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Fatty acid, tocopherol and squalene contents of Rosaceae seed oils

Botanical StudiesAn International Journal201455:48

DOI: 10.1186/s40529-014-0048-4

Received: 11 March 2014

Accepted: 10 May 2014

Published: 5 June 2014

Abstract

Background

The aim of current study is to establish the composition of these seeds belong to Rosaceae family with respect to fatty acid, tocopherol and squalene content.

Results

The oil contents of seeds varied between 3.49 (Cotoneaster bullatus) to 46.15 g/100 g (Prunus tenella). The main fatty acids of seed oils were oleic (6.50 - 67.11 %), linoleic (22.08 - 68.62 %) and 20:1n-7 (0.10 - 61.59 %). As observed, the oils of seed were rich in linoleic and oleic acids. Total tocopherol contents ranged between 7.06 mg/100 g (Prunus tenella) to 165.74 mg/100 g (Potentilla glandulosa ssp. pseudorupestris). The major tocopherols were γ-tocopherol, ranging from 2.08 mg/100 g to 106.01 mg/100 g; α-tocopherol ranging from 2.86 mg100 g to 74.26 mg/100 g and δ-tocopherol ranging used in this experiment were found between 0.02 mg/100 g (Alchemilla caucasica) to o.29 mg/100 g (Cotoneaster simonsii).

Conclusions

These results show that Rosaceae seed oils can be a potential saurce of valuable oil which might be useful for the evaluation of dietary information in important food crops and other industrial applications.

Keywords

Rosaceae Oil content Fatty acid Tocopherol Squalen

Background

Some seed oils are already used for several purposes: blending higly saturated edible oils to provide new oils with modified nutritional values, as ingredients in paint and varnish formulations, surface coating and oleo-chemicals and as oils for cosmetic purposes (Helmy [1990]). Several species of Rosaceae presently have great commercial value as oil crops, e.g. Aronia melanocarpa L., Rosa canina, severeal and Rubus spp (Pourrat and Carnat [1981]; Johansson et al. [1997]; Xu et al. [2006]; Oh et al. [2007]). Plant seeds are important sources of oils of nutritional, industrial and pharmaceutical importance. No oil from any single source has been found to be suitable for all purposes because oils from different sources generally differ in their fatty acid composition. The fatty acid composition of the endogenous fats plays an important role in determining shelf life, nutrition and flavor of food products (Gao and Mazza [1995]). The study of oil seeds for their minor constituents is useful in order that both the oil and its minor constituents be used effectively (Ramadan and Mörsel [2002]). Tocopherols and squalene are components present in the unsaponifiable lipid fraction of foods. α- Tocopherol, the most common form of vitamin E present in nature, is the most biologically active (Bjorneboe et al. [1990]), and is preferentially retained in large quantities and transported to body components (Traber et al. [1990]; Ching and Mohamed [2001]). Konings et al. ([1996])) developed a HPLC method for determination of tocopherols and tocotrienols in margarine, infant foods and vegetables. The main biochemical function of the tocopherols is believed to be the protection of polyunsaturated fatty acids aganist peroxidation (Beringer and Dompert [1976]; Kamel-Eldin and Andersson [1997]). They have vitamin E properties and display antioxidant activity, which protect the body tissues aganist the damaging effects caused by the free radicals that results from many normal metabolic functions (Lopez Ortiz et al. [2006]). The major fatty acids composing the oils were linoleic (41-70%), linolenic (13-36%), and oleic (11-19%) acids (Pourrat and Carnat [1981]; Johansson et al. [1997]; Oomah et al. [2000]; Bushman et al. [2004]). At the same time, tocopherols, the major vitamin of vitamin E are fat-soluble antioxidants that function as scavengers of lipid peroxyl radicals (Ryan et al. [2007]).

Squalene, a 30 carbon isoprenoid, is a key intermediate in cholesterol biosynthesis and is abundant in shark liver oil and olive oil (Ryan et al. [2007]). More recently, squalene has been shown to act as an antidote to reduce accidental drug-induced toxicities (Aguilera et al. [2005]; Senthilkumar et al. [2006]; Ryan et al. [2007]). The protective effect of squalene may be attributed to its ability to serve as an antioxidant (Ryan et al. [2007]). To achieve the most economical and efficient utilization of these seeds, more information on the varieties, properties and composition is required. Therefore, the present study attempted to establish the composition of these seeds belong to Rosaceae family with respect to fatty acid, tocopherol and squalene content.

Methods

Seeds

About 26 variety of plants belong to Rosaceae family were collected from plants growing in Botanical Garden of Germany (Alchemilla caucasica, Cotoneaster bullatus, Cotoneaster dielsianus, Cotoneaster francheti, Cotoneaster moupinensis, Cotoneaster simonsii, Dryas drummondii, Exochorda racemosa, Geum elatum,Geum magellanicum, Geum pyrenaicum, Potentilla alchimilloides, Potentilla ambigua, Potentilla argyrophylla var.leucochroa, Potentilla atrosanguinea, Potentilla aurea, Potentilla glandulosa, Potentilla grammopetala, Potentilla hippiana, Potentilla pyrenaica, Potentilla speciosa, Potentilla tridentate, Potentilla visianii, Prinsepia uniflora, Prunus tenella and Rosa palustris) in August, 2007 year. The seeds were cleaned in air screen cleaner to remove immature and broken seeds, dried by air condition. The seeds were stored in paper bags at +4°C temperature.

Reagents

Petroleum ether (40–60°C) was of analytical grade (>98%; Merck, Darmstadt, Germany). Heptane and tert-butyl methyl ether were of HPLC grade (Merck, Darmstadt, Germany). Tocopherol and tocotrienol standard compounds were purchased from CalBiochem (Darmstadt, Germany).

Oil content

The oil content was determined according to the method ISO 659:1998 (ISO,1998). About 2 g of the seeds were ground in a ball mill and extracted with petroleum ether in a Twisselmann apparatus for 6 h. The solvent was removed by a rotary evaporator at 40°C and 25 Torr. The oil was dried by a stream of nitrogen and stored at – 20°C until used.

Fatty acid composition

The fatty acid composition was determined following the ISO standard ISO 5509:2000 (ISO 2000). In brief, one drop of the oil was dissolved in 1 mL of n-heptane, 50 μg of sodium methylate was added, and the closed tube was agitated vigorously for 1 min at room temperature. After addition of 100 μL of water, the tube was centrifuged at 4500 g for 10 min and the lower aqueous phase was removed. Then 50 μL of HCl (1 mol with methyl orange) was added, the solution was shortly mixed, and the lower aqueous phase was rejected. About 20 mg of sodium hydrogen sulphate (monohydrate, extra pure; Merck, Darmstadt, Germany) was added, and after centrifugation at 4500 g for 10 min, the top n-heptane phase was transferred to a vial and injected in a Varian 5890 gas chromotograph with a capillary column, CP-Sil 88 (100 m long, 0.25 mm ID, film thickness 0.2 μm). The temperature program was as follows: from 155°C; heated to 220°C (1.5°C/min), 10 min isotherm; injector 250°C, detector 250°C; carrier gas 36 cm/s hydrogen; split ratio 1:50; detector gas 30 mL/min hydrogen; 300 mL/min air and 30 mL/min nitrogen; manual injection volume less than 1 μL. The peak areas were computed by the integration software, and percentages of fatty acid methyl esters (FAME) were obtained as weight percent by direct internal normalization.

Tocopherols

For determination of tocopherols, a solution of 250 mg of oil in 25 mL of n-heptane was directly used for the HPLC. The HPLC analysis was conducted using a Merck-Hitachi low-pressure gradient system, fitted with a L-6000 pump, a Merck-Hitachi F-1000 fluorescence sp ectrophotometer (detector wavelengths for excitation 295 nm, for emission 330 nm), and a D-2500 integration system. The samples in the amount of 20 μL were injected by a Merck 655-A40 autosampler onto a Diol phase HPLC column 25 cm × 4.6 mmID (Merck, Darmstadt, Germany) used with a flow rate of 1.3 mL/min. The mobile phase used was n-heptane/tert-butyl methyl ether (99 + 1, v/v).

Results and discussion

Percentages of the lipidic fraction of the 26 plant seeds belong to Rosaceae familya re given in Table 1. Oil contents of samples changed between 3.49 g/100g and 46.15 g/100g. On average terms, seeds contained 19.45%. However, due to the economical value of oil content, they are both valuable as raw material for oil extraction. The authors found numerous references in the literature composition of the lipidic fraction for some Rosaceae seeds. Studies based on varieties give results that ranged between 9.0 and 23% (Pourrat and Carnat [1981]; Johansson et al. [1997]; Zlatanov [1999]; Oomah et al. [2000]; Bushman et al. [2004]; Oh et al. [2007]).
Table 1

Oil contents of some Rosaceae seeds

Samples

Oil contents (%)

Alchemilla caucasica

25.99

Cotoneaster bullatus

3.49

Cotoneaster dielsianus

7.56

Cotoneaster francheti

5.22

Cotoneaster moupinensis

5.29

Cotoneaster simonsii

3.91

Dryas drummondii

21.82

Exochorda racemosa

19.56

Geum elatum

17.38

Geum magellanicum

19.04

Geum pyrenaicum

14.53

Potentilla alchimilloides

20.23

Potentilla ambigua

9.71

Potentilla argyrophylla var.leucochroa

17.48

Potentilla atrosanguinea

23.81

Potentilla aurea

28.93

Potentilla glandulosa

28.95

Potentilla grammopetala

19.01

Potentilla hippiana

28.60

Potentilla pyrenaica

23.92

Potentilla speciosa

15.09

Potentilla tridentate

18.41

Potentilla visianii

23.80

Prinsepia uniflora

41.82

Prunus tenella

46.15

Rosa palustris

16.06

The most abundant fatty acids in seed oils were oleic, linoleic and 20:1n-7 acids, accounting for 96.63 to 99.80% in seed oils. The oils extracted from Rosaceae seeds were composed of 3.25-9.17% palmitic, 1.19-4.27% stearic, 6.50-67.11% oleic, 22.08-68.62% linoleic and 0.10-61.59% eicosenoic acids (Table 2). The proportion of linoleic acid in the seed oil of Exochorda racemosa was higher than that in the seed oil of Potentilla hippiana. This proportion was also higher than those of in other some seed oils (Pourrat and Carnat [1981]; Bushman et al. [2004]; Matthaus and Ozcan [2005]; Oh et al. [2007]). The erucic acid species of this genus contain from the linolenic acid (Table 2). As can be observed, the oils of all seed oils used in this experiment had higher linoleic acid content than those of other fatty acids. On the other hand, oleic acid contents of seed oils varied between 6.5% (Potentilla argyrophylla var. leucochroa) to 67.11% (Prunus tenella).
Table 2

Fatty acid compositions of Rosaceae seed oils (%)

Samples

Fatty acids

Palmitic

Palmitoleic

Stearic

Oleic

Vaccenic

Linoleic

Linolenic

Eicosenoic

20:1n-7

Alchemilla caucasica

4.15

0.07

1.96

10.54

0.31

31.29

-

0.24

50.29

Cotoneaster bullatus

7.89

0.29

1.45

20.57

1.26

60.04

3.30

-

0.46

Cotoneaster dielsianus

9.17

0.13

4.27

29.81

0.28

51.89

0.67

-

0.42

Cotoneaster francheti

8.77

0.16

1.37

16.67

0.49

66.60

0.77

-

0.62

Cotoneaster moupinensis

6.66

0.21

1.48

26.59

0.44

59.85

0.88

-

0.53

Cotoneaster simonsii

6.81

0.25

1.19

19.52

0.49

64.64

1.47

-

0.94

Dryas drummondii

5.92

0.30

1.73

22.72

0.40

56.82

0.05

1.31

6.20

Exochorda racemosa

6.84

0.18

2.50

18.54

0.43

68.62

0.47

-

0.16

Geum elatum

8.19

0.17

2.06

20.30

0.40

39.25

0.06

0.06

27.20

Geum magellanicum

4.73

0.06

2.07

17.62

0.39

29.69

0.03

0.13

43.23

Geum pyrenaicum

6.06

0.18

3.43

34.45

0.51

22.61

0.07

0.08

30.28

Potentilla alchimilloides

6.09

0.09

2.44

7.89

0.40

26.74

-

0.16

55.02

Potentilla ambigua

5.65

0.18

0.98

13.13

0.57

22.67

0.37

0.12

52.70

Potentilla argyrophylla

4.46

0.15

1.44

6.50

0.41

28.04

-

0.63

57.25

Potentilla atrosanguinea

4.20

0.13

1.44

11.31

0.43

32.84

-

0.14

48.59

Potentilla aurea

5.16

0.13

1.59

10.91

0.35

26.17

-

0.84

53.78

Potentilla glandulosa

4.37

0.22

1.22

13.41

0.51

25.91

-

0.82

52.20

Potentilla grammopetala

5.32

0.09

2.00

9.77

0.36

27.89

-

0.52

52.91

Potentilla hippiana

4.64

0.12

1.40

10.80

0.70

22.08

0.03

0.16

57.89

Potentilla pyrenaica

4.93

0.08

1.99

12.90

0.29

29.65

-

0.86

48.28

Potentilla speciosa

7.81

0.13

2.07

19.21

0.55

26.73

-

0.11

40.94

Potentilla tridentate

4.30

0.13

1.88

14.13

0.39

40.85

-

0.60

36.53

Potentilla visianii

3.25

0.05

1.55

8.14

0.33

23.27

-

0.70

61.59

Prinsepia uniflora

5.20

0.17

1.75

28.22

0.41

60.92

0.34

-

0.44

Prunus tenella

3.48

0.23

-

67.11

-

26.76

0.16

-

0.10

Rosa palustris

5.04

0.19

1.74

15.77

0.56

27.56

0.15

0.83

45.37

Nutritionally unfavorable is the high content of saturated fatty acids, consisting of palmitic acid, which amounted to between 3.25% (Potentilla visianii) to 9.17% (Cotoneaster dielsianus), and stearic acid, which was found in a very small range between 1.19% (Cotoneaster simonsii) to 4.27% (Cotoneaster dielsianus). However, Rosaceae seed oil used in this experiment contain more linoleic and 20:1 n-7 (except for a few seed oils) acids and less stearic and palmitic acids. Also, the oils of some seed, contained a high propertion of 20:1 n-7. The main fatty acids in bramble seed oils are C18:2n −6 (51.0-66.1%), C18:3n-3 (9.70-35.6%), C18:1n-9 (9.85-16.3) and C16:0 (2.01-5.73%) (Xu et al. [2006]). In general, high amounts of linoleic acid are unsuitable for oil-food products due to its instability and reversion of flavor associated with autoxidation (Green [1986]; Singh et al. [1998]). So, these seed oils may be a suitable oil seed crop for the various industry due to its very low content of linolenic and high content of linoleic acid (Singh et al. [1998]). Those observations are in agreement with the data reported earlier about the fatty acid composition of some seed oils (Tiscornia et al. [1976]; Zlatanov et al. [1997]; Zlatanov [1999]).

Most plants deriveted foods contain low to moderate levels of vitamin E activity. However, oving to the abundance of plant-derived foods in our diets, they provide a significant and consistent source of vitamin E (Eitenmiller and Lee [2004]; Ryan et al. [2007]). The tocopherol contents of seed oils researched in present study are listed in Table 3. All the seeds analysed exhibited differences in their tocopherol contents and the differences were found. The major tocopherol was γ-tocopherol in all the varieties of Rosaceae seed oils, which was higher in Potentilla glandulosa (106.01 mg/100 g) than in Cotoneaster simonnsii (2.08 mg/100 g). The contents of α-tocopherol in seed oil of Cotoneaster simonsii (74.26 mg/100 g) were about 26x that of Prunus tenella (2.86 mg/100 g), and the content of tocopherol in Potentilla aurea seed oil (73.59 mg/100 g) was also hipher than that in Alchemilla caucasica (0.60 mg/100 g) oil. The total tocopherol in Potentilla glandulosa seed oil (165.74 mg/100 g) was higher than that in Prunus tenella (7.06 mg/100 g). Our results are higher than those of other authors (α-tocopherol and β + γ-tocopherol) (Ryan et al. [2007]). The major tocopherol in all bramble seed oils of 10 varieties was γ-tocopherol. The composition (mg/100 g) was as follows: α-tocopherol 7.65-52.6, γ-tocopherol 46.9-106, δ-tocopherol 3.1-9.50, and the active vitamin E 15.9-61.5 among the varieties (Xu et al. [2006]). In the tocopherol fraction (55.5 mg/kg in chokeberry oil, 249.6 mg/kg in black currant oil and 89.4 mg/kg in rose hip oil), α-tocopherol predominated in chokeberry oil (70.6 mg/kg). γ-Tocopherol was the main component in black currant oil (55.4 mg/kg) and rose hip oil (71.0 mg/kg) (Zlatanov [1999]). The content of tocopherols is 360 mg/100 g in the hexane extract oil of raspberry seed and the main component is the isomer (Oomah et al. [2000]). In cold- pressed raspberry seed oil, the total tocopherols are 88.9 mg/100 g (Parry et al. [2005]). So, because of the nutritional and antioxidant properties of tocopherols, Rosaceae seed oils should be taken into account. As a healthy product, the fatty acids and tocopherols in the seed oil are the major components (Oomah et al. [2000]).
Table 3

Tocopherol contents of some Rosaceae seed oils (mg/100 g)

 

α

α-T3

β-T

γ-T

β-T3

P8

γ-T3

Δ-T

Δ-T3

Sum

Alchemilla caucasica

6.17

5.64

0.00

15.90

0.00

0.00

0.00

0.60

0.00

28.31

Cotoneaster bullatus

53.56

56.84

0.00

285.49

0.00

0.00

0.00

0.00

0.00

138.88

Cotoneaster dielsianus

21.87

21.29

0,00

11,77

0,00

0,00

0,00

0,68

0,00

55,61

Cotoneaster francheti

34.10

29.11

1,72

28,38

0,00

0,00

0,00

3,97

0,00

97,27

Cotoneaster moupinensis

27.33

0.00

7,14

0,00

0,00

0,00

0,00

0,00

0,00

34,47

Cotoneaster simonsii

74.26

0,00

74,72

2,08

0,00

5,10

0,00

1,57

0,00

157,73

Dryas drummondii

10.47

0,00

0,37

13,68

0,00

0,42

0,00

0,69

0,00

25,63

Exochorda racemosa

25,48

0,00

0,00

87,09

0,00

0,00

0,00

4,21

0,00

116,78

Geum elatum

42,92

10,03

3,43

12,40

0,00

0,22

0,19

1,70

0,00

70,89

Geum magellanicum

23,16

7,75

2,71

41,94

0,00

0,65

0,51

5,21

0,00

81,93

Geum pyrenaicum

32,86

11,81

0,82

24,59

0,00

0,54

0,37

0,99

0,00

71,97

Potentilla alchimilloides

11,67

10,17

0,50

27,48

0,00

0,36

0,39

4,98

0,00

55,55

Potentilla ambigua

20,43

17,02

0,41

58,10

0,00

0,00

0,00

2,69

0,00

98,64

Potentilla argyrophylla

12,51

10,14

1,21

48,55

0,00

0,23

0,27

44,56

0,00

117,45

Potentilla atrosanguinea

9,88

7,75

99,00

37,11

0,00

0,95

0,47

25,33

0,00

82,48

Potentilla aurea

7,58

5,54

1,54

39,38

0,00

0,29

0,38

73,59

0,00

128,30

Potentilla glandulasa

5,89

0,00

0,28

106,01

0,00

0,46

0,16

52,94

0,00

165,74

Potentilla grammopetala

8,06

0,00

0,41

33,42

0,00

0,29

0,47

3,96

0,00

46,61

Potentilla hippiana

5,76

0,00

0,00

58,16

0,00

0,45

0,24

41,28

0,00

105,89

Potentilla pyrenaica

10,13

8,05

1,41

15,04

0,00

0,30

0,25

68,30

0,53

104,01

Potentilla speciosa

22,75

13,34

0,49

50,77

0,00

0,00

0,51

2,85

0,00

90,71

Potentilla tridentata

10,96

9,97

0,18

21,83

0,00

0,42

0,44

0,83

0,00

44,63

Potentilla visianii

9,17

7,50

0,39

55,99

0,00

0,31

0,25

9,28

0,00

82,89

Prinsepia uniflora

6,11

0,00

0,00

39,79

0,00

0,00

0,29

2,85

0,00

49,04

Prunus tenella

2,86

0,00

0,16

2,57

0,00

0,00

0,70

0,78

0,00

7.06

Rosa palustris

11.55

0.00

0.60

43.05

0.00

0.59

0.26

1.90

0.72

58.67

Squalene was determined in some Rosaceae seed oils employed in the present study; levels of squalene were found between 0.02 mg/100 g (Alchemilla caucasica) and 0.29 mg/100 g (Cotoneaster simonsii) (Table 4). Squalene, a biosynthetic precurson to all steroids both in plant and animal cells, also exists with phytosterols and tocopherols in the unsaponifiable fraction of foods. There is an obvious scarcity of data on squalene content in foods (Ryan et al. [2007]).
Table 4

Squalene contents of some Rosaceae seeds

Samples

Concentrations (%)

Alchemilla caucasica

0.02

Cotoneaster bullatus

0.22

Cotoneaster dielsianus

0.07

Cotoneaster francheti

0.13

Cotoneaster moupinensis

0.16

Cotoneaster simonsii

0.29

Dryas drummondii

0.09

Exochorda racemosa

0.14

Geum elatum

0.09

Geum magellanicum

0.05

Geum pyrenaicum

0.13

Potentilla alchimilloides

0.05

Potentilla ambigua

0.12

Potentilla argyrophylla var.leucochroa

0.05

Potentilla atrosanguinea

0.04

Potentilla aurea

0.04

Potentilla glandulosa

0.05

Potentilla grammopetala

0.07

Potentilla hippiana

0.03

Potentilla pyrenaica

0.05

Potentilla speciosa

0.07

Potentilla tridentate

0.05

Potentilla visianii

0.06

Prinsepia uniflora

0.04

Prunus tenella

-

Rosa palustris

0.10

In the tocopherol fraction (55.5 mg/kg in chokeberry oil, 249.6 mg/kg in black currant oil and 89.4 mg/kg in rose hip oil), α-tocopherol predominated in chokeberry oil (70.6 mg/kg). Γ-tocopherol was the main component in black currant oil (55,4 mg/kg) and rose hip oil (71.0 mg/kg) (Zlatanov [1999]).

Among plant foods, amaranth, a pseudo cereal grain, contains relatively high amounts of squalene, approximately 132 mg/100 g to 424 mg/100 g (Berganza et al. [2003]). Another exceptionally rich source of squalene is olive oil, which is reported to contain 2000 to 7000 μg/g oil (Liu et al. [1976]). In another study, Ryan et al. ([2007])) identified 58.4 and 89.0 mg/100 g squalene in quinoa and pumpkin seed, respectively. The contents of other samples ranged between 0.2 barley to 8.8 mg/100 (Millet). As a result, the squalene content of Rosaceae seed oils employed in the present study is lower than that of the squalene content reported for poppy, mustard pumpkin, sesame, millet, quinoa, spelt, lentils, peas and especially olive (Liu et al. [1976]; Ryan et al. [2007]). In addition, several experimental studies demonstrated the detoxifying activities of squalene against a wide range of chemicals such as arsenic, hexacholorobengene and Phenobarbital (Kamimara et al. [1992]; Fan et al. [1996]; Ryan et al. [2007]).

Conclusion

The oil contents of seeds varied between 3.49 (Cotoneaster bullatus) to 46.15 g/100 g (Prunus tenella). The main fatty acids in seed oils were oleic (6.50-67.11%) and linoleic (22.08-68.62%). The concentrations of total tocopherol ranged between 7.06 mg/100 g (Prunus tenella) to 165.74 mg/100 g (Potentilla glandulosa ssp. pseudorupestris). Squalene was determined in some Rosaceae seed oils employed in the present study; levels of squalene were notably low between 0.02 mg/100 (Alchemilla caucasica) to 0.29 mg/100 g (Cotoneaster simonsii). The present study indicates that some Rosaceae seeds are good natural sources of oil. In addition, fatty acids, tocopherol and squalene in particular seem to have a very important effect on health.

Declarations

Acknowledgements

This work was supported by The Scientific and Technical Research of Turkey (TÜBITAK) and Deutsche Forschungs Gemeinschaft (DFG, Almanya). We are grateful to Dr J. Fiebig (Head of Institue). The authors also thank to Mrs E. Claudia, Miss E. Uda and Miss B. Bielefeld for skilful technical assistance with the GLC and HPLC.

Authors’ Affiliations

(1)
Institute fur for Lipid Research, Federal Research Center for Nutrition and Food
(2)
Department of Food Engineering, Faculty of Agriculture, Selcuk Universty

References

  1. Aguilera Y, Dorado ME, Prada FA, Martinez JJ, Quesada A, Ruiz-Gutierrez V: The protective role of squalene in alcohol damage in the chick embryo retina. Experim. Eye Res. 2005, 80: 535–543. 10.1016/j.exer.2004.11.003View ArticleGoogle Scholar
  2. Berganza BE, Moran AW, Rodriguez G, Coto NM, Santamaria M, Bressani R: Effect of variety and location on the total fat, fatty acids and squalene content of Amaranth. Plant Food Hum. Nutr. 2003, 58: 1–6. 10.1023/B:QUAL.0000041143.24454.0aView ArticleGoogle Scholar
  3. Beringer H, Dompert BWU: Fatty acid and tocopherol pattern in oil seeds. Fette Seifen Anst. 1976, 78(6):228–231. 10.1002/lipi.19760780603View ArticleGoogle Scholar
  4. Bjorneboe A, Bjorneboe G, Drevon C: Absorption, Transport and distribution of vitamin E. J. Nutr. 1990, 120: 233–242.PubMedGoogle Scholar
  5. Bushman BS, Phillips B, Isbell T, Ou B, Crane JM, Knapp SJ: Chemical composition of caneberry ( Rubus spp.) seeds and oils and their antioxidant potential. J. Agric. Food Chem 2004, 52: 7982–7987. 10.1021/jf049149aView ArticlePubMedGoogle Scholar
  6. Ching LS, Mohamed S: Alpha-Tocopherol content in 62 edible tropical plants. J. Agric. Food Chem. 2001, 49: 3101–3105. 10.1021/jf000891uView ArticlePubMedGoogle Scholar
  7. Eitenmiller RR, Lee J: Vitamin E: Food chemistry, composition and analysis. Marcel Dekker, New York; 2004.View ArticleGoogle Scholar
  8. Fan S, Ho I, Yeoh FL, Lin C, Lee T: Squalene inhibits sodium arsenite-induced sister chromatid exchanges and micronuclei in Chinese hamster ovary-KI cells. Mutat Res. 1996, 368: 165–169. 10.1016/S0165-1218(96)90058-0View ArticlePubMedGoogle Scholar
  9. Gao L, Mazza G: Characterization, quantitation, and distribution of anthocyanins and colorless phenolics in sweet cherries. J. Agric. Food Chem. 1995, 43: 343–346. 10.1021/jf00050a015View ArticleGoogle Scholar
  10. Green AG: Genetic control of polyunsaturated fatty acid biosynthesis in flax ( Linum usitatissimum ) seed oil. Theor Appl. Gen. 1986, 72: 654–666. 10.1007/BF00289004View ArticleGoogle Scholar
  11. Helmy HE: Studies on the pigments of some citrus, prune and cucurbit seed oils when processed with or without cottonseed oil. J. Am. Oil Chem. Soc. 1990, 67: 376–380. 10.1007/BF02539694View ArticleGoogle Scholar
  12. Johansson AK, Kuusisto PH, Lakkso PH, Derome KK, Sepponen PJ, Katajisto JK: Geographical variations in seed from Rubus chamaemorus and Empetrum nigrum . Phytochem. 1997, 44(8):1421–1427. 10.1016/S0031-9422(96)00762-5View ArticleGoogle Scholar
  13. Kamel-Eldin A, Andersson RA: A multivariate study of the correlation between tocopherol content and fatty acid compostion in vegetable oils. J. Am. Oil Chem. Soc. 1997, 74: 375–380. 10.1007/s11746-997-0093-1View ArticleGoogle Scholar
  14. Kamimara H, Koga N, Oguri K, Yoshimura H: Enhanced elimination of theophylline, phenobarbital and strychnine from the bodies of rats and mice by squalene treatment. J. Pharm. 1992, 15: 215–221.Google Scholar
  15. Konings EJM, Romans HHS, Beljaars PR: Liquid chromotographic determination of tocopherols and tocotrienols in margarine, infant foods, and vegetables. J. AOAC Int. 1996, 79(4):902–906.PubMedGoogle Scholar
  16. Liu GCK, Ahjrens EH, Schreibman PH, Crouse JR: Measurement of squalene in human tissues and plasma: validation and application. J. Lipid Res. 1976, 17: 38–45.PubMedGoogle Scholar
  17. Lopez Ortiz CM, Prats Moya MS, Berenguer Navarro V: A rapid chromatographic method for simultaneous determination of β-sitositerol and tocopherol homologues in vegetable oils. J. Food Comp. Analyses 2006, 19: 141–149. 10.1016/j.jfca.2005.06.001View ArticleGoogle Scholar
  18. Matthaus B, Özcan M: Glucosinolates and fatty acid, sterol and tocopherol composition of seed oils from Capparis spinosa var. spinosa and Capparis ovata Desf. vr. canescens (Coss.) Heawood. J Agric Food Chem 2005, 53: 7136–7141. 10.1021/jf051019uView ArticlePubMedGoogle Scholar
  19. Oh HH, Hwanng KT, Shin MK: Oils in the seeds of Caneberries produced in Korea. J. Am. Oil Chem. Soc. 2007, 84: 549–555. 10.1007/s11746-007-1065-1View ArticleGoogle Scholar
  20. Oomah BD, Ladet S, David VG, Liang J, Girard B: Characteristics of raspberry ( Rubus idaeus L.) seed oil. Food Chem 2000, 69: 187–193. 10.1016/S0308-8146(99)00260-5View ArticleGoogle Scholar
  21. Parry J, Su L, Luther M, Zhou K, Yurawecz MP, Whittaker P: Fatty acid composition and antioxidant properties of cold-pressed marionberry, red raspberry, and blueberry seed oils. J. Agric. Food Chem. 2005, 53: 566–573. 10.1021/jf048615tView ArticlePubMedGoogle Scholar
  22. Pourrat H, Carnat AP: Chemical composition of raspberry seed oil ( Rubus idaeus L. Rosaceae). Rev. Franh Crops and Grass 1981, 28: 477–479.Google Scholar
  23. Ramadan MF, Mörsel JT: Neutral lipid classes of black cumin ( Nigella sativa L.) seed oils. Eur. Food Res.Technol. 2002, 214: 202–206. 10.1007/s00217-001-0423-8View ArticleGoogle Scholar
  24. Ryan E, Galvin K, O’Connor TP, Maguire AR: Phytosterol, squalene, tocopheral content and fatty acid profile of selected seeds, grains, and legumes. Plants Food Human Nutr. 2007, 62: 85–91. 10.1007/s11130-007-0046-8View ArticleGoogle Scholar
  25. Senthilkumar S, Devaki T, Manohar BM, Babu MS: Effect of squalene on cyclophosphamide-induced toxicity. Clinica Chim. Acta 2006, 364: 335–342. 10.1016/j.cca.2005.07.032View ArticleGoogle Scholar
  26. Singh SP, Shukla S, Khanna KR, Dixit BS, Banerji R: Variation of major fatty acids in F8 generation of Opium poppy ( Papaver somniferum x Papaver setigerum ) genotypes. J. Sci. Food Agric. 1998, 76: 168–172. 10.1002/(SICI)1097-0010(199802)76:2<168::AID-JSFA919>3.0.CO;2-XView ArticleGoogle Scholar
  27. Tiscornia E, Camurat F, Gastaldo P, Pagano M: La frazione sterolica dele olio di pomodoro. Riv. Italaly Sost. Grasse 1976, 53: 119–129.Google Scholar
  28. Traber MG, Burton GV, Ingold KU, Kayden HJ: RRR- and SRR- alpha-tocopherols are secreted without discrimination in human cylomicrons, but RRR-alpha-tocopherol is preferentially secreted in very low-density lipoproteins. J. Lipid Res. 1990, 31: 675–685.PubMedGoogle Scholar
  29. Xu Y, Zhang Y, Chen M, Tu P: Fatty acids, tocopherols and proanthocyanidins in bramble seeds. Food Chem. 2006, 99: 586–590. 10.1016/j.foodchem.2005.08.059View ArticleGoogle Scholar
  30. Zlatanov MD: Lipid composition of Bulgarian chokeberry, black currant and rose hip seed oils. J. Sci. Food Agric. 1999, 79: 1620–1624. 10.1002/(SICI)1097-0010(199909)79:12<1620::AID-JSFA410>3.0.CO;2-GView ArticleGoogle Scholar
  31. Zlatanov M, Ivanov S, Antova G, Kouleva L: Study of phospholipids composition of Rosaceae seed oils. Riv. Ital. Sost. Grasse 1997, LXXIV(settebre):409–410.Google Scholar

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© Matthaus and Ozcan; licensee Springer 2014

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