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~ 1393 ~
International Journal of Chemical Studies 2018; 6(2): 1393-1397
P-ISSN: 2349–8528
E-ISSN: 2321–4902
IJCS 2018; 6(2): 1393-1397
© 2018 IJCS
Received: 25-01-2018
Accepted: 28-02-2018
Shubham Yadav
Ph.D. Scholar, Division of
Agricultural Chemicals, ICAR-
Indian Agricultural Research
Institute, New Delhi, India
Correspondence
Shubham Yadav
Ph.D. Scholar, Division of
Agricultural Chemicals, ICAR-
Indian Agricultural Research
Institute, New Delhi, India
Edible oil adulterations: Current issues, detection
techniques, and health hazards
Shubham Yadav
Abstract
Edible oils are used as cooking or frying medium, salad oil or in food products formulation. They are
important from nutritional point of view but ensuring their purity is a concern since old times. Because of
their greater demand in national and international market adulteration in high price oil with low price oil
is a major issue. It can affect the health of consumers adversely. Mustard oil adulterated with argemone
oil and butter yellow has been reported to cause gall bladder cancer. Similarly, argemone oil mixed with
edible oils can lead to epidemic dropsy, glaucoma and loss of eyesight. Therefore there is an urgent need
for authentication and prevention of adulteration for the sake of consumers. A spectrophotometric
method for detection and quantification of adulteration of sunflower, corn and soybean oils in olive oil
was developed. ESI-MS fingerprinting analysis has also been applied to differentiate olive oil from the
five other edible oils. GC/MS is used to classify five kinds of edible oils into five groups for authenticity
assessment. Argemone oil adulteration in mustard oil can be determined by HPTLC. The HPTLC
fingerprinting can also be used for identification and estimation of mineral oil in various vegetable oils.
The presence of palm kernel olein as adulterant in virgin coconut oil can be successfully detected by
using FTIR spectroscopy. as health of the consumers is top priority so the purity of edible items is of
utmost concern. Utilizing advance techniques for adulteration detection, we can help to reduce
consumer’s health risks.
Keywords: Edible oil adulterations, authentications, health hazards, adulteration detection techniques
Introduction
Edible oils are a food substance of whatever origin, source or composition that is
manufactured for human consumption wholly or in part from a fat or oil other than milk and
dairy product. India is an importer of edible oil due to their less net domestic availability. The
total production of edible oil in India was 25.3 million tonnes in 2015-16 and total area under
edible oils was 26.13 million hectare. Maximum production of edible oils were reported in
2013-14 which was 32.75 million tonnes from area 28.05 million hectares. India imported
148.2 lakh tonnes of edible oils in 2015-16 and net domestic availability was 86.37 lakh tonnes
(ICAR, 2016) [14]
. Because of their greater demand in national and international market
adulteration in high price oil with low price oil is a major issue. Therefore there is an urgent
need for authentication and prevention of adulteration for the sake of consumers. Purity of
edible oils is generally ascertained using saponification value, iodine value, acid value,
specific gravity, refractive index etc. but these techniques are not sensitive in sophisticated
adulterations so advance techniques are required. Further, it is possible to use oil’s both major
and minor components as adulteration detection tool. As health of the consumer’s detection,
we can help to reduce consumer’s health risks. Oils are liquid at room temperature and is top
priority so the purity of edible items is of utmost concern.
~ 1394 ~
International Journal of Chemical Studies
Source: ICAR. Handbook of Agriculture, Sixth edition,
Directorate of Information and Publication of Agriculture, New
Delhi, 2016, 1120-1194.
Fig : Net Domestic availability and Import of Edible Oils (Lakh
Tonnes)
Current issues in edible oil adulterations
Admixing cold press oil with refined one: Refined oils are
used in the adulterations of cold press oil. During refining
processes, trans fatty acids and steradienes are formed which
are generally absent in cold press oil. Trans fatty acids are not
essential and they do not promote good health. The
consumption of trans fatty acids increases risk of coronary
heart disease. Trans fats from partially hydrogenated oils are
more harmful than naturally occurring oils (Damirchi and
Torbati, 2015) [3]
.
Mustard oil adulterated with argemone oil: In number of
cases, adulteration of Argemone mexicana (Family:
Papaveraceae) seed oil in edible oils has been reported as
cause of epidemic dropsy. Sanguinarine and
dihydrosanguinarine are toxic principles (alkaloids) present in
Argemone (Das and Khanna, 1997) [4]
.
High price oil adulterations with low price oil: The
substitution of more expensive oil by cheaper one is so
profitable for producers and there are inspires to do it oil. the
substitution of expensive oil by lower price one is usual
respecting economic point of view. Some oils are more prone
to be adulterated due to their higher price and limited
accessibility. Because of the high price of virgin olive oil,
there is a great temptation to adulterate it with oils with
similar fatty acid and sterol profiles (Damirchi and Torbati,
2015) [3]
.
Loose edible oil adulterations: The poor who buy loose
edible oil across the country run the risk of cancer, paralysis,
liver damage and cardiac arrest as such oils are heavily
adulterated [11]
.
Besides these reputed brands also found to be adulterated with
ordinary palm oil or other cheap oils. In many cases it has
been found that Mineral oil, karanja oil, castor oil, and
artificial colours are heavily used in edible oil adulterations
(Navya et al., 2017) [20]
.
The Report by Consumer Voice
Highest adulteration found is 85%- coconut oil, 74.07% -
cottonseed oil, 74%-sesame oil and 71.77% in mustard oil.
New Delhi: Consumer Voice, the Voluntary Consumer
Organization working in interest of consumer education and
rights of consumers has recently done laboratory tests of loose
edible oils of 8 varieties namely Mustard, Sesame, Coconut,
Sunflower, Palmolein, Soybean, Groundnut and Cottonseed.
1, 015 samples of loose edible oils were taken from 15 states
including Delhi. The base of the tests was both on quality and
safety parameters as per FSSAI standards and samples were
tested at NABL accredited laboratory. The 15 states covered
for the samples collections are Delhi, Haryana, Uttar Pradesh,
Gujarat, West Bengal, Bihar, Jharkhand, Maharashtra, Kerala,
Tamil Nadu, Andhra Pradesh, Telangana, Karnataka,
Rajasthan and Madhya Pradesh (Consumer voice, 2016) [7]
.
Table 1
Edible Oils Total Failed % Failure
Coconut Oil 149 126 84.56%
Cottonseed Oil 54 40 74.07%
Sesame Oil 50 37 71.77%
Mustard Oil 124 89 71.77%
Groundnut 152 90 59.21%
Palmolein 50 16 32%
Soyabean 230 46 20%
Sunflower 206 34 16.5%
1,015 478 47.09%
Source: Consumer Voice New Delhi, 2016
~ 1395 ~
International Journal of Chemical Studies
Edible oil Adulterations and its effects
Adulteration usually refers to mixing other matter of an
inferior and sometimes harmful quality with edible oil
intended to be sold. As a result of adulteration, oil becomes
impure and unfit for human consumption. [10]
Fig : Techniques for edible oils adulterations detections
Saponification Value: It is the number of milligrams of KOH
required to completely saponify one gram of edible oil. Since
each carboxyl group of a fatty acid reacts with one mole of
KOH during saponification, therefore, the amount of alkali
needed to saponify certain weight of edible oil depends upon
the number of fatty acids present per weight. Thus, edible oil
containing short-chain acids will have more carboxyl groups
per gram than long chain fatty acids and consume more alkali,
i.e., will have higher saponification number.
Iodine Value: It is the number of grams of iodine absorbed
by 100 grams of edible oil. It is a measure for the degree of
unsaturation of the edible oil, as a natural property for it.
Unsaturated fatty acids absorb iodine at their double bonds,
therefore, as the degree of unsaturation increases iodine
number and hence biological value of the edible oil increase.
It is used for identification of the type of edible oil, detection
of adulteration and determining the biological value of edible
oil.
Acid Value: It is the number of milligrams of KOH required
to neutralize the free fatty acids present in one gram of edible
oil. It is used for detection of hydrolytic rancidity because it
measures the amount of free fatty acids present.
Specific Gravity: Specific gravity is the ratio of the density
of a substance to the density of a reference substance;
equivalently, it is the ratio of the mass of a substance to the
mass of a reference substance for the same given volume.
Apparent specific gravity is the ratio of the weight of a
volume of the substance to the weight of an equal volume of
the reference substance. It can be observed that the
substitution of the edible oil with other types of edible oil, the
specific gravity is increasing or decreasing greater than the
maximum allowable value for the specific gravity. It can be
observed a positively correlation between the substitution of
edible oil and specific gravity.
Refractive Index: In optics, the refractive index or index of
refraction of a material is a dimensionless number that
describes how light propagates through that medium. It is
defined as: n= c/v
Where c is the speed of light in vacuum and v is the phase
velocity of light in the medium. According to the EU
regulations, the refractive index for extra virgin olive oil
(EVOO) must range between 1.467 and 1.470. The EVOO
substation with groundnut oil (in all the substitution
percentages) decreases the value of the refractive index. The
substitution of EVOO with 10%, 20%, 30%, 40% and 50%
corn oil and sunflower oil maintain the refractive index at
normal levels. The substitution of EVOO with sunflower oil
had the highest influence on the refractive index.
Limitations
These are Insensitive at lower concentration and time
consuming. They usage chemicals and requires maximal
Sample preparations. They are insensitive in sophisticated
adulterations.
Major Advance Techniques for Adulteration Detection in
Edible Oils and Fat, as reported in the literature from
2005 to 2015
Source: Gromadzka and Wardencki, 2011
Fig
Fourier transform infrared (FTIR) spectroscopy is used in
detecting adulteration of virgin coconut oil with palm kernel
olein. Multi-bounce attenuated total reflectance measurements
were made on pure and adulterated samples of virgin coconut
oil. Detection of adulteration up to 1% was possible.
Discriminant analysis using 10 principal components was able
~ 1396 ~
International Journal of Chemical Studies
to classify pure and adulterated samples on the basis of their
spectra (Manaf et al., 2007) [18]
.
Table 1: Fatty Acid composition (%) of Virgin coconut oil and Palm
kernel olein
Fatty acid Virgin coconut oilPalm kernel olein
Iodine value 4.9 21.0
C6-C8 11.91 9.0
C12 49.69 45.0
C14 19.94 13.0
C16 8.83 9.0
C18 2.06 3.0
C18:1 6.36 19.0
C18:2 1.21 2.0
Source: Manaf et al., 2007
In number of cases, adulteration of Argemone mexicana seed
oil in mustard oils has been reported as cause of epidemic
dropsy. Oils are extracted from the seed and samples were
analysed by HPTLC and it determined argemone oil
adulteration up to lower concentration 0.5% v/v. Further
quantitative evaluation may be used as quality control tool at
manufacturer’s level and public health laboratories (Sheler et.
al., 2011) [22]
.
HPTLC fingerprinting is used for Adulteration detection of
vegetable oil by mineral oils. Due to scarcity of vegetable
oils, often it is adulterated with mineral oils. Mineral oils are
listed as group 1 carcinogens to humans. The proposed
HPTLC method was found to be simple, rapid, accurate and
reproducible for the identification and estimation of mineral
oil in various vegetable oils (Kumar and shree, 2014) [17]
.
The detection of adulteration of high priced oils is a particular
concern in food quality and safety 28 fatty acids were
identified and employed to classify five kinds of edible oils by
using GC/MS. Fatty acid profiles of these edible oils could
classify five kinds of edible vegetable oils into five groups
and are therefore employed to authenticity assessment.
Moreover, adulterated oils were simulated by Monte Carlo
method to establish simultaneous adulteration detection model
for five kinds of edible oils by random forests (Zhang et. al.,
2014) [26]
.
A spectrophotometric method for detection and quantification
of adulteration of olive oil with sunflower, corn and soybean
oils was developed. This was done by measuring the
characteristics of the absorption bands between 200 and 400
nm. It was found that max absorbance frequencies related to
conjugated diene and triene systems which characterize the
chemical composition of sunflower, corn and soybean refined
oils was a wave length 268 nm. If the absorbance measured is
higher than 0.2, this indicate that the sample is subjected to
adulteration with other seeds and vegetables oils since olive
oil at this wave length doesn't show high absorption values at
268 nm referring to the lack of poly unsaturated fatty acids
(Amereih et. al., 2014) [1]
.
Table : Fatty acid composition of olive oil
Type of oil (%)
Type of fatty acid Olive oil Corn oil Soybean Sunflower
Stearic acid 05-5 2.0-5.0 0.3-4.1 1-7
Oleic acid 55-83 19.0-49.0 2.4-23.3 14-40
Linoleic acid 3.5-21 34.0-62.0 2.6-52.2 48-74
Linolenic acid 0-1.5 0-1 3.5-5.6 0.09-0.12
Absorbance at 268nm 0.17 1.97 2.5 1.49
Source: Amereih et al., 2014
Electrospray ionization mass spectrometry (ESI-MS) is used
to analyse vegetable oils. This fingerprinting analysis was
applied to genuine samples of olive, soybean, corn, canola,
sunflower, and cottonseed oil, to admixtures of these oils, and
samples of aged soybean oil. ESI-MS fingerprints in the
negative ion mode clearly differentiate olive oil from the five
other refined oils. The method is also shown to detect aging
and adulteration of vegetable oils (Catharino et. al., 2005) [2]
.
Conclusion
It can be concluded that there is constant development of
advance techniques for edible oil adulteration detection such
as ESI-MS fingerprinting analysis which is applied to genuine
samples of olive, soybean, corn, canola, sunflower, and
cottonseed oil, to admixtures of these oils, and samples of
aged soybean oil. ESI-MS fingerprints in the negative ion
mode clearly differentiate olive oil from the five other oils.
This method also detect aging and adulteration of vegetable
oils. Now a days new advance techniques are appearing which
use modern instruments, which are partially or fully
automated. Most often their main advantage is the simplicity
of performance and short times needed for individual
analysis. Such methods include chromatographic techniques
such as GC/MS, which is used to detect adulteration of edible
oil with other vegetable oils about the level of 10% in peanut,
sunflower, sesame, soybean and rapeseed oils. This model
could identify five kinds of edible oils. This is very popular
techniques in vegetable oil analysis. Spectrophotometric
method for detection and quantification of adulteration of
olive oil with sunflower, corn and soybean oils was
developed. HPTLC method is developed for the identification
of mineral oil and argemone oil in various vegetable oils. The
presence of palm kernel olein as adulterant in virgin coconut
oil can be successfully detected by using FTIR spectroscopy.
A multivariate classification method such as discriminant
analysis was able to classify pure and adulterated virgin
coconut oil samples successfully down to an adulterated level
of 1%.
Path/ Future prospects ahead
Edible oil adulteration detection by advance techniques, based
on fatty acid profile is not so popular, so it should be
considered in future research. Similarly, Geographical and
seasonal variations in fatty acid profile of edible oils other
than olive oil should also be considered in future research for
authentication of edible oils.
References
1. Amereih S, Barghouthi Z, Marowan O. Detection and
quantification of adulteration in olive oil using a uv-
spectrophotometric method. Palestine Technical
University Research Journal. 2014; 2:l14-19.
2. Catharino RR, Haddad R, Cabrini LG, Cunha IBS,
Sawaya ACHF, Eberlin MN. Characterization of
vegetable oils by electrospray ionization mass
spectrometry fingerprinting: Classification, quality,
adulteration, and aging. American Chemical Society
Analytical Chemistry, 2005; 77:7429-7433.
3. Damirchi SA, Torbati M. Adulterations in some edible
oils and fats and their detection methods. Journal of food
quality and hazard control. 2015; 2:38-44.
4. Das M, Khanna SK. Clinico epidemiological,
toxicological, and safety evaluation studies on argemone
oil. Critical reviews in toxicology, 1997; 27(3):273-297.
~ 1397 ~
International Journal of Chemical Studies
5. Gromadzka J, Wardencki W. Trends in edible vegetable
oils analysis. Part B. Application of different analytical
techniques. Polish Journal of Food and Nutrition
Sciences. 2011; 61(2):89-99.
6. Hong E, Lee SY, Jeong JY, Park JM, Kim BH, Kwon K,
et al. Modern analytical methods for the detection of food
fraud and adulteration by food category. Journal of the
science of food and agriculture. 2017.
7. http://caiindia.org/edible-oils-adulterated-finds-study/
8. http://foodnetindia.in/blog/2017/10/02/902/ Widespread
Edible Oil Adulteration in India
9. http://vikaspedia.in/health/health-campaigns/beware-of-
adulteration/methods-for-detection-of-common-
adulterants-in-food.
10. https://en.wikipedia.org/wiki/adulterations.
11. https://timesofindia.indiatimes.com ›... › loose edible oil
adulterated: Study
12. https://timesofindia.indiatimes.com/india/...adulteration...
edible-oil.../52661878.cms
13. https://www.thehindubusinessline.com/bline/2003/06/10/.
../2003061000361100.htm
14. ICAR. Handbook of Agriculture, Sixth edition,
Directorate of Information and Publication of Agriculture,
New Delhi, 2016, 1120-1194.
15. Indelicato S, Bongiorno D, Pitonzo R, Stefano VD,
Calabrese V, Indelicato S et al. Triacylglycerols (TAGs)
in edible oils: Determination, characterization,
quantitation, chemometric approach and evaluation of
adulterations. Journal of Chromatography a. 2017;
17:31144-5.
16. Khan A, Sankhyan P, Kumar S. Biochemical
characterization of Mustard Oil (Brassica campestris L.)
with special reference to its fatty acid composition. Asian
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17. Kumar UP, Shree ABR. A rapid technique for detection
and quantification of mineral oil in vegetable oils used as
vehicles in ayurvedic formulations. International Journal
of Herbal Medicine. 2014; 2:20-22.
18. Manaf MA, Man YBC, Hamid NSA, Ismail A, abiding
SJ. Analysis of adulteration of origin coconut oil by palm
kernel olein using FTIR spectroscopy. Journal of food
lipid. 2007; 14:111-121.
19. Mishra V, Mishra M, Ansari KM, Chaudhari BP, Khanna
R, Das M. Edible oil adulterants, argemone oil and butter
yellow, as aetiological factors for gall bladder cancer.
European Journal of Cancer, 2012; 48(13):2075-2085.
20. Navya P, Raju K, Sukumaran MK. Analysis of Food
Adulterants in Selected Food Items Purchased From
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in Scientific Research. 2017; 3(07):82-89.
21. Oroian M, Leahu A. Olive oil adulteration with other
edible oils: Influence of substitution on physicochemical
properties. Food and Environment Safety, 2014; 8:263-
266.
22. Shelar MK, Bafna AR, Wahile AM, Tupkar SV.
Evaluation of edible oils for Argemone mexicana seed oil
adulteration. Research Journal of Pharmaceutical
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23. Shukla AK, Dixit AK, Singh RP. Detection of
adulteration in edible oils. Journal of Oleo Science. 2005;
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cooking-oils.../196856.html
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Edible oil adulterations

  • 1. ~ 1393 ~ International Journal of Chemical Studies 2018; 6(2): 1393-1397 P-ISSN: 2349–8528 E-ISSN: 2321–4902 IJCS 2018; 6(2): 1393-1397 © 2018 IJCS Received: 25-01-2018 Accepted: 28-02-2018 Shubham Yadav Ph.D. Scholar, Division of Agricultural Chemicals, ICAR- Indian Agricultural Research Institute, New Delhi, India Correspondence Shubham Yadav Ph.D. Scholar, Division of Agricultural Chemicals, ICAR- Indian Agricultural Research Institute, New Delhi, India Edible oil adulterations: Current issues, detection techniques, and health hazards Shubham Yadav Abstract Edible oils are used as cooking or frying medium, salad oil or in food products formulation. They are important from nutritional point of view but ensuring their purity is a concern since old times. Because of their greater demand in national and international market adulteration in high price oil with low price oil is a major issue. It can affect the health of consumers adversely. Mustard oil adulterated with argemone oil and butter yellow has been reported to cause gall bladder cancer. Similarly, argemone oil mixed with edible oils can lead to epidemic dropsy, glaucoma and loss of eyesight. Therefore there is an urgent need for authentication and prevention of adulteration for the sake of consumers. A spectrophotometric method for detection and quantification of adulteration of sunflower, corn and soybean oils in olive oil was developed. ESI-MS fingerprinting analysis has also been applied to differentiate olive oil from the five other edible oils. GC/MS is used to classify five kinds of edible oils into five groups for authenticity assessment. Argemone oil adulteration in mustard oil can be determined by HPTLC. The HPTLC fingerprinting can also be used for identification and estimation of mineral oil in various vegetable oils. The presence of palm kernel olein as adulterant in virgin coconut oil can be successfully detected by using FTIR spectroscopy. as health of the consumers is top priority so the purity of edible items is of utmost concern. Utilizing advance techniques for adulteration detection, we can help to reduce consumer’s health risks. Keywords: Edible oil adulterations, authentications, health hazards, adulteration detection techniques Introduction Edible oils are a food substance of whatever origin, source or composition that is manufactured for human consumption wholly or in part from a fat or oil other than milk and dairy product. India is an importer of edible oil due to their less net domestic availability. The total production of edible oil in India was 25.3 million tonnes in 2015-16 and total area under edible oils was 26.13 million hectare. Maximum production of edible oils were reported in 2013-14 which was 32.75 million tonnes from area 28.05 million hectares. India imported 148.2 lakh tonnes of edible oils in 2015-16 and net domestic availability was 86.37 lakh tonnes (ICAR, 2016) [14] . Because of their greater demand in national and international market adulteration in high price oil with low price oil is a major issue. Therefore there is an urgent need for authentication and prevention of adulteration for the sake of consumers. Purity of edible oils is generally ascertained using saponification value, iodine value, acid value, specific gravity, refractive index etc. but these techniques are not sensitive in sophisticated adulterations so advance techniques are required. Further, it is possible to use oil’s both major and minor components as adulteration detection tool. As health of the consumer’s detection, we can help to reduce consumer’s health risks. Oils are liquid at room temperature and is top priority so the purity of edible items is of utmost concern.
  • 2. ~ 1394 ~ International Journal of Chemical Studies Source: ICAR. Handbook of Agriculture, Sixth edition, Directorate of Information and Publication of Agriculture, New Delhi, 2016, 1120-1194. Fig : Net Domestic availability and Import of Edible Oils (Lakh Tonnes) Current issues in edible oil adulterations Admixing cold press oil with refined one: Refined oils are used in the adulterations of cold press oil. During refining processes, trans fatty acids and steradienes are formed which are generally absent in cold press oil. Trans fatty acids are not essential and they do not promote good health. The consumption of trans fatty acids increases risk of coronary heart disease. Trans fats from partially hydrogenated oils are more harmful than naturally occurring oils (Damirchi and Torbati, 2015) [3] . Mustard oil adulterated with argemone oil: In number of cases, adulteration of Argemone mexicana (Family: Papaveraceae) seed oil in edible oils has been reported as cause of epidemic dropsy. Sanguinarine and dihydrosanguinarine are toxic principles (alkaloids) present in Argemone (Das and Khanna, 1997) [4] . High price oil adulterations with low price oil: The substitution of more expensive oil by cheaper one is so profitable for producers and there are inspires to do it oil. the substitution of expensive oil by lower price one is usual respecting economic point of view. Some oils are more prone to be adulterated due to their higher price and limited accessibility. Because of the high price of virgin olive oil, there is a great temptation to adulterate it with oils with similar fatty acid and sterol profiles (Damirchi and Torbati, 2015) [3] . Loose edible oil adulterations: The poor who buy loose edible oil across the country run the risk of cancer, paralysis, liver damage and cardiac arrest as such oils are heavily adulterated [11] . Besides these reputed brands also found to be adulterated with ordinary palm oil or other cheap oils. In many cases it has been found that Mineral oil, karanja oil, castor oil, and artificial colours are heavily used in edible oil adulterations (Navya et al., 2017) [20] . The Report by Consumer Voice Highest adulteration found is 85%- coconut oil, 74.07% - cottonseed oil, 74%-sesame oil and 71.77% in mustard oil. New Delhi: Consumer Voice, the Voluntary Consumer Organization working in interest of consumer education and rights of consumers has recently done laboratory tests of loose edible oils of 8 varieties namely Mustard, Sesame, Coconut, Sunflower, Palmolein, Soybean, Groundnut and Cottonseed. 1, 015 samples of loose edible oils were taken from 15 states including Delhi. The base of the tests was both on quality and safety parameters as per FSSAI standards and samples were tested at NABL accredited laboratory. The 15 states covered for the samples collections are Delhi, Haryana, Uttar Pradesh, Gujarat, West Bengal, Bihar, Jharkhand, Maharashtra, Kerala, Tamil Nadu, Andhra Pradesh, Telangana, Karnataka, Rajasthan and Madhya Pradesh (Consumer voice, 2016) [7] . Table 1 Edible Oils Total Failed % Failure Coconut Oil 149 126 84.56% Cottonseed Oil 54 40 74.07% Sesame Oil 50 37 71.77% Mustard Oil 124 89 71.77% Groundnut 152 90 59.21% Palmolein 50 16 32% Soyabean 230 46 20% Sunflower 206 34 16.5% 1,015 478 47.09% Source: Consumer Voice New Delhi, 2016
  • 3. ~ 1395 ~ International Journal of Chemical Studies Edible oil Adulterations and its effects Adulteration usually refers to mixing other matter of an inferior and sometimes harmful quality with edible oil intended to be sold. As a result of adulteration, oil becomes impure and unfit for human consumption. [10] Fig : Techniques for edible oils adulterations detections Saponification Value: It is the number of milligrams of KOH required to completely saponify one gram of edible oil. Since each carboxyl group of a fatty acid reacts with one mole of KOH during saponification, therefore, the amount of alkali needed to saponify certain weight of edible oil depends upon the number of fatty acids present per weight. Thus, edible oil containing short-chain acids will have more carboxyl groups per gram than long chain fatty acids and consume more alkali, i.e., will have higher saponification number. Iodine Value: It is the number of grams of iodine absorbed by 100 grams of edible oil. It is a measure for the degree of unsaturation of the edible oil, as a natural property for it. Unsaturated fatty acids absorb iodine at their double bonds, therefore, as the degree of unsaturation increases iodine number and hence biological value of the edible oil increase. It is used for identification of the type of edible oil, detection of adulteration and determining the biological value of edible oil. Acid Value: It is the number of milligrams of KOH required to neutralize the free fatty acids present in one gram of edible oil. It is used for detection of hydrolytic rancidity because it measures the amount of free fatty acids present. Specific Gravity: Specific gravity is the ratio of the density of a substance to the density of a reference substance; equivalently, it is the ratio of the mass of a substance to the mass of a reference substance for the same given volume. Apparent specific gravity is the ratio of the weight of a volume of the substance to the weight of an equal volume of the reference substance. It can be observed that the substitution of the edible oil with other types of edible oil, the specific gravity is increasing or decreasing greater than the maximum allowable value for the specific gravity. It can be observed a positively correlation between the substitution of edible oil and specific gravity. Refractive Index: In optics, the refractive index or index of refraction of a material is a dimensionless number that describes how light propagates through that medium. It is defined as: n= c/v Where c is the speed of light in vacuum and v is the phase velocity of light in the medium. According to the EU regulations, the refractive index for extra virgin olive oil (EVOO) must range between 1.467 and 1.470. The EVOO substation with groundnut oil (in all the substitution percentages) decreases the value of the refractive index. The substitution of EVOO with 10%, 20%, 30%, 40% and 50% corn oil and sunflower oil maintain the refractive index at normal levels. The substitution of EVOO with sunflower oil had the highest influence on the refractive index. Limitations These are Insensitive at lower concentration and time consuming. They usage chemicals and requires maximal Sample preparations. They are insensitive in sophisticated adulterations. Major Advance Techniques for Adulteration Detection in Edible Oils and Fat, as reported in the literature from 2005 to 2015 Source: Gromadzka and Wardencki, 2011 Fig Fourier transform infrared (FTIR) spectroscopy is used in detecting adulteration of virgin coconut oil with palm kernel olein. Multi-bounce attenuated total reflectance measurements were made on pure and adulterated samples of virgin coconut oil. Detection of adulteration up to 1% was possible. Discriminant analysis using 10 principal components was able
  • 4. ~ 1396 ~ International Journal of Chemical Studies to classify pure and adulterated samples on the basis of their spectra (Manaf et al., 2007) [18] . Table 1: Fatty Acid composition (%) of Virgin coconut oil and Palm kernel olein Fatty acid Virgin coconut oilPalm kernel olein Iodine value 4.9 21.0 C6-C8 11.91 9.0 C12 49.69 45.0 C14 19.94 13.0 C16 8.83 9.0 C18 2.06 3.0 C18:1 6.36 19.0 C18:2 1.21 2.0 Source: Manaf et al., 2007 In number of cases, adulteration of Argemone mexicana seed oil in mustard oils has been reported as cause of epidemic dropsy. Oils are extracted from the seed and samples were analysed by HPTLC and it determined argemone oil adulteration up to lower concentration 0.5% v/v. Further quantitative evaluation may be used as quality control tool at manufacturer’s level and public health laboratories (Sheler et. al., 2011) [22] . HPTLC fingerprinting is used for Adulteration detection of vegetable oil by mineral oils. Due to scarcity of vegetable oils, often it is adulterated with mineral oils. Mineral oils are listed as group 1 carcinogens to humans. The proposed HPTLC method was found to be simple, rapid, accurate and reproducible for the identification and estimation of mineral oil in various vegetable oils (Kumar and shree, 2014) [17] . The detection of adulteration of high priced oils is a particular concern in food quality and safety 28 fatty acids were identified and employed to classify five kinds of edible oils by using GC/MS. Fatty acid profiles of these edible oils could classify five kinds of edible vegetable oils into five groups and are therefore employed to authenticity assessment. Moreover, adulterated oils were simulated by Monte Carlo method to establish simultaneous adulteration detection model for five kinds of edible oils by random forests (Zhang et. al., 2014) [26] . A spectrophotometric method for detection and quantification of adulteration of olive oil with sunflower, corn and soybean oils was developed. This was done by measuring the characteristics of the absorption bands between 200 and 400 nm. It was found that max absorbance frequencies related to conjugated diene and triene systems which characterize the chemical composition of sunflower, corn and soybean refined oils was a wave length 268 nm. If the absorbance measured is higher than 0.2, this indicate that the sample is subjected to adulteration with other seeds and vegetables oils since olive oil at this wave length doesn't show high absorption values at 268 nm referring to the lack of poly unsaturated fatty acids (Amereih et. al., 2014) [1] . Table : Fatty acid composition of olive oil Type of oil (%) Type of fatty acid Olive oil Corn oil Soybean Sunflower Stearic acid 05-5 2.0-5.0 0.3-4.1 1-7 Oleic acid 55-83 19.0-49.0 2.4-23.3 14-40 Linoleic acid 3.5-21 34.0-62.0 2.6-52.2 48-74 Linolenic acid 0-1.5 0-1 3.5-5.6 0.09-0.12 Absorbance at 268nm 0.17 1.97 2.5 1.49 Source: Amereih et al., 2014 Electrospray ionization mass spectrometry (ESI-MS) is used to analyse vegetable oils. This fingerprinting analysis was applied to genuine samples of olive, soybean, corn, canola, sunflower, and cottonseed oil, to admixtures of these oils, and samples of aged soybean oil. ESI-MS fingerprints in the negative ion mode clearly differentiate olive oil from the five other refined oils. The method is also shown to detect aging and adulteration of vegetable oils (Catharino et. al., 2005) [2] . Conclusion It can be concluded that there is constant development of advance techniques for edible oil adulteration detection such as ESI-MS fingerprinting analysis which is applied to genuine samples of olive, soybean, corn, canola, sunflower, and cottonseed oil, to admixtures of these oils, and samples of aged soybean oil. ESI-MS fingerprints in the negative ion mode clearly differentiate olive oil from the five other oils. This method also detect aging and adulteration of vegetable oils. Now a days new advance techniques are appearing which use modern instruments, which are partially or fully automated. Most often their main advantage is the simplicity of performance and short times needed for individual analysis. Such methods include chromatographic techniques such as GC/MS, which is used to detect adulteration of edible oil with other vegetable oils about the level of 10% in peanut, sunflower, sesame, soybean and rapeseed oils. This model could identify five kinds of edible oils. This is very popular techniques in vegetable oil analysis. Spectrophotometric method for detection and quantification of adulteration of olive oil with sunflower, corn and soybean oils was developed. HPTLC method is developed for the identification of mineral oil and argemone oil in various vegetable oils. The presence of palm kernel olein as adulterant in virgin coconut oil can be successfully detected by using FTIR spectroscopy. A multivariate classification method such as discriminant analysis was able to classify pure and adulterated virgin coconut oil samples successfully down to an adulterated level of 1%. Path/ Future prospects ahead Edible oil adulteration detection by advance techniques, based on fatty acid profile is not so popular, so it should be considered in future research. Similarly, Geographical and seasonal variations in fatty acid profile of edible oils other than olive oil should also be considered in future research for authentication of edible oils. References 1. 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