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Quality Changes of Shrimp Crac

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Int Aquat Res (2016) 8:227–238

DOI 10.1007/s40071-016-0138-x

ORIGINAL RESEARCH

Quality changes of shrimp cracker covered with fish


gelatin film without and with palm oil incorporated
during storage
Krisana Nilsuwan . Soottawat Benjakul . Thummanoon Prodpran

Received: 24 March 2016 / Accepted: 2 July 2016 / Published online: 22 July 2016
Ó The Author(s) 2016. This article is published with open access at Springerlink.com

Abstract Impact of fish gelatin film incorporated without and with palm oil on the quality changes of fried
shrimp cracker stored for 15 days at room temperature was investigated, in comparison with nylon/linear low-
density polyethylene (nylon/LLDPE) film. The moisture content and water activity of shrimp cracker pack-
aged with all films increased during storage (p \ 0.05). The lowest moisture content and water activity were
found in the sample packaged with nylon/LLDPE film throughout the storage (p \ 0.05). Sample packaged
with fish gelatin films incorporated with palm oil generally had lower moisture content than those without oil
added during the first 12 days of storage (p \ 0.05). During 15 days of storage, shrimp cracker packaged with
nylon/LLDPE film generally had the lower PV and TBARS value as well as volatile compounds, except for n-
nonanal, than those stored in fish gelatin films, regardless of oil incorporation. The decrease in crispiness and
increase in toughness occurred in all samples during the 15 days of storage. Nevertheless, the lower changes
were observed in the sample packaged with nylon/LLDPE film. Overall, gelatin film showed excellent oxygen
barrier property, which was associated with the retardation of lipid oxidation. The incorporation of oil into
gelatin film could lower WVP, but negatively increased oxygen permeability of the resulting film. Thus, the
improvement of gelatin film is still required.

Keywords Quality changes  Gelatin film  Nylon/LLDPE film  Shrimp cracker

Abbreviations
GF and EF Fish gelatin film incorporated without and with palm oil
Nylon/LLDPE Nylon/linear low-density polyethylene
FFS Film-forming solution
FFD Film-forming dispersion
TS Tensile strength
EAB Elongation at break
WVP Water vapour permeability
OTR Oxygen transmission rate
PV Peroxide value

K. Nilsuwan  S. Benjakul (&)


Department of Food Technology, Faculty of Agro-Industry, Prince of Songkla University, Hat Yai, Songkhla 90112,
Thailand
e-mail: soottawat.b@psu.ac.th

T. Prodpran
Department of Material Product Technology, Faculty of Agro-Industry, Prince of Songkla University, Hat Yai,
Songkhla 90112, Thailand

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228 Int Aquat Res (2016) 8:227–238

TBARS Thiobarbituric acid reactive substances


aw Water activity

Introduction

During the last decade, there has been an increasing interest in edible or biodegradable films based on
biopolymers. The main advantage of biopolymers over synthetic polymers is their biodegradability.
Biopolymers such as polysaccharides and proteins have been used as biodegradable and/or edible food
packaging materials (Artharn et al. 2009; Gennadios et al. 1997). Proteins are important biopolymers pos-
sessing good film-forming ability. Among proteins, fish gelatin has been used as film-forming material
(Gómez-Guillén et al. 2009). Properties of fish gelatin-based films depend on various factors such as the
source of gelatin, concentration of gelatin, plasticisers and substances incorporated into the film-forming
solutions (Jongjareonrak et al. 2006; Limpisophon et al. 2010; Tongnuanchan et al. 2012). Gelatin film
generally has good mechanical and oxygen barrier properties. However, it has high water absorptivity due to
hydrophilicity of gelatin molecules and the presence of hydrophilic plasticisers such as glycerol (Gennadios
et al. 1994; Krochta and De Mulder-Johnston 1997; McHugh and Krochta 1994). To improve water vapour
barrier properties of the gelatin films, hydrophobic substances such as fats and oils have been added (Bertan
et al. 2005; Tongnuanchan et al. 2012). Recently, gelatin film incorporated with palm oil has been prepared by
Tongnuanchan et al. (2015) and it had the lowered water vapour permeability. With the improved water
vapour barrier property, the gelatin films incorporated with fats and oils could become an environmental
friendly edible packaging, which could be used to maintain the quality of foods, especially those prone to the
textural changes induced by moisture absorption. Thus, the aim of this work was to study the effect of the
gelatin films incorporated without and with palm oil on the quality of shrimp cracker during the extended
storage.

Materials and methods

Materials and chemicals

Glycerol, soy lecithin (HLB = 4.0) and trichloroacetic acid were obtained from Merck (Darmstadt, Germany).
Ammonium thiocyanate and 1,1,3,3-tetramethoxypropane (MDA) were purchased from Sigma-Aldrich (St.
Louis, MO, USA). All chemicals were of analytical grade. Fish gelatin from tilapia skin (*240 bloom) was
procured from Lapi Gelatine S.p.A (Empoli, Italy). Palm oil was obtained from OLEEN Company Limited
(Bangkok, Thailand).

Preparation of films from fish gelatin incorporated without and with palm oil

Preparation of film-forming solution and dispersion

Film-forming solution and dispersion were prepared according to the method of Tongnuanchan et al. (2015)
with slight modifications. Gelatin (3.5 g) was dissolved in 90 mL of distilled water and then heated at 70 °C
for 30 min. Glycerol was added into solution to obtain the concentration of 30 g/100 g gelatin. The mixture
was stirred using a magnetic stirrer for 5 min. The resulting solution was termed as ‘film-forming solution,
FFS’. For another portion of gelatin solution, glycerol was added to gelatin solution at the level of 10 g/100 g
protein. Palm oil was mixed with soy lecithin at a level of 50 g/100 g palm oil and then transferred into the
prepared gelatin solution to obtain the palm oil concentration of 75 g/100 g protein. The volume was adjusted
to 100 mL using distilled water. The mixture was homogenised at a speed of 22,000 rpm for 3 min using a
rotor–stator homogeniser (IKA Labortechnik homogeniser, Selangor, Malaysia). The coarse emulsion was
passed through a Microfluidiser (Model HC-5000, Microfluidiser, Newton, MA, USA) at 20.68 MPa for two

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Int Aquat Res (2016) 8:227–238 229

passes. Fine emulsion was referred to as ‘film-forming dispersion, FFD’. Both FFS and FFD were subjected to
film preparation.

Film casting and drying

Prior to casting, FFS and FFD were subjected to air removal by a vacuum pump (Diaphragm vacuum pump,
Wertheim, Germany) for 30 min at room temperature. FFS or FFD (4 mL) were cast onto a rimmed silicone
resin plate (50 9 50 mm2) and air-blown for 12 h at room temperature (28–30 °C) prior to further drying at
25 °C and 50 ± 5 % relative humidity (RH) for 24 h in an environmental chamber (WTB Binder, Tuttlingen,
Germany). The resulting films were manually peeled off and subsequently analysed.

Determination of film properties

Film thickness The thickness of film was measured using a micrometer (Mitutoyo, Model ID-C112PM,
Serial No. 00320, Mitutoyo Corp., Kawasaki-shi, Japan). Five random locations around each film of ten film
samples were used for determination of average thickness.

Mechanical properties Prior to testing, films were conditioned for 48 h at 25 °C and 50 ± 5 %RH. Tensile
strength (TS) and elongation at break (EAB) were determined as described by Iwata et al. (2000) using the
Universal Testing Machine (Lloyd Instrument, Hampshire, UK) equipped with tensile load cell of 100 N. Ten
samples (2 9 5 cm2) with an initial grip length of 3 cm were used for testing. Cross-head speed was set at
30 mm/min.

Water vapour permeability (WVP) WVP was measured using a modified ASTM method (ASTM 1989) as
modified by Shiku et al. (2004). The films were sealed on an aluminium permeation cup containing dried silica
gel (0 %RH) with silicone vacuum grease and a rubber gasket to hold the films in place. The cups were placed
in a desiccator containing the distilled water at 30 °C. The cups were weighed at 1-h intervals over a 10-h
period. WVP of the film was calculated as follows:

wl
WVP ðg/m s PaÞ ¼
AtðP2  P1 Þ

where w is the weight gain of the cup (g); l is the film thickness (m); A is the exposed area of film (m2); t is the
time of gain (s); P2 - P1 is the vapour pressure difference across the film (4242.31 Pa at 30 °C).

Oxygen transmission Oxygen transmission rate (OTR) of films was measured according to the ASTM
D3985-05 method. An Oxygen Permeation Analyser (Illinois model 8000, Illinois Instruments Inc., USA) was
used to measure oxygen transmission rates through the film. Each film was placed on a stainless steel mask.
The mask was then placed in a test cell and exposed to an oxygen atmosphere flow on one side and a nitrogen
atmosphere flow on the other. Oxygen transmission rates were measured at 25 ± 1 °C and 50 ± 2 %RH. The
film was allowed to equilibrate for 10 h before measurements.

Preparation of shrimp cracker

Dried shrimp crackers were obtained from a local market in Songkhla, Thailand. They had an average
diameter of 5 mm with thickness of 1.5 mm. Crackers were fried using an electric deep fryer containing 4 L of
frying oil. Palm oil used as a frying medium was preheated to 180 °C before frying. Samples were placed in
the frying basket and immersed into the oil for 30 s until samples are completely puffed. Thereafter, fried
samples were placed on the screen to drain the oil for 5 min. The fried shrimp cracker was blotted with paper
towels to remove an excess oil on the surface and allowed to cool at room temperature (26–28 °C),
approximately 15 min before being packaged.

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230 Int Aquat Res (2016) 8:227–238

Study on quality changes of fried shrimp cracker during storage

Fried shrimp cracker (1.4 g) was placed into an aluminium cup and covered with fish gelatin films incor-
porated without and with palm oil or nylon/LLDPE film. Fried shrimp cracker stored in aluminium cup
without packaging was prepared as the control. The samples were stored at 28 ± 0.5 °C and 65 ± 5 %RH.
Shrimp cracker samples were taken every 3 days for totally 15 days for analyses.

Moisture content and water activity

Moisture content was determined by the method of AOAC (2000). Water activity (aw) was measured using a
water activity meter (4TEV, Aqualab, Pullman, WA, USA).

Peroxide value

Peroxide value (PV) was determined as per the method of Richards and Hultin (2000) with a slight modifi-
cation. Ground shrimp cracker (1 g) was homogenised at a speed of 13,500 rpm for 2 min in 11 mL of
chloroform/methanol (2:1, w/v). Homogenate was filtered using Whatman No. 1 filter paper. Two millilitres of
NaCl (5 g/L) were added to 7 mL of the filtrate. The mixture was vortexed at a moderate speed for 30 s and
then centrifuged at 30009g for 3 min to separate the sample into two phases. Two millilitres of cold chlo-
roform/methanol mixture (2:1) were added to 3 mL of the lower phase. Twenty-five microlitres of ammonium
thiocyanate and 25 lL of iron(II) chloride were added to the mixture (Shanta and Decker 1994). Reaction
mixture was allowed to stand for 20 min at room temperature prior to reading the absorbance at 500 nm. A
standard curve was prepared using cumene hydroperoxide at a concentration range of 0.5–50 ppm. PV was
expressed as mg cumene hydroperoxide/kg sample.

Thiobarbituric acid-reactive substances (TBARS)

TBARS values were determined as described by Buege and Aust (1978). Ground shrimp cracker (0.2 g) was
mixed with 2.5 mL of a TBA solution containing 3.75 g/L thiobarbituric acid, 150 g/L trichloroacetic acid
and 0.25 N HCl. The mixture was heated in a boiling water bath (95–100 °C) for 10 min to develop a pink
colour, cooled with running tap water and then sonicated for 30 min, followed by centrifugation at 50009g at
25 °C for 10 min. The absorbance of the supernatant was measured at 532 nm. A standard curve was prepared
using 1,1,3,3-tetramethoxypropane (MDA) at the concentration ranging from 0 to 10 ppm and TBARS value
was expressed as mg MDA equivalent/kg sample.

Textural properties

Textural property of shrimp cracker was measured at room temperature by a compressive test using a texture
analyser (Stable Micro Systems, Guildford, UK). Ottawa cell with flat square probe was used to determine the
crispiness, in which the maximum force required to break the shrimp cracker samples was recorded.
Toughness was determined by measuring the area under the curve during compressing. The studies were
conducted using a pre-test speed of 1.0 mm/s, test speed of 2.0 mm/s, distance of 5.0 mm, and load cell of
50 kg.

Volatile compounds

Volatile compounds in fried shrimp cracker samples were determined using a solid-phase micro-extraction gas
chromatography–mass spectrometry (SPME-GC–MS) following the method of Iglesias and Medina (2008)
with a slight modification.

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Int Aquat Res (2016) 8:227–238 231

Extraction of volatile compounds by SPME fibre

To extract volatile compounds, 1 g of sample was mixed with 4 mL of deionised water and stirred contin-
uously to disperse the sample. The mixture was heated at 60 °C in 20 mL headspace vial with equilibrium
time of 10 h. The SPME fibre (50/30 lm DVB/CarboxenTM/PDMS StableFlexTM) (Supelco, Bellefonte, PA,
USA) was conditioned at 270 °C for 15 min before use and then exposed to the headspace. The 20-mL vial
(Agilent Technologies, Palo Alto, CA, USA) containing the sample extract and the volatile compounds were
allowed to absorb into the SPME fibre at 60 °C for 1 h. The volatile compounds were then desorbed in the GC
injector port for 15 min at 270 °C.

GC–MS analysis

GC–MS analysis was performed in a HP 5890 series II gas chromatography (GC) coupled with HP 5972 mass-
selective detector equipped with a splitless injector and coupled with a quadrupole mass detector (Hewlett
Packard, Atlanta, GA, USA). Compounds were separated on a HP-Innowax capillary column (Hewlett
Packard, Atlanta, GA, USA) (30 m 9 0.25 mm ID, with film thickness of 0.25 lm). The GC oven temper-
ature program was: 35 °C for 3 min, followed by an increase of 3 °C/min to 70 °C, then an increase of 10 °C/
min to 200 °C, and finally an increase of 15 °C/min to a final temperature of 250 °C and holding for 10 min.
Helium was employed as a carrier gas, with a constant flow of 1 mL/min. The injector was operated in the
splitless mode and its temperature was set at 270 °C. Transfer line temperature was maintained at 260 °C. The
quadrupole mass spectrometer was operated in the electron ionisation (EI) mode and source temperature was
set at 250 °C. Initially, full scan mode data were acquired to determine appropriate masses for the later
acquisition in scan mode under the following conditions: mass range, 25–500 amu and scan rate, 0.220 s/scan.
All the analyses were performed with ionisation energy of 70 eV, filament emission current at 150 lA, and the
electron multiplier voltage at 500 V.

Analyses of volatile compounds

Identification of volatile compounds in the samples was done by consulting ChemStation Library Search
(Wiley 275.L). Identification of compounds was performed, based on the retention time and mass spectra in
comparison with those of standards from ChemStation Library Search (Wiley 275.L). Quantification limits
were calculated to a signal-to-noise (S/N) ratio of 10. The identified volatile compounds were expressed in the
terms of relative abundance.

Statistical analysis

All experiments were run in triplicate with different three lots of films. Data were subjected to analysis of
variance (ANOVA) and mean comparisons were carried out by Duncan’s multiple range test. Analysis was
performed using the SPSS package (SPSS for windows, Inc., Chicago, IL, USA).

Results and discussions

Properties of different films

Films from fish gelatin incorporated without and with palm oil and nylon/linear low-density polyethylene
(nylon/LLDPE) had varying properties as shown in Table 1. Different films showed various thickness. Film
from fish gelatin incorporated with palm oil (EF) showed the higher thickness, whilst gelatin film (GF) had the
lowest thickness (p \ 0.05). For tensile strength (TS) and elongation at break (EAB), nylon/LLDPE film had
the highest values (p \ 0.05). When comparing between GF and EF samples, the latter showed the higher TS
and EAB than the former (p \ 0.05). Oil droplet incorporated in matrix might strengthen the resulting films.
Oil droplets might reduce the interaction between gelatin chains as indicated by higher EAB. This reduction in
protein–protein interaction might take place at appropriate degree, which brought about the increased

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Table 1 Thickness, tensile strength (TS), elongation at break (EAB), water vapour permeability (WVP) and oxygen transmission
rate (OTR) of films from fish gelatin incorporated without (GF) and with (EF) palm oil and nylon/linear low-density polyethylene
(nylon/LLDPE) film
Films Thickness (mm) TS (MPa) EAB (%) WVP (910-12 g/m s Pa) OTR (cc/m2 day)

Nylon/LLDPE 0.080 ± 0.001*b 48.75 ± 1.06a 132.5 ± 3.70a 0.81 ± 0.16c 92.50 ± 3.70a
c c c a
GF 0.055 ± 0.002 26.90 ± 1.19 40.17 ± 1.37 23.90 ± 0.69 3.53 ± 0.28c
a b b b
EF 0.086 ± 0.001 41.00 ± 0.47 59.65 ± 1.11 4.50 ± 0.04 63.20 ± 4.42b
Different superscript lowercase letters in the same column indicate significant differences (p \ 0.05)
* Mean ± SD (n = 3)

extension of film before breaking. Upon film stretching without breaking, gelatin molecule in the film matrix
could undergo more orientation, which could withstand more tensile load. This led to the increased strength
(i.e. TS) of the palm oil-incorporated gelatin film, compared to control film. For water vapour permeability
(WVP), nylon/LLDPE film, which is the synthetic film, had the lowest value (p \ 0.05). Gelatin film showed a
decrease in WVP when oil was incorporated in the film (EF). Oil droplets distributed in film acted as barrier
against water vapour adsorption and migration through the film. Overall, film from nylon/LLDPE had the
highest oxygen transmission rate (OTR) (p \ 0.05). In general, protein-based film showed higher oxygen
barrier properties than the plastic films such as nylon/metallocene-catalysed linear low-density polyethylene
(nylon/mLLDPE), low-density polyethylene (LDPE) and high-density polyethylene (HDPE) films (Cho et al.
2010; Rhim et al. 2006). Amongst all films, GF had the lowest OTR (p \ 0.05). Gelatin-based film has been
reported to possess excellent oxygen barrier property (Jongjareonrak et al. 2006). It was noted that the
incorporation of oil increased OTR of gelatin film. When oil was added, the matrix was disconnected and the
hydrophobicity of gelatin film generally increased, which could increase adsorption or solubility of oxygen, a
non-polar molecule, in the film. This brought about the lowering of oxygen barrier property of the film. The
increasing oxygen transmission rate of films incorporated with oil was related to the microstructural changes,
in which the film became more porous with the addition of oil (Altiok et al. 2010).

Quality changes of shrimp cracker during storage as affected by various films

Moisture content and water activity

Moisture contents of fried shrimp cracker kept in aluminium cup covered with fish gelatin films incorporated
without (GF) and with palm oil (EF) in comparison with nylon/linear low-density polyethylene (nylon/
LLDPE) film during 15 days of storage are shown in Fig. 1a. The initial moisture content of cracker was
1.13 %. In general, the moisture content of fried shrimp cracker in aluminium cup covered with all films
drastically increased within the first 3 days of storage (p \ 0.05). The moisture content was increased to a
higher extent for the sample packaged in both gelatin films (GF and EF) than that found in sample packaged in
nylon/LLDPE film throughout the 15 days (p \ 0.05). At 15 days of storage, samples packaged with GF, EF
and nylon/LLDPE film showed the increase in moisture content by 8.40, 8.46, and 4.54-fold, respectively. The
result was in agreement with the lowest WVP of nylon/LLDPE film (Table 1). When comparing moisture
content of shrimp cracker covered with GF and EF, the former showed the higher moisture content (p \ 0.05).
The result confirmed that the incorporation of oil could lower the migration of water vapour to the sample.
This was in accordance with the lower WVP of EF in comparison with GF (Table 1).
For water activity (Fig. 1b), fried shrimp cracker covered with EF showed lower water activity than those
covered with GF during 3–9 days of storage (p \ 0.05). Initial water activity of fried crackers was 0.22. Much
lower water activity was also found in sample packaged with nylon/LLDPE film throughout the 15 days of
storage (p \ 0.05). The result indicated that water vapour barrier property of gelatin film was lower than that
of nylon/LLDPE film. Generally, water vapour barrier property of gelatin film was poorer than that of other
biopolymer films, especially for non-hydrophilic material or synthetic polymer, due to the hydrophilic nature
of gelatin and hydrophilic plasticiser required for film preparation (Limpisophon et al. 2009). The increase in
moisture content and water activity of fried shrimp cracker was due to the diffusion of water vapour from the

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Int Aquat Res (2016) 8:227–238 233

12.0 (a)

10.0

Moisture content (%)


8.0

Air
6.0
Nylon/LLDPE
GF
4.0
EF

2.0

0.0
0 3 6 9 12 15
Storage time (Days)

0.8
(b)
0.7

0.6
Water activity

0.5
Air
0.4
Nylon/LLDPE
0.3 GF
EF
0.2

0.1

0.0
0 3 6 9 12 15
Storage time (Days)

Fig. 1 Changes in moisture content (a) and water activity (b) of fried shrimp cracker packaged with GF, EF and nylon/LLDPE
films during storage of 15 days at 28 ± 0.5 °C and 65 ± 5 %RH. Air fried shrimp cracker without packaging. Bars represent the
standard deviation (n = 3). GF and EF fish gelatin film incorporated without and with palm oil, respectively, nylon/LLDPE
nylon/linear low-density polyethylene film

surrounding atmosphere through the packaging material. Generally, the incorporation of hydrophobic sub-
stances such as oil improved the water vapour barrier property of gelatin film (Tongnuanchan et al. 2015).
Therefore, the incorporation of palm oil could improve the water vapour barrier property of gelatin film, as
evidenced by the lower moisture content and water activity of fried shrimp cracker during the storage.
Amongst all samples, that stored in air (without film covering) had the higher moisture content and water
activity. Therefore, films, either synthetic or gelatin films, were able to serve as the barrier against water
vapour migration, in which the quality changes of cracker could be retarded.

Peroxide value and TBARS

Lipid oxidation of fried shrimp cracker stored in aluminium cup covered with GF and EF in comparison with
nylon/LLDPE film during the 15 days of storage was monitored as shown in Fig. 2a, b. PV of samples covered
with either GF or EF increased during the 15 days of storage (p \ 0.05). During storage, the samples
packaged with nylon/LLDPE film had no difference in PV, compared with those packaged with GF

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234 Int Aquat Res (2016) 8:227–238

25.0 (a)

20.0

PV (mg cumene/kg sample) 15.0


Air
Nylon/LLDPE
10.0
GF
EF
5.0

0.0
0 3 6 9 12 15
Storage time (Days)

5.0 (b)
TBARS (mg MDA/kg sample)

4.0

3.0
Air
Nylon/LLDPE
2.0
GF
EF
1.0

0.0
0 3 6 9 12 15
Storage time (Days)

Fig. 2 Changes in peroxide value (a) and TBARS (b) of fried shrimp cracker packaged with GF, EF and nylon/LLDPE films
during storage of 15 days at 28 ± 0.5 °C and 65 ± 5 %RH. Air fried shrimp cracker without packaging. Bars represent the
standard deviation (n = 3). GF and EF fish gelatin film incorporated without and with palm oil, respectively, nylon/LLDPE
nylon/linear low-density polyethylene film

(p [ 0.05). It was found that sample covered with EF had similar PV to the control throughout the storage
(p [ 0.05). Oxidative changes in crackers were initiated by the formation of free radicals, the precursors for
the hydroperoxides, which were the primary oxidation products (Maisuthisakul et al. 2007). Crackers are
susceptible to lipid oxidation due to the large surface area in contact with the air, in which carbonyl com-
pounds and hydroperoxides are generated (Noomhorm et al. 1997). Due to the excellent oxygen barrier
property of GF, the PV was expected to be lower in the sample covered with GF. Nevertheless, GF had the
poorer WVP than nylon/LLDPE film. As a consequence, the water in the cracker was increased. The higher
amount of water might facilitate the movement of reactants, especially prooxidant. Thus, the oxidative
reaction was increased although the amount of oxygen used for oxidation was limited.
Continuous increases of TBARS value were observed in all samples throughout the storage of 15 days.
Lower TBARS values were obtained in sample stored with nylon/LLDPE film during 9–12 days of storage
(p \ 0.05). Lipid oxidation can be accelerated at high RH since more water molecules can act as reaction
media (Partanen et al. 2008). As the moisture content and water activity of all samples increased during the
15 days of storage, lipid oxidation could be promoted, especially for the samples covered with EF. However,

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Int Aquat Res (2016) 8:227–238 235

there was no difference in TBARS value between sample covered with GF and nylon/LLDPE films at day 15
(p [ 0.05). The result was in agreement with PV. Thus, packaging materials used was a prime factor affecting
water vapour and oxygen permeability, thereby influencing oxidative stability. The result suggested that the
incorporation of palm oil into gelatin could lower water vapour migration, but it decreased the barrier property
toward oxygen molecule (Table 1).

Textural properties

Crispiness (force necessary to break a product) and toughness (area under the curve during compressing) of
fried shrimp cracker stored in aluminium cup, covered with GF and EF in comparison with nylon/LLDPE film
during 15 days of storage are shown in Fig. 3a, b. Physical properties, such as density, shrinkage and porosity,
are the main factors affecting the texture and transport phenomena of fried foods (Ziaiifar et al. 2010).
Crispiness is related to the deformation and fracturing of subsequent layers in a cell structure of food products
(Luyten et al. 2004). Crispiness of samples packaged with all films sharply decreased with the first 3 days of

25000 (a)

20000
Crispiness (g force)

15000
Air
Nylon/LLDPE
10000
GF
EF
5000

0
0 3 6 9 12 15
Storage time (Days)

12000 (b)

10000
Toughness (g force s)

8000

Air
6000
Nylon/LLDPE
GF
4000
EF

2000

0
0 3 6 9 12 15
Storage time (Days)

Fig. 3 Changes in crispiness (a) and toughness (b) of fried shrimp cracker packaged with GF, EF and nylon/LLDPE films during
storage of 15 days at 28 ± 0.5 °C and 65 ± 5 %RH. Air fried shrimp cracker without packaging. Bars represent the standard
deviation (n = 3). GF and EF fish gelatin film incorporated without and with palm oil, respectively, nylon/LLDPE nylon/linear
low-density polyethylene film

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236 Int Aquat Res (2016) 8:227–238

storage (p \ 0.05), except that covered with nylon/LLDPE film. Similar rate of decrease in crispiness was
observed during 3–15 days of storage. During storage, shrimp cracker covered with nylon/LLDPE film
showed the higher crispiness than others (p \ 0.05). No difference in crispiness between samples packaged
with GF and EF was observed (p [ 0.05). Crispiness of sample covered with gelatin films was similar to that
of the control. On the other hand, the toughness of shrimp cracker samples covered with GF and EF and that
kept in air markedly increased within the first 3 day of storage (p \ 0.05). No change in toughness of sample
packaged with nylon/LLDPE film was obtained during the first 6 days of storage (p [ 0.05). When storage
time was increased, the water vapour might migrate through the films and contact with the sample surface to a
higher extent. Water more likely reduced the strength of air cell structure of cracker (Luyten et al. 2004).
Water might fluidise the cracker network, where it became tougher in texture. The change was coincidental
with the increase in toughness of cracker. Thus, packaging with the ability in lowering water vapour migration
was required for crispy cracker, in which textural property could be maintained. Although the incorporation of
palm oil into gelatin film in this study could lower WVP of resulting film to some degree, the film still showed
the lower barrier property toward water vapour, in comparison with the commercial nylon/LLDPE film.

Volatile compounds

Selected volatile compounds in freshly fried shrimp cracker and those stored in aluminium cup covered with
GF and EF in comparison with nylon/LLDPE film after 15 days of storage are shown in Table 2. At day 0,
fried shrimp cracker contained some volatile compounds including aldehyde (hexanal, n-nonanal and 2-de-
cenal), alcohol (1-pentanol and 2-Furanmethanol), nitrogen-containing compounds (2,6-dimethylpyrazine),
and noncyclic hydrocarbons (n-tridecane and n-undecane). The result suggested that shrimp cracker under-
went lipid oxidation to some degree during frying. After 15 days of storage, volatile compounds were also
found in all fried shrimp cracker, but the abundance and types of compounds varied. Aldehydes have been
used as the index of lipid oxidation in a number of foods, because they possess low threshold values and are

Table 2 Selected volatile compounds in freshly prepared shrimp cracker and those stored with different films after 15 days
Volatile compounds Day 0 Day 15
Air Nylon/LLDPE GF EF

Aldehydes
Hexanal 0.7 25.7 2.6 3.9 16.1
n-Nonanal 0.5 13.2 3.9 1.8 12.3
2-Decenal 2.8 8.1 2 1.9 7.5
2,4-Decadienal ND 3.2 0.8 0.4 3
Alcohols
1-Methoxy-2-propanol ND 7.1 ND ND ND
1-Pentanol 1.9 5.8 2.5 2.6 2.8
2-Furanmethanol 0.3 1.5 0.4 0.5 1.0
Nitrogen-containing compounds
Methylpyrazine ND 0.8 ND ND ND
2,5-Dimethylpyrazine ND 7 4.4 5 4.9
2,6-Dimethylpyrazine 2.5 1.3 0.5 0.5 0.6
Ethylpyrazine ND 1.1 0.5 0.8 0.8
Noncyclic hydrocarbons
Heptane ND 5.1 0.8 3.8 5.0
n-Tridecane 0.4 9.5 8.8 9.3 9.2
n-Dodecane ND 19.6 18.4 19.0 20.2
n-Undecane 2.8 19.0 13.0 18.1 18.8
ND non-detectable, GF and EF fish gelatin film incorporated without and with palm oil, respectively, nylon/LLDPE nylon/linear
low-density polyethylene film, Air fried shrimp cracker without packaging
* Values are expressed as abundance (9109)

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Int Aquat Res (2016) 8:227–238 237

the major contributors to off-odour and off-flavour (Ross and Smith 2006). Numerous aldehydes produced
during oxidation included octanal, nonanal, pentanal, hexanal, etc. (Ross and Smith 2006). Amongst all
aldehydic compounds, hexanal and n-nonanal were found as the major aldehydes in all stored shrimp cracker
samples, followed by 2-decenal and 2,4-decadienal (Table 2). Sample stored in air had the highest abundance
of all aldehydes. It was noted that sample packaged with GF showed similar profile to that stored with nylon/
LLDPE film. Nevertheless, some differences in hexanal and n-nonanal were noticeable. This reconfirmed the
excellent oxygen barrier property of GF film (Table 1). Alcohols are the secondary products produced by the
decomposition of hydroperoxide (Eymard et al. 2009). The 1-pentanol and 2-furanmethanol were found in
shrimp cracker samples (Table 2). All shrimp cracker samples after 15 days of storage showed the higher
abundance of those alcoholic compounds than freshly prepared sample. It was postulated that higher lipid
oxidation and greater decomposition of hydroperoxide occurred. Higher abundance of volatile lipid oxidation
products found in fried shrimp cracker without packaging correlated well with high TBARS value as shown in
Fig. 2b. 1-Methoxy-2-propanol was found only in sample stored in air after 15 days of storage. Four nitrogen-
containing compounds mainly pyrazine derivatives, were found in fried shrimp cracker. The 2,5-dimethyl-
pyrazine was detected in all samples after 15 days of storage. Conversely, 2,6-dimethylpyrazine was formed
only in freshly prepared sample (day 0). Pyrazines were reported to be formed by Maillard reaction from
degradations of various nitrogen sources such as amino acids (Jaffrès et al. 2011). Methylpyrazine was found
only in fried shrimp cracker kept without packaging (air), whilst ethylpyrazine was detected only in the stored
shrimp cracker. The presence of pyrazine indicated that browning reaction mediated by Maillard reaction
occurred in shrimp cracker samples during the 15 days of storage. Furthermore, some hydrocarbon com-
pounds including heptane, n-tridecane, n-dodecane and n-undecane were found in fried shrimp cracker after
15 days of storage. The abundance of those compounds increased after 15 days of storage. Alkanes are mainly
formed from lipid auto-oxidation of fatty acids released from triglycerides (Latorre-Moratalla et al. 2011).
Based on volatile compounds, fried shrimp cracker stored with different packaging showed varying volatile
compounds.

Conclusion

Fish gelatin films incorporated with palm oil could lower the increase in moisture content and water activity of
fried shrimp cracker to some extent, but its capability was still lower than nylon/LLDPE film. The preventive
effect toward lipid oxidation of films from fish gelatin was equivalent to nylon/LLDPE film. However, fish
gelatin film could not maintain the textural property of cracker during storage. Therefore, the improvement of
barrier property against water and oxygen of fish gelatin film is still needed.
Author contribution SB developed the initial idea and designed the study. KN was responsible for con-
ducting experiments and analysis of data. SB and KN carried out the analytical work. KN wrote the manu-
script with assistance from SB and TP. SB and TP read and approved the final manuscript.

Acknowledgments The authors would like to thank the Graduate School of Prince of Songkla University, Thailand, for the
financial support. The TRF Distinguished Research Professor Grant was also acknowledged.

Compliance with ethical standards

Conflict of interest The authors declare that they have no competing interests.

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://
creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided
you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if
changes were made.

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