Thermal Effect, Diffusion, and
Thermal Effect, Diffusion, and
Thermal Effect, Diffusion, and
Article
Thermal Effect, Diffusion, and Leaching of Health-Promoting
Phytochemicals in Commercial Canning Process of Mango
(Mangifera indica L.) and Pineapple (Ananas comosus L.)
Palitha C. Arampath 1, * and Matthijs Dekker 2
Canning of mango and pineapple is a major preservation techniques [5]. Natural fruit
juices or mixed juices and sugar syrups with arange of concentrations, 10–22 ◦ Bx are used as
the filling media in the canning of fruits or fruit pieces. The syrup is classified on the basis
of its cut-out strength, as extra light syrup (>10◦ Bx), light syrup (>14 ◦ Bx), heavy syrup
(>18 ◦ Bx), or extra heavy syrup (>22 ◦ Bx). This liquid medium facilitates heat penetration,
inactivation of enzymes, and destruction of pathogenic microorganisms [6,7]. Quality
parameters, beneficial phytochemicals, and sensory attributes of canned products are
mainly affected by leaching, the formation and degradation of compounds, non-enzymatic
browning reactions, and pigment destruction [8,9]. Phytochemicals are considered as
bioactive non-nutrient plant compounds with health benefits. These bioactive non-nutrients
are available in fruits, grains, vegetables, and other plant foods [10].
Mango is a rich source of macronutrients, micronutrients (vitamins and minerals), and
non-nutritive phytochemicals such as phenolic compounds, carotenoids, flavonoids, and
other polyphenols [11]. Flavonoids represent 60% of dietary polyphenols in plants and
potentially possess human cancer preventive abilities [12,13].
Several authors have reported that a diet rich in polyphenolic compounds is associated
with protective effects against some chronic degenerative diseases related to oxidative
stress, such as cancer and cardiovascular diseases [14]. Gallic acid (major polyphenol) and
hydrolysable tannins (p-OH-benzoic acid, m-coumaric acid, p-coumaric acid, and ferulic
acid) are present in mangoes [15].
Pineapple is a good source of several phytochemicals, such as flavonoids; coumaric
acid, ellagic acid, ferulic acid, chlorogenic acid, and micronutrients and dietary fiber. These
nutritional and non-nutritional constituents vary depending on the cultivar and several
pre- and post-harvest management practices [16].
Several varieties of canned pineapple products are available on the market, such as
chunks, titbits/pieces, and slices. A clinical study on the consumption of canned pineapple
reported reductions in the duration and incidence of infection in school children [17].
Kinetic models of thermal treatment are important to maintain new food process designs
and to assure the quality and safety of food production [18]. The degradation of, or damage
to, nutrients during thermal treatment can be predicted by determining the kinetic behavior
of these compounds. Kinetic studies on several compounds in fruits and juices have been
conducted, e.g., in orange juice [19], and raspberry pulp [20]. Improvement of food quality
with variable retort temperatures [21], global optimization of process conditions in the
batch thermal sterilization of food [22], optimization of the sterilization process of canned
food using temperature distribution [6], and heat transfer simulation and retort program
adjustment for thermal processing [7] have been reported. Studieson degradation kinetic
parameters of anthocyanins and mathematical models and estimation of activation energy
(Ea), and z-value during the thermal processing of foods and storage were reviewed [10].
Although studies on the process optimization and thermal processing of canning have
been reported, information on the fate of the beneficial bioactive compounds during the
canning of mango and pineapple is scant. In this study, processing effects on beneficial
phytochemicals, retention of compounds, and the kinetics and activation energy of bioactive
compounds were determined based on pilot-scale commercial canning of mango and
pineapple.
dCc,i
= −k l .Cc,i . (1)
dt
Cc,l = 1 − Cci (2)
where
Cc,i : fraction of intact cells (-),
Cc,l : fraction of lysed cells (-),
kl : lysis rate constant (min−1 ),
t: time (min).
For the leaching of water-soluble components to occur, cells must lyse and the compo-
nents must diffuse to the surrounding water. Due to the heterogeneous size and shape of
the fruit particles, the diffusion process is difficult to model exactly. For practical reasons, it
is therefore assumed that the lysis and diffusion processes can be described together by
first-order equations and mass balance (Equations (1) and (2)). The lysis rate constant, in
fact, is a lumped parameter also including the diffusion process. The resulting parameter
(kl ) is therefore called the leaching parameter. By making this assumption, the transfer of
components to the surrounding water can be described by a mass balance of the amount of
water in the fruit (in intact cells and lysed cells) and the surrounding water.The volume
of the free water phase (surrounding water plus water in lysed cells), in fact, increases as
more cell are lysed. This process can be described by the following relation (Equation (3)):
dMw dC
= − c,i .M f ,0 = k l .Cc,i . M f ,o (3)
dt dt
where
Mw : mass of free water (g),
Mf,0 : initial mass of fruit (g).
According to this model, the leaching of water-soluble components is a direct conse-
quence of cell lysis. The contents of the cells that lyse are added to the free water phase. To
describe this process mathematically, one has to take into account the amount of compo-
Foods 2021, 10, 46 5 of 18
nents from the lysed cells as well as the diluting effect caused by the increase in the mass
of free water caused by this lysis (Equation (4)):
" #
k l . C c,i . M f ,0 .Cv k l . C c,i . M f ,0 k l . C c,i . M f ,0 . (C f − Cw )
dCw
IL = − Cw . = (4)
dt Mw Mw Mw
where
L: refers to the fact that this component represents the change due to leaching only,
Cw : component concentration in the free water (µmol/g),
Cf : component concentration in the intact part of the fruit (µmol/g).
Thermal breakdown is described by first-order kinetics, similar to previous studies [30].
Since breakdown rates can be different in fruit and the surrounding water, different rate
constants can be used (Equations (5) and (6)):
dC f
= −k d, f .C f (5)
dt
dCw
IB = −k d,w .Cw (6)
dt
where
B: refers to the fact that this component is the change due to breakdown only,
kd,f : breakdown rate constant in fruit (min−1 ),
kd ,w : breakdown rate constant in water (min−1 ).
All estimations of the reaction rates were performed on the respective, experimentally
determined individual concentrations of each canning experiment and not by using the
average values of the three consecutive runs, effectively accounting for sample variability.
The rate constants for leaching and degradation are temperature-dependent. This fact is
described by a modified Arrhenius equation, which determines the rate constant relative
to a reference temperature (Equation (7)):
( ERa )( T 1 − 1
T)
k d = k d,re f e re f (7)
All equations were fitted to data of individual concentrations in both water and fruit
pieces simultaneously using the Athena Visual Workbench software (Athena Visual Studio,
Inc, Naperville, IL, USA). Reaction kinetics were studied by multi-response modelling
using the determinant criterion [31]. Multi-response modelling implies that more than one
reactant or product is taken into account. The determinant criterion is then more suitable
than the familiar least-squares criterion. Athena Visual Workbench was used for numerical
integration of differential equations, as well as parameter estimation of the rate constants
in the differential equations, following minimization of the determinant in order to obtain
the reaction kinetic parameters (rate constant ka and activation energy Ea ). The goodness
of fit of the models, describing first-order degradation, was calculated using the Pearson
chi-square test.
111 °C 111 °C
Vitamin C (mg/100g 25 115 °C 30 115 °C
Vitamin C (mg/100g
20 119 °C 25 119 °C
124 °C 20 124 °C
15
FW)
FW)
15
10 10
5 5
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
60
60
50 50
40
FW)
40
FW)
30 111 °C 30 111 °C
20 115 °C 20 115 °C
10 119 °C 119 °C
124 °C
10
0 124 °C
21, 10, x FOR PEER REVIEW 0 7 of 18
0 50
0 20 40 60
Time (min) Time (min)
6 111 °C 6 111 °C
115 °C 5 115 °C
5
ß-Carotene μg/g FW)
119 °C
ß Carotene (μg/g FW)
119 °C
4 124 °C 4 124 °C
3 3
2 2
1 1
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
10 111 °C 8 111 °C
115 °C 115 °C
8 6 119 °C
119 °C
TEAC (μmol/g FW)
TEAC (μmol/g FW)
6 124 °C 124 °C
4
4
2
2
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
Mango Pineapple
Figure C,
Figure 1. Vitamin 1. Vitamin C, total
total phenols, phenols, β-carotene,
β-carotene, and troloxantioxidant
and trolox equivalent equivalent capacity
antioxidant capacity
(TEAC) (TEAC)
in pieces (closed symbols)
in pieces (closed symbols) and syrup (open symbols) during the canning of mango and pineapple
and syrup (open symbols) during the canning of mango and pineapple at different temperatures. The legend represents the
at different temperatures. The legend represents the steady state coldest spot temperature in the
steady state coldest spot temperature in the can measured by the iButton.
can measured by the iButton.
hydrolysable polyphenols being leached from pieces to the syrup with the progression of
heat treatment.
3.3. β-Carotene
The β-carotene content in fresh mango (5.65 µg/g FW) was within the range 1.7–
18 µg/g reported by [40]. The β-carotene content determined in fresh pineapple (4.82µg/g
FW) was higher than that reported [28,41]. The retention percentage of β-carotene in
mango and pineapple pieces was 56–14% and 47–20%, respectively at 115–130 ◦ C following
retorting for 40 min. Further, the degradation of β-carotene increased with the duration
of thermal treatment. Leaching of β-carotene from pieces to sugar syrup occurs during
canning (Figure 1). β-Carotene contents in sugar syrup of 1.25 µg/g FW and 0.91 µg/g
FW were measured at 115 ◦ C after 10 min of retorting in canned mango and pineapple,
respectively. A loss of β-carotene, 17% in canned mango was reported [42], and the value
was comparable with our finding at 130 ◦ C.
3.5. Flavonoids
3.5.1. Mango Fruit Pieces
Flavonoids measured in canned fruit pieces and sugar syrup at different thermal
treatments are shown in Figures 2 and 3. In fresh mango, catechin (42.36 µg/g), tannic
acid (48.32 µg/g), chlorogenic acid (18.14 µg/g), epicatechin (26.35 µg/g), and gallic acid
(24.53 µg/g) were measured in FW. The content of gallic acid in mango was higher than
the previously reported value of 6.9 µg/g [44]. The concentrations of these compounds
reduced substantially during fruit preparation for canning and can exhausting followed by
retorting. Therefore, the values were 50% lower than the values in fresh fruits after 10 min.
A retention rate of catechin, 9–20% was observed in both mango and pineapple pieces at
115 and 130 ◦ C.
21, 10, x FOR PEER REVIEW 9 of 18
15 111 °C 10 111 °C
115 °C 115 °C
6
4
5
2
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
25 111 °C 20 111 °C
115 °C 115 °C
20 119 °C
15 119 °C
124 °C
124 °C
15
10
10
5
5
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
10 111 °C 8 111 °C
Chlorogenic acid (μg/g
115 °C
Chlorogenic acid (μg/g
115 °C
8 119 °C 6 119 °C
124 °C 124 °C
6
FW)
4
FW)
4
2
2
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
Mango Pineapple
Figure 2. tannic
Figure 2. Catechin, Catechin, tannic
acid, acid, and chlorogenic
and chlorogenic acid concentrations
acid concentrations in mango
in mango and and pineapple
pineapple pieces (closed symbols) and
pieces (closed symbols) and syrup (open symbols) during canningat different temperatures.
syrup (open symbols) during canningat different temperatures.
Retention of tannic acid in canned mango pieces was greater than retention of catechin
(Figure 2). The retention rate of chlorogenic acid was 19–34% in canned mango pieces
following treatment at 115 and 130 ◦ C for 40 min. However, the retention rate of epicatechin
was greater than that of the other flavonoid compounds17–44% (epicatechin) compared
with 11–27% (gallic acid) at 115–130 ◦ C for 40 min in both canned mango and pineapple.
A non-flavonoid compound 5-hydroxymethylfurfural (HMF) was detected in canned
fruit pieces and syrup. HMF was formed due to the thermal effect with available sugars,
and the quantity was increased with an increasing retort temperature and time. In this
experiment, the HMF levelincreased by sixfold from 115 (10 min) to 130 ◦ C (40 min) in
mango pieces (Figure 3).
Foods 2021, 10, 46 10 of 18
15 111 °C 10 111 °C
115 °C 115 °C
5 4
2
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
20 111 °C 15 111 °C
115 °C
Gallic acid (μg/g FW)
115 °C
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
15 111 °C 20 111 °C
115 °C
HMF (μg/g FW)
115 °C
HMF (μg/g FW)
119 °C 15
10 119 °C
124 °C 124 °C
10
5
5
0 0
0 20 40 60 0 20 40 60
Time (min) Time (min)
Mango Pineapple
Figure 3. Epicatechin, gallic acid, and Hydroxymethylfurfural (HMF) concentrations in mango
Figure 3. Epicatechin, gallic acid, and Hydroxymethylfurfural (HMF) concentrations in mango and pineapple pieces (closed
and pineapple pieces (closed symbols) and syrup (open symbols) during canningat different tem-
symbols) and syrup (open symbols) during canningat different temperatures.
peratures.
120 111 °C
100 115 °C
119 °C
40
20
0
0 10 20 30 40 50
Time (min)
120 111 °C
115 °C
100
119 °C
TEAC (μmol/g FW)
80 124 °C
60
40
20
0
0 10 20 30 40 50
Time (min)
Figure
Figure 4. Percentages
4. Percentages of vitamin
of vitamin C and
C and TEAC
TEAC in in pineapple
pineapple pieces
pieces expressed
expressed asas percentages
percentages ofof the
the
original content in initial fruit during canning at different temperatures. Lines are fitted to a
original content in initial fruit during canning at different temperatures. Lines are fitted to a modelmodel
describing first-order degradation using Equations (1)and(2).
describing first-order degradation using Equations (1) and (2).
TheThe vitamin
vitamin C content
C content in pineapple
in pineapple pieces
pieces decreased
decreased astemperature
as the the temperature and retort-
and retorting
ing time increased. The highest degradation rate was evident at an internal
time increased. The highest degradation rate was evident at an internal can temperature can tempera-
of 124 ◦
ture ofC. 124 °C.A similar
A similar findingfinding for the thermal
for the thermal degradation
degradation of vitamin
of vitamin C in squeezedor-
C in squeezedoranges
anges
heated 120–150at◦120–150
atheated °C was [46].
C was reported reported [46]. However,
However, a simple first-order
a simple first-order degradationdegradation
model
model
does does not
not always always describe
properly properlythe describe the degradation
degradation kinetics ofkinetics
vitaminofC.vitamin C. In our
In our experi-
experiments,
ments, theeffect
the thermal thermal effect
on the on the degradation
degradation kinetics
kinetics of the of the has
compounds compounds has been
been described
by described by a modelthe
a model combining combining thekinetic
first-order first-order
modelkinetic modelbalance
and mass and mass balance applicable
applicable for cell
for cell lysis/leaching
lysis/leaching and degradation
and degradation during theduring
canningtheofcanning of fruit
fruit pieces pieces (Equations
(Equations (1)–(7)). (1)–
(7)).
Table 1. Goodness of fit test statistics (X 2 ), and associated significant probabilities (in parenthesis) of
theTable
fitted curves for vitamin
1. Goodness C and
of fit test statistics (𝑋 ), and associated
trolox equivalent antioxidant capacity(TEAC)
significant at different
probabilities internal
(in parenthesis)
canoftemperatures
the fitted curves fordifferent
for the vitamin thermal
C and trolox equivalent
treatment antioxidant
durations shown incapacity(TEAC)
Figure 5. at different
internal can temperatures for the different thermal treatment durations shown in Figure 5.
Internal Can Temperature (◦ C)
Compound
Internal can temperature (°C)
Compound 111 115 119 124
111 115 119 124
Vitamin C 7.87(0.55) 12.22(0.20) 4.01(0.91) 5.43(0.79)
Vitamin C
TEAC
7.87(0.55)
6.03(0.74)
12.22(0.20)
8.60(07)
4.01(0.91)
5.77(0.76)
5.43(0.79)
19.20(0.02)
TEAC 6.03(0.74) 8.60(0.47) 5.77(0.76) 19.20(0.02)
Foods 2021, 10,
Foods 2021, 10, 46
x FOR PEER REVIEW 13 of
13 of 18
18
Vitamin C
Vitamin C and
and TEAC
TEAC concentrations
concentrations inin pineapple
pineapple pieces
pieces and
and syrup
syrup during
during canning
canning
are given
are given in
in Figure
Figure 5.
5. The
The lines
lines were
were fitted
fitted to
to aa model
model describing
describing cell
cell lysis,
lysis, leaching,
leaching, and
and
Equations(1)–(7).
degradation by Equations (1)–(7). Degradation
Degradation can can occur
occur in
in fruit
fruit pieces and sugar syrup,
model.Degradation and leaching of vitamin
as described by the model.Degradation vitamin C C in
in canned
canned pineapple
pineapple
pieces gradually increased as thethe internal
internal can
can temperature
temperature increased.
increased. The
The lowest
lowest vitamin
vitamin
C content
content (1.45
(1.45 mg/100
mg/100g)g)in pineapple pieces was measured
in pineapple pieces was measured at at 124 ◦
°CC after 40 min. In
40 min. In
sugar syrup
contrast, the vitamin C content in the sugar syrup ofof pineapple
pineapple cans
cans gradually
gradually increased
increased
lysis occurring
due to cell lysis occurring in the
the pieces
pieces followed
followed by by leaching
leaching to
to the
the surrounding
surrounding liquid
liquid
matrix.
30.0
111 °C
25.0 115 °C
119 °C
20.0
Vitamin C (mg/100g FW)
124 °C
15.0
10.0
5.0
0.0
0.0 10.0 20.0 30.0 40.0 50.0
Time (min)
9.00
111 °C
8.00
115 °C
7.00
119 °C
6.00
TEAC (μmol T/g FW)
124 °C
5.00
4.00
3.00
2.00
1.00
0.00
0.0 10.0 20.0 30.0 40.0 50.0
Time (min)
Figure 5. Vitamin
Vitamin CC and
and TEAC
TEACconcentrations
concentrationsininpineapple
pineapplepieces
pieces(closed
(closedsymbols)
symbols)andandsyrup
syrup
(open
(open symbols)
symbols) duringduring canningat
canningat differentdifferent temperatures.
temperatures. Lines
Lines are fittedare
to fitted
a modelto adescribing
model describing
degradation
degradation
and leaching and leaching
using using
Equations (1)Equations
and (2). (1)and(2).
Leached vitamin
vitaminCCininthe
the sugar syrup
sugar is subjected
syrup to further
is subjected degradation
to further during
degradation ther-
during
mal treatment
thermal at 111,
treatment 115,
at 111, 119,
115, and
119, and ◦
124°C.
124 C.TheThedata
datarecorded
recordedfor
forsugar
sugarsyrup
syrup fitted the
the
model describing cell lysis, leaching, and degradation (Figure 5). Comparatively,
Comparatively, aa higher
higher
content of vitamin C was measured in the syrup at 111 ◦°C
at 111 after 10
C after 10 min,
min, while
while the
the lowest
lowest
was measured
content was measured atat 124 ◦
124 °Cafter
C after 40 min. AA similar
similar trend was shown in the fitted
fitted data
data
sugar syrup.
for TEAC measured in the sugar syrup.
Foods 2021, 10, 46 14 of 18
In our experiments, it is evident that the application of thermal treatment at the lowest
temperature preserves a comparatively high content of beneficial health compounds in
both fruit pieces and syrup. Therefore, selection of the optimal minimumtime–temperature
combination considering microbiological safety is one of the best strategies to ensure the
maximal occurrence of healthpromoting compounds in canned fruit products.
The antioxidant activity, as measured by TEAC, in the pieces and syrup is affected
by leaching and degradation of compounds. The occurrence of vitamin C and TEAC in
fruit pieces and syrup showed similar trends with slight changes. Greater degradation
of TEAC in pineapple pieces occurred at 124 ◦ C than at 111–119 ◦ C. The TEAC in sugar
syrupshowed a similar trendafter the first 10 min, while more prominent reduction after
10 min was evident at 124 ◦ C than at 111 and 115 ◦ C. The TEAC in pineapple pieces and
syrup was stable at 111 ◦ C.β-Carotene, catechin, tannic acid, chlorogenic acid, epicatechin,
and gallic acid values measured in both the fruit pieces and sugar syrup are shown in
Figures 1–3. The degradation kinetics of these compounds were almost the same as those
described and shown for vitamin C and TEAC (Figure 5).
The total polyphenol content was comparatively stable. It increased during thermal
treatment, as elaborated previously. There is a lack of recent literature on the reaction
kinetics of canned mango and pineapple. However, color degradation kinetics during
thermal processing of mango and pineapple puree have been reported [47,48].
The degradation rate constant (ka ) and activation energy (Ea ) of vitamin C, TEAC,
β-carotene, and flavonoids are shown in Table 2. The thermo stability is described by
both Ea and ka values. A reaction with a higher Ea indicates a strong dependency of
the rate constant on temperature. Compounds with higher Ea and lower ka values and
vice versa show thermo stability. In exceptional situations, higher Ea and ka values in
an unstable compound are also associated with thermo stability. In mango pieces, the
estimated Ea value for vitamin C, 109 ± 6 kJ mol−1 , was higher than that in pineapple pieces
(Ea 81 ± 6 kJ mol−1 ), while ka (2.4 ± 0.1 × 10−2 min−1 ) was similar in both fruits. In mango
pieces, the estimated Ea value for β-carotene (148 ± 4 kJ mol−1 ) was higher than that in
pineapple pieces (92 ± 5 kJ mol−1 ), while ka value in mango (0.9 ± 0.0 × 10−2 min−1 ) was
lower than that in pineapple (1.3 ± 0.1 × 10−2 min−1 ). Therefore, the thermo stability of
β-carotene is higher in canned mango pieces, and 56% retention in mango was found to be
higher than that in pineapple (46%) after thermal treatment at 115◦ C for 10 min. Similarly,
the higher values of Ea for gallic acid (73 ± 3 kJ mol−1 ) and TEAC (106 ± 8 kJ mol−1 ) in
pineapple pieces indicate lower dependency of the degradation rate constants for canned
mango pieces.
Ea values vary based on the type of fruit [20,49]). Variation in the Ea value (35.9–
94.0 kJ mol−1 ) for ascorbic acid degradation has been reported [37]. The Ea values, de-
termined for vitamin C in this study, 81 ± 6 kJ mol−1 (mango) and 109 ± 6 kJ mol−1
(pineapple) are within the range previously reported. Leaching or migration of compounds
is mainly due to thermal effects on the cell walls and membranes and the exposure of the
cut surfaces of fruit to sugar syrup with a low soluble solid content (15 ◦ Bx).The leaching
and degradation of vitamin C in pineapple piecesgradually increased as the temperature
increased.
In pineapple, the degradation rate constant at 111 ◦ C (kd111 ) values of catechin, tannic
acid, chlorogenic acid, and epicatechin were higher than those in mango, while the Ea
values were lower than those in mango (Table 2). Therefore, canned mango pieces retain
greater amounts of the above tested flavonoids compared with canned pineapple pieces. In
canned mango pieces, retention rates of 27% (vitamin C), 78% (polyphenols), 45% (TEAC),
and 56% (β-carotene) were determined at 111 ◦ C (40 min), whereas in canned pineapple
pieces, there were retention rates of only 31%, 79%, 26%, and 46%, respectively, for the
same compounds.
Foods 2021, 10, 46 15 of 18
Table 2. Kinetic parameters for the degradation of compounds in pineapple and mango during
canning (first-order model). Values are given with their 95% confidence intervals.
Pineapple Mango
Constituent kd,111 Ea kd,111 Ea
(10−2 ) min−1 kJ mol−1 (10−2 ) min−1 kJ mol−1
Vitamin C 2.4 ± 0.1 81 ± 6 2.4 ± 0.1 109 ± 6
β-carotene 1.3 ± 0.1 92 ± 5 0.9 ± 0.0 148 ± 4
Catechin 3.5 ± 0.1 35 ± 3 1.4 ± 0.1 62 ± 4
Tannic acid 3.5 ± 0.1 44 ± 2 1.0 ± 0.0 83 ± 4
Chlorogenic acid 2.7 ± 0.1 31 ± 3 1.2 ± 0.0 96 ± 4
Epicatechin 2.1 ± 0.0 25 ± 2 0.9 ± 0.0 82 ± 3
Gallic acid 2.5 ± 0.1 73 ± 3 1.4 ± 0.0 51 ± 4
TEAC 2.2 ± 0.1 106 ± 8 1.5 ± 0.1 61 ± 5
4. Conclusions
The retention of health-promoting compounds was found to be higherin canned
mango than in canned pineapple based on the kinetic parameters (ka and Ea ) determined.
Foods 2021, 10, 46 16 of 18
Higher temperature treatments may facilitate the cell lysis and leaching of health-promoting
compounds into sugar syrup. The estimated Ea values of vitamin C were 109 ± 6 (mango)
and 81 ± 6 kJ mol−1 (pineapple) and the ka value, 2.4 ± 0.1 × 10−2 min−1 , was the
same for both fruits. The total phenolic content in mango increased from 77% (115 ◦ C)
to 118% (130 ◦ C) after 40 min, while in pineapple, the content was 79% and 152%. The
greater retention at 130◦ C is due to release of soluble free and hydrolysable bound phenolic
compounds in the cellular matrices of both fruit pieces during the expended thermal
treatment. There were evidences of leaching and degradation of β-carotene and flavonoids.
Accumulation of HMF was highly temperature dependent, and 13.7 and 14.6 µg/g FW
in the sugar syrup of both fruit cans processed at 130 ◦ C (40 min) were measured. The
first-order degradation model in combination with the modified Arrhenius equation fitted
the experimental data very well, as reflected by the goodness of fit test statistic (X 2 )
for all variables with the exception of TEAC at 124 ◦ C. The estimated parameters for
the degradation kinetics clearly show the differences in behavior of the compounds in
different fruits. Processing of mango and pineapple at the lowest optimal temperature with
the minimum liquid content in the cans, without disturbing the heat transfer would be
applicable for better retention of health promoting phytochemicals. Further, in order to
minimize higher thermal treatment and prolong thermal process time, pretreatments such
as steam blanching of fruit pieces and microwave treatment can be applied to partial or
complete destruction of pathogenic microorganisms and inactivation of enzyme activities
in fruit pieces. These pretreated fruit pieces and sugar syrup or fruit juice (heated and
cooled previously) are filled in to the sterile cans, followed by conventional canning
process. Similarly fruit pieces can be retorted using retort pouches filled with syrup of fruit
juices. The suggest technique can reduce the thermal effect on fruit pieces substantially
and be able toretain the bioactive phytochemicals in comparison to conventional canning
process. However future investigation and scale up studies should be conducted on
mango, pineapple and other potential fruits to optimize the process control parameters
for commercial operations. The research finding presented is valuable information for
the optimization and retention of these bioactive phytochemicals compounds through
applicable process design.
Author Contributions: Conceptualization, P.C.A. and M.D.; methodology, P.C.A.; software, M.D.;
validation, P.C.A. and M.D.; formal analysis, P.C.A.; investigation, P.C.A.; resources, M.D.; data
curation, P.C.A.; writing—original draft preparation, P.C.A.; writing—review and editing, P.C.A. and
M.D.; visualization, P.C.A.; supervision, M.D.; project administration, M.D.; funding acquisition,
M.D. All authors have read and agreed to the published version of the manuscript.
Funding: This research was funded by the Sandwich Ph.D. programme of Wageningen University,
the Netherlands.
Acknowledgments: The authors acknowledge the technical assistance provided by the Food Quality
and Design Group, Department of Agrotechnology and Food Sciences, Wageningen University,
The Netherlands.
Conflicts of Interest: The authors declare no conflict of interest. The funders had no role in the design
of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or
in the decision to publish the results.
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