DOI: 10.31038/NDN.2019113

Abstract

The current interest in the healthfulness of fruits may be linked to its antioxidant capacity, related to the presence of bioactive compounds. Freeze-drying opens up new alternatives for fruit processing, mainly due to the scarce heat damage to the product. Nevertheless, the high cost of this process may recommend some pre-drying treatment. In this study, the effect that using pre-microwaves or hot air partial drying prior to freeze-drying has on the vitamin A, C and E content and antioxidant capacity of kiwifruit puree, with or without the presence of gum Arabic and tricalcium phosphate, was studied. Powders obtained from kiwifruit purees with solutes added showed a significant (p<0.05) higher content of vitamins and greater antioxidant capacity. Gum Arabic and tricalcium phosphate protect against loss caused by any studied drying treatments. Nevertheless,  microwaves and especially hot air partial drying treatments prior to freeze-drying caused significant vitamin and antioxidant capacity loss.

Keywords

microwaves; hot air; freeze-drying; antioxidant capacity; vitamins A, E and C

Introduction

Every day, our body is subjected to attack by many reactive oxygen species (ROS), formed not only during the physiological metabolism of energetic nutrients but also under infection, smoking, and pollution threaten [1, 2]. When the normal antioxidant defences are overwhelmed, ROS bring about a condition of oxidative stress [3], which means that ROS attack and oxidize portions of lipids, nucleic acids, and proteins, with the consequent impairment of physiological functions and the appearance of pathologies [1]. The contribution of antioxidant nutrients becomes of vital importance to rescuing the body from oxidative stress conditions [4]. Fresh vegetables are relevant reservoirs of vitamins and phenol compounds [5]. If introduced into the body at every meal, those nutrients provide consistent protection to physiological macromolecules by increasing the antioxidant capacity of the plasma [6, 7]. The kiwifruit is the edible berry of a cultivar group of the woody vines of several Actinidia species. The most common commercially available, green-fleshed kiwifruit is the ‘Hayward’ cultivar, which belongs to the Actinidia deliciosa species [8]. Kiwifruit are often promoted for their high vitamin C content, which probably contributes to the health benefits that include antioxidant, antiatherogenic and anticarcinogenic activities, as well as immunomodulation [9]. However, kiwifruit also contain other vitamins and minerals that may contribute to possible health benefits, including folate, potassium and magnesium, dietary fibre and phytochemicals [10]. The effects of kiwifruit consumption on hypertension and dyslipidemia have been tested in human trials. [11] found that the consumption of green kiwifruit resulted in a small but significant reduction in diastolic and systolic blood pressure in male smokers, the effect being strongest in those with hypertension. On the other hand, in subjects that were hypercholesterolemic, kiwifruit consumption did have a favourable effect on plasma high-density lipoprotein cholesterol (HDL-C) concentrations and the total cholesterol (TC): HDL-C ratio [12]. These results support the earlier findings that kiwifruit consumption increased HDL-C and decreased the TC: HDL-C ratio and also decreased the plasma triglyceride concentrations [13, 14].

In addition to the “mainstream” health targets commonly used to define the benefits from functional food, a small number of studies demonstrate more novel bioactive effects of kiwifruit, such as “natural” sleep aid or wound healingThe consumption of “Hayward” kiwifruit in the evening has been shown to improve sleep onset, duration, and efficiency in adults with self-reported sleep disturbances [15]. In addition, the application of kiwifruit fresh slices to burns has been shown to improve the healing process [16].

However, many people are not able to consume fresh fruit every day, due to their work conditions, distance from the markets of fresh products, or having very little time for shopping and cooking [17]. Therefore, they buy processed fruit and consume them every day. Powdered fruit products may be an alternative means of increasing fruit consumption in response to the increased demand for ready-to-eat foodstuffs. The benefits of handling, packaging and transporting fruit powder, the great stability of the product and the ease of final consumption could contribute to this end. Freeze-drying (FD) emerged as a drying method which generates high quality products with very low moisture content, good sensory and nutritional properties and a good capacity for rehydration. However, long processing times and high operation costs are necessary to obtain freeze-dried products with an adequate level of quality (18).  Different studies have been carried out into how to reduce processing costs, for example abolishing the cost of vacuum generation, combining technologies prior to or during FD operation or enhancing heat transfer [19–21]. On the other hand, freeze-dried fruit products are highly hygroscopic and are prone to suffering changes in their physical properties brought about by the environment and time. Therefore, adding biopolymers and other solutes has been shown to be necessary in order to increase the product stability by acting as a barrier to water adsorption [22, 23]. The aim of this study was to evaluate the impact of both the use of microwave (MW) or hot-air drying (HA) as pre-drying treatments prior to freeze-drying and the presence of gum Arabic (GA) and tricalcium phosphate (TCP) on both the vitamins and antioxidant capacity of kiwifruit powders.

Materials and Methods

Sample preparation and treatments

Kiwifruit (Actinidadeliciosa var. Hayward) was purchased in a local market in Valencia (Spain). The mean values (with standard deviation in brackets) of pH, ºBrix and water content of the kiwifruit used were 3.32 (0.09), 13.6 (0.7) and 84.0 (0.8) g/100g, respectively. The fruit pieces were peeled, washed with distilled water and triturated in a Thermomix (TM 21, Vorwerk, Spain). The obtained puree was divided into two parts and GA (Sigma CAS: 9000-01-5, Spain) along with TCP (Sigma CAS: 7758-87-04, Spain) were added to one of them. The quantities employed were: 1 kg GA/kg soluble solids of the liquid phase of the product [24] and 0.02 kg TCP/kg soluble solids of the liquid phase of the product [25, 26]. As a result, two different samples were obtained: kiwifruit and kiwifruit with solutes. A part of each sample was freeze-dried. To this end, a layer (5 mm thickness) of each sample was placed in a standardised aluminium plate (15 cm diameter and 5 cm height). Consecutively, samples were stored in a CVF 525/86 cryo freezer (-86ºC) (Ing. Climas, Spain) for the 24 h before being freeze-dried in a Lioalfa-6 Lyophyliser (Telstar, Spain) at 0.026 mbar and -56.6 ºCat condenser for 24 h. The obtained cakes were crushed (Thermomix TM 21, Vorwerk, Spain) to obtain kiwifruit powders, with and without solutes, which were named KS and K, respectively.

The rest of the samples of kiwifruit and kiwifruit with solutes was submitted to two different pre-drying methods, prior to FD, in order to reduce the initial water content: MW and HAD. According to preliminary experiments (data not shown), the final water content for pre-treatments was set at 65 g water/100 g sample. This moisture level led to a sample of good appearance with noticeable water loss, without the need for an excessively long pre-treatment time. To ensure this water content in the samples, their weight was recorded during the process. It allowed for the calculation of the water content at different drying times, provided the initial water content is known. Puree samples of kiwifruit and kiwifruit with solutes (300 g) were placed in standard recipients (25 cm diameter and 3 cm depth) made of Teflon (Mecaplast, Spain) or aluminium for MW and HAD, respectively. A household microwave (3038GC, Norm, China), set at a microwave power of 2 W/g and an oven (5141 AFW2, Moulinex, China), set at an air temperature of 40 ºC and an air velocity of 1.5 m/s, were used to carry out the drying pre-treatments. Microwave power and air temperature were selected by taking into account the minimal loss of antioxidant capacity obtained in preliminary experiments (data not shown). The treated samples were immediately cooled in ice water until the puree reached 30 °C. All four samples were freeze-dried as described above to obtain the corresponding powders, thus becoming freeze-dried kiwifruit puree with and without solutes added, pre-dried by MW or HAD, named as follows: KMW, KHAD, KSMW and KSHAD, respectively.

Analytical determinations

All the analyses described below were carried out in triplicate on fresh and freeze-dried kiwifruit samples. Despite the obtained results being referred to 100 g of each sample, the losses of vitamins, total phenolic compounds and antioxidant capacity suffered by the samples were calculated and also referred to 100 g of the kiwifruit’s own solutes (KS) in order to compare them(equations 1 and 2).

where: x_w^p is the water content of the powder (w/w), x_GS/TS is the mass fraction of the grapefruit’s own solutes (GS) to total sample solutes, m_GA, m_CMC and m_L are the mass of gum Arabic, carboxymethyl cellulose and liquidized grapefruit, respectively, in the sample and x_w^L is the water content of the liquidized grapefruit (w/w).

The mass fraction of water was obtained by vacuum drying the samples in a vacuum oven (Vaciotem, J.P. Selecta, Spain) at 60 ± 1 ºC under a pressure of < 100 mm Hg until constant weight. To determine the total solute content (TS) of the freeze-dried samples, the methodology described by [27] was followed. In turn, 1.5 g of each powder were rehydrated, in triplicate, and the TS of the bulk suspension were determined by oven drying (Vaciotem, J.P. Selecta, Spain) at 60 ºC until constant weight.

Vitamins A, C and E

The vitamins were determined by HPLC (Jasco equipment, Italy). The procedure employed to determine vitamin C was the reduction of dehydroascorbic acid to ascorbic acid, using DL-dithiothreitol as reductant reagent according to Igual et al., 2016. The HPLC method and instrumentation were: Ultrabase-C18, 5 μm (4.6×250 mm) column (AnálisisVínicos, Spain); mobile phase 0.1 % oxalic acid, volume injection 20 μL, flow rate 1mL/min, detection at 243 nm and at 25 ºC. AA standard solution (Panreac, Spain) was prepared.

Vitamins A and E were extracted twice in the hexane phase and the collected extract was dried under a stream of liquid nitrogen [28]. The dried extract was solubilized in 0.2 mL methanol. The HPLC method and instrumentation were: Ultrabase-C18, 5 μm (4.6 × 250 mm) column (Spain); mobile phase methanol/acetonitrile/chloroform (47:42:11, v/v/v), volume injection 20 μL, flow rate 1 mL/min, detection at 326 and 296 for vitamins A and E, respectively at 25 ºC. Standard curves of each reference compound (Fluka-Biochemika, USA) were used for quantification purposes.

Antioxidant capacity

Antioxidant capacity (AOC) was assessed using the free radical scavenging activity of the samples evaluated with the stable radical 2, 2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH). Briefly, the samples were diluted in methanol, homogenized and centrifuged (Selecta Medifriger-BL, Spain) at 400 x g for 10 min at 4 °C. 0.1 mL of supernatant was added to 3.9 mL of DPPH (Sigma-Aldrich, Germany) diluted in methanol (0.030 g/L). At 30 s intervals, a UV-visible spectrophotometer was used to measure the absorbance at 25 ºC and515 nm until the reaction reached the steady state. The percentage of DPPH was calculated following Eq. (3).

where A_control is the absorbance of the control (initial time) and A_sample the absorbance of the sample at the steady state.

The final results were expressed as mmol trolox equivalents (TE) per 100 g sample using a trolox calibration curve in the range of 6.25–150 mM (Sigma-Aldrich, Germany).

Statistical analysis

An analysis of variance (ANOVA) was carried out to evaluate the differences among samples. When the p value was lower than 0.05, significant differences between samples were assumed. Furthermore, an analysis of the correlation between AOC and all the studied vitamins, with a 95 % significance level, was carried out. All statistical analyses were performed using Stat graphics Centurion XVI.II for Windows.

Results and discussion

Kiwifruit characterization

The vitamin A content (0.029 (0.002) mg/100 g) was lower than that of the rest of the quantified bioactive compounds. The vitamin E content was 2.10 (0.13) mg/100 g, similar to the values of this vitamin shown by [29] (2.5 mg /100g,). In general, citric fruit are considered a good source of vitamin C. However, the amount of vitamin C in kiwifruit (105 (5) mg/100 g) is about three times more than that present in 100 g of grapefruit [30] or twice more than orange [31]. The obtained results coincide with the values shown for kiwifruit var. Hayward by other authors [32–35]. One of the predominant mechanisms of the protective action of bioactive compounds is their antioxidant activity and the capacity to scavenge free radicals [36]. Kiwifruit showed 15.63 (0.15) mmol TE/100g of AOC.

The effect of solute addition and pre-drying on bioactive compound variation of freeze-dried kiwifruit powder

The losses of vitamins and AOC suffered by the samples as a consequence of each drying step have been plotted in Fig. 1 – 4. The loss of each component (ΔMi), referred to the fresh kiwifruit content, were calculated according to equations 4 and 5.

where: M_i: mass of compound i in the sample referred to the kiwifruit’s own solutes and superscripts: FK: fresh kiwifruit, P: pre-treated (mixed with the solutes and/or pre-dried by MW or HAD), FD: freeze-dried.

Figure 1. Mean value and standard deviation of Vitamin C losses suffered by the samples as a consequence of each process studied.

Letters indicate homogeneous groups established by the ANOVA (p < 0.05) for total process variation.

Figure 2. Mean value and standard deviation of Vitamin A losses suffered by the samples as a consequence of each process studied

Letters indicate homogeneous groups established by the ANOVA (p < 0.05) for total process variation.

Figure 3. Measn value and standard deviation of Vitamin E losses suffered by the samples as a consequence of each process studied

Letters indicate homogeneous groups established by the ANOVA (p < 0.05) for total process variation

Figure 4. Mean value and standard deviation of antioxidant capacity losses suffered by the samples as a consequence of each process studied.

Letters indicate homogeneous groups established by the ANOVA (p < 0.05) for total process variation.

As regards the vitamins studied (Figures 1 – 3), FD was observed to bring about the greatest vitamin loss in sample K. When comparing samples K and KS, a loss of all three of the vitamins studied was observed due to the mixing process when solutes were added to the kiwifruit puree. Nevertheless, solutes reduced the losses caused by FD. In general, the application of MW or HAD pre-treatment led to an increase in vitamin losses, especially when no solutes were present. In this way, GA+TCP can be confirmed to exert a protective effect on the vitamins studied throughout FD.As regards pre-drying treatments, the loss of vitamins A or C due to MW or HAD pre-treatments was of the same order, while the loss of vitamin E was greater when HAD was used. In fact both the KMW and KHAD samples even lost the entire amount of vitamin A present in the fresh kiwi. In these KMW and KHAD samples, the additional loss of the remaining vitamin C brought about by the freeze-drying process was almost negligible, while the loss of vitamin E was also promoted in sample KMW. When comparing these samples with KSMW and KSHAD, the loss of vitamins was reduced in the samples with solutes added, so that for vitamins A and C the loss was reduced in the range of 30 and 20 %, respectively and for vitamin E from 15 % to 40%, depending on whether the HAD or the MW pre-treatment was applied, respectively. As regards AOC (Fig. 4), a loss of about 5 % was observed caused by FD (sample K) or simply by sample formulation (sample KS). A 50–60 % loss of AOC was observed in pre-treated KMW and KHAD samples, due just to FD or to HAD and FD, respectively. This loss was reduced to 20–25 % when solutes were present (KSMW and KSHAD samples). Added solutes help the retention of nutritive properties of kiwifruit during pre-treatments and FD. Maltodextrins and gums are added during the production of food powders in order to act as encapsulating or wall materials, contributing to keeping the desired functional properties in the finished product, such as stability against oxidation, ease of handling, improved solubility, controlled release and extended shelf-life [37]. GA is the gum most often used as a flavour encapsulating material, mainly due to its solubility, low viscosity, emulsification characteristics and its good retention of volatile compounds [38–40].

Table 1 shows the mean value of vitamins and AOC contained in 15 g of the different obtained kiwifruit powders. About 15 g of kiwifruit powder is the equivalent to a fresh kiwi-fruit (≈85 g). The highest vitamin intake is provided by sample KS, despite the highest AOA being supplied by sample K. An intake of 15 g of K or KS powders or ≈ 23 g of any of the other powders is enough to meet the daily amount of vitamin C recommended by the World Health Organization (≈40 mg). KMW, KHAD and KSHAD samples also showed the lowest AOC. In order to explain the relationship among the different vitamins quantified in this study themselves and also between them and the AOC of the samples, correlation statistical analyses were performed using all the obtained data (Table 2). A significant relationship (p>0.05) between the AOC and any of the studied vitamins was observed, as was a closer relationship among the vitamins.

Table 1. Mean values (with standard deviation) of vitamins (mg/15 g) and antioxidant capacity (AOC) (mmolTE/15 g) of obtained powders: K (kiwifruit powders without solutes), KS (kiwifruit powders with solutes), KMW (kiwifruit powder without solutes added pre-dried by microwaves), KHAD (kiwifruit powder without solutes added pre-dried by hot air), KSMW (kiwifruit powder with solutes added pre-dried by microwaves) and KSHAD (kiwifruit powder with solutes added pre-dried by hot air).

The same letter in superscript within columns indicates homogeneous group established by ANOVA (p<0.05).

Table 2. Pearson correlation coefficients among all studied components

* Correlation is significant at the 0.05 level.

Conclusions

An encapsulating effect of GA+TCP was observed both for the mixing with solutes and/or the pre-drying treatment and for the freeze-drying process. When solutes are present, a pre-drying treatment with MW may be recommended instead of HAD for the purposes of obtaining a freeze-dried product, as vitamin E and AOC are better preserved. Nevertheless, despite the fact that the pre-treatment will shorten the subsequent freeze-drying time and so reduce the energy costs, if the maximum preservation of the vitamin content and AOC is desired, the use of microwave or hot air drying pre-treatment should be avoided.

Acknowledgments

The authors thank the Ministerio de Economía y Competitividad for the financial support given through the Project AGL 2017-89251-R (AEI/FEDER-UE).

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