem mass spectrometry analysis showed that all major milk proteins were present in all foulant streams. Proteins did appear to be the major cause of membrane fouling. Proteomics analysis of the foulants indicated elevated levels of serum proteins as compared with milk in the foulant fractions collected from the adsorption study. Caseins were preferentially introduced into the fouling layer during MF, when transmembrane pressure was applied, as confirmed both by proteomics and mineral analyses. The knowledge generated in this study advances the understanding of fouling mechanisms in cold MF of skim milk and can be used to identify solutions for minimizing membrane fouling and increasing the efficiency of milk MF.     

Physical properties and sensory evaluation of WPI films of varying thickness

The effect of varying thickness on the water barrier properties, tensile properties and sensory characteristics of glycerol-plasticised whey protein isolate (WPI) films was investigated. Thickness was varied by preparing films with increasingly dilute film forming WPI solutions in the range 9.5-2.3 g protein/100 g. All films had a glycerol to protein ratio of 0.37 (Gly: Pro). Tensile strength (TS), elastic modulus (EM) and film permeance were unaffected by film thickness but maximum load (ML) and % elongation (E) decreased (P<0.05) with decreasing thickness. In a sensory test with crackers and melted cheese, panelists could readily detect the thickest films (79 μm) but not the thinnest films (23 μm) (P<0.05). The results indicate that reducing the thickness of glycerol plasticised WPI films makes them less perceptible in a food system while maintaining moisture barrier and certain tensile properties.     

Mate (Ilex paraguariensis St. Hilaire) saponins induce caspase-3-dependent apoptosis in human colon cancer cells in vitro

Saponins are naturally occurring metabolites associated with several health benefits. The objective was to quantify and purify saponins from mate dry leaves, and to assess their anti inflammatory and apoptotic mechanisms in human colon cancer cells in vitro. Matesaponins were extracted with methanol from dry leaves, partially purified and quantified. Leaves contained 10–15 mg/g dry weight total saponins, predominantly matesaponins 1 and 2. HPLC and LC/ESI-MS-MS identified saponins in six preparative chromatographic fractions (A, B, C, D, E, and F). Major matesaponins were identified as 1 [M–H]⁻ = 911 and 2 [M–H]⁻ = 1057, with trace amounts of 3 [M–H]⁻ = 1073, 4 [M–H]⁻ = 1219, and 5 [M–H]⁻ = 1383. Fractions D, E, and F significantly inhibited iNOS (IC₃₅ = 36.3, 29.5, 43.7 μM), PGE₂ (IC₃₅ = 23.1, 22.3, 11.7 μM) and COX-2 (IC₃₅ = 45.7, 32.4, 17.0 μM). Fraction F reduced nuclear translocation of nuclear factor-κB subunits p50 (49.8%) and p65 (49.0%) and induced apoptosis through suppression of Bcl-2 and increased Bax protein expressions and activated caspase-3 activity. Saponins in leaves of mate prevent inflammation and colon cancer in vitro.     

The microstructure of almond (Prunus dulcis (Mill.) D.A.Webb cv. ‘Nonpareil’) cotyledon

Microstructure of almond (Prunus dulcis (Mill.) D.A. Webb cv. ‘Nonpareil’) cotyledon was observed with light, scanning and transmission electron microscopy. The objective of this study was to characterise almond cotyledon surfaces as well as to describe internal and subcellular organisation. The testa has an outer epidermis, which consists of relatively large thin-walled cells, which range from 100 to 300 μm in width. The major portion of the testa consists of approximately 14-20 layers of flattened parenchymal cells with the total thickness of the layers ranging from 80 to 120 μm. The remainder of the testa was comprised of a small amount of vascular tissue. The embryo consisted primarily of parenchymal tissue with relatively thin cell walls (1-3 μm in thickness) and a small amount of provascular tissue. Protein bodies up to 12 μm in width and spaces once occupied by lipid bodies up to 3 μm in width were present in all cells of the embryo.     

Physiochemical, antioxidant and whitening properties of extract from root cortices of mulberry as affected by membrane process

Extract from root cortices of mulberry (Morus alba, L.) was separated into permeate and retentate fractions using a membrane system equipped with either a microfiltration membrane or one of four molecular weight cut-off ultrafiltration membranes. The effects of membrane process at volume concentration ratio (VCR)=4 on the physiochemical characteristics, the contents of active compounds, antioxidant ability, and whitening capability (tyrosinase inhibitory activity) in permeate and retentate were evaluated. The clarification degree, antioxidant effects, and whitening capability of the permeates increased as compared to those of feed. In addition, permeate treated with a 0.45 μm microfiltration membrane exhibited less fouling layer and specific resistance (αpC_B=622.8 m⁻²×10⁻⁶) and thus had a higher permeate flux than treated with other ultrafiltration membranes (αpC_B=786.1-1025.3 m⁻²×10⁻⁶). A higher content of active compounds, such as chlorogenoic acid and p-hydroxybenzoic acid may explain higher antioxidant and whitening capabilities in permeate of extracts from root cortices of mulberry.     

The relationship of Central Corneal Thickness (CCT) to Thinnest Central Cornea (TCC) in healthy adults

Purpose

The aim of the study was to precisely quantify the relationship between the central corneal points, namely the pupillary centre and the thinnest point in the central cornea, in terms of their thickness and location in healthy adults.

Methods

120 eyes of 60 healthy adult volunteers underwent pachymetry with a Scheimpflug imaging system (Pentacam). The thickness at the pupillary centre (Central Corneal Thickness, CCT) and the thickness at the Thinnest Central Corneal (TCC) point were measured. One eye of each patient was used to analyse the mean difference between CCT and TCC. Unpaired t-test (one tailed) was used to test significance and 95% confidence limits were used. The precise location of the TCC in relation to the corneal apex was measured using vector algebraic and trigonometric calculations.

Results

The mean CCT was 520 ± 33 μm and the TCC was 515 ± 36 μm. The difference between CCT and TCC was found to be 5.57 μm (0-15.9 μm, 95% CI; P = 0.1909). The TCC location was inferotemporal to the corneal apex in 58/60 (96.7%) of the right eyes and in 49/60 (81.7%) of the left eyes. The average vector location of TCC of both eyes was inferotemporal. This coordinate was found to lie 0.62 mm (right eye) and 0.79 mm (left eye) from the corneal apex subtending and angle of 45.5° (right eye) and −10.9° (left eye) from the horizontal.

Conclusion

The study has identified the parameters of TCC and its relationship to CCT in terms of the location and thickness. For clinical usage, they can be interchangeable as there is no significant difference between the two. The consistency in the (inferotemporal) location of the TCC merits further research in this regard to the development of corneal ectasia.     

Dietary molasses increases ruminal pH and enhances ruminal biohydrogenation during milk fat depression

Feeding high-concentrate diets has the potential to cause milk fat depression, but several studies have suggested that dietary sugar can increase milk fat yield. Two experiments were conducted to evaluate the ability of dietary molasses to prevent milk fat depression in the presence of a 65% concentrate diet. In trial 1, molasses replaced corn grain at 0, 2.5, or 5% of diet dry matter in diets fed to 12 second-lactation Holstein cows (134 ± 37 d in milk) in a 3 × 3 Latin square design. Trial 1 demonstrated that replacing up to 5% of dietary dry matter from corn with molasses had positive effects on de novo fatty acid synthesis, increasing the yield of short- and medium-chain fatty acids during diet-induced milk fat depression. Increasing inclusion rate of molasses increased milk fat concentration, but decreased milk yield and milk protein yield. Trial 2 used 7 ruminally cannulated, multiparous, late-lactation Holstein cows (220 ± 18 d in milk) to evaluate effects of dietary molasses on ruminal parameters and milk composition, and also to assess whether increased metabolizable protein supply would alter these responses. Cows were randomly assigned to a dietary treatment sequence in a crossover split plot design with 0 and 5% molasses diets. Dietary treatments were fed for 28 d, with 16 d for diet adaptation, and the final 12 d for 2 abomasal infusion periods in a crossover arrangement. Abomasal infusions of water or AA (5 g of l-Met/d + 15 g of l-Lys-HCl/d + 5 g of l-His-HCl-H₂O/d) were administered 3 times daily for 5 d, with 2 d between infusion periods. Administration of AA had no effect on concentration or yield of any milk components. Addition of molasses increased milk fat concentration (2.71 vs. 2.94 ± 0.21%), but had no effect on yields of milk fat or protein. Dietary molasses decreased total volatile fatty acid concentration (141 vs. 133 ± 4.6 mM), decreased the molar proportion of propionate, and increased the molar proportion of butyrate in ruminal fluid. Molasses also increased ruminal pH (5.73 vs. 5.87 ± 0.06), decreased the yield of trans-10 C18:1, and increased the yield of trans-11 C18:1 in milk fat. These data provide evidence that molasses may promote mammary de novo fatty acid synthesis in cows fed high-energy rations by moderating ruminal pH and altering ruminal fatty acid biohydrogenation pathways.     

Microwave-assisted extraction and determination of dicyandiamide residue in infant formula samples by liquid chromatography-tandem mass spectrometry

A simple, precise, accurate, and validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the determination of dicyandiamide residue in infant formula samples. Following microwave-assisted extraction with 5% formic acid and clean-up on a Sep-Pak AC-2 SPE cartridge, samples were separated on a ZIC-HILIC HPLC column (150 × 2.1 mm i.d., 5-µm film thickness; Merck KGaA, Darmstadt, Germany) with 20 mM ammonium acetate solution-acetonitrile as mobile phase at a flow rate of 0.25 mL/min. A linear calibration curve was obtained in the concentration range from 1.0 to 50 ng/mL. Infant formula samples were fortified with dicyandiamide at 3 levels, producing average recovery yields of 83.6 to 95.7%. The limits of detection and quantification of dicyandiamide were 3 and 10 μg/kg, respectively. Due to its simplicity and accuracy, the straightforward method is particularly suitable for routine dicyandiamide detection.     

Upgrading of discarded oranges through fermentation using kefir in food industry

Upgrading of orange pulp suspension by enrichment with kefir was investigated and the effects of initial sugar concentration, pH, aeration and the addition of molasses on kefir growth were monitored. Higher maximum growth rate μ_max for kefir was observed when initial sugar used was 75 g/l. Both 75 g/l and 90 g/l initial sugar contents of kefir resulted in higher final biomass concentration and daily biomass productivity. At an initial sugar concentration >75 g/l, however, high residual sugar and ethanol concentrations were observed. Air flow rate and pH affected kefir’s μ_max, while the addition of molasses had no effect on growth. Potential application of upgraded orange pulp in bread-making was examined. Bread produced by immobilized kefir on orange pulp had an improved aromatic profile in comparison with bread produced by baker’s yeast, and preliminary sensory evaluation of the produced bread was acceptable.     

Detection of alkaline phosphatase by competitive indirect ELISA using immunoglobulin in yolk (IgY) specific against bovine milk alkaline phosphatase

Immunoglobulin in yolk (IgY) (with a titer of 1.3 × 10⁶) specific against bovine milk (BM) alkaline phosphatase (ALP) was obtained by intramuscularly immunizing hens on the thigh and was used as the primary antibody to conduct competitive indirect enzyme-linked immunosorbent assay (CI-ELISA) to determine BMALP in ALPs from BM and Escherichia coli sources. A relationship between the ELISA value and the BMALP level (0.01–10 μg/mL) in whole milk (R² = 0.9019) or in skimmed milk (R² = 0.9402) was observed. The maximal inhibition (%) of BMALP on the microtiter plate by free BMALP at 10 μg/mL whole milk (3.89 mU/μg BMALP) was about 50%, while no inhibition (%) of BMALP by free E. coli ALP at concentrations between 0.01 to 10 μg/mL (60 mU/μg E. coli ALP) was determined. At BMALP levels higher than 0.1 μg/mL, CI-ELISA was proved to be effective in differentiating between BMALP and E. coli ALP and quantifying BMALP in whole milk or skimmed milk in the presence of E. coli ALP with an activity of 0.6 U/mL. Higher inhibition (about 70%) of BMALP on the microtiter plate by free BMALP in diluted (10¹–10⁴ fold) milk samples was observed. The optimal conditions for CI-ELISA in determining BMALP (0.1–10 μg/mL) from ALPs in milk samples were using 10³-fold diluted crude IgY specific against BMALP as primary antibody and 10³-fold diluted goat anti-chicken IgG–ALP conjugate as the secondary antibody.     

Pilot-scale crossflow-microfiltration and pasteurization to remove spores of Bacillus anthracis (Sterne) from milk

High-temperature, short-time pasteurization of milk is ineffective against spore-forming bacteria such as Bacillus anthracis (BA), but is lethal to its vegetative cells. Crossflow microfiltration (MF) using ceramic membranes with a pore size of 1.4 μm has been shown to reject most microorganisms from skim milk; and, in combination with pasteurization, has been shown to extend its shelf life. The objectives of this study were to evaluate MF for its efficiency in removing spores of the attenuated Sterne strain of BA from milk; to evaluate the combined efficiency of MF using a 0.8-μm ceramic membrane, followed by pasteurization (72°C, 18.6 s); and to monitor any residual BA in the permeates when stored at temperatures of 4, 10, and 25°C for up to 28 d. In each trial, 95 L of raw skim milk was inoculated with about 6.5 log₁₀ BA spores/mL of milk. It was then microfiltered in total recycle mode at 50°C using ceramic membranes with pore sizes of either 0.8 μm or 1.4 μm, at crossflow velocity of 6.2 m/s and transmembrane pressure of 127.6 kPa, conditions selected to exploit the selectivity of the membrane. Microfiltration using the 0.8-μm membrane removed 5.91 ± 0.05 log₁₀ BA spores/mL of milk and the 1.4-μm membrane removed 4.50 ± 0.35 log₁₀ BA spores/mL of milk. The 0.8-μm membrane showed efficient removal of the native microflora and both membranes showed near complete transmission of the casein proteins. Spore germination was evident in the permeates obtained at 10, 30, and 120 min of MF time (0.8-μm membrane) but when stored at 4 or 10°C, spore levels were decreased to below detection levels (≤0.3 log₁₀ spores/mL) by d 7 or 3 of storage, respectively. Permeates stored at 25°C showed coagulation and were not evaluated further. Pasteurization of the permeate samples immediately after MF resulted in additional spore germination that was related to the length of MF time. Pasteurized permeates obtained at 10 min of MF and stored at 4 or 10°C showed no growth of BA by d 7 and 3, respectively. Pasteurization of permeates obtained at 30 and 120 min of MF resulted in spore germination of up to 2.42 log₁₀ BA spores/mL. Spore levels decreased over the length of the storage period at 4 or 10°C for the samples obtained at 30 min of MF but not for the samples obtained at 120 min of MF. This study confirms that MF using a 0.8-μm membrane before high-temperature, short-time pasteurization may improve the safety and quality of the fluid milk supply; however, the duration of MF should be limited to prevent spore germination following pasteurization.     

Dose-effect study on the antioxidant properties of leaves and outer bracts of extracts obtained from Violetto di Toscana artichoke

Artichoke (Cynara scolymus L.) is an edible vegetable largely used in the Mediterranean diet and in folk medicine. The present paper discusses the analysis of the polyphenol content of leaves and outer bracts of Violetto di Toscana artichoke using different extraction procedures with the aim of establishing a correlation between polyphenol subclasses and antioxidant activity measured on human LDL oxidized by copper ions. HPLC/DAD and HPLC/MS analyses revealed that both the matrixes contain identical polyphenol subclasses, with mainly quantitative differences. The antioxidant effect of four artichoke extracts decreases in the following order when the sum of total phenolic compounds was considered: ethanolic extract from leaves (IC₅₀ = 2.92 ± 0.46 μM); ethanolic extract from outer bracts (IC₅₀ = 4.04 ± 0.21 μM); ethyl acetate extract from leaves (IC₅₀ = 4.91 ± 0.11 μM); ethyl acetate extract from outer bracts (IC₅₀ = 10.18 ± 1.6 μM). IC₅₀ were also calculated considering the concentrations of single polyphenol subclasses. In both cases, the potency of antioxidant properties was not related to the amount of total polyphenols or the single subclasses.