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Journal of the Science of Food and Agriculture J Sci Food Agric 86:944–952 (2006)
DOI: 10.1002/jsfa.2442
Abstract: The purpose of this work was to determine the chemical and sensory stability of roasted peanuts
prepared with a high-oleic cultivar, Granoleico (GO-RP), in comparison to a regular cultivar, Tegua
(T-RP), from Argentina. Consumer test of fresh products, oxidative stability estimated by chemical
indicators (peroxide and p-anisidine values, conjugated dienes and trienes) and descriptive analyses
during storage (at 23 and 40 ◦ C) were performed on the roasted peanuts. GO-RP did not differ from T-RP
as regards consumer acceptance. Chemical indicator values and oxidized and cardboard flavors showed
lower increments for GO-RP than T-RP during storage. Roasted peanutty flavor decreased for both
samples at 23 and 40 ◦ C. Using prediction equations, roasted peanuts prepared with kernels of high-oleic
contents had shelf lives of 25 (at 23 ◦ C) and 10 (at 40 ◦ C) times longer than those elaborated with normal
peanuts.
2006 Society of Chemical Industry
∗ Correspondence to: Nelson R Grosso, Quimica Biologica, Facultad de Ciencias Agropecuarias (UNC), IMBIV-CONICET, CC 509, 5000
Cordoba, Argentina
E-mail: nrgrosso@agro.uncor.edu
Contract/grant sponsor: CONICET
Contract/grant sponsor: SECYT-UNC
(Received 29 December 2004; revised version received 23 May 2005; accepted 8 August 2005)
Published online 1 March 2006
2006 Society of Chemical Industry. J Sci Food Agric 0022–5142/2006/$30.00 944
Chemical and sensory stability of roasted high-oleic peanuts
peanuts were inspected; damaged and bruised kernels (volume in mL of Na2 S2 O3 ) × (0.1 N) × (1000) ×
were manually removed. (g oil−1 ). The oil was obtained from two extractions
with 50 mL of n-hexane (Anedra, San Fernando,
Preparation of samples Buenos Aires, Argentina) from samples (20 g) dur-
Peanuts of ‘Granoleico’ and ‘Tegua’ cultivars were ing 12 h by maceration at room temperature in a dark
roasted at 170 ◦ C in an oven (Memert, model 600, room. The extracted oils were dried over anhydrous
Schwabach, Germany) for 30 min. Peanuts were sodium sulfate and the solvent was removed under
heated to a medium roast or an average Hunter color reduced pressure in a rotary film evaporator.21
lightness (L) value of 50 ± 1.0.17
In the final product, the moisture content was p-Anisidine value (AV)
23 g kg−1 . To determine moisture, the peanuts were This method is commonly used as a measurement
milled and dried in an oven at 130 ◦ C for 1 h following for lipid oxidation products. The procedure was
AOAC methods.18 described by IUPAC.22 0.5–4.0 ± 0.001 g of peanut
oil sample was dissolved with 25 mL of n-hexane in a
Fatty acid composition of roasted peanuts volumetric flask. The absorbance (Ab) of the solution
Fatty acid methyl esters were prepared from oils was measured at 350 nm in a spectrophotometer (UV-
from roasted peanuts (GO-RP and T-RP) by V diode array spectrophotometer Hewlett Packard
transmethylation with a solution of 30 g L−1 sulfuric HP 8452 A, USA), using n-hexane as blank. In a test
acid in methanol, as previously described.19 The fatty tube, 5 mL of the fat solution was mixed with 1 mL of
acid methyl esters of total lipids were analyzed on a p-anisidine reagent (2.5 g p-anisidine hydrochloride,
Hewlett Packard HP-6890 gas–liquid chromatograph BDH Laboratory Reagents, Poole, UK, L−1 glacial
(Palo Alto, CA, USA) equipped with a flame acetic acid). The absorbance of this solution (As)
ionization detector (FID HP-3398). An HP-INNO was measured at 350 nm after exactly 10 min, using
wax capillary column (30 m × 0.32 mm × 0.5 nm, a mixture of 5mL of n-hexane and 1mL p-anisidine
with polar polyethylene glycol) was used. Column reagent as blank. The p-anisidine value was given by
temperature was programmed from 200 ◦ C (held for the formula: AV = 25 × (1.2As − Ab) × (m−1 ), where
1 min) to 230 ◦ C (20 ◦ C min−1 ). Injector and detector as is absorbance of the fat solution after reaction
temperatures were 260 ◦ C. The carrier (nitrogen) with the p-anisidine reagent, Ab is the absorbance
had a flow rate of 3.8 mL min−1 . Volume of sample of the fat solution and m is the mass of the peanut
injected was 1 µL. The separated fatty acid methyl oil (g).
esters were identified by comparing their retention
times with those of authentic samples, which were Conjugated dienes and trienes (CD and CT)
purchased from Sigma Chemical Co. (St Louis, Weighed oil samples were dissolved in 6 mL of n-
MO, USA). Quantitative fatty acids analysis was hexane; conjugated diene and triene absorbances were
performed using heptadecanoic acid methyl ester measured at 232 nm and 268 nm, respectively, in a
(Sigma Chemical Co.) as internal standard. spectrophotometer (UV-V diode array spectropho-
tometer, Hewlett Packard HP 8452 A), using n-hexane
Storage conditions and samplings as blank. The results were reported as the sample
After preparation of GO-RP and T-RP, samples were extinction coefficient E (1%, 1cm).23,24
packaged in 27 × 28 cm plastic bags (Ziploc, Johnson
& Son, Buenos Aires, Argentina). The samples were Sensory methods
stored at 23 ◦ C (room temperature) to reproduce Consumer analysis
normal storage conditions of peanut products and Panelists (n = 100) were from Cordoba (Argentina)
at 40 ◦ C (oven) to reproduce accelerated storage and were recruited under the following criteria: ages
conditions to obtain a wide range of difference in between 18 and 65, non-smokers, presenting no
sensory attributes.5,20 Samples of each product were food allergies and who consume roasted peanuts
removed from storage for chemical and descriptive and/or peanut products at least twice per week. For
analyses. Sampling days were: 0, 28, 56, 84 and sample evaluation, 5 g of the peanut samples were
112 days at 23 and 40 ◦ C. placed into plastic cups with lids, coded with 3-digit
random numbers. Samples consisting of GO-RP and
Chemical analysis T-RP (three replications of each) were prepared for
Peroxide value (PV) each panelist. Samples were presented to panelists
PV was evaluated following AOAC method 28.022,18 in random order during the test day. Samples were
using 5 g of oil of each sample. It consisted of presented with water and paper ballots on a plastic
reaction in darkness of a mixture of oil and chlo- tray. Panelists were instructed to consume the whole
roform/acetic acid 2:3 (v/v) with saturated potassium sample and rinse their mouths with water between
iodide solution. The iodine formed was titrated with samples to minimize any residual effect. A 9-point
0.1 N Na2 S2 O3 . PV was expressed as milliequivalents hedonic scale ranging from 1 = dislike extremely
of active oxygen per kilogram of oil (meqO2 kg−1 ) to 9 = like extremely was used to evaluate overall
and calculated using the formula PV (meqO2 kg−1 ) = acceptance from the samples.25
Table 2. Standard reference and warm up intensity ratings used in descriptive tests for roasted peanuts
Appearance
1. Brown color Cardboard 40 27
Aromatics
2. Roasted peanutty Dry-roasted peanuts (JL SA, Ticino, 69 69
Córdoba, Argentina)
3. Oxidized Rancid peanuts 53 8
4. Cardboard Moist cardboard 52 11
5. Raw/beany Raw peanuts 69 13
Tastes
6. Sweet 20 g kg−1 sucrose solution 20 25
50 g kg−1 sucrose solution 50
100 g kg−1 sucrose solution 100
150 g kg−1 sucrose solution 150
7. Salty 2 g kg−1 NaCl solution 25 19
3.5 g kg−1 NaCl solution 50
5 g kg−1 NaCl solution 85
8. Sour 0.5 g kg−1 citric acid solution 20 9
0.8 g kg−1 citric acid solution 50
1.5 g kg−1 citric acid solution 100
9. Bitter 0.5 g kg−1 caffeine solution 20 7
0.8 g kg−1 caffeine solution 50
1.5 g kg−1 caffeine solution 100
Texture
10. Hardness Almonds (Grandiet, Cordoba, 56 41
Argentina)
11. Crunchiness Corn flakes (Granix, Buenos Aires, 102 60
Argentina)
12. Toothpack Raw peanuts 66 43
a Intensity ratings are based on 150 mm unstructured line scales.
b Medium (lightness value, L = 50 ± 1.0) roasted peanuts (Blanched Runner).
Table 3. Fatty acid composition of Tegua and Granoleico roasted not have an effect on the acceptability of the roasted
peanuts (T-RP and GO-RP) products.
Composition (g kg−1 fatty acids)
Chemical and sensory results from stored
Fatty acids T-RP GO-RP roasted peanuts
Chemical analyses
Palmitic acid (C16:0) 89 49
The changes in peroxide and p-anisidine values during
Stearic acid (C18:0) 25 25
Oleic acid (C18:1) 458 790 storage at 23 and 40 ◦ C of the samples GO-RP
Linoleic acid (C18:2) 333 46 and T-RP are shown in Fig. 1. Conjugated dienes
Arachidic acid (C20:0) 13 13 and trienes are shown in Fig. 2. Peroxide and p-
Eicosenoic acid (C20:1) 17 25 anisidine values and conjugated dienes and trienes
Behenic acid (C22:0) 30 27 increased with storage time in both products at both
Lignoceric acid (C24:0) 20 20 temperatures. The increase of these variables was more
Oleic/linoleic ratio 1.4 17.2 noticeable at 40 ◦ C than at 23 ◦ C.
Saturated/unsaturated ratio 0.22 0.16 T-RP had higher peroxide values and showed
significant differences (α = 0.05) since day 28 with
respect to GO-RP at both temperatures. GO-RP did
Consumer analysis not show significant differences in peroxide value
Significant differences (α = 0.05) in consumer accep- during storage at 23 and 40 ◦ C. T-RP showed higher
tance tests among the products (GO-RP and T-RP) peroxide values at 23 ◦ C than at 40 ◦ C since day 42.
were not found. In general, the products had consumer Peroxide values (meqO2 kg−1 ) of GO-RP were from
acceptances of about 6 (like slightly) in a hedonic scale 0.5 ± 0.1 (day 0) to 4.1 ± 0.0 (day 112) at 23 ◦ C and
of 9 points. The overall acceptance means in GO-RP from 0.5 ± 0.2 (day 0) to 11.8 ± 0.0 (day 112) at
and T-RP were 5.6 ± 1.6 and 5.7 ± 1.5, respectively. 40 ◦ C. T-RP sample showed PV from 2.4 ± 0.3 (day
In other studies5,21 similar overall acceptances were 0) to 55.5 ± 6.1 (day 112) at 23 ◦ C and from 2.1 ± 0.1
found in roasted and cracker-coated peanut products (day 0) to 85.7 ± 6.2 (day 112) at 40 ◦ C.
of between 6.0 and 6.4. The differences in the chem- p-Anisidine values were from 0.9 ± 0.3 (day 0) to
ical composition of peanut cultivars (GO and T) did 1.1 ± 0.5 (day 112) in GO-RP at 23 ◦ C, from 1.5 ± 0.1
6
GO-RP-23ºC
T-RP. These results are presented in Table 4. Except
5 for roasted peanutty, the other sensory attributes from
GO-RP-40ºC
4 the descriptive analysis showed no significant dif-
T-RP-23ºC
3 ferences (α = 0.05) between GO-RP and T-RP at
2
T-RP-40ºC day = 0, indicating that the difference in peanut culti-
1 var did not influence the panel scores. The intensity of
0 roasted peanutty attribute used to characterize peanut
0 28 56 84 112 flavor in peanut products was 64 ± 11 in GO-RP
days and 57 ± 8 in T-RP (scale 0–150), showing signif-
icant differences. Grosso and Resurreccion5 found
Figure 1. (a) Peroxide value (PV), (b) p-anisidine value (AV) in
that the roasted peanutty intensity was 67 and 63 in
Granoleico (GO-RP) and Tegua (T-RP) roasted peanuts during
storage time at 23 and 40 ◦ C.
roasted peanuts and cracker-coated peanuts, respec-
tively.
In other studies,2,3,5 an increase of the intensity
14
ratings of cardboard and oxidized and a decrease of
Conj. Dienes (E1%, 232nm)
(a)
12 roasted peanutty in peanut products during storage
10 time was observed. In this work, the sensory attributes
GO-RP-23ºC
that changed during storage time were also roasted
8 GO-RP-40ºC peanutty and those attributes related to the lipid
6 T-RP-23ºC oxidation, such as oxidized and cardboard. The
4 T-RP-40ºC other attributes did not show significant variations
2 (α = 0.05) during storage. The changes of these
0
0 28 56 84 112 Table 4. Means of sensory attribute intensities from descriptive
days analysis in fresh (storage time = 0 days) Granoleico (GO-RP) and
Tegua (T-RP) roasted peanuts
1,2
Conj. Trienes (E1%, 268nm)
30
25
GO-RP-23ºC from 57 ± 2 to 40 ± 3 in T-RP at 23 ◦ C, and from
GO-RP-40ºC
20 64 ± 3 to 53 ± 3 on day 112 in GO-RP, and from
T-RP-23ºC
15 T-RP-40ºC
57 ± 2 to 39 ± 3 on day 112 in T-RP at 40 ◦ C.
10
5 Correlation and regression analysis
0 The variables of interest in this study were PV,
0 28 56 84 112 AV, CD, CT, and oxidized, cardboard and roasted
days peanutty flavors. Correlation coefficients are presented
35
in Table 5. Positive correlations higher than 0.70
(b) were observed among the following variables: PV,
30
AV, CD, CT, oxidized and cardboard flavors. All
Intensity rating
60
GO-RP-23ºC
55 presented in Tables 6 (23 ◦ C) and 7 (40 ◦ C).
GO-RP-40ºC
50 T-RP-23ºC
The dependent variables (PV, AV, CD, CT,
45 T-RP-40ºC oxidized, cardboard and roasted peanutty) showed
40 R2 > 0.60 in both products (GO-RP and T-RP)
35 and temperatures (23 and 40 ◦ C), indicating that
30
these variables are good predictors. Therefore, these
0 28 56 84 112 regression equations could be used to predict the
days effect of storage time at 23 and 40 ◦ C on these peanut
products.
Figure 3. Intensity rating of sensory attributes: (a) oxidized,
(b) cardboard and (c) roasted peanutty in Granoleico (GO-RP) and
Bett and Boylston3 detected that cardboard flavor
Tegua (T-RP) roasted peanuts during storage time at 23 and 40 ◦ C. intensity had a linear increase across storage time
in roasted peanuts, while roasted peanutty flavor
intensity decreased as storage time increased. Muego-
attributes in GO-RP and T-RP are represented in Gnanasekharan and Resurreccion33 detected that
Fig. 3. Oxidized and cardboard intensities increased oxidized and cardboard flavor intensities exhibited
with storage time. The intensities of oxidized flavor a linear increase during storage time in peanut
were from 5 ± 1 on day 0 to 15 ± 3 on day 112 paste. Warner and others31 observed that oxidized
in GO-RP at 23 ◦ C, and to 19 ± 4 on day 112 at flavor intensity increased and roasted peanutty flavor
40 ◦ C. The intensities of cardboard flavor were from decreased during storage time in ground roasted
10 ± 1 on day 0 to 19 ± 4 on day 112 in GO-RP at peanuts, but a regression equation was not presented
23 and 40 ◦ C. The ratings of these attributes were in their work.
higher in T-RP. Significant differences (α = 0.05) In the Food Code from Argentina, 10 meqO2 kg−1
between GO-RP and T-RP in oxidized and cardboard is the maximum level of peroxide value allowed for
intensities were observed since day 28 at 23 and peanut oil.34 Peroxide values of 10 meqO2 kg−1 may
40 ◦ C. be useful as an endpoint of quality for roasted peanuts.
Roasted peanutty flavor can be attributed to Therefore, shelf life was estimated as the time to
the presence of pyrazines.29,30 Bett and Boylston3 reach the peroxide value of 10 meqO2 kg−1 from linear
found that roasted peanutty flavor intensity and regression of the peroxide value–time curves.21 Using
alkylpyrazines decreased in stored roasted peanuts. the prediction equations, peroxide values higher than
Warner et al.31 and Brannan et al.32 also found that 10 meqO2 kg−1 were reached after 202 days in GO-RP
roasted peanutty flavor decreased in stored roasted at 23 ◦ C, 8 days in T-RP at 23 ◦ C, 99 days in GO-RP
peanuts. In this study, the intensity ratings of roasted at 40 ◦ C and 10 days in T-RP at 40 ◦ C. Thus, the shelf
peanutty in GO-RP and T-RP decreased during life was of 25 (at 23 ◦ C) and 10 (at 40 ◦ C) times longer
storage time and GO-RP had higher intensities of for GO-RP than T-RP.
Table 5. Correlation coefficients among the variables: peroxide (PV) and p-anisidine (AV) values, conjugated dienes and trienes (CD and CT) and
sensory attributes in Granoleico (GO-RP) and Tegua (T-RP) roasted peanuts
Correlation coefficientsa
Table 6. Regression coefficients and R2 from prediction equations of peroxide (PV) and p-anisidine (AV) values, conjugated dienes and trienes (CD
and CT), and sensory attributes in Granoleico and Tegua roasted peanuts at 23 ◦ C
Regression coefficientsa
Table 7. Regression coefficients and R2 from prediction equations of peroxide (PV) and p-anisidine (AV) values, conjugated dienes and trienes (CD
and CT), and sensory attributes in Granoleico and Tegua roasted peanuts at 40 ◦ C
Regression coefficientsa
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