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Food Science and Technology

Print version ISSN 0101-2061On-line version ISSN 1678-457X

Food Sci. Technol (Campinas) vol.35 no.3 Campinas July/Sept. 2015  Epub Aug 25, 2015 

Research Paper

Phenolic content and antioxidant capacity in organically and conventionally grown eggplant (Solanum melongena) fruits following thermal processing

Erika Leonor Zambrano-Moreno 1  

Rosa Nilda Chávez-Jáuregui 1   2   *  

María de Lurdes Plaza 1   2  

Linda Wessel-Beaver 2  

1Food Science and Technology Program, University of Puerto Rico, Puerto Rico, USA

2Department of Crops & Agroenvironmental Sciences, University of Puerto Rico, Puerto Rico, USA


Thermal processing and production practices used in vegetables can cause changes in their phytochemical contents. Eggplant is characterized by its high antioxidant content. The objective of this work was to determine levels of anthocyanins, polyphenols, and flavonoids and antioxidant capacity in organically and conventionally grown eggplant prepared fresh or subjected to one of three thermal preparation methods: boiling, baking or steaming. The soluble and hydrolyzable polyphenols and flavonoids content were quantified by Folin-Ciocalteu and Aluminum chloride methods, respectively. Anthocyanins were quantified according to the pH differential method. Antioxidant capacity was determined by DPPH and ORAC methods. The results showed differences between organic and conventional eggplant for some variables although cultivation method did not have a consistent effect. Hydrolysable polyphenol content was greater, and soluble and hydrolysable antioxidant capacities were higher in organically grown eggplant, while anthocyanin content was greater in conventionally grown eggplant. Fresh eggplant produced under conventional cultivation had a much greater content of anthocyanins compared to that of other cultivation method-thermal treatment combination. In general, steamed eggplant contained higher total polyphenol and flavonoid levels as well as greater antioxidant capacity. Steamed eggplant from both conventional and organic systems also had high amounts of anthocyanins compared to other thermal treatments.

Keywords:  eggplant; antioxidant capacity; organic; boiled; steamed, baked

1 Introduction

Nutritional quality of vegetables can vary depending on the cultivation method used. Organic cultivation is a growing trend world-wide with 164 countries producing organic products in 2014, and a total value of $64 billion of products being sold (Willer & Lernoud, 2014). Whether there are greater nutritional benefits in organic compared to conventional fruits and vegetables is still a much-debated subject.

The beneficial influence of fruit on human health is linked with the presence of specific phytochemicals. Determining the nature of these compounds in different products, and the influence of preharvest, postharvest and processing treatments have been major areas of study in food research (Cools et al., 2011).

Fruits are most commonly consumed raw; however, vegetables often undergo some type of processing before being ingested. Cooking is often the final step in at-home food processing. Vegetables are commonly cooked either by simple boiling, microwaving or stir-frying before being consumed. Cooking processes induce significant changes in the physical characteristics as well as chemical composition of the vegetables and thus influence the concentration and bioavailability of compounds (Zhang & Hamauzu, 2004; Azizah, 2009; Donado-Pestana et al., 2012).

Following exposure to certain cooking processes, fruits and vegetables can present significant losses of some antioxidants such as ascorbic acid and some carotenoids. However, polyphenol and flavonoid content can increase and show certain stability when they are exposed to high temperatures, a quality that is reflected in the preservation of their antioxidant capacity (Faller & Fialho, 2009). For example, Dewanto et al. (2002) found significant increases in the content of total free phenolics in sweet corn after thermal treatment involving increased heating times and temperatures.

Eggplant is among the top ten vegetables for its oxygen radical absorbance capacity due to its phenolic constituents, which have important health benefits (Singh et al., 2009; Akanitapichat et al., 2010). Eggplant needs to be cooked before being eaten. It is generally consumed after frying, boiling in water or grilling. Some recent studies have shown that thermal treatment increases its antioxidant content (Braga et al., 2011; Das et al., 2011). However, it is not known how antioxidant content and activity might vary depending on how eggplant is produced at the field level, nor what, if any interactions might occur between the eggplant production system and postharvest thermal treatment of this vegetable. Therefore, the objective of this work was to determine the total polyphenol, flavonoid and anthocyanin content and their antioxidant capacity in organically and conventionally produced eggplant subjected to three thermal treatments (boiling, steaming and baking) compared to fresh eggplant used as a control (no thermal treatment).

2 Materials and methods

2.1 Preparation of samples and thermal treatments

Eggplant fruits (cv. Dancer) were obtained from two commercial farms near Guánica, Puerto Rico, one using organic and the other using conventional cultivation practices. Sixteen mature eggplant fruits were selected from each cultivation system. Fruits were washed with potable water, disinfected with 200 mg/L sodium hypochlorite, washed again, and dried with paper towels. Four fruits from each cultivation system were randomly assigned to each of four treatments (fresh-control, boiling, steaming and baking). For fresh, boiled or steamed treatments, fruits were cut into approximately 1 cm2 cubes. For baking treatment, fruits were cut in half longitudinally. Cooking times for boiling, steaming and baking were determined by preliminary tests adapted from the methodology proposed by Faller & Fialho (2009). A covered stainless steel pot was used to boil 100 g of sample in 200 ml water for seven minutes. After boiling, water was drained and samples were cooled to room temperature using a cold water bath in a stainless steel receptacle. In a similar manner, 100 g of sample was steamed for seven minutes in a food steamer, then drained and cooled as previously described. In the baking treatment, samples were placed into a conventional oven at 180 °C for 25 minutes, transferred to a stainless steel and cooled in a water bath as above. In order to minimize possible oxidation, processed samples were packed into plastic Ziploc® bags. Air was manually removed from the bags before sealing and then immediately stored at -80 °C until elaboration of extracts.

2.2 Chemicals and reagents

Potassium chloride, Sodium acetate, Methanol, Sodium carbonate, Sodium hydroxide, Hydrochloric acid and acetone reagents were purchased from VWR Advanced Instruments, LLC (Manatí, Puerto Rico, USA). Folin-Ciocalteu, 2,2-Diphenyl-1-picrylhydrazyl (DPPH), 6-Hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox) and (+)-Catechin reagents were purchased from Sigma–Aldrich (St. Louis, MO, USA). Gallic acid, Sodium nitrite, Aluminum chloride, Fluorescein and 2,2’-Azobis [2-amidinopropane] dihydrochloride (AAPH) were purchased from Fisher Scientific (Pittsburgh, PA, USA). All other reagents were of analytical quality grade.

2.3 Preparation of extracts

Approximately 5 g of each processed fruit was macerated with 40 ml methanol:HCl 12 M (99:1, v/v) for determination of anthocyanins, 20 ml methanol:water (50:50, v/v) for determination of soluble polyphenols and flavonoids, and 20 ml methanol-water:HCl 1.2 M (50:50, v/v) for hydrolyzable polyphenols and flavonoids. Samples were quantitatively transferred to centrifuge tubes and stirred for 60 min at 38±2.0 ºC. Polyphenols and flavonoids detained were carried to a second extraction with 20 ml acetone:water (70:30, v/v). After this procedure, the solutions were centrifuged at 1200 g for 30 min and were filtered on WhatmanTM #1 paper (GE Healthcare Bio- Sciences, Pittsburgh, Pennsylvania, USA) using a vacuum pump. Supernatants from extractions were combined and made up to 50 ml with distilled water (Todaro et al., 2009; Rufino et al., 2010).

2.4 Phytochemical analysis

2.4.1 Total anthocyanins

Total anthocyanins content was determined using the pH differential method according to official method AOAC 37.1.68 (Association of Official Analytical Chemists, 2006). Two different dilutions of samples were prepared, one with pH 1.0 buffer solution (Potassium chloride 0.025 M) and the second with pH 4.5 buffer solution (Sodium acetate 0.4 M). The pH was adjusted with concentrated Hydrochloric acid. The appropriate dilution factor was determined by diluting the extract with pH 1.0 buffer, the absorbance at 530 nm should be less than 1.2. Using this dilution factor, were prepared two dilutions of the samples, one with pH 1.0 buffer and the other with pH 4.5 buffer. After 20 min, the absorbance was measured at 530 nm and 700 nm using a Spectronic Genesys TM8 spectrophotometer (Thermo Electron Scientific Instruments, Madison, Wisconsin, USA). Total anthocyanin content was calculated using the Equation 1:

Total anthocyanin=A*MW*DF*1000ɛ*L (1)

where, MW is anthocyanin cyanidin-3-glucoside molecular weight (= 449.2 g/mol), DF is the dilution factor, ε is the molar absorptivity coefficient (= 34,300 L/mol*cm) and L is the pathlength (= 1 cm). Results were expressed as cyanidin-3-glucoside equivalents (Cyd-3-gluE) in mg per 100 g fresh weight (mg Cyd-3-gluE/100 g FW).

2.4.2 Determination of polyphenol content

Soluble and hydrolysable total polyphenols content were determined using the microscale protocol named Folin-Ciocalteu colorimetry (Waterhouse, 2002). A 20 µl volume of blank, standard or extract was placed into an assay tube to which was added 1580 µl distilled water and 100 µl Folin-Ciocalteu reagent. The mixture was allowed to stand for 6 min in darkness at room temperature. After this time, 300 µl of 20% sodium carbonate solution was added and the mixture was swirled and incubated for 120 min at room temperature. Finally, the absorbance was measured at 760 nm using a Spectronic Genesys TM8 spectrophotometer (Thermo Electron Scientific Instruments, Madison, Wisconsin, USA). Soluble and hydrolyzable total polyphenols contents were calculated using a standard curve of gallic acid. The results were expressed as gallic acid equivalents (GAE) in mg per 100 g fresh weight (mg GAE/100 g FW) (Akanitapichat, et al., 2010).

2.4.3 Flavonoids analysis

Soluble and hydrolysable total flavonoids content were determined using the aluminum chloride colorimetric method. A 500 µl volume of blank, standard or extract, was mixed with 1250 µl distilled water and 75 µl of 5% sodium nitrite solution and the mixture was allowed to stand for 6 min in darkness at room temperature. Then, 150 µl of 10% aluminum chloride solution was added and the mixture was allowed to stand for another 5 min before adding 500 µl of 1 M sodium hydroxide solution and made up to 3000 µl. The absorbance was measured at 510 nm using a Spectronic Genesys TM8 spectrophotometer (Thermo Electron Scientific Instruments, Madison, Wisconsin, USA). The soluble and hydrolyzable total flavonoids contents were calculated using a standard curve of (+)-catechin and the results were expressed as catechin equivalents (CE) in mg per 100 g fresh weight (mg CE/100 g FW) (Akanitapichat, et al., 2010).

2.4.4 Oxigen Radical Absorbance Capacity (ORAC)

Antioxidant capacity was determined using the ORAC method (Oxygen Radical Absorbance Capacity), accord to methodology described by Cao & Prior (Cao & Prior, 1999) and Huang et al. (2002). A fMax 96-well plate fluorometer (Molecular Devices, Sunnyvale, California, USA) was utilized with an excitation wavelength of 485 nm and an emission wavelength of 538 nm with the AscentTM Software version 2.6 (Thermo Scientific). A 50 µl volume of blank (pH 7.0 buffer solution (Potassium 0.75 M and Sodium 0.75 M)), standard or extract, 100 µl of 500 nM fluorescein solution and 50 µl of 900 mg per 10 ml AAPH solution (2,2’-Azobis [2-amidinopropane] dihydrochloride), were directly placed into the 96-well plate. The reduction of fluorescein was recorded for 70 min. The antioxidant capacity was calculated using a standard curve of Trolox and the results were expressed as Trolox equivalents (TE) in µmol per g fresh weight (µmol TE/g FW).

2.4.5 DPPH radical-scavenging capacity

Antioxidant capacity was also determined using the DPPH modified method (2,2-Diphenyl-1-picrylhydrazyl radical) described by Faller & Fialho (2009). A 100 µM DPPH solution was prepared with 80% methanol giving approximately an absorbance of 1.0 ± 0.1 at 515 nm. A 200 µl volume of blank (80% methanol), standard or extract was mixed with 2800 µl DPPH solution. After 20 min, absorbance was measured using a Thermo Spectronic Genesys TM8 spectrophotometer (Thermo Electron Scientific Instruments, Madison, Wisconsin, USA). The percentage radical scavenging capacity (%RSC) was calculated with the Equation 2:

%RSC=A0-AfA0 (2)

where A0 is the absorbance of the DPPH solution alone measured at time zero and Af is the absorbance for each sample after 20 minutes following the addition of the DPPH solution. The antioxidant capacity was calculated using a standard curve of %RSC vs. Trolox concentration and the results were expressed as Trolox equivalents (TE) in µmol per g fresh weight (µmol TE/g FW) (Leyva, 2009).

2.5 Statistical analysis

Data were analyzed as a completely randomized 2 x 4 factorial (2 cultivation systems x 4 processing methods) design with four replications. Both factors were considered to be fixed effects. Analysis of variance was performed using InfoStat (Di Rienzo et al., 2013). The significance of the interaction and main effects were determined using an F test, and means were separated using Fisher’s least significant difference multiple comparison test.

3 Results and discussion

With one exception (total monomeric anthocyanins, Table 1), there were no significant cultivation system by thermal treatment interactions (Tables 2 and 3). In general, relative differences between preparation methods were the same whether fruits came from the organic or conventional cultivation system. Even in the case of total monomeric anthocyanins, the relative ranking of thermal treatments were similar under the two cultivation systems: fresh and steamed eggplant had the highest amounts of anthocyanin, and boiled and baked eggplant had the lowest amounts of anthocyanin under both cultivation systems (Table 1).

Table 1 Mean total monomeric anthocyanins in fresh and cooked eggplant grown under conventional and organic cultivation systems in Puerto Rico. 

Treatment1 Total monomeric anthocyanins
(mg Cyd-3-gluE/100 g FW)
Cultivation system x thermal treatment interaction
Conventional – fresh (control) 6.31 d
Conventional - boiled 2.5 b
Conventional - baked 0.16 a
Conventional - steamed 4.2 c
Organic - fresh (control) 1.19 ab
Organic - boiled 0.42 a
Organic - baked 0.27 a
Organic - steamed 2.46 b
LSD (0.05) 1.58
Significance of F test
Cultivation system **
Thermal treatment **
Interaction **
CV 49.4%

1Due to the presence of a significant interaction, only cultivation system by thermal treatment means are presented.

Cyd-3-gluE = Cyanidin-3-glucoside equivalents. LSD = Fishers least significant difference test at the 0.05 probability level. Means followed by the same letter are not significantly different.

**= Significant at the 0.05 and 0.01 probability level.

Table 2 Mean total polyphenol and flavonoid content (soluble and hydrolysable) in fresh and cooked eggplant grown under conventional and organic cultivation systems in Puerto Rico. 

Treatment Total soluble polyphenols
(mg GAE/100 g FW)
Total hydrolysable polyphenols
(mg GAE/100 g FW)
Total soluble flavonoids
(mg CE/100 g FW)
Total hydrolysable flavonoids
(mg CE/100 g FW)
Cultivation system
Conventional 63.99 a 71.95 a 49.34 a 41.45 a
Organic 77.20 a 100.00 b 50.80 a 49.89 a
LSD (0.05) 15.55 21.28 9.65 9.89
Thermal treatment
Fresh (control) 38.95 a 66.88 a 14.71 a 30.08 a
Boiled 62.93 b 76.26 a 52.42 b 45.38 b
Baked 75.65 b 80.57 a 52.38 b 39.03 ab
Steamed 104.84 c 120.19 b 80.75 c 68.20 c
LSD (0.05) 21.98 30.10 13.64 13.99
Significance of F tests
Cultivation system NS * NS NS
Thermal treatment ** ** ** **
Interaction NS NS NS NS
CV 30.2% 33.9% 26.4% 29.7%

GAE = Gallic acid equivalents; CE = Catechin equivalents.

LSD = Fishers least significant difference test at the 0.05 probability level. Within columns and main effects, means followed by the same letter are not significantly different at the 0.05 probability level according to Fishers LSD.

NS, *, ** = Not significant, and significant at the 0.05 and 0.01 probability levels, respectively.

Table 3 Mean antioxidant capacity (ORAC and DPPH) in fresh and cooked eggplant grown under conventional and organic cultivation systems in Puerto Rico. 

Treatment Soluble antioxidant capacity (ORAC)
(μmol TE/g FW)
Hydrolyzable antioxidant capacity (ORAC)
(μmol TE/g FW)
Anthocyanin antioxidant capacity (ORAC)
(μmol TE/g FW)
Soluble antioxidant capacity (DPPH)
(μmol TE/g FW)
Hydrolyzable antioxidant capacity (DPPH)
(μmol TE/g FW)
Anthocyanin antioxidant capacity (DPPH)
(μmol TE/g FW)
Cultivation system
Conventional 36.61 a 47.71 a 68.18 a 48.06 a 67.38 a 97.95 a
Organic 50.60 b 75.06 b 68.79 a 62.41 a 62.11 a 73.25 a
LSD (0.05) 11.96 16.61 14.92 14.97 16.00 31.79
Thermal treatment
Fresh (control) 12.56 a 37.93 a 49.03 a 15.89 a 51.70 a 59.35 a
Boiled 49.32 b 62.74 b 66.74 a 59.15 b 65.87 ab 72.35 a
Baked 43.66 b 52.46 ab 63.52 a 61.3 b 61.48 ab 77.26 a
Steamed 68.88 c 92.40 c 94.65 b 84.61 c 79.93 b 133.44 b
LSD (0.05) 16.92 23.48 21.10 21.17 22.63 44.95
Significance of F tests
Cultivation system * ** NS NS NS NS
Thermal treatment ** ** ** ** NS *
Interaction NS NS NS NS NS NS
CV 37.6% 37.1% 29.9% 37.1% 33.9% 50.9%

ORAC = Oxygen radical absorbance capacity method; DPPH = 1,1-Diphenyl-2-picrylhydrazyl radical method; TE = Trolox equivalents.

LSD = Fishers least significant difference test at the 0.05 probability level. Within columns and main effects, means followed by the same letter are not significantly different at the 0.05 probability level according to Fishers LSD.

NS, *, ** = Not significant, and significant at the 0.05 and 0.01 probability levels, respectively.

Organic eggplant had only about a third as much total monomeric anthocyanins compared to conventionally produced eggplant (Table 1). However, In contrast, organic eggplant had a significantly higher content of hydrolysable polyphenols (Table 2) and higher soluble and hydrolysable antioxidant capacities when the ORAC method was used (Table 3). There was no difference between organic and conventionally grown eggplant for the other phenolic content and antioxidant capacities measured (Tables 2and 3).

Among thermal preparation methods, steamed eggplant had the highest levels of polyphenols and flavonoids (Table 2). Fresh eggplant had the lowest levels of these two phenolics, although the difference was not always significantly different from levels in boiled or baked eggplant. Total monomeric anthocyanin levels among the four preparation methods were affected by the type of cultivation system (significant interaction, p = 0.0007) (Table 1). Overall, anthocyanin levels were considerably higher in conventionally grown eggplant, and levels were significantly different for each preparation method. The highest amount of anthocyanin was found in fresh eggplant, followed by steamed, boiled and baked eggplant. In organically grown eggplant, anthocyanin levels on average were much lower with the highest level observed in steamed eggplant, and no differences observed among the other three preparation methods.

Total anthocyanin content in fresh eggplant fruit produced under conventional cultivation (6.31 mg Cyd-3-gluE/100 g) was more than five times greater than under organic cultivation (1.19 mg Cyd-3-gluE/100 g) (Table 1). Boiled and steamed fruits from conventional cultivation also had high anthocyanin content. Skin color of fruits produced under conventional cultivation was noticeably less faded in color, possibly due to these fruits being harvested earlier on average than fruits produced under the organic production system. Eggplant skin color fades when harvest of fruit is delayed as was possibly the case in the organically grown eggplant. Anthocyanin content observed in organically produced fresh eggplant in this study (1.19 mg Cyd-3-gluE/100 g) (Table 1) was comparable to the amount reported by Sadilova et al. (2006) (1.65 mg Del-3-gluE/100 g). Anthocyanin content in the conventionally grown fresh eggplant (6.31 mg Cyd-3-gluE/100 g) was similar to results reported by Braga et al. (2011) (7.0 Cyd-3-gluE/100 g) and Koponen et al. (2007) (7.5 mg Cyd-3-gluE/100 g). Large differences in anthocyanin content observed in this and previous studies suggest that not only differences in cultivation practices between an organic and conventional system, but differences in harvest practices between any two cultivation systems may have an impact on anthocyanin content in eggplant.

Hydrolysable polyphenol content was significantly higher in organic eggplant compared to conventional eggplant. A similar, although non-significant, trend was observed for soluble polyphenols and soluble and hydrolysable flavonoids: their content was higher in organic versus conventional eggplant (Table 2). Lima et al. (2008) and Raigón et al. (2010) also reported greater polyphenols and flavonoids content in organic eggplant. Raigón et al. (2010) concluded that polyphenols and flavonoids content is lower in conventionally grown eggplant due to higher levels of fertilization, especially nitrogen, which results in phenolic content reduction. The presence of pathogens in organic agriculture due to minimal use of pesticides might also explain higher content of polyphenols since these substances can be used as a mechanism of pest protection in plants (Asami et al., 2003).

Soluble polyphenol content in this study (38.95 mg AGE/100 g) was 19% less than that reported by Raigón et al. (2008) (48.26 mg AGE/100 g), although those authors studied several different eggplant varieties and did not include the variety in our study. Hydrolysable polyphenol content in the current study (66.88 mg AGE/100 g) was 12% higher than reported by Concellón et al. (2012). Soluble and hydrolysable flavonoid contents in this study were lower than those reported by Fategbe et al. (2012). The variability in soluble and hydrolysable flavonoid content can depend on the eggplant variety used and the predominant flavonoid type, an observation also point out by Cao et al. (2010).

Soluble antioxidant capacity by the ORAC method in fresh eggplant (12.56 µmol TE/g, Table 3) was similar to results reported by Isabelle et al. (2010) (12.78 µmol TE/g). However, Isabelle et al. (2010) values were higher than those reported by Cao et al. (1996) (3.9 µmol TE/g). Hydrolysable antioxidant capacity in fresh eggplant (37.93 µmol TE/g) was higher than reported by Wu et al. (2004) (25.09 µmol TE/g). The conditions under which a crop is grown affects antioxidant capacity (Huang et al., 2009) and could explain these contrasting results.

Our study was conducted using the same cultivar (‘Dancer’) under both organic and conventional cultivation systems. Nevertheless, the inferences that can be made concerning the effect of cultivation system (organic vs. conventional) are limited due to the fact that the fruit was produced at a single location and in only one cultivation year. Cultural practices within a particular organic or conventional system can also vary widely. The authors were not able to obtain detailed information concerning, for example, total amounts of nutrients applied in the two cultivation systems sampled in the study, although it is likely that larger amounts of nutrients (nitrogen in particular) were applied in the conventional system. Previous studies comparing organic and conventional systems have suffered from similar design deficiencies. A study sampling eggplant produced from multiple organic and conventional farms in various locations is needed to make stronger inferences about the differences between these two systems in terms of phenolic compounds content and antioxidant capacity.

In general, anthocyanin content decreased with cooking treatments, except with the steaming treatment in organically grown eggplant (Table 1). Baking resulted in a greater loss of anthocyanins (94%) than boiling (61%) and steaming (11%). An anthocyanin loss after boiling was also reported by Braga et al. (2011). The reduction in content might be explained by the fact that anthocyanin is present primarily in the eggplant peel which is in more direct contact with heat that causes its decomposition.

Soluble and hydrolysable polyphenols and flavonoids generally increased when eggplant was subjected to thermal treatments whether the fruits came from the organic or conventional cultivation system (Table 2). Compared to fresh eggplant, soluble polyphenols content increased up to almost 60% with the boiling treatment, 94% with the baking treatment and as much as 169% with the steaming treatment. Braga et al. (2011)reported that boiled eggplant had 77% more polyphenols than fresh eggplant. These increases are due to the release of antioxidants that occurs following the thermal destruction of the cellular wall and subcellular compartments. In addition, increased content of polyphenols results from the reduction in oxidation of phenolic products that occurs with the thermal inactivation of oxidative enzymes such as polyphenol oxidase (Jiménez-Monreal et al., 2009; Braga, et al., 2011; Mennella et al., 2012).

Compared to fresh eggplant, soluble flavonoid content was about 3.5 times greater in baked and boiled eggplant and about 5.5 times greater in steamed eggplant (Table 2). Hydrolysable flavonoid content was about 1.5 times greater with boiling and more than two times greater with steaming. Baking did not increase hydrolysable flavonoid content compared to fresh eggplant. Grajek & Olejnik (2010) studied hot air-dried tomato and observed up to two times the lycopene content compared to fresh fruit. Increases in flavonoid content are a result of cellular wall rupture and the breaking of bonding forces between antioxidant substances and the tissue matrix.

The antioxidant capacity by the methods ORAC and DPPH had similar values in soluble and hydrolysable polyphenol and flavonoid content. Overall, the antioxidant capacity methods detected differences among cooking treatments. Other authors have noted a high correlation between the phenolic compound content and their antioxidant capacity (Wu et al., 2004).

4 Conclusions

There is a growing interest in how organic production might affect the nutritional characteristics of vegetables and how these effects might vary with different thermal preparation methods. Organic production has been promoted as a way to produce more nutritional foods. Our study did not find consistent differences in polyphenol and flavonoid content and antioxidant capacity of eggplant fruit produced under organic versus conventional cultivation systems. In fact, total monomeric anthocyanin content was three times greater in conventionally produced eggplant compared to fruit produced in the organic system. Phenolic and anthocyanin content, as well as antioxidant capacity, was greater in steamed eggplant compared to fresh, boiled and baked fruit. These differences were consistent no matter the cultivation system used to produce eggplant fruits. While our study was limited to the use of a single eggplant cultivar (‘Dancer’) and production location, other eggplant cultivars may be more responsive to organic production systems.


This project was supported by the Food Science and Technology Program, University of Puerto, Mayagüez Campus.

Practical Application: Eggplant is characterized by its high antioxidant content. In order to elucidate the possible benefits of the consumption of organic eggplant as part of a whole diet, information is needed on anthocyanin and polyphenol content as well as antioxidant capacity in organically and conventionally grown eggplant prepared fresh or subjected to one of three thermal preparation methods: boiling, baking, or steaming. Results from this study could be used as a part of a database providing information on the effects of different cooking methods on the antioxidant potential of eggplant.


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Received: February 28, 2015; Accepted: June 06, 2015

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