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ABSTRACT
INTRODUCTION
Retail fruit prices in the United States showed the steepest price increase of
all food products from 1982 to 1997; nonetheless, fruit consumption steadily
grew regardless of economic considerations, probably due to the growing public
awareness of the associated health benefits. This was also confirmed by an
increase of 23 % in the consumption of fresh fruits compared to a 2 % increase
in the consumption of processed fruit during the same period, even though fresh
fruit prices increased 138% while processed fruit prices only increased 54%
(USDA 1999). Pears are primarily consumed as fresh fruit (Kadam ef al. 1995).
-
Consumption of fresh pears increased 30% in the United States between 1980
and 1997 while processed pear consumption decreased -31 % over the same
period (USDA 1999). The increased consumer demand for foods as natural and
as fresh as possible (Sloan 2001) and the demand for fresh-like, high quality
products, and at the same time, products that are convenient and ready-to-eat,
requires the development of minimally processed fruits and vegetables that can
sustain a natural and fresh quality for extended periods of time.
The development of minimally processed, ready-to-eat fruits is unfortunate-
ly difficult since fresh-cut products are vulnerable to faster deterioration due to
the removal of natural protective skin and the resulting damage to cells and
tissues, causing degradation in the color, texture, and flavor of fruits (Watada
and Qi 1999), which greatly reduces shelf-life (Watada ef al. 1996). Fresh-cut
pears can undergo quality deterioration processes such as browning, microbial
spoilage, weight loss, and textural changes.
Disruption of the fruit tissue causes browning by exposing suitable
substrates such as phenolic compounds to the oxidizing action of oxygen,
coenzymes (e.g., copper), and oxidizing enzymes (Ahvenainen 1996).
Antioxidants such as sulfur-containing amino acids, carboxylic acids, ascorbic
acid, 4-hexylresorcinol, honey, and pineapple juice can be used to reduce or
prevent browning (Iyengar and McEvily 1992; Lozano ef al. 1993; Monsalve-
Gonzalez ef al. 1993; Gil el al. 1998; Sapers and Miller 1998; Buta e? al. 1999;
Chen ef al. 2000; Son ef al. 2001; Lee ef al. 2003).
Increase of the exposed surface of fruits due to slicing greatly improves the
chances for microbial spoilage, because high-moisture, high-sugar-content
surfaces represent a great opportunity for microorganisms to colonize and grow
(Nguyen-The and Carlin 1994). To avoid microbial spoilage of fresh cut fruits,
antimicrobials like benzoic acid, sodium benzoate, potassium sorbate, and
propionic acid may be used (Baldwin er al. 1995). However, diffusion of the
preservative into the fruit can decrease its effectiveness over time (Vojdani and
Torres 1990).
Decline of the texture of fresh-cut fruits has been related to loss of turgor
caused by water loss and to degeneration of the structure of the lamella media
in intercellular regions. The onset of this defect can be delayed by controlling
water migration and by the addition of calcium chloride (Rocha ef al. 1998;
Poovaiah ef al. 1988; Ponting ef al. 1971, 1972), which strengthens plant cell
walls through its ability to cross link with pectins (Sams 1999).
Considering all the previously discussed factors that promote quality loss,
edible coatings may offer a means of extending the shelf-life of fresh-cut pears.
Edible coatings can be applied to fresh pear wedges to regulate transfer of
moisture, oxygen, carbon dioxide, aroma, and flavor compounds, thus retarding
EDIBLE COATINGS TO PRESERVE QUALITY OF PEAR WEDGES 30 1
The study was conducted using Anjou pears obtained from a local
supermarket at the commercial ripeness stage. Pears were stored at 4C and 90%
RH until used. A total of 31 pears were used. Each pear was cut into eight
wedges. Slicing was accomplished with a stainless-steel slicer. Fresh-cut pear
wedges were immediately subjected to one of the following treatments:
Since eight wedges per pear were available, two wedges were randomly
treated with each of four treatments so that the variation among pears could be
302 G.I. OLIVAS, J.J. RODRIGUEZ and G . V . BARBOSA-CANOVAS
blocked out. Pear wedges were then stored for posterior analysis. The whole
process was repeated independently on three separate days as replications.
Coating Preparation
A method adapted from that described by Kamper and Fennema (1984) and
Quezada er al. (2000) was employed for the preparation of coatings. To prepare
the methylcellulose solution, 100 g of methylcellulose (MC) molecular weight
14,000 (Aldrich Chemical Company Inc., Milwaukee, WI) were solubilized in
500 mL of distilled water at 90C under magnetic stirring for 10 min to wet the
powder and to obtain consistent dispersion. While stirring, 12.5 g of polyethyl-
ene glycol molecular weight 1,450 (Sigma Chemical Co., St. Louis, MO) and
1.03 g of potassium sorbate were added to the solution. Distilled water (250
mL) and absolute ethanol (250 mL) (AAPER Alcohol and Chemical Co.,
Shelbyville, KY), both at IOC, were added to the solution and hence decreased
the solution temperature to 70C. The solution was stirred for 5 min and then
stored overnight at 5C to reduce the amount of air trapped in the solution. The
solution was then degassed in a vacuum oven VRW 1410 (Sheldon Manufactur-
ing, Cornelius, OR) at 5 in Hg absolute pressure.
Methylcellulose-stearic acid (MC-SA) solution was prepared similarly to
methylcellulose solution, except 10 g of stearic acid (SA) (Sigma Chemical Co.,
St. Louis, MO) were added prior to stirring the solution for last 5 min; also 1
g of glycerol alpha-monostearate (TCI America, Portland, OR) was added to
increase the stability of the emulsion. Previous studies (unpublished observa-
tions) showed that higher amounts of SA in the coating solution produced a thick
white film on the pear surface that was visually unacceptable. The solution was
homogenized for 1 min at 20,000 rpm in a Benchtop Homogenizer PT 10/35
(Brinkmann Instruments, Westbury, NY).
Methylcellulose (MC) of low molecular weight was chosen for the
elaboration of the coatings because oxygen permeability (OP) and water vapor
permeability (WVP) increase as the molecular weight of the MC increases (Park
er al. 1993). A high molecular weight PEG was used because high molecular
weight plasticizers improve the vapor barrier properties of the film (Donhowe
and Fennema 1993). Ethanol was used in the coating solution to reduce drying
time and to obtain transparent and shiny films (Quezada er al. 2000).
Coating Application
Coating was applied by dipping the pear wedges in corresponding solutions
depending on the treatment. In the first treatment (control) wedges were
submerged for 3 s in water, while in the second treatment (VitC-CaC1,-PS)
wedges were submerged in a solution of ascorbic acid (1 %), calcium chloride
(0.25 %), and potassium sorbate (0.1 %). For treatments VitC-CaC1, + MC and
EDIBLE COATINGS TO PRESERVE QUALITY OF PEAR WEDGES 303
VitC-CaC1, + MC-SA, the pear wedges were submerged first for 3 s into a
solution of ascorbic acid (1%) and sodium chloride (0.25%), and then dipped
for 4 s into the methylcellulose (MC) solution for treatment VitC-CaC1, + MC
or into the methylcellulose-stearic acid (MC-SA) solution for treatment VitC-
CaCl, + MC-SA. After dipping, pear wedges were drained for 10 min and
those coated with MC and MC-SA solutions were dried at 37C for 25 and 30
min, respectively, in a food dehydrator (Excalibur 3924T) (Sacramento, Ca).
Pear wedges were put on plastic trays and stored in controlled chambers at 4C
and 78% (f 2) RH for 12 days for subsequent analysis.
Weight Loss
To determine the effectiveness of the applied treatments as moisture-
barriers, the weight of eight pear wedges from each treatment was monitored
during the storage period. It was considered that weight loss corresponded
almost exclusively to water loss since migration of other components such as
aromas or flavors is practically imperceptible in terms of weight. Weight percent
loss relative to the initial weight was calculated by weighing the samples every
two days, in triplicate.
Texture
Texture parameters of pears were determined with a Universal Texture
Analyzer TA.XT2 (Stable MicroSystems) using a texture profile analysis (TPA)
at days 0, 3, 6, 9, and 12. The studied attributes were hardness, adhesiveness,
springiness, cohesiveness, chewiness, and gumminess. Three cylinders
measuring 10 mm diameter each were obtained from each wedge by using a
powered rotating core borer (cylinder orientation perpendicular to the core of the
pear). Three wedges per treatment were used obtaining a total of nine cylinders
per repetition. The height of the specimen was adjusted at 15 mm using a
parallel-bladed trimming saw. A flat plate applying 25% compression was used.
Pretest speed, test speed, and posttest speed were all set at 1 d s . Triplicates
of each treatment were evaluated.
Microbial Analysis
Quantification of aerobic mesophilic microorganisms, molds, and yeast was
conducted initially and at day 7. Two pear wedges (one set) per treatment were
removed from the storage room using sterile plastic bags. Special care was taken
during sampling to avoid microbial contamination. From each set of pear
wedges, 25 g were obtained and placed on a filter stomacher bag (Seeward,
Ltd., London) containing 225 mL of sterilized peptone water (0.1 %), which was
then blended for 90 s using a stomacher, model 400 Lab Blender (Seeward,
304 (3.1. OLIVAS. J.J. RODRIGUEZ and G.V. BARBOSA-CANOVAS
Color
The effect of the studied coatings on the browning of pear wedges was
determined by characterizing its surface color using a Minolta CM-2002
colorimeter (Minolta Camera Co., Osaka). Readings were obtained in CIELAB
scale (L*,a*, b*). Three wedges per treatment were taken and six color
measurements made at three locations in each sample, totaling eighteen
measurements per treatment per replicate. Triplicates of each treatment were
measured. Coatings were not removed from pears prior to testing. Color was
measured every 3 days for 12 days. The browning index (BI) was calculated and
used as an indicator of the intensity of brown color (Guerrero et al. 1996). The
Browning Index was calculated as follows:
X*( 100- % W J
V=
100
where X is the value for soluble solids or malic acid obtained from pear juice
before weight loss compensation. %Wis the percentage of weight loss at time
t , and V is the corresponding true value for soluble solids or malic acid content
after weight loss compensation.
Volatiles
Concentration of volatiles in pear tissues was determined by gas chromatog-
raphy using the solid phase microextraction (SPME) technique. Samples of pear
juice were taken initially and at days 4, 8, and 12 of storage. The initial samples
were taken 3 h after treatments were applied. Pear juice was obtained and
weight loss compensated for by the same method described in acidity analyses.
A 4.0 mL sample vial was used with 0.65 g NaCl stirred on a stirring plate
mixed with 2.0 mL of pear juice. A SPME device (Supelco Co., Bellefonte,
PA) with a fused silica fiber coated with 65 pm polydimethylsiloxane/
divinylbenzene was exposed to the headspace of the sample for approximately
1h before GC injection. SPME injection was achieved through splitless injection
for 2 min at 200C into a Hewlett-Packard 589011/5970 GC/MSD equipped with
a DB-1 60 m column. Chromatographic conditions were as described by
Mattheis et al. (1991), however the transfer line temperature and ion source was
held at 250C.
Statistical Analysis
The experiment was conducted as a split plot model. All determinations
were conducted in triplicate. Treatments were considered as the whole plot
factor and time as the subplot factor. Data analysis of variance using PROC
GLM of the Statistical Analysis System (SAS Institute, Cary, NC) was
conducted. Specific differences were determined by preplanned orthogonal
contrasts. All comparisons were made at a 5% level of significance (a= 0.05).
All three studied treatments delayed the loss of quality in pear wedges
during refrigeration when compared to the control. The observed effect of
treatments included reduced weight loss, delayed hardness loss, and retarded
onset of browning. Since no difference in the hardness and browning index
among the three studied treatments was found, it can be hypothesized that there
306 G.I. OLIVAS. J.J. RODRIGUEZ and G.V. BARBOSA-CANOVAS
is no effect from the coating on these parameters and that extension of shelf-life
was only due to the presence of ascorbic acid and sodium chloride. If we
consider the possibility of the salt solutions being partially washed away by this
subsequent immersion in the coating solution, then this delay of browning and
hardness loss in the case of the coated pears could result from a combined effect
between the salt solution and the coating. Pear slices immersed in water were
used as a control since the presence of water alone could have reduced the
degradation rate, compared to merely sliced pears. Lee and Krochta (2001)
found that a water-soluble edible coating retarded the oxidation of peanuts, but
also discovered that water alone delayed oxidation.
Results of microbial analyses showed no differences among treatments. Both
aerobic mesophile microorganisms and molds and yeast counts were < 250
CFU for all treatments from initial sampling through day 7.
Weight Loss
Slicing of fruits causes an increment of skinless surface area, making it
conducive to substantial weight loss. Edible coatings can help prevent water loss
by acting as water loss barriers, causing high relative humidity in the surround-
ing atmosphere of the sliced fruits and thus reducing the gradient to the exterior.
Although a significant amount of work can be found in the literature regarding
the use of edible films to reduce moisture loss in fruits (Amarante el al. 2001a;
Garcia et al. 1998; Baldwin et al. 1999; Cameron et al. 1995; McHugh and
Senesi 2000), most has focused on the coating of whole fruits. Figure 1 shows
the weight loss of the studied pear wedges during storage. Treatment Vit C-
CaCl, + MC-SA showed the best properties as a water vapor barrier ( P c
0.05), maintaining 12.55% more weight than the rest of the treatments at the
end of the storage period, which is in agreement with Wong et al. (1994) who
found that coatings containing emulsions of mixed components seem to perform
best as vapor barriers. Vojdani in 1987 found that stearic acid increases the
barrier properties of methylcellulose films. Here, the methylcellulose seems to
provide a network for the stearic acid to disperse.
Treatments Vit C-CaC1,-PS and Vit C-CaCl, + MC performed similarly
to the control ( P < 0.05), allowing water to migrate out of the pear wedges.
Methylcellulose-only coatings showed a low capacity to work as water vapor
barriers, probably due to the high water activity of pear wedges (0.98).
Although methylcellulose is the least hydrophilic of the water-soluble cellulose
ethers [therefore the most resistant to the passage of water vapor (Vojdani
1987)], it seems it is unable to form good films under high relative humidity
conditions. When working under high relative humidity, hydrophilic coatings
may incorporate water into the film structure, increasing their permeability
(McHugh and Krochta 1994). Moisture loss results obtained in this study are
EDIBLE COATINGS TO PRESERVE QUALITY OF PEAR WEDGES 307
supported by the work realized by Wong et af. (1994), who found that coatings
containing protein or polysaccharide alone provided no detectable protection
against water loss in cut surfaces, where water from the cell tissues is simply
drawn through the coating.
10 , -C Control
--t VitC-CaCI, t MC
-
- -X-
VitC-CaCI,PS
- VitC-CaCI MC-SA
0 T
0 2 4 6 8 10 12
Time (days)
FIG. 1. WEIGHT LOSS FROM PEAR WEDGES STORED 12 DAYS AT 4C AND 78% RH
Control: pear wedges immersed in water. ViC-CaC1,-PS: pear wedges dipped in a solution
containing ascorbic acid, calcium chloride, and potassium sorbate. ViC-CaCI, + MC: pear wedges
dipped in a methylcellulose solution after immersion in a solution containing ascorbic acid and
calcium chloride. VitC-CaC1, + MC-SA: pear wedges dipped in a methylcellulose and stearic acid
solution after immersion in a solution containing ascorbic acid and calcium chloride.
Texture
Texture has been used as an index of fruit quality in both fresh and
processed fruits (Huxsoll el af. 1989). Texture of fruits depends on cellular
organelles and biochemical constituents, water content, and cell wall composi-
tion; any external factors affecting fruits can modify the texture and change the
final product quality (Sams 1999). Changes in texture occur mainly as a result
of changes in the chemistry of the primary cell wall components: cellulose,
pectin, and hemicelluloses. Results of TPA analyses during storage of pear
wedges showed no differences in adhesiveness, springiness, and cohesiveness,
among treatments during storage (P < 0.5) (Table 1).
308 (3.1. OLIVAS, J.J. RODRIGUEZ and G.V. BARBOSA-CANOVAS
TABLE 1 .
CHANGES IN SOME TEXTURE PARAMETERS OF ANJOU PEAR WEDGES COATED
WITH SELECTED FORMULATIONS DURING STORAGE AT 4C FOR 12 DAYS
Treated pear wedges differed from the control in hardness (Fig. 2). Since
there was no difference among the three studied treatments (P < 0.05),calcium
addition may have been responsible for the higher values of hardness during
storage regardless of the applied coating. Textural changes in maturing fruits
have been attributed to pectin-degrading enzymes, and calcium can maintain the
structure in fruits by interacting with pectic acid in the cell walls, forming
calcium pectate (Rolle and Chism 1987). Ponting el al. (1972) found ascorbic
acid and calcium chloride to have a synergistic effect in maintaining color and
texture in refrigerated fresh apple slices. The behavior of pear wedges regarding
chewiness and gumminess throughout the storage period is also shown in Fig.
2. Control values were always lower throughout the storage period (P < 0.05).
Although Vit C-CaC1,-PS and Vit C-CaCl, + MC showed the same water
loss as the control, the presence of ascorbic acid and calcium chloride probably
helped prevent a decrease in chewiness and gumminess to the level reached by
the control. The positive effect of calcium chloride on texture might be
extended, if instead of immersing the wedges in a calcium chloride solution and
afterwards in an edible coating solution, the additives were included in the
coating solution, thus avoiding the dilution effect. After day 9, an increase in
chewiness and gumminess of the control is observed (P < 0.05),probably due
to loss of water to a critical point at which a compact structure is formed,
causing an increase in chewiness and gumminess beyond this point. According
to Krokida ef al. (2000), the maximum stress at a given compression decreases
EDIBLE COATINGS TO PRESERVE QUALITY OF PEAR WEDGES 309
26
22
18
14
10
Chewiness (N.m)
2 1 I 1 1 1
0 2 4 6 8 10 12
Time (days)
Meheriuk and Lau (1985) showed that whole Anjou pears had higher
firmness values than the control when coated with Pro-long@and Nutri-
Save@coatings. When coated with wax, whole pears were firmer over time
than nonwaxed pears (Sornsrivichai et al. 1990). Application of Nutri-Save@
solutions to Mchtosh apples at concentrations of 1.5% (wt/v) or less showed no
significant retention of fruit firmness when stored at 3C,however, a 2% coating
3 10 G.I. OLNAS, J.J. RODRIGUEZ and G.V. BARBOSA-CANOVAS
caused retention of firmness, although lower than the quality retention found in
conventional controlled atmospheres (Elson et al. 1985). Amarante ef al.
(2001b) found that a small reduction in the internal oxygen partial pressure ( p i )
in pears can substantially delay color change but not softening, which would
require a much lower reduction in p ; for substantial reduction.
Color
Physical injury as from slicing disrupts the cellular integrity of fruits,
causing browning (Vhmos-Vigyhzo 1981). Injuries allow the interaction of
polyphenol oxidase (PPO) and phenolic compounds that are normally separated
by the cell compartments of intact fruits (Luo and Barbosa-Cinovas 1996). PPO
is considered responsible for the browning of pears when cut (Kadam ef al.
1995). Reduction of O2 levels to near 0% is necessary to inhibit browning
caused by this enzyme in many fresh-cut fruit products (Gorny 1997). Browning
index (BI) of pear wedges significantly increased during the first three days of
storage (Fig. 3). From then on, BI of the control was considerably higher
compared to all other treatments (P C 0.05). Vit C-CaC1,-PS, Vit C-CaC12
+ MC, and Vit C-CaCl, + MC-SA had significantly lower browning values
but there was no difference among them (P < 0.05). Most likely, ascorbic acid
was the principal factor responsible for delaying browning, although the addition
of calcium chloride has been known to enhance browning inhibition (Ponting ef
al. 1972; Sapers and Miller 1998; Lee ef al. 2003). Previous works show that
alternative treatments can be used to preserve cut pears from browning. Sodium
erythorbate, calcium chloride, and 4-hexylresorcinol, in combination with a
modified atmosphere, have been successfully used to retard the browning of cut
Anjou pears (Sapers and Miller 1998).
45 1 T
40
25
0 2 4 6 8 10 I2
Time (days)
Volatiles
Pears produce large amounts of volatiles during ripening and storage, the
principal compounds being ethyl, propyl, butyl, and hexyl acetates, which
account for 70.6% of total volatiles (Tress1 et al. 1975; Kadam e? al. 1995). In
this study, changes in the content of ethanol, ethyl acetate, butyl acetate, and
hexyl acetate were monitored throughout storage, since postharvest handling can
significantly affect aroma production in fruits (Suwanagul 1996). Provided the
application of edible films limits the contact of the fruit with atmospheric
oxygen, and since low 0, and/or high CO, atmospheres generally reduce acetate
ester synthesis in fruits (Fellman and Mattheis 1995; Ke et al. 1994), the flavor
and aroma of the pear wedges could be affected by the presence of the films.
Ethyl Acetate. Ethyl acetate was found to be part of a group of odor active
compounds that correlate well with flavor intensity and general acceptability of
pears (Suwanagul 1996). Low O2 and/or high CO, atmospheres enhance the
activity of enzymes such as pyruvate decarboxylase (PDC) and alcohol
dehydrogenase (ADH) resulting in the accumulation of ethanol, which is used
to synthesize ethyl acetate (Ke er al. 1994). In this study, there was a higher
concentration of ethyl acetate in pears coated with treatment Vit C-CaC1, +
MC-SA ( P < 0.05) compared to the other studied treatments and the control
during storage (Fig. 5 ) . Considerably higher values of ethyl acetate in treatment
Vit C-CaC1, + MC-SA (particularly on the fourth day) could be due to
metabolization of the ethanol that remained in the initial coating to ethyl acetate.
Figure 4 shows the abrupt loss in ethanol with treatment Vit C-CaCl, + MC-
SA during the first four days. Compared to similar processes, it has been found
that presence of ethanol in apples produces an increase in the amount of ethyl
acetate (Knee and Hatfield 1981; Mattheis et al. 1991) since apples have been
demonstrated to metabolize exogenously applied ethanol to esters (Knee and
Hatfield 1981; Berger and Drawert 1984). Although ethyl acetate increased
considerably at day four, at the end of storage (12 days) there was no significant
difference between Vit C-CaC1, + MC-SA and all the other treatments and
control.
50
-Control
---c-VitCCaCl,+ MC
- VitC-CaCI;PS
- -x- - %tC-CaCI,+ MC-SA
O J I
0 2 4 6 8 10 12
Time (days)
FIG. 4. CHANGES IN ETHANOL CONTENT OF PEAR WEDGES STORED AT
4C AND 78% RH FOR 12 DAYS
Control: pear wedges immersed in water. VitC-CaCI,-PS: pear wedges dipped in a solution
containing ascorbic acid, calcium chloride, and potassium sorbate. VitC-CaCI, + MC: pear wedges
dipped in a methylcellulose solution after immersion in a solution containing ascorbic acid and
calcium chloride. VitC-CaCI, + MC-SA: pear wedges dipped in a methylcellulose and stearic acid
solution after immersion in a solution containing ascorbic acid and calcium chloride.
- -x- - vitc-caaI+MC-SA
25 i -MIC-C~C\ + MC
*p- - -.
0
0 2 4 6 8 10 12
Time (days)
CONCLUSIONS
0.016-
h Days: 0 0 0 4 0 8
a 1 0.012
.3
0
Control VitC-CaCli VitC-CaCG + VitC-CaC{ +
PS MC MC-SA
To obtain a good coating for fresh cut fruits it is necessary to look, not only
for an efficient barrier to moisture loss that has selective permeability to gases
and good carrier properties, but also is important to consider that the compo-
nents forming the edible coating can interact with fruit components and thus
affect flavor through the production of secondary volatiles when in contact with
wounded tissue. The use of edible coatings as carriers of aroma compounds or
aroma-precursors is another important role edible coatings can play to control
the quality of minimally processed fruits.
REFERENCES