Lebensm.-Wiss. u.-Technol.
, 29, 573–577 (1996)
Research Note
 Utilization of Jojoba Oil for Deep-fat Frying of Foods
                                     I.S. Saguy*, A. Shani, P. Weinberg and N. Garti
 I.S. Saguy, P. Weinberg: Department of Biochemistry, Food Science and Nutrition, The Hebrew University of
                                  Jerusalem, P.O. Box 12, Rehovot 76100 (Israel)
      A. Shani: Department of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva 84105 (Israel)
   N. Garti: Casali Institute for Applied Chemistry, The Hebrew University of Jerusalem, Jerusalem (Israel)
                             (Received September 22, 1995; accepted October 26, 1995)
Jojoba oil is a mixture of long chain esters comprising C18, C20, C22 and C24 monounsaturated acids and alcohols, but in particular
two ester molecules containing 40 and 42 carbon atoms which make up to 80% of the oil. Five quality parameters of Jojoba oil
were compared with cotton oil in time–temperature conditions simulating abusive industrial deep-fat frying. In four out of five
quality criteria, namely, colour index, oxidation index, peroxide value and viscosity, Jojoba oil was found to be superior to cotton
oil, while free fatty acids showed comparable low values, within the range expected, in industrial frying operations. Oil uptake of
a deep-fried restructured potato product was significantly higher in Jojoba oil as compared to cotton oil. The enhanced stability
during deep-fat frying of Jojoba oil could play a part in improving the shelf-life of fried foods.
©1996 Academic Press Limited
Introduction                                                       (9). Additional applications include a mixture of JO
                                                                   and glyceride oils (80:20 by wt.) for frying scrambled
Reduction of calories derived from oils and fats from              eggs (10), and others (11–15).
37% to 20–30% is a health and nutritional goal yet to              The utilization of JO to replace frying fat in large- or
be met (1). In addition, cholesterol in blood serum                small-scale food frying operations is still not feasible,
causes concern and measures taken toward lowering its              nevertheless its application could be advantageous as it
level below 200 mg/dL are to be viewed positively. To              is triglyceride-free and does not break down as com-
facilitate reducing these nutritional risks, numerous              pared to regular fats, and could be used for extended
fatty substitutes have been developed in recent years,             industrial frying periods (16).
most of them based on protein and carbohydrates.                   The main objectives of this study were to assess the
However, these substitutes usually cannot replace oils             performance of JO for deep-fat frying of foods and to
used in cooking, baking and frying (2). Jojoba liquid              compare its oxidation stability with cottonseed oil.
wax (Simmondsia chinensis Buxaceae; jojoba ‘oil’, JO),
produced by the seeds of the female plant of the once
wild bush is a narrow mixture of long-chain esters,                Materials and Methods
composed mainly of monounsaturated C18, C20, C22 and
C24 acids and alcohols, in particular two ester molecules          Frying
containing 40 and 42 carbon atoms which make up to                 An extruded restructured potato product (17), cylinder-
80% of the oil (3).                                                shaped (0.02 m diameter 3 0.03 m length), was fried in
Jojoba oil is scarcely hydrolysed by pancreatic lipases            a bench-top deep-fat fryer (0.12 m depth), containing
(4). Only ca. 40% is digested when incorporated into               2.5 L oil. Cotton oil was obtained from a local
animal diets at significant and practical levels (5), and          manufacturer and compared to jojoba oil (Jojoba
its caloric value (in terms of nutrition) could be even            Israel, Ltd., Tel Aviv). Both oils were exposed to an
lower (6). Although JO cannot be used in foods until               extended frying process carried out in two stages,
proper approval by EC authorities or the FDA (7),                  lasting 22.3 h (Table 1). In stage I, restructured potato
several applications have been reported, including                 samples (triplicate) were fried individually (to mini-
coating of foodstuffs (e.g. chocolate, dried fruit), which         mize temperature drop) at 175, 185 and 195 °C, for 300
greatly improved stability and reduced moisture loss               s. Fryer time and temperature are listed in Table 1.
even in comparison with hydrogenated oil coating (8).              Samples were removed from the fryer, and allowed to
Beneficial results were also demonstrated in studies               cool to room temperature (23 ± 2 °C) on a paper towel.
focusing on replacing edible fats and oil by JO in                 In stage II, the same oil used in stage I was heated to
margarine and mayonnaise (4), and for deep-fat frying              205 °C and kept at this temperature for more than 19 h.
                                                                   To simulate a controlled frying process (Table 1), 2 mL
*To whom correspondence should be addressed.                       water in the form of small drops was added with a
                              0023-6438/96/050573 + 05$18.00/0     ©1996 Academic Press Limited
                                                              573
                                                                                                                                                      lwt/vol. 29 (1996) Nos. 5 & 6
      Table 1 Effect of abusive time–temperature conditions simulating deep-fat frying on oil quality parameters
                                                       Jojoba oil                                        Cotton oil
                                   Oxidation         Peroxide                            Oxidation              Peroxide
      Time     Temp.     Colour      index     FFA    value   Viscosity       Colour       index      FFA        value    Viscosity
       (h)      (°C)     index     (mmol/L)    (%) (mEq.O2/kg) (mPa s)        index      (mmol/L)     (%)     (mEq.O2/kg) (mPa s)     Comments
        0        175      0.789      4.97       0.19      0.84         28       0.528      13.26       0.08        0.60      40.      Oil break-in
        2.3      175      0.100      4.68       0.20      2.22         29       0.701      38.50       0.13        5.52      45       Sample frying
        3.0      185      0.072      4.47       0.21      2.45         30       0.748      41.79       0.14        6.36      47       Sample frying
        3.6      195      0.054      6.57       0.24      2.68         31       0.760      58.90       0.15        7.67      48       Sample frying
        8.6      205      0.068      7.03       0.29      2.83         34       0.954      56.03       0.18        7.67      53       +2 mL water
       11.8      205      0.080      7.99       0.35      3.10         35       1.120      66.29       0.20        5.60      60       +2 mL water
574
       15.1      205      0.084      8.52       0.41      3.22         41       1.419      71.75       0.25        4.83      68       +2 mL water
       18.3      205      0.101     10.31       0.48      2.91         42       1.670      68.46       0.24        5.13      75       +2 mL water
       22.3      205      0.130      8.44       0.60      2.91         45       2.066      74.50       0.41        3.45      83       +2 mL water
                                                                                                   lwt/vol. 29 (1996) Nos. 5 & 6
Pasteur pipette after 8.6, 11.8, 15.1, 18.3 and 22.3 h        initial yellow colour to a clear almost colourless fluid.
(Table 1). Oil samples were withdrawn periodically            Even after extensive and abusive time–temperature
(Table 1) and analysed in duplicate. Sampling routine         exposure (175 to 205 °C for up to 22.3 h), the colour
for both oils was identical.                                  index remained as low as 0.130 ( ± 0.002). This colour
                                                              reduction is a distinct characteristic of JO not matched
                                                              by any other frying oil. On the other hand, cotton oil
Colour index                                                  showed a marked increase in colour index with frying
Absorption at 420 nm was determined on a spec-                time. The increase is probably due to oxidation typically
trophotometer and read against water as blank.                resulting in the generation of hydroperoxides, conju-
                                                              gated dienoic acids, epoxides, hydroxides and ketones.
                                                              These compounds could undergo further oxidation, and
Oxidation index                                               fission into smaller fragments or may remain in the
Oxidation index, defined as the absorption of conju-          triglyceride molecule and cross-link with each other,
gated dienes, was followed spectrophotometrically             leading to dimeric and higher polymeric triglycerides
(UV/Visible Philips Cambridge, U.K.) at 234 nm (18).          (22). Fats can also produce dimeric acids, and form
The oil sample was diluted (1:240 and 1:1200 for JO and       polymers of higher molecular weight, causing a darker
cotton oil, respectively) with hexane (HPLC grade). An        colour and a deposit of yellow or brown pigments (23).
extinction coefficient of 29,000 mol/L (19) was utilized      The oxidation process and polymerization of cotton oil
to quantify the concentration of conjugated dienes            was accompanied by a viscosity increase(40 ± 2 to
formed during oxidation.                                      83 ± 5 mPa.s), while JO viscosity remained relatively
                                                              low (28 ± 2 to 45 ± 2 mPa.s).
                                                              Free fatty acid (FFA) is one of the indicators utilized to
Free fatty acid (FFA)                                         assess oil quality during the frying process. It can be
Oil samples were titrated with 0.01 mol/L KOH (20).           used to determine the total content of reactive acid
Data are expressed as percent of oleic acid.                  groups in the oil. Although FFA is not a good
                                                              parameter for comparing different frying processes or
                                                              oil stability, it could be used as an indicator to show
Peroxide value (PV)                                           whether the process is in control. Therefore, the values
Standard method (20) was utilized. Data are expressed         reported, although somewhat higher for JO, are still
as peroxide value (mEq.O2/kg).                                within the range expected during a regular industrial
                                                              frying operation.
                                                              The level of oil primary oxidation is measured by
Viscosity                                                     peroxide value. However, as peroxides are very unsta-
A Brookfield LV (Brookfield Engineering Lab.                  ble at typical frying temperatures, PV content is often a
Stoughton, MA) equipped with an SC4-19 spindle was            criterion of the peroxides generated during the cooling
used to measure the viscosity of the oil samples at 30        process. Hence, to compare the two oils, identical
°C. The shear rate ranged from 10 to 50 s–1 and the           sampling and cooling procedures were applied. The
Newtonian viscosity was determined.                           data (Table 1) clearly show a difference between the
                                                              two oils. While cotton oil showed a rapid increase (from
                                                              0.60 ± 0.03 to 7.67 ± 0.21 mEq.O2/kg) after only 3.6 h,
Other analyses                                                JO reached its maximum (from 0.84 ± 0.04 to
Moisture content, oil uptake and UR criterion (defined        3.22 ± 0.15 mEq.O2/kg) after a much longer time (15.1
as the weight ratio (g/g) between the amount of oil           h) and higher frying temperatures (195 to 205 °C). As
uptake and water removed) were determined as                  expected, in both cases, PV reached a peak and levelled
described previously (21). Oil uptake is expressed as         off. A more reliable method than the PV method for
g/100 g dry matter, excluding fat. All data were              comparing oil stability is the active oxygen method
statistically analysed using Statistix (Analytical Soft-      (AOM). Dienoic acids, such as linoleic acid, are much
ware, St. Paul, NM). When treatment effects were              more sensitive towards oxygen and the rate of peroxide
significant (α = 0.01), the least significance difference     formation is much faster (24). Typical AOM values are
(LSD) test was used.                                          14, 45, and 40 to 50 h for cotton oil, high oleic sunflower
                                                              oil (25) and JO (Jojoba Israel, Ltd.), respectively.
                                                              The above values are not surprising if they are related
Results and Discussion                                        to the oils chemical structure. There are two major
                                                              differences between cottonseed oil and JO. Cottonseed
The effect of frying time and temperature on oil              oil is a triglyceride while JO is a narrow mixture of long
characteristics is listed in Table 1. The data show a clear   chain esters. The degree of unsaturation in the fatty
distinction between cotton oil and JO in colour,              acids (and alcohols in JO) is also different. Three major
oxidation indexes, FFA, peroxide values and viscosity.        fatty acids comprise cotton oil (saturated palmitic acid
However, the differences are not consistant, and each         22–26%, monounsaturated oleic acid 16–19% and
characteristic should be evaluated separately.                diunsaturated linoleic acid 49–58%) (23). The compo-
The colour index of JO decreased significantly from its       nents of JO are monounsaturated entities, thus it is
                                                        575
lwt/vol. 29 (1996) Nos. 5 & 6
more like a high oleic sunflower oil (i.e. palmitic acid,          of long chain esters exhibiting high stability at frying
8%; oleic acid, 80%; and linoleic acid, 12%) (25).                 temperatures manifested by its light colour and an
Hyderoperoxides resulting from oxidation of the diene              order of magnitude lower oxidation index measured as
system in linoleic acid are later cleaved to yield short           conjugated dienes that absorb UV. The enhanced
chain volatile aldehydes and hydrocarbons (26) which               chemical stability may make a significant contribution
evaporate during the frying process (24). Simultane-               to improving the shelf-life of fried food products by
ously, longer diunsaturated aldehydes (e.g. 2,4-decan-             reducing the deterioration reactions related to fat
dienals) are left behind and may increase the PV of                oxidation.
fried linoleic-rich oil (24). Such products are produced
less during frying of oleic acid, and the hydroperoxides
formed from the monounsaturated acid remain their
original length. This might furnish an explanation for             References
the lower values of PV observed in JO. Furthermore,
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