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Original Article
2 (
2
); 95-99
doi:
10.1016/j.arabjc.2009.10.004

Selenium content in selected foods from the Saudi Arabia market and estimation of the daily intake

Department of Chemistry, Girls College of Education, King Abdulaziz University, Jeddah, Saudi Arabia
Disclaimer:
This article was originally published by Elsevier and was migrated to Scientific Scholar after the change of Publisher.

Abstract

This study was conducted to create a selenium database for the representative food items in Saudi diet and to estimate the dietary selenium intake of Saudi Arabians. Three samples for each food item selected were purchased from the markets. Each pooled sample was analyzed in triplicate by ICP–MS after thorough homogenization. The rich sources of selenium were meats (0.216–0.658 μg/g), eggs (0.226 μg/g) and cereals and cereals products (0.043–0.165 μg/g). Vegetables and fruits contained trace amounts of selenium (0.001–0.067 μg/g). The major food sources of selenium intake were cereals and cereals products (30.2%), legumes (24.7%) and meats (20%). The daily intake of Se was calculated taking into account the concentration of this element in the edible part and the daily consumption data which were derived from two sources, (a) the food balance sheet of KSA given by Food and Agriculture Organization (FAO) and (b) from questionnaires distributed among 200 families in Jeddah. The results showed that the daily intake of Se according to the two sources is 75.00–121.65 μg/person/day.

Keywords

Selenium
Determination
Food
ICP–MS
1

1 Introduction

The trace mineral selenium (Se) is an essential nutrient of fundamental importance to human health, but it is required only in small amounts (Thomson, 2004). Selenium is also toxic and, therefore, could cause selenium poisoning in humans and animals when intake exceeds the safe and adequate level (Hartikainen, 2005). Selenium is incorporated into proteins to make selenoproteins (Fragra, 2005), and several selenoproteins defend against oxidative stress (Goldhaber, 2003). Selenium deficiency can lead to heart disease, hypothyroidism and a weakened immune system (Combs, 2000; Ellis and Salt, 2003). Keshan disease and Kashin–Beck disease were found in China where the selenium content was very low in the soil (Cheng and Qian, 1990; Yang et al., 1993), while selenium has toxic effects in high amounts (Pappa et al., 2006). Chronic toxicity of selenium in humans results in selenosis, characterized by hair loss and nail brittleness, gastrointestinal problems, skin rash, ‘‘garlic-breath” odor and nervous system abnormalities (Yang et al., 1983; Yang and Zhou, 1994).

The dietary intake of selenium depends on its concentration in food and the amount of food consumed (Pappa et al., 2006). The selenium content of food varies depending on the content of the element in the soil where the animal was raised or the plant was grown (IOM, 1998; Uden et al., 2004; Barclay et al., 1995). Food is the main source of selenium for humans. In particular, meat and seafood are key sources, because animals require selenium, unlike plants (Klapec et al., 2004; Sirichakwal et al., 2005). The dietary intake of selenium varies considerably across populations around the world because of the large variability of the selenium content of foods (McNaughton and Marks, 2002). Therefore, it is necessary to monitor the selenium content in representative and widely consumed foods in each country.

Precise determination of selenium content in the food is quite important because there is a narrow margin of safety between adequate amount and overconsumption. To analyze trace selenium, there are various methods currently available (Foster and Sumar, 1995) including neutron activation analysis (Slejkovec et al., 2000), atomic fluorescence spectrometry (Pappa et al., 2006; Semenova et al., 2003; Tinggi et al., 1992), atomic absorption spectrometry (AAS) using either electrothermal atomization (Hussein and Bruggeman, 1999) or hydride generation method (Tinggi et al., 1992; Mindak and Dolan, 1999), and inductively coupled plasma spectrometry (ICP) (Kim et al., 1990; Masson et al., 2005; Featherstone et al., 2004) and ICP/mass spectrometry (MS) (Park and Kim, 2001). For this study, ICP–MS for the analysis of selenium has been optimized and applied because of the low detection limit and high efficiency.

In spite of many concerns about selenium intake, the data for the selenium in foods is very limited in Kingdom of Saudi Arabia. Therefore this study was carried out to produce a finite food selenium and to assess the dietary intake of selenium for the Saudi Arabian population in a limited manner based on the data from the food balance sheet of KSA given by Food and Agriculture Organization (FAO) and from questionnaire.

2

2 Experimental

2.1

2.1 Materials and methods

2.1.1

2.1.1 Food lists

Samples from local foodstuff of Saudi Arabia (KSA) were collected during January–February 2009.

Three kilograms of each fresh sample were collected from market in Jeddah in polyethylene container to avoid contamination.

The groups of food stuff studied are:

Cereals and Cereals products:

Wheat–Rice–Maize–Barley–Macaroni–Cookies–Cakes–Bread.

Legumes:

Broad Beans–Chick pea–Cowpea–Fenugreek seeds–Lentils–Peas garden.

Leafy vegetables:

Jews mallow–Spinach–Garden rocket–Lettuce–Parsley–Cabbage–Mint–Sweet basil.

Non-leafy vegetables:

Squash–Okra–Green pepper sweet–Eggplant (Black)–String beans–Cucumber–Cauliflower–Onions–Radish.

Tubers:

Potatoes–Sweet potatoes–Carrots.

Fruits:

Fresh dates–Dried dates–Oranges–Apples–Bananas–Grapes–Figs–Tomatoes–Mandarin–Pumpkin–Melon sweet–Mango.

Meats:

Chicken–Lamp–Beef–Camel–Fish.

Eggs:

Chicken eggs.

Fats and oils:

Butter–Corn oil–Margarine–Olive oil.

Milk and products dairy:

Cow milk powder–Cheddar cheese–Salted cheese–Sweet cheese–White cheese–Cream.

Nuts:

Almonds–Coconut–Hazel nuts–Peanut–Pine nuts–Pistachio nuts.

2.1.2

2.1.2 Sampling and preparation

For processed foods, those brands commanding a high share of the domestic market were purchased. Three samples for each food item were purchased from January to February 2009.

The samples were dried at 100 °C till constant weight and ground with special mills, with provision to prevent contamination (wearing parts made of aluminum and titanium), into a homogenous matter. A 150 g of the sample has been taken and stored in air-tight polyethylene bottles at −18 °C until analysis.

2.1.3

2.1.3 Chemical analysis

2.1.3.1
2.1.3.1 Apparatus and reagents

Double deionized distilled water of high quality used and all reagents were of analytical grade from (BDH). Measurements were done against metal standard solution specpure from Alfa–Aesar–Ubichem, England. All the vessels were washed with 10% (v/v) HNO3 and rinsed with deionized distilled water before use.

2.1.3.2
2.1.3.2 ICP–MS analysis

A portion (10 g) of finely ground sample was weighed precisely into a beaker and digested with 40 ml of nitric acid for 4 h by heating (150 °C) on a hot plate (PC-351, Corning Incorporated Life Sciences, Lowell, MA, USA). The same pretreatment procedure was repeated until the darkness of solution disappeared. After cooling, the digested solution was diluted with deionized distilled water and transferred to a 50-ml volumetric flask. The diluted solution was filtered through a filter paper into a plastic tube designed for the auto sampler of Agilent 4500 Series ICP–MS (Agilent, Palo Alto, CA, USA) that was used for the analysis of selenium content. Selenium concentrations of the samples were calculated from the regression line (r2 = 0.9998) obtained using selenium standard solution.

2.1.3.3
2.1.3.3 Estimation of dietary selenium intake

The selenium intake per person per day was estimated by the food balance sheet of KSA given by Food and Agriculture Organization (FAO) and from questionnaire which was distributed among two hundred families in Jeddah. The answer on the quantities of food they consumed indigently of financial situation were collected and the mean values were calculated.

3

3 Results

The number of selected food items in each food group was as follows: cereals and cereals products (n = 8), legumes (n = 6), leafy vegetables (n = 8), non-leafy vegetables (n = 9), tubers (n = 3), fruits (n = 12), meats (n = 5), eggs (n = 1), fats and oils (n = 4), milk and products dairy (n = 6) and nuts (n = 6).

An analytical quality assurance test was performed. Then, the results obtained were compared with the results obtained from the standard reference material and they were satisfactory (recovery: 101.5%). The instrumental quantitative detection limit of selenium was 0.3 ng. Selenium content in various foods is shown in Table 1. The highest values were found in meats (0.216–0.658 μg/g), eggs (0.226 μg/g), and cereals and cereals products (0.043–0.165 μg/g). Legumes (0.220–0.045 μg/g), fruits (0.004–0.032 μg/g), vegetables (0.001–0.067 μg/g), tubers (0.001–0002 μg/g), fats and oils (0.002–0.007 μg/g), milk and dairy products (0.024–0.039 μg/g) and nuts (0.015–0.145 μg/g) contained very low levels of selenium.

Table 1 Selenium content in representative Saudi diet.
No. Kind of food Sample Concentration (μg/g ± S.D.)
1 Cereals and cereals products Wheat 0.165 ± 0.0012
2 Rice 0.072 ± 0.0004
3 Maize 0.110 ± 0.0085
4 Barley 0.069 ± 0.0029
5 Macaroni 0.043 ± 0.0013
6 Cookies 0.124 ± 0.0242
7 Cakes 0.108 ± 0.0512
8 Bread 0.052 ± 0.0041
9 Legumes Broad beans 0.031 ± 0.0056
10 Chick pea 0.029 ± 0.0044
11 Cowpea 0.045 ± 0.0092
12 Fenugreek seeds 0.022 ± 0.0029
13 Lentils 0.076 ± 0.0043
14 Peas garden 0.037 ± 0.0091
15 Leafy vegetables Jew’s mallow 0.011 ± 0.0032
16 Spinach 0.007 ± 0.0002
17 Garden rocket 0.006 ± 0.0008
18 Lettuce 0.010 ± 0.0042
19 Parsley curly 0.007 ± 0.0005
20 Cabbage 0.009 ± 0.0002
21 Mint 0.014 ± 0.0027
22 Sweet basil 0.011 ± 0.0019
23 Non-leafy vegetables Squash 0.032 ± 0.0023
24 Okra 0.027 ± 0.0018
25 Green pepper sweet 0.052 ± 0.0016
26 Eggplant (black) 0.067 ± 0.0024
27 String beans 0.034 ± 0.0029
28 Cucumber 0.021 ± 0.0007
29 Cauliflower 0.025 ± 0.0009
30 Onions 0.043 ± 0.0022
31 Radish 0.033 ± 0.0013
32 Tubers Potatoes white 0.001 ± 0.0003
33 Sweet potatoes 0.001 ± 0.0002
34 Carrots 0.002 ± 0.0004
35 Fruits Fresh dates 0.022 ± 0.0072
36 Dates dried 0.030 ± 0.0021
37 Oranges 0.028 ± 0.0017
38 Apples 0.011 ± 0.0044
39 Bananas 0.024 ± 0.0019
40 Grapes 0.023 ± 0.0026
41 Figs 0.032 ± 0.0009
42 Tomatoes 0.015 ± 0.0006
43 Mandarin 0.009 ± 0.0001
44 Pumpkin 0.012 ± 0.0011
45 Melon sweet 0.004 ± 0.0008
46 Mango 0.005 ± 0.0002
47 Meats Chicken 0.353 ± 0.0074
48 Lamp 0.425 ± 0.0053
49 Beef 0.390 ± 0.0081
50 Camel 0.216 ± 0.0029
51 Fish 0.658 ± 0.0063
52 Eggs Chicken eggs 0.226 ± 0.0035
53 Fats and oils Butter 0.005 ± 0.0002
54 Corn oil 0.007 ± 0.0002
55 Margarine 0.002 ± 0.0005
56 Olive oil 0.002 ± 0.0003
57 Milk and dairy products Cow milk powder 0.039 ± 0.0024
58 Cheddar cheese 0.033 ± 0.0027
59 Cheese salted 0.035 ± 0.0032
60 Cheese sweet 0.030 ± 0.0008
61 Cheese white 0.031 ± 0.0017
62 Cream 0.024 ± 0.0043
63 Nuts Almonds 0.015 ± 0.0019
64 Coconut 0.093 ± 0.0021
65 Hazel nuts 0.047 ± 0.0028
66 Peanut 0.145 ± 0.0063
67 Pine nuts 0.102 ± 0.0082
68 Pistachio nuts 0.036 ± 0.0017

Considering the amount of food consumed, the major food sources of selenium intake for Saudi were cereals and cereals products (30.2%), legumes (24.7%), meats (20.3%), milk and dairy products (9.2%), eggs (6.9%), non-leafy vegetables (3.4%), leafy vegetables (2.8%), Fruits (1.2%), tubers (0.5%), fats and oils (0.5%) and nuts (0.3%) as shown in (Fig. 1). The selenium intake of the Saudi Arabia population was estimated by multiplying the mean intake of each food item by the selenium content in each food.

The contribution of food group on selenium intake of Saudi Arabian (% of total estimated selenium intake).
Figure 1
The contribution of food group on selenium intake of Saudi Arabian (% of total estimated selenium intake).

As a result, the estimated selenium intake of Saudi Arabia was 121.65 μg/person/day by using food balance sheet of KSA FAO (1994–1996) The results which are shown in Table 2 reflect the Se daily intake according to the food balance of KSA shown by FAO and 75.00 μg/person/day by using questionnaire data as shown in Table 3. Results obtained were similar to the values reported for Netherlands, Japan, China, USA and Australia as seen in Table 4 which shows the estimated amounts of daily dietary selenium intakes in other countries.

Table 2 Selenium daily intake in correlation with food balance of KSA given by FAO.
No. Sample Daily consumption of food (g) Daily intake of Se (μg/person/day)
1 Chicken meat 78.10 27.579
2 Lamb meat 20.80 8.840
3 Beef meat 11.80 4.602
4 Camel meat 6.50 1.404
5 Fish meat 17.80 11.712
6 Vegetables 289.50 6.948
7 Potatoes 47.60 0.048
8 Carrots 0.26 0.005
9 Mandarins 56.00 0.504
10 Dry dates 74.70 2.241
11 Pumpkin 16.40 0.197
12 Tomatoes 82.50 1.238
13 Wheat 332.00 54.780
14 White cheese 50.00 1.550
Sum 121.648
Table 3 Selenium daily intake in correlation with questionnaire.
No. Kind of food Daily consumption of food (g) Daily intake of Se (μg/person/day)
1 Cereals and cereals products 78.10 27.579
2 Legumes 20.80 8.840
3 Leafy vegetables 11.80 4.602
4 Non-leafy vegetables 6.50 1.404
5 Tubers 17.80 11.712
6 Fruits 289.50 6.948
7 Meats 47.60 0.048
8 Eggs 0.26 0.005
9 Fats and oils 56.00 0.504
10 Milk and dairy products 74.70 2.241
11 Nuts 16.40 0.197
Sum 75.00
Table 4 Comparison of the estimated selenium intake of population in various countries.
No. Country Se intake (μg/day) References
1 Netherlands 72 Van Dokkum et al. (1989)
2 Sweden 44 Becker and Kumpulainen (1991)
3 Canada 113–224 Health Canada (1992)
4 Italy 51 Amodio-Cocchieri et al. (1995)
5 Japan 129 Hirai et al. (1996)
6 Egypt 49 Hussein and Bruggeman (1999)
7 UK 29–39 Food Standards Agency (2008)
8 China 69 Zang et al. (2001)
9 USA 114 Department of Health and Human Services (2002)
10 Australia 58–85 Food Standards Australia and Zealand (2003)
11 Greece 39 Pappa et al. (2006)
12 Korea 57.5 Choi et al. (2009)
13 Saudi Arabia 75–122 This study
4

4 Discussion

The food and nutrition database is quite important for an accurate evaluation of nutrient intake from dietary intake surveys. Therefore, the selenium content database of the foods frequently consumed by Saudi people was developed for the estimation of selenium intake by them. Most animal foods such as fish, meats, and eggs have a high selenium content, which has previously been reported (Sirichakwal et al., 2005). On the other hand, vegetables and fruits are assumed to contain very low level of selenium unlike foods of animal origin, because selenium is not an essential element for the growth of plants as it is for animals (Klapec et al., 2004). Our data are similar to those of an Australian study, which reported selenium levels of 0.63 μg/g in fish and 0.38 μg/g in meats (McNaughton and Marks, 2002). Also similar to the reported study by Korean, which reported selenium levels of 0.448–0.788 μg/g in fish, 0.169–0.324 μg/g in meats, 0.267 μg/g in eggs, 0.043–0.216 μg/g in cereals, 0.006–0.052 μg/g in vegetables, 0.003–0.028 μg/g in fruits, 0.008 μg/g in fats and oils and 0.013–0.146 μg/g in nuts (Choi et al., 2009).

According to the database of the United States Department of Agriculture National Nutrient, foods with the high content of selenium are Brazil nuts (19.2 μg/g), wheat flour (0.71 μg/g) and barley (0.38 μg/g). Due to the presence of many types of food with higher selenium content in the United States than in Saudi Arabia, the selenium intake of the Americans is considered higher than that of Saudi Arabia. Recently, efforts have been made to increase the selenium content of plants by adding selenium to the soil; selenium-fortified food products can be found on Saudi Arabia markets.

In this study it was found that, the major food source of selenium intake in the Saudi Arabia diet was cereals and cereals products (30.2%) followed by legumes (24.7%) and meats (20.3%) (Fig. 1), because these groups are consumed in a very large amount by the Saudi.

Other studies have also reported that the major contributors to selenium intake are cereals and bakery products followed by fish and shellfish, meats and meat products, and dairy products (Gonzalez et al., 2006). Moreover, it has been pointed out in some reports that the heavy metals in fish interact with selenium, resulting in low bioavailability (Robinson and Tomson, 1983). Therefore, further study is necessary to consider the bioavailability of selenium in foods to correctly determine the bioavailable selenium intake value.

The estimated selenium intake of Saudi in this study was 75–122 μg/person/day, and this level was quite close to the recommended intake (72 μg/person/day, Van Dokkum et al., 1989), and 58–85 μg/person/day (Food Standards Australia and Zealand, 2003). More detailed estimation of selenium intake by merging selenium content data with individuals’ food intake data would be necessary to develop a nutrition program tailored for the particular needs of specific group. This was not attempted because it goes beyond the scope of this study.

Comparing to the cases of other countries, the selenium intake of Saudi falls in the middle of ranges reported and is considerably lower than that of the Canadian and Japanese and higher than Greece, Korea, UK, Egypt, Italy and Sweden (Table 4). Before comparing the intake levels among different countries, it is necessary to reach a consensus on the issues such as standard principles or criteria for matching of food items of different countries.

5

5 Conclusions

By analyzing the selenium content in representative food items in Saudi Arabia, a selenium database was made on a limited scale. The food balance sheet of KSA given by Food and Agriculture Organization (FAO) were utilized to select foods for analysis. Wheat, meat and vegetables turned out to be the major sources of selenium for Saudi.

References

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