Open access peer-reviewed chapter

Food Fortification through Innovative Technologies

Written By

Vlaic Romina Alina, Mureşan Crina Carmen, Muste Sevastita, Mureşan Andruţa, Muresan Vlad, Suharoschi Ramona, Petruţ Georgiana and Mihai Mihaela

Submitted: 14 September 2018 Reviewed: 25 October 2018 Published: 18 January 2019

DOI: 10.5772/intechopen.82249

From the Edited Volume

Food Engineering

Edited by Teodora Emilia Coldea

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Abstract

The chapter aims to approach food fortification naturally as a result of the need for nutritional improvement and therefore underlines sustainable activities that would facilitate effective fortification. The need to fortify food is due to the close link between human, health, and food. The WHO and FAO and other internationally recognized organizations have recognized that there are over 2 billion people worldwide suffering from a variety of micronutrient deficiencies. The interest in the fortification of foods is largely due to bioactive compounds, such as vitamins, minerals, sugars, organic acids, dietary fiber, phenolic compounds, essential amino acids, and antioxidants. The most effective and accessible way of securing the population with vitamins and micronutrients is to fortify additional food and consumer products daily. At the same time, the technology for the fortification of bakery products will also be presented.

Keywords

  • food
  • fortification
  • nutrients
  • advanced technologies

1. Introduction

In accordance with the General Principles for the Addition of Essential Nutrients to Foods [1] Codex, the term fortification or enrichment is synonymous to the addition of one or several essential nutritional elements for a food product, regardless of whether it is or not habitually contained in foods, toward the prevention or correction of proven deficiencies in one or more nutrients, either for the entire population or certain specific groups. The General Principles Codex further states as the primary condition mentioned in the fulfillment of any such fortification program to be the initial demonstration of the requirement for an increase in the nutrient intake essential to the population or to the target group. This demonstration can rely on real clinical or subclinical studies of deficiency, estimates of the low levels of nutrient intake, or possible deficiencies triggered by changes in standard food products [1].

Food fortification has been implemented for a long period of time in industrialized countries to achieve the successful control of vitamin A and D deficiencies, several B vitamins (thiamine, riboflavin, and niacin), as well as iodine and iron. Salt irrigation was introduced in the early 1920s both in Switzerland [2] and the United States [3] and has progressively expanded worldwide since salt iodine is presently used in most countries. Since the early 1940s, the fortification of cereal products with thiamine, riboflavin, and niacin has become a common practice. Margarine was fortified with vitamin A in Denmark, while milk was fortified with vitamin D in the United States. Foods for young children were fortified with iron, thus substantially reducing the risk of iron-deficiency anemia in this age group. In recent years, folic acid fortification has become widespread in America, a strategy undertaken by Canada and around 20 Latin American countries [4]. These approaches have proven to be effective in reducing the prevalence of many diseases due to deficiencies, such as goiter (iodine), xerophthalmia (vitamin A), rickets (vitamin D), and anemia (iron). Foods from around the world have begun to be fortified with calcium, iron, phosphorus, and vitamins (especially A, B, C, and D), depending on the chemical composition of the basic foods [5].

The need for food fortification is also presented by the WHO and FAO, among many other nationally recognized organizations. They have acknowledged the micronutrient deficiencies of more than 2 billion people, largely caused by a dietary deficiency of vitamins and minerals. The importance of these deficiencies for public health depends on their magnitude and spread, but the most vulnerable are pregnant women and young children, as fetal and child development, cognitive development, and resistance to infections are affected. Although the entire world population suffers from various nutritional deficiencies, people with low incomes are the most affected, particularly in developing countries, due to unsafe food consumption. Poverty, the lack of access to a variety of foods, and the lack of knowledge on appropriate dietary practices represent major drawbacks for socioeconomic development while also contributing to a vicious circle of underdevelopment. As such, long-term effects on health, learning, and productivity are significant, while they also generate a high level of social and public costs from reduced work capacity due to high rates of illness and disability [4].

It was also in less industrialized countries that fortification has become more and more appealing in recent years, so much that the planned programs have advanced more rapidly throughout the implementation phase than initially estimated. Bearing in mind the success of the relatively long program to fortify sugar with vitamin A in Central America, where the prevalence of vitamin A deficiency has been greatly reduced, there are similar initiatives in other regions of the world. Currently, the first attempt to fortify sugar in South Africa is taking place in Zambia, and if successful, it will be implemented elsewhere. Darnton-Hill and Nalubola [5] identified at least 27 developing countries that could benefit from programs to fortify one or more foods.

According to research conducted by Svetlana [6], the most efficient and accessible way of providing the population with vitamins and micronutrients is their additional fortification using these substances in consumer food products and daily foods, especially flour and bakery products. The fortification of foods should not diminish their nutritional qualities and quality, especially not to substantially alter the taste or assimilation of other nutrients contained therein, not to reduce shelf life or to change product harmlessness characteristics.

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2. Biofortification

People require at least 22 mineral elements for their well-being [7]. These micronutrients can be delivered through a proper diet. However, over 60% of the world’s population is estimated to be iron-deficient(Fe), more than 30% are zinc-deficient (Zn), while 30% are iodine-deficient and 15% selenium-deficient (Se). In addition, calcium (Ca), magnesium (Mg), and copper (Cu) deficiencies are common in many developed and developing countries [8]. These deficits influence many biochemical pathways directly or indirectly [9]. This is due to the production of crops in areas with low mineral bioavailability and/or (sporadic) crop consumption with inherent tissue mineral concentrations, accompanied by the lack of fish or food products [7] or low-micronutrient crops [10]. At present, mineral malnutrition is considered to be one of the most serious global challenges that is active but avoidable [11]. Mineral malnutrition can be addressed by dietary diversification, mineral supplements, food fortification and/or increased mineral concentration in edible crops (biofortification).

The term biofortification refers to the increase of the micronutrient concentration in the edible part of the plant and can be achieved both by using fertilizers and by stimulating the absorption of these minerals in the plant [12], while the use of micronutrient fertilizers was effective in increasing the micronutrient content in plants [13].

Practically, the fortification of food is closely linked with the biofortification of plants (raw materials for food); the higher the nutritional value of the raw material, the smaller the need for fortification. Thus, from increasing the productivity of the cultivated varieties nowadays, the necessity of obtaining varieties with high nutritional value has become a very important task for agronomists, as almost half of the world population suffers from deficiencies in zinc, iron, and selenium [14].

In some countries, selenium wheat biofortification is achieved by using selenium-based fertilizers, as wheat is considered a major source of selenium for our daily diet [15]. As such, selenium is considered to be an essential micronutrient for the human body, which can reduce the risk of degenerative diseases, including cancer [16]. A study by Wu [17] based on the consumption of common wheat biscuits biofortified with selenium through fertilization showed that although the levels of selenium in blood plasma increased, there were no significant changes of degenerative disease-specific biomarkers and of the health condition in general. Another method of biofortification that aimed at the development of wheat varieties enriched with some micronutrients was based on interactions between genotypes and environmental factors and led to good iron and zinc levels in humans [18, 19].

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3. Food fortification

Government agencies, as well as food policy makers, support food enrichment and fortification to different degrees, in order to lower the deficiency rate in populations on a large scale, this proving to be an efficient approach [20]. It is estimated that 2 billion people worldwide suffer from micronutrient malnutrition [21]. From a public health standpoint, it is estimated that micronutrient deficiencies account for approximately 7.3% of global diseases.

The most important elements used for food fortification are:

3.1 Iron

The greatest part of the iron in the human body is found in erythrocytes as hemoglobin, where its main function is to carry oxygen from the lungs onto the tissues. Iron deficiency causes anemia, the most common and widespread nutritional disorder in the world and a public health problem in both industrialized and nonindustrialized countries [22]. As a component of myoglobin, a protein that supplies oxygen to the muscles, iron supports metabolism [23]. Additionally, iron is necessary for growth, development, normal cellular function, and the synthesis of hormones and the connective tissue [23]. Dietetic iron has two main forms: heme and nonheme [24]. Iron-fortified plants and foods contain only nonheme iron, while meat, seafood, and poultry contain both heme and nonheme iron [23].

People normally lose small amounts of iron through the urine, feces, gastrointestinal tract, and skin. Losses are higher in menstrual women due to blood loss. Hepcidin, a circulating peptide hormone, is the key element in regulating iron absorption and iron distribution in the body, including plasma [23, 24, 25].

Hemoglobin concentrations lower than 13 g/dL in men and 12 g/dL in women indicate the incidence of iron-deficiency anemia (IDA) [26].

The Recommended Dietary Allowance (RDA) is shown in Table 1; RDA for vegetarians is 1.8 times higher than for those who eat meat. This is because iron from meat is more bioavailable than the iron in herbal foods, while meat, poultry, and seafood increase iron absorption through nonheme [26].

Age/nutrient Iron(mg/d) Vitamin A (μg/d) Iodine (μg/d) Folate (μg/d) Vitamin B12 (μg/d) Thiamin (mg/d) Riboflavin (mg/d) Niacin (mg/d) Vitamin B6 (mg/d) Vitamin C (mg/d) Vitamin D (μg/d) Calcium (mg/d) Selenium (μg/d) Total fiber (g/d) Protein (g/d) Fat (g/d)
Infants 0–6 months 0.27 400 110 65 0.4 0.2 0.3 2 0.1 40 10 200 15 ND 9.1 31
6–12 months 11 500 130 80 0.5 0.3 0.4 4 0.3 50 10 260 20 ND 11 30
Children 1–3 years 7 300 90 150 0.9 0.5 0.5 6 0.5 15 15 700 20 19 13 ND
4–8 years 10 400 90 200 1.2 0.6 0.6 8 0.6 25 15 1000 30 25 19 ND
Males 9–13 years 8 600 120 300 1.8 0.9 0.9 12 1 45 15 1300 40 31 34 ND
14–18 years 11 900 150 400 2.4 1.2 1.3 16 1.3 75 15 1300 55 38 52 ND
19–30 years 8 900 150 400 2.4 1.2 1.3 16 1.3 90 15 1000 55 38 56 ND
31–50 years 8 900 150 400 2.4 1.2 1.3 16 1.3 90 15 1000 55 38 56 ND
51–70 years 8 900 150 400 2.4 1.2 1.3 16 1.7 90 15 1000 55 30 56 ND
70+ years 8 900 150 400 2.4 1.2 1.3 16 1.7 90 20 1200 55 30 56 ND
Females 9–13 years 8 600 120 300 1.8 0.9 0.9 12 1 45 15 1300 40 26 34 ND
14–18 years 15 700 150 400 2.4 1 1 14 1.2 65 15 1300 55 26 46 ND
19–30 years 18 700 150 400 2.4 1.1 1.1 14 1.3 75 15 1000 55 25 46 ND
31–50 years 18 700 150 400 2.4 1.1 1.1 14 1.3 75 15 1000 55 25 46 ND
51–70 years 8 700 150 400 2.4 1.1 1.1 14 1.5 75 15 1200 55 21 46 ND
70+ years 8 700 150 400 2.4 1.1 1.1 14 1.5 75 20 1200 55 21 46 ND
Pregnancy 14–18 years 27 750 220 600 2.6 1.4 1.4 18 1.9 80 15 1300 60 28 71 ND
19–30 years 27 770 220 600 2.6 1.4 1.4 18 1.9 85 15 1000 60 28 71 ND
31–50 years 27 770 220 600 2.6 1.4 1.4 18 1.9 85 15 1000 60 28 71 ND
Lactation 14–18 years 10 1200 290 500 2.8 1.4 1.6 17 2 115 15 1300 70 29 71 ND
19–30 years 9 1300 290 500 2.8 1.4 1.6 17 2 120 15 1000 70 29 71 ND
31–50 years 9 1300 290 500 2.8 1.4 1.6 17 2 120 15 1000 70 29 71 ND
References [26] [26] [26] [27] [27] [27] [27] [27] [27] [28] [29] [29] [30] [31] [31] [31]

Table 1.

Nutrient RDA by age.

ND—not determined.

The richest sources of heme iron in the diet include lean meats and seafood. Dietary nonheme iron sources include nuts, beans, vegetables, and fortified cereal products. In the United States, about half of the food is derived from bread, cereals, and other cereal products [23, 26]. Breast milk contains highly bioavailable iron but in quantities that are not sufficient to meet the needs of infants over 4–6 months [23, 32]. In the United States, Canada, and many other countries, wheat and other types of flour are fortified with iron [33]. Also, infant formulas are fortified with 12 mg iron per liter [32].

According to EFSA average iron intake ranged between 2.6 and 6.0 mg/day (0.9–1.9 mg/MJ) in infants (< 1 year, four surveys), between 5.0 and 7.0 mg/day (1.2–1.6 mg/MJ) in children aged 1 to <3 years (five surveys), between 7.5 and 11.5 mg/day (1.1–1.7 mg/MJ) in children aged 3 to <10 years (seven surveys), between 9.2 and 14.7 mg/day (1.1–1.7 mg/MJ) in children aged 10 to <18 years (seven surveys), and between 9.4 and 17.9 mg/day (1.2–2.1 mg/MJ) in adults (≥ 18 years) (eight surveys). Average daily intakes were in most cases slightly higher in males (Appendix D) than in females (Appendix E), mainly owing to larger quantities of food consumed per day [34]. Tolerable upper intake levels for iron fall between 40 and 45 mg [26].

A study conducted in the United States, for example, revealed that iron supplements during pregnancy have reduced the number of premature births or the incidence of low birth weight [35]. In Vietnam, fortifying fish sauce with iron and consuming 10 ml per day of the sauce fortified with 100 mg iron (as NaFeEDTA) for 100 ml significantly improve the iron deficiency of the group of women tested, compared to the placebo group after just 6 months [36]. In China, a series of studies have been carried out to evaluate the efficacy of fortifying soy sauce with iron (as NaFeEDTA). The daily consumption of 5 mg or 20 mg of iron in fortified sauce has been reported to be very effective in the treatment of iron-deficiency anemia in children; positive effects were recorded within 3 months of starting the study or 6 months on a sample of 10,000 children and women suffering from anemia [37]. In a South African iron deficiency group, fortifying the curry powder with NaFeEDTA led to significant improvements in blood hemoglobin and the prevalence of iron-deficiency anemia in women declined from 22% to just 5% during the 2 years of study [38].

3.2 Vitamin A

Vitamin A is the name of a group of retinoids soluble in fats, including retinol, retinal, and retinyl esters. Vitamin A represents an essential nutrient, thus necessary in small amounts for the normal functioning of the visual system in human beings, maintenance of cell growth function, epithelial cell integrity, immune function, and reproduction. Dietary vitamin A requirements are normally provided by a combination of preformed vitamin A (retinol), which is present in food of animal origin, and provitamin A carotenoids, which are derived from foods of plant origin, which have to be converted into retinol by tissues such as the intestinal mucosa and the liver, in order to be used by cells [39, 40, 41]. Vitamin A deficiency is based on a frequent evaluation of serum or plasma retinol [42], and a deficit affects visual function, as vitamin A status indicators have traditionally been based on visual changes, especially night blindness and xerophthalmia [43]. The World Health Organization (WHO) estimated that over 254 million preschool children worldwide have low serum retinol levels, and therefore these indicators may be considered clinically or subclinically deficiencies in vitamin A [42].

Two forms of vitamin A are available in the human diet: preformed vitamin A (retinol and its esterified form, retinyl ester) and provitamin A carotenoids [26, 39, 40, 41]. Preformed vitamin A is found in food from animal sources, including dairy products, fish, and meat (especially the liver). The most important provitamin A carotenoid is beta-carotene; other provitamin A carotenoids are alpha-carotene and beta-cryptoxanthin. The body transforms these pigments into vitamin A. Both provitamin A and preformed vitamin A should be metabolized intracellularly within the retina and retinoic acid, the active forms of vitamin A, to support the vital biological functions of the vitamin [40, 41]. Other carotenoids found in foods, such as lycopene, lutein, and zeaxanthin, are not turned into vitamin A.

Commonly, vitamin A deficiency occurs with a diet low in vitamin A sources (e.g., dairy products, eggs, fruits, and vegetables), poor nutritional status, and a high rate of infection, especially measles and diarrheal diseases. The best sources of vitamin A are foods of animal origin, especially liver, eggs, and dairy products containing vitamin A in the form of retinol, a form that can be easily used by the body. In fact, it is difficult for children to meet their vitamin A requirements if their diet is low in foods of animal origin [26, 40] and, similarly, if their diet is low in fat. Fruits and vegetables contain vitamin A in the form of carotenoids, the most important being β-carotene. In a mixed diet, the conversion rate of β-carotene to retinol is about 12: 1. The conversion of other carotenoids to retinol is less effective, the corresponding conversion rate being 24: 1. Different food preparation techniques, such as cooking, grinding, and adding oil, can improve the absorption of synthetic β-carotene food carotenoid in the oil, also widely used in vitamin A supplements. The latter has a conversion ratio of 2: 1 to retinol, while the synthetic β-carotene forms, commonly used to fortify foods, have a conversion ratio of 6: 1.

Analyses have shown that high-dose vitamin A supplements can reduce measles mortality by up to 50%. Another analysis found that improving vitamin A deficiencies, either by supplements or by fortification, decreased mortality by 23% in children aged 6 months to 5 years, irrespective of the cause [44]. Another study on a group of preschoolers who consumed 27 g of vitamin A-fortified margarine for 6 months reported a reduction in the prevalence of low serum retinol concentrations from 26 to 10% [45].

A plasma retinol concentration lower than 0.70 micromoles/L (or 20 micrograms/mcg/dL) reflects vitamin A deficiency in a population, whereas concentrations of 0.70–1.05 micromoles/L could be marginal in some people [5]. RDA for men and women is 900 and 700 μg retinol activity equivalent/day. Tolerable upper intake levels for preformed vitamin A in adults are set at 3000 μg [26].

3.3 Iodine

Iodine is present in the body in small amounts, mainly in the thyroid gland, while its only confirmed role is in the synthesis of thyroid hormones. Iodine deficiency is a major public health problem for populations around the world but especially for young children and pregnant women. In some areas, it is a significant threat to national, social, and economic development, as the devastating result of iodine deficiency is mental retardation: currently one of the main causes of cognitive impairment that can be prevented. This is the primary reason behind the current global mission to eliminate iodine deficiency-related disorders [4].

Iodine is an essential component of thyroid hormones, thyroxine, and triiodothyronine. Thyroid hormones regulate many important biochemical reactions, including protein synthesis and enzymatic activity, as critical determinants of metabolic activity [26, 46]. These are also necessary for an adequate development of the central nervous system and skeletal system in the fetus and infants [46].

Food iodine and iodine salt are present in several chemical forms, including sodium and potassium salts, inorganic iodine, iodate, and iodide, the reduced iodine form [47]. Iodine rarely appears as an element but rather as a salt. For this reason, it is called iodide and not iodine. Iodine is rapidly and almost completely absorbed in the stomach and duodenum. Iodate is reduced in the gastrointestinal tract and absorbed as iodide [26, 48]. When the iodide enters the circulation, the thyroid gland concentrates it in quantities adequate for thyroid hormone synthesis, and most of the remaining amount is excreted in the urine [26]. Healthy adults with sufficient iodine amounts exhibit approximately 15–20 mg of iodine, 70–80% of which are contained in the thyroid [49].

Average urinary iodine concentrations of 100–199 mcg/L in children and adults, 150–249 mcg/L in pregnant women, and > 100 mcg/L in nursing women indicate adequate iodine intake. Values lower than 100 mcg/L in children and adults who are not pregnant indicate insufficient iodine intake, although iodine deficiency is not classified as severe until the urinary iodine level is lower than 20 mcg/L [47].

One of the best sources of iodine is marine algae, but its content is variable according to species [48]. Other good sources include seafood, dairy products, cereal products, and eggs [50]. Iodine is also present in human breast milk [26, 48] and in infant formulas.

3.4 Folate (vitamin B9)

Folate (vitamin B9) is important in the synthesis and methylation of nucleotides that intervene in cell multiplication and tissue growth. Its role in protein synthesis and metabolism is closely interrelated to that of vitamin B12.

The main sources of dietary folate are leafy vegetables, fruits, yeast, and liver [4]. The total body content of folate is estimated at 10–30 mg; about half of this amount is stored in the liver [51, 52], while the rest in the blood and body tissues. A serum folate concentration is commonly used to assess folic acid status, with a value greater than 3 ng/ml being adequate [26, 51]. The follicular erythrocyte concentration above 140 ng/ml indicates an adequate folate status [26, 53], although some researchers have suggested that superior values are optimal for preventing neural tube defects [54].

Folate is naturally found in a wide variety of foods, including vegetables (especially leafy green vegetables), fruits and fruit juices, nuts, beans, peas, dairy products, poultry and meat, eggs, sea food, and cereal. Spinach, liver, yeast, asparagus, and brussels sprouts are among the foods with the highest levels of folic acid [52, 55].

In January 1998, the US Food and Drug Administration (FDA) began to require producers to add folic acid to enriched bread, cereals, flour, corn, pasta, rice, and other cereal products [56]. Since cereals are widely consumed in the United States, they have become very important contributors to folic acid intake for the American diet. The fortification program was designed to increase the folic acid intake in the United States by about 100 mcg/day but eventually succeeded an increase of about 190 mcg/day [57]. In April 2016, the FDA approved the voluntary addition of folic acid to corn meal at levels compatible with other enriched cereal products [58]. The Canadian Government has also called for the addition of folic acid to many cereals, including white flour, enriched pasta, and corn flour, as of November 1, 1998 [59]. Other countries, including Costa Rica, Chile, and South Africa, have also established compulsory programs for the folic acid fortification [60].

3.5 Vitamin B12

Vitamin B12 (cobalamin) is a cobalt-containing vitamin that is synthesized by microorganisms and exists in various chemical forms in food, particularly that of animal origin, such as milk, cheese and eggs, as well as artificially fortified foods [61]. B12 deficiency can cause neurological damage, megaloblastic anemia, increase of homocysteine in plasma, and possibly impairment of the immune function. In infants and young children, it can cause serious developmental delays [4]. Approximately 56% of an oral B12 dose of 1 mcg is absorbed, but absorption decreases drastically when the intrinsic factor capacity is exceeded (for 1–2 μm of vitamin B12) [62].

Vitamin B12 is systematically evaluated through B12 serum or plasma levels. Approximate values below 170–250 pg/ml (120–180 picomoles/L) for adults [26] indicate a vitamin B12 deficiency. Increased levels of methylmalonic acid (values>0.4 micromole/l) could be a more reliable indicator of vitamin B12 status, as they indicate a metabolic change that is highly specific to vitamin B12 deficiency [26, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64].

Vitamin B12 is naturally found in animal products, including fish, meat, poultry, eggs, milk, and dairy products. Generally, vitamin B12 is not present in plant foods, but fortified breakfast cereals are an available vitamin B12 source with high bioavailability for vegetarians. Some nutritional products from yeast also contain vitamin B12 [26, 65].

3.6 Other B vitamins (thiamine, riboflavin, niacin, and vitamin B6)

In recent years, due to increased evidence that some B vitamins can prevent the occurrence of developmental disorders, as well as chronic degenerative and neoplastic diseases, special attention has been paid to their possibilities of employment [66]. Moreover, vitamin B complexes are of utmost importance for energy metabolism. Specifically, thiamine (vitamin B1), riboflavin (vitamin B2), niacin (vitamin B3), and vitamin B6 are required for decarboxylation, transamination, acylation, oxidation, and reduction of substrates that are ultimately employed in energy consumption. One or several of these vitamins are also important for amino acid, fatty acids, cholesterol, steroid, and glucose synthesis [67]. In fact, thiamine plays a critical role in energy metabolism and hence in cell growth, development, and function. Important sources can be found in wheat germs and yeast extracts, the edible organs of most animals, legumes, and green vegetables [68]. The main sources of riboflavin are milk and dairy products, bread and bakery products, mixed meat-based foods, ready-to-eat cereals, and mixed grain-based foods [27, 69]; good sources of niacin are liver, meat and meat products, fish, peanuts, and whole grains [70]. The richest sources of vitamin B6 include fish, beef liver and other organs, potatoes, and other starchy vegetables, and fruits (other than citrus fruits) [27, 71]. Fortification of foods for nutrient recovery such as the vitamin B complex is effective in basic foods or spices [72], in wheat flour [73, 74], fish sauce [75], and rice [76]. RDAs are presented in Table 1.

3.7 Vitamin C

Vitamin C is a redox system composed of ascorbic acid and dehydroascorbic acid, which acts as an electron donor. Its main metabolic function is to maintain collagen formation. Additionally, it functions as an important antioxidant. Vitamin C is widely available in food of plant and animal origin, but the best sources are fresh fruits and vegetables and the edible organs of animals. However, since vitamin C is unstable when exposed to an alkaline environment or to oxygen, light, and heat, losses can be substantial during storage and cooking [4]. Foods fortified with vitamin C include milk and baby food [77], juices [78], jelly, and candies [79].

Acute vitamin C deficiency leads to scurvy. Scurvy evolution time varies with vitamin C levels, but signs may occur within 1 month after the decrease or absence of vitamin C consumption (below 10 mg/day) [80].

3.8 Vitamin D

Vitamin D deficiency can lead to musculoskeletal diseases such as rickets and osteomalacia, but vitamin D supplements and fortified foods can prevent extraskeletal disorders such as respiratory tract infections, asthma exacerbations, pregnancy complications, and premature death. Vitamin D has a unique metabolism as it is mainly synthesized in the skin under the influence of sunlight (i.e., ultraviolet radiation-B), while nutritional intake traditionally plays a relatively minor role. The recommended target concentrations range from ≥25 to ≥50 nmol/L (≥ 10–20 ng/ml), corresponding to a daily vitamin D dose of 10–20 μg (400–800 international units). Worldwide, vitamin D food fortification has already been introduced in the United States, Canada, India, and Finland with effective results [81]. As such, foods recommended to be fortified with vitamin D include milk, dairy products, and margarine [82].

Very few natural foods contain vitamin D. Fatty fish (such as salmon, tuna, and mackerel) and fish liver oils are among the best sources [28, 65]. Small amounts of vitamin D are found in beef liver, cheese and egg yolks, and certain mushroom varieties [83].

In the American diet, fortified foods provide most of the vitamin D intake [28, 83]. For example, almost all US milk is voluntarily fortified with 100 IU/cup. (In Canada, milk is fortified by law with 35–40 IU/100 ml, similar to margarine with ≥530 IU/100 g.) In the 1930s, a milk fortification scheme was implemented in the United States to fight rickets, considered to be a major public health problem. Other dairy products such as cheese are generally not fortified. Ready-to-eat breakfast snacks often contain vitamin D, similar to some brands of orange juice, yoghurt, margarine, and other foods. Both the United States and Canada require vitamin D-fortified formula for infants: 40–100 IU/100 kcal in the United States and 40–80 IU/100 kcal in Canada [28].

3.9 Calcium

Calcium is an essential element for the growth, activity, and maintenance of the human body [84]. Bone health is a major public concern. Each year, approximately 9 million people worldwide suffer from fractures due to osteoporosis [85]. Insufficient calcium and vitamin D absorption, an inadequate lifestyle, food choices, and genetics play an important role in the development of osteoporosis. Calcium absorption is controlled homeostatically by vitamin D regulation. Calcium deficiency can also lead to reduced blood clotting conditions, weak teeth, and some other symptoms [86]. People with lactose intolerance have decreased calcium intake due to absent dietary intake of calcium-dairy products [87], while the availability of calcium from nondairy sources is affected by the presence of the phytic acid, oxalic acid, and fiber [88]. Calcium is used for fortification in the form of calcium carbonate, calcium lysinate, and tricalcium phosphate in foods such as rice extrudates and noodles [89], tuna bone powder crackers [90], cookies [91], biscuits [92], yoghurt [84], etc.

The percentage of calcium absorbed depends on the total amount of elemental calcium consumed at one time; as the amount increases, the absorption percentage decreases. The absorption is highest in doses ≤500 mg. For example, someone who takes 1000 mg of calcium daily as supplements could divide the dose and take 500. The average dietary calcium intake for men over 1 year old is between 871 and 1266 mg/day, depending on the age group, while for females the interval is between 748 and 968 mg/day mg at two separate times during the day [29].

3.10 Selenium

Selenium (Se) is an essential micronutrient for both humans and animals. It forms an important component of glutathione peroxidase, a well-known antioxidant that counteracts cellular oxidative destruction. Furthermore, it plays an important role in catalyzing the production of the active thyroid hormone [93, 94], and it is required to improve human immunity and sperm motility [95]. Epidemiological studies have indicated that Se deficiency is positively correlated with the incidence of cancer [96]. The average daily recommended dose for an adult is 60 μg/day [97]. Selenium content in foods of plant origin varies with soil selenium content [98]. The most prevalent selenium fortification is that of the cooking salt, which significantly reduced the prevalence of Keshan disease in China [99], but there are other foods that can be fortified with selenium, such as yoghurt [100].

3.11 Fibers

Constipation has a negative impact on the quality of life and is defined as a difficult evacuation accompanied by discomfort and pain, while long-term constipation entails serious health problems. This is due to a decrease in dietary fiber consumption, which is directly proportional to excessive food processing [101].

Food fibers can be classified as soluble and insoluble fibers. Both types of fiber have many health benefits including maintaining intestinal and overall health integrity, lowering blood cholesterol levels, controlling blood sugar levels, and providing a non-caloric volume that can help weight loss by replacing caloric food components such as fat. According to the Dietary Guidelines for Americans, dietary fiber is consumed by most adults indicating that fortification of fiber foods might bring health benefits. Numerous studies [102, 103, 104, 105] have shown that sausage fiber fortification (2–3 g/portion) can be achieved without any negative impact on sausage sensory quality. Alongside the increased fiber intake, products also come with other advantages such as fat replacement, increased water holding capacity, and improved oxidative stability when the fiber source is associated with phenolic antioxidants [103, 106], bran bread [107], and fiber-containing yoghurt [108].

3.12 Proteins

Proteins belong to a category of biologically active compounds that are essential to life through their specific action. They are the building blocks for the formation of tissues in the human body (cell walls, muscles, blood, hair, internal organs such as the heart and the brain, etc.), hormones, enzymes and antibodies, and replacement of waste cells. The essential amino acids are those that the body cannot produce by itself, and thus, they must be secured from food. Nonessential amino acids are amino acids that can be synthesized by the human body from essential acids or by cleavage of proteins [109]. The quality of plant proteins (vs. those from animal sources) has become a very debatable topic due to the consumption of plant products, which is increasingly promoted in the “world of nutrition.” As the presence of essential amino acids in the body is of utmost importance, nutritionists recommend the right combination between the two sources (plant and animal). An advantage can be found in the addition of a vegetable matrix to meat preparation. This improves the mineral profile of the product and brings a supply of vitamins to the finished product, for example, mushroom sausages, meat products with soy protein isolate, and whey or wheat protein [110, 111], but also the fortification of plant products with plant proteins, for example, the fortification of wheat flour with cottonseed, chickpeas, amaranth, quinoa, and lentils [12].

3.13 Fatty acids

Essential fatty acids are important nutrients for the human body, especially for maintaining the health of the cardiovascular system. Several sources of information suggest that human beings have evolved on a diet that included a ratio of omega-6 to omega-3 fatty acids (EFA) of ∼ 1, while western diets include a ratio of 15/1–16.7/1. Western diets exhibit omega-3 fatty acid deficiency, while they also include excessive amounts of omega-6 compared to the diet that human beings have evolved on and which set the foundation for their genetic patterns [112]. Products fortified with fatty acids in balanced proportions include meat, oil, jelly, various sauces, etc.

3.14 Multiple fortifications

Based on what is known about the prevalence of individual micronutrient deficiencies, there are generally multiple deficiencies of common micronutrients or in different population groups. Micronutrient deficiencies are more common in people on a diet low in foods of animal origin and therefore low in iron and bioavailable zinc intake, as well as calcium, retinol (vitamin A), vitamin B2 (riboflavin), vitamin B6, and vitamin B12 intakes. Commonly, poor diets, lacking fresh fruits and vegetables, yield deficiencies of vitamin C (ascorbic acid), β-carotene (provitamin A), and folic acid. Grain milling eliminates several nutrients, especially iron and zinc, various B complex vitamins (i.e., thiamine, riboflavin, and niacin), and folate. People on refined grain diets are at increased risk of deficiency in all these micronutrients. [4] Thus, fortifications are cumulated, such as vitamin A and iron, the vitamin B complex, calcium, and vitamin D, if micronutrients are separated. If fortification is achieved with the addition of different raw or auxiliary materials, the finished product will benefit from multiple fortifications, for example, the fortification of bread or sausages with mushrooms—this product will additionally have the nutritional value for protein and fiber content [110], while bakery products with the addition of nut paste come with a high intake of lipids, fibers, and minerals [12]. Most of the products fortified with unprocessed vegetable additions exhibit multiple fortifications.

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4. Advanced applied technologies for the fortification of bakery products

The lentil flour was obtained by grinding the lentils, thus obtaining a fine consistency; then flour mixtures were created according to Figure 1 [113].

Figure 1.

The technological chart for the production of bread fortified with lentil flour, according to [113].

Several aspects need to be taken into account throughout the technological process of obtaining fortified bakery products. This process of obtaining different types of fortified bread, including lentil bread, can be achieved through a single-phase process, since the amount (10–30%) of lentil flour is always introduced into the process by uniform distribution in the flour mass before adding the wet components (Figure 1) or through a two-phase process [113].

The use of compressed yeast as suspension in water facilitates the even distribution of yeast cells in the dough, thereby contributing to the improvement of product quality. As such, preparing the compressed yeast involves performing several operations such as suspending, filtering the suspension, and activating the yeast [114, 115]. The dosing aims at obtaining the dough with the optimal rheological properties and the appropriate composition of the product. The dosing of the raw materials used for dough preparation is performed taking into account their physical characteristics [113].

During the kneading process, an amount of air is included in the dough, required to meet its rheological attributes. The physical processes that take place in the dough at its kneading are the mechanical action during the kneading that ensures the water penetration into the flour mass and the temperature increase of the dough [116]. During the process of kneading itself, wet clumps of flour stick together under the influence of the mechanical kneading action, surface water penetrates deep, proteins become hydrated, the amount of bound water increases, and the dough increases its consistency and gradually acquires its elastic properties [117].

The fermenting operation is aimed at obtaining a risen dough that would produce suitable well-risen products with the right volume, as well as a porous and elastic core. Therefore, during this operation, various dough substances are accumulated in the dough, which impart the taste and aroma of bakery products. During dough fermentation, the yeast multiplication process continues, the predominant process being alcoholic fermentation, which releases carbon dioxide, ethyl alcohol, and a small amount of heat [116].

A well-risen product can only be obtained if the dough forms large amounts of gas. Ultimate leavening is the operation where the leavening of the dough reaches the maximum. The gases formed affect the gluten skeleton and thus the porosity of the dough by increasing or decreasing mesh size [116]. The biochemical processes formed during fermentation are hydrolysis of starch and gluten amylolysis or proteolysis, respectively. The microbiological processes refer to the multiplication of yeasts and their fermentative activity, as well as that of lactic bacteria that make up dough microbiota. Colloidal processes are the continuation of the gluten-forming process and gluten peptization [115].

Some of the gas present in the dough is lost during modeling, and as a result, the spongy structure of the dough is largely destroyed, the internal surface is reduced, and its specific weight increased [115].

A significant part of the carbon dioxide accumulated in the dough is eliminated during the division and modeling operations. Therefore, the dough must be subjected to a new fermentation for the restoration of its porous structure. As such, the products rise and the volume develops [116]. The main goal of the final leavening of the dough is the rise by the accumulation of carbon dioxide that is formed during yeast alcoholic fermentation and conditions the volume and structure of the porosity of products [115].

Colloidal processes condition the dough to be transformed into the inner crumb and modify the water binding state so that the crumb, although exhibiting a higher moisture than the initial humidity of the dough, appears dry due to thermal hydrophilic modifications. During coagulation, protein clotting and the gelatinization of starch occur [116]. The protein coagulation process starts at temperatures slightly above 50° C and proceeds at a maximum speed of 60–70° C, thus accelerating to continue the heating of the dough. After coagulation, proteins become more easily attackable by enzymes, both digestive enzymes and the proteolytic ones in the dough. The gelatinization of the starch takes place in two stages: granule swelling and gelatinization itself. Swelling occurs due to the penetration of water groups within the starch granule that distances the protein chains. This is achieved by increasing the kinetic energy of water molecules by heating the dough. The gelatinization is accomplished by breaking the existing H2 bonds between the amylose and amylopectin chains and dispersing these chains between the molecules of water previously penetrated into the granule. Biochemical processes formed during baking are amylolysis and proteolysis. Microbial processes during baking include alcoholic fermentation and lactic fermentation [117].

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5. Results obtained in food fortification

After lentil flour was employed in 10%, 15%, 20%, and 30% proportions for the fortification of bread, the increase in mineral elements was found to be up to 4 times the control sample, and protein content increased from 6.55% to 10.50% and fibers from 0.6% to 4.7%, while the ratio of ω-6 and ω-3 fatty acids decreased from 16.66 to 7.86 [113].

For 10%, 20%, and 30% flax fiber fortified biscuits, the results showed that the total content of polyunsaturated fatty acids increased significantly from 10.50% to 20.50%, while the total content of saturated fatty acids decreased significantly from 48.22% to 40.20%, showing that the omega-3 content of fortified flax seed biscuits was significantly higher than biscuits lacking flax seeds, while the ω-6/ω-3 dropped significantly from 8.50 to 1.00. Furthermore, the calcium content increased significantly from 25.6 mg/100 g for the control sample to 168.3, 175.0, and 179.1 mg/100 g, respectively [92].

Examples may continue for different products: mushroom sausages [110], mushroom powder pastes [118], marc bread [119], chestnut flour bread [120], spirulina paste [121], inulin- and lactobacilli-fortified juice [122], tortillas fortified with iron and folic acid [123, 124], bread fortified with zinc and iron [19], etc.

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6. Conclusion

The benefits of food fortification positively impact the entire life cycle of mankind. Thus, food fortification may be one of the most effective ways to overcome malnutrition and various diseases, especially in children and pregnant women and their children, preventing the birth of intellectually impaired children with malformations or deficiencies. Efforts to fortify food must be integrated in the context of each country’s public health and nutrition plans and as part of a comprehensive strategy to include different micronutrients in staple foods to meet the social, physiological, and economic goals of millions of people worldwide.

References

  1. 1. Codex Alimentarius Commission. General Principles for the Addition of Essential Nutrients to Foods CAC/GL 09-1987 (amended 1989, 1991). Rome, Joint FAO/WHO Food Standards Programme, Codex Alimentarius Commission, 1987 (http://www.codexalimentarius.net/download/standards/299/CXG_009e.pdf [Accessed: Oct 1, 2018])
  2. 2. Burgi H, Supersaxo Z, Selz B. Iodine deficiency diseases in Switzerland one hundred years after Theodor Kocher’s survey: A historical review with some new goitre prevalence data. Acta Endocrinologica. 1990;123:577-590. DOI: 10.1530/acta.0.1230577
  3. 3. Marine D, Kimball OP. Prevention of simple goiter in man. Archives of Internal Medicine. 1920;25:661-672. DOI: 10.1001/archinte.1920.00090350088005
  4. 4. Lindsay A, de Benoist B, Dary O, Hurrell R. Guidelines on Food Fortification with Micronutrients. Geneva, Switzerland: WHO Library; 2006. http://www.who.int/entity/nutrition/publications/guide_food_fortification_micronutrients.pdf. [Accessed: Oct 1, 2018]
  5. 5. Mozaffarian D, Rosenberg I, Uauy R. History of modern nutrition science—Implications for current research, dietary guidelines, and food policy. BMJ. 2018;361(k2392):1-6. DOI: 10.1136/bmj.k2392
  6. 6. Darnton-Hill I, Nalubola R. Fortification strategies to meet micronutrient needs: Successes and failures. The Proceedings of the Nutrition Society. 2002;61:231-241. DOI: 10.1079/PNS2002150
  7. 7. Samoraj M, Tuhy Ł, Dmytryk A, Chojnacka K. Biofortification of food with trace elements. In: Recent Advances in Trace Elements. Wiley Online Library. 2018;21:443-456. DOI: 10.1002/9781119133780.ch21
  8. 8. Fageria NK, Moraes MF, Ferreira EP, Knupp AM. Biofortification of trace elements in food crops for human health. Communications in Soil Science and Plant Analysis. 2012;43(3):556-570. DOI: 10.1080/00103624.2012.639431
  9. 9. Salem HM, El–Gizawy NK. Importance of micronutrients and its application methods for improving maize (Zea mays L.) yield grown in clayey soil. Chemist-Analyst. 2012;12(7):954-959. DOI: 10.5829/idosi.aejaes.2012.12.07.1759
  10. 10. Shi R, Zhang Y, Chen X, Sun Q, Zhang F, Römheld V, et al. Influence of long-term nitrogen fertilization on micronutrient density in grain of winter wheat (Triticum aestivum L.). Journal of Cereal Science. 2010;51(1):165-170. DOI: 10.1016/j.jcs.2009.11.008
  11. 11. Kumar N, Kumar RJ, Kumar CV, Jain S, Rajesh. Backcross breeding for enhancing minerals (iron and zinc) content in rice (Oryza sativa L.). International Journal of Current Microbiology and Applied Sciences. 2018;7(5):3593-3603. DOI: 10.20546/ijcmas.2018.705.415
  12. 12. Pǎucean A. Tendinţe modern privind creşterea valorii nutritive a fǎinii de grâu şi a produselor de panificaţie. Cluj Napoca: Editura Mega; 2017
  13. 13. Velu G, Ortiz–Monasterio I, Cakmak I, Hao Y, Singh RP. Biofortification strategies to increase grain zinc and iron concentrations in wheat. Journal of Cereal Science. 2014;59(3):365-372. DOI: 10.1016/j.jcs.2013.09.001
  14. 14. Osendarp SJM, Martinez H, Garrett GS, Neufeld LM, De-Regil LM, Vossenaar M, et al. Large-scale food fortification and biofortification in low- and middle-income countries: A review of programs, trends, challenges, and evidence gaps. Food and Nutrition Bulletin. 2018;39(2):315-331. DOI: 10.1177/0379572118774229
  15. 15. Saha S, Chakraborty M, Padhan D, Saha B, Murmu S, Batabyal K, et al. Agronomic biofortification of zinc in rice: Influence of cultivars and zinc application methods on grain yield and zinc bioavailability. Field Crops Research. 2017;210:52-60. DOI: 10.1016/j.fcr.2017.05.023
  16. 16. Lidon FC, Oliveira K, Ribeiro MM, Pelica J, Pataco I, Ramalho JC, et al. Selenium biofortification of rice grains and implications on macronutrients quality. Journal of Cereal Science. 2018;81:22-29. DOI: 10.1016/j.jcs.2018.03.010
  17. 17. Wu J, Salisbury C, Graham R, Lyons G, Fenech M. Increased consumption of wheat biofortified with selenium does not modify biomarkers of cancer risk, oxidative stress, or immune function in healthy Australian males. Environmental and Molecular Mutagenesis. 2009;50:489-501. DOI: 10.1002/em.20490
  18. 18. Naz S, Yousaf B, Tahir MA, Qadir A, Yousaf A. Iron and zinc bio-fortification strategies in wheat crop by exogenous application of micronutrients. Food Science and Quality Management. 2015;35:49-55
  19. 19. Ciccolini V, Pellegrino E, Coccina A, Fiaschi AI, Cerretani D, Sgherri C, et al. Biofortification with iron and zinc improves nutritional and nutraceutical properties of common wheat flour and bread. Journal of Agricultural and Food Chemistry. 2017;65(27):5443-5452. DOI: 10.1021/acs.jafc.7b01176
  20. 20. The World Health Report 2002. Reducing Risks, Promoting Healthy Life: Overview. Geneva: World Health Organization; 2002. Available from: http://www.who.int/whr/2002/en/
  21. 21. Liu OR, Molina R, Wilson M, Halpern BS. Global opportunities for mariculture development to promote human nutrition. PeerJ. 2018;6:e4733. DOI: 10.7717/peerj.4733
  22. 22. Joosten E. Iron deficiency anemia in older adults: A review. Geriatrics & Gerontology International. 2017;18(3):373-379. DOI: 10.1111/ggi.13194
  23. 23. Erdman JW, MacDonald AI, Steven HZ. Present Knowledge in Nutrition. 10th ed. Vol. 33. Hong Kong: Wiley-Blackwell; 2012. pp. 506-520. DOI: 10.1002/9781119946045
  24. 24. Doran L. Echocardiography Audit on Patients with Hereditary Haemochromatosis. Masters thesis. DIT; 2016
  25. 25. Drakesmith H, Prentice AM. Hepcidin and the iron-infection axis. Science. 2012;338:768-772. DOI: 10.1126/science.1224577
  26. 26. Trumbo P, Yates AA, Schlicker S, Poos M. Dietary reference intakes. Journal of the American Dietetic Association. 2001;101(3):294-301. DOI: 10.1016/s0002-8223(01)00078-5
  27. 27. Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC, USA: National Academy of Sciences; 1998
  28. 28. Institute of Medicine. Food and Nutrition Board. Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC: National Academy Press; 2010
  29. 29. Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Food and Nutrition Board, Institute of Medicine. Dietary Reference Intakes for Calcium and Vitamin D. Washington, DC: National Academy Press; 2010
  30. 30. Institute of Medicine, Food and Nutrition Board. Dietary Reference Intakes. Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington DC: National Academy Press; 2000
  31. 31. Institute of Medicine. Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids. National Academy Press. Food and Nutrition Board, Institute of Medicine, National Academies. 2005
  32. 32. Baker RD, Greer FR. Diagnosis and prevention of iron deficiency and iron-deficiency anemia in infants and young children (0–3 years of age). Pediatrics. 2010;126:1040-1050. DOI: 10.1542/peds.2010-2576
  33. 33. Whittaker P, Tufaro PR, Rader JI. Iron and folate in fortified cereals. Journal of the American College of Nutrition. 2001;20:247-254. DOI: 10.1080/07315724.2001.10719039
  34. 34. Andrew TG, Huchzermeyer KDA, Mbeha BC, Nengu SM, Arthur JR. Scientific opinion on dietary reference values for iron. EFSA Journal. 2015;13(10):4254. DOI: 10.2903/j.3efsa.2015.4254
  35. 35. Cogswell ME, Parvanta I, Ickes L, Yip R, Brittenham GM. Iron supplementation during pregnancy, anemia, and birth weight: A randomized controlled trial. The American Journal of Clinical Nutrition. 2003;78(4):773-781. DOI: 10.1093/ajcn/78.4.773
  36. 36. Thuy PV, Berger J, Davidsson L, Khan NC, Lam NT, Cook JD, et al. Regular consumption of NaFeEDTA-fortified fish sauce improves iron status and reduces the prevalence of anemia in anemic Vietnamese women. The American Journal of Clinical Nutrition. 2003;78(2):284-290. DOI: 10.1093/ajcn/78.2.284
  37. 37. Mannar V, Boy Gallego E. Iron fortification: Country level experiences and lessons learned. The Journal of Nutrition. 2002;132:856S-858S. DOI: 10.1093/jn/132.4.856S
  38. 38. Ballot DE, MacPhail AP, Bothwell TH, Gillooly M, Mayet FG. Fortification of curry powder with NaFe(111)EDTA in an iron-deficient population: Report of a controlled iron-fortification trial. The American Journal of Clinical Nutrition. 1989;49(1):162-169. DOI: 10.1093/ajcn/49.1.162
  39. 39. Johnson EJ, Russell RM. Beta-carotene. In: Coates PM, Betz JM, Blackman MR, et al., editors. Encyclopedia of Dietary Supplements. 2nd ed. London and New York: Informa Healthcare; 2010. pp. 115-120
  40. 40. Ross CA. Vitamin A. In: Coates PM, Betz JM, Blackman MR, et al., editors. Encyclopedia of Dietary Supplements. 2nd ed. London and New York: Informa Healthcare; 2010. pp. 778-791
  41. 41. Ross A. Vitamin A and carotenoids. In: Shils M, Shike M, Ross A, Caballero B, Cousins R, editors. Modern Nutrition in Health and Disease. 10th ed. Baltimore, MD: Lippincott Williams & Wilkins; 2006. pp. 351-375
  42. 42. Global Prevalence of Vitamin A Deficiency. Micronutrient Deficiency Information System working paper No. 2. Geneva, World Health Organization. 1995. Available from: http://www.who.int/nutrition/publications/micronutrients/iodine_deficiency/54015_mdis_workingpaper1/en/
  43. 43. Indicators for Assessing Vitamin A Deficiency and their Application in Monitoring and Evaluating Intervention Programmes. Geneva: World Health Organization; 1996. Available from: http://www.who.int/nutrition/publications/micronutrients/vitamin_a_deficiency/WHO_NUT_96.10/en/
  44. 44. Beaton GH, Martorell R, Aronson KJ, Edmonston B, McCabe G, Ross AC, et al. Effectiveness of Vitamin a Supplementation in the Control of Young Child Morbidity and Mortality in Developing Countries. Geneva: Administrative Committee on Coordination—Sub-Committee on Nutrition; 1992. Available from: https://www.unscn.org/web/archives_resources/files/Policy_paper_No_13.pdf
  45. 45. Solon FS, Solon MS, Mehansho H, West KP, Sarol J, Perfecto C, et al. Evaluation of the effect of vitamin A-fortified margarine on the vitamin A status of preschool Filipino children. European Journal of Clinical Nutrition. 1996;50:720-723
  46. 46. National Research Council. Committee to Assess the Health Implications of Perchlorate Ingestion. Health Implications of Perchlorate Ingestion. Washington, DC: The National Academies Press; 2005
  47. 47. World Health Organization. United Nations Children’s Fund & International Council for the Control of Iodine Deficiency Disorders. Assessment of Iodine Deficiency Disorders and Monitoring their Elimination. 3rd ed. Geneva, Switzerland: WHO; 2007
  48. 48. Zimmermann MB. Iodine deficiency. Endocrine Reviews. 2009;30(4):376-408. DOI: 10.1210/er.2009-0011
  49. 49. Zimmermann MB, Jooste PL, Pandav CS. Iodine-deficiency disorders. Lancet. 2008;372(9645):1251-1262. DOI: 10.1016/S0140-6736(08)61005-3
  50. 50. Murray CW, Egan SK, Kim H, Beru N, Bolger PM. US Food and Drug Administration’s total diet study: Dietary intake of perchlorate and iodine. Journal of Exposure Science & Environmental Epidemiology. 2008;18(6):571-580. DOI: 10.1038/sj.jes.7500648
  51. 51. Bailey LB, Gregory JF 3rd. Folate. In: Bowman B, Russell R, editors. Present Knowledge in Nutrition. Washington, DC: International Life Sciences Institute; 2006. pp. 278-301
  52. 52. Carmel R. Folic acid. In: Shils M, Shike M, Ross A, Caballero B, Cousins R, editors. Modern Nutrition in Health and Disease. Baltimore, MD: Lippincott Williams & Wilkins; 2005. pp. 470-481
  53. 53. Yetley EA, Pfeiffer CM, Phinney KW, Fazili Z, Lacher DA, Bailey RL, et al. Biomarkers of folate status in NHANES: A roundtable summary. The American Journal of Clinical Nutrition. 2011;94(1):303-312. DOI: 10.3945/ajcn.111.013011
  54. 54. Colapinto CK, O’Connor DL, Dubois L, Tremblay MS. Folic acid supplement use is the most significant predictor of folate concentrations in Canadian women of childbearing age. Applied Physiology, Nutrition, and Metabolism. 2012;37(2):284-292. DOI: 10.1139/h11-161
  55. 55. U.S. Department of Agriculture Agricultural Research Service. USDA National Nutrient Database for Standard Reference, Release 252012. DOI: 10.13140/RG.2.1.1551.1284
  56. 56. U.S. Food and Drug Administration. Food standards: Amendment of standards of identity for enriched grain products to require addition of folic acid. Federal Register. 1996;61(44)
  57. 57. Choumenkovitch SF, Selhub J, Wilson PWF, Rader JI, Rosenberg IH, Jacques PF. Folic acid intake from fortification in United States exceeds predictions. The Journal of Nutrition. 2002;132(9):2792-2798. DOI: 10.1093/jn/132.9.2792
  58. 58. Food and Drug Administration. Final rule: Food additives permitted for direct addition to food for human consumption; folic acid. Federal Register. 2016;81(73):22176-22183
  59. 59. Wilson RD, Désilets V, Wyatt P, Langlois S, Gagnon A, et al. Pre-conceptional vitamin/folic acid supplementation 2007: The use of folic acid in combination with a multivitamin supplement for the prevention of neural tube defects and other congenital anomalies. Journal of Obstetrics and Gynaecology Canada. 2007;29(12):1003-1013. DOI: 10.1016/s1701-2163(16)32685-8
  60. 60. Centers for Disease Control and Prevention. CDC grand rounds: Additional opportunities to prevent neural tube defects with folic acid fortification. MMWR. Morbidity and Mortality Weekly Report. 2010;59(31):980-984
  61. 61. Moll R, Davis B. Iron, vitamin B12 and folate. Medicine. 2017;45(4):198-203. DOI: 10.1016/j.mpmed.2017.01.007
  62. 62. Carmel R. How I treat cobalamin (vitamin B12) deficiency. Blood. 2008;112:2214-2221. DOI: 10.1182/blood-2008-03-040253
  63. 63. Vitamin and Mineral Requirements in Human Nutrition. Report of a Joint FAO/WHO Expert Consultation on Human Vitamin and Mineral Requirements. Bangkok, Thailand, 21–30 September 1998. 2nd ed. Geneva: World Health Organization; 2004. Available from: http://apps.who.int/iris/bitstream/handle/10665/42716/9241546123.pdf?sequence=1
  64. 64. Andrès E, Federici L, Affenberger S, Vidal-Alaball J, Loukili NH, Zimmer J, et al. B12 deficiency: A look beyond pernicious anemia. The Journal of Family Practice. 2007;56:537-542
  65. 65. U.S. Department of Agriculture, Agricultural Research Service. USDA National Nutrient Database for Standard Reference, Release 24. . Nutrient Data Laboratory Home Page. 2011
  66. 66. Ezzati M, Riboli E. Behavioral and dietary risk factors for noncommunicable diseases. The New England Journal of Medicine. 2013;369:954-964. DOI: 10.1056/NEJMra1203528
  67. 67. Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes. The B Vitamins and Choline: Overview and Methods. Washington, DC, USA: National Academies Press; 1998
  68. 68. Ortigoza-Escobar JD, Alfadhel M, Molero-Luis M, Darin N, Spiegel R, de Coo IF. Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors. Annals of Neurology. 2017;82(3):317-330. DOI: 10.1002/ana.24998
  69. 69. European Food Safety Authority (EFSA). Dietary reference values for riboflavin. EFSA Journal. 2017;18:4919
  70. 70. European Food Safety Authority (EFSA). Scientific opinion on dietary reference values for niacin. EFSA Journal. 2014;12:3759
  71. 71. European Food Safety Authority (EFSA). Dietary reference values for vitamin B6. EFSA Journal. 2016;14:4487
  72. 72. Rosenberg IH, Abrams SA, Beecher GR, et al. Dietary reference intakes: Guiding principles for nutrition labeling and fortification. Nutrition Reviews. 2004;62:73-79
  73. 73. Swaminathan S, Thomas T, Kurpad AV. B-vitamin interventions for women and children in low income populations. Current Opinion in Clinical Nutrition and Metabolic Care. 2015;18:295-306. DOI: 10.1097/MCO.0000000000000166
  74. 74. Scholey A. Vitamin B1 deficiency; vitamins in human nutrition—Social aspects; vitamins—Health aspects; vitamin B deficiency; health—Physiological aspects. The Australian Journal of Pharmacy. 2018;1175:58-64
  75. 75. Whitfield KC, Karakochuk CD, Kroeun H, Sokhoing L, Chan BB, Borath M, et al. Household consumption of thiamin-fortified fish sauce increases erythrocyte thiamin concentrations among rural Cambodian women and their children younger than 5 years of age: A randomized controlled efficacy trial. The Journal of Pediatrics. 2017;181:242-247. DOI: 10.1016/j.jpeds.2016.10.066
  76. 76. FAO. FAOSTAT. Food Balance Sheet Cambodia. 2011. Available from: http://www.fao.org/faostat/en/#country/115
  77. 77. Reidy KC, Bailey RL, Deming DM, O'Neill L, Carr BT, Lesniauskas R, et al. Food consumption patterns and micronutrient density of complementary foods consumed by infants fed commercially prepared baby foods. Nutrition Today. 2018;53(2):68-78. DOI: 10.1097/NT.0000000000000265
  78. 78. Thakur NS, Thakur N, Hamid, Kumar P, Thakur A. Formulation and optimization of vitamin C rich ready-to-serve juice based beverage from wild aonla fruits and its quality evaluation during storage. Journal of Pharmacognosy and Phytochemistry. 2018;7(1):1796-1802
  79. 79. Mohammadi T, Azandeh S, bijan Nejad D, Shamseddini lori N. Effect of vitamin C on bioavailability and differentiation potential of human umbilical cord Wharton’s jelly-derived mesenchymal stem cells. Qom University of Medical Sciences Journal. 2018;11(11):1-11
  80. 80. Wang AH, Still C. Old world meets modern: A case report of scurvy. Nutrition in Clinical Practice. 2007;22:445-448. DOI: 10.1177/0115426507022004445
  81. 81. Pilz S, März W, Cashman KD, Kiely ME, Whiting SJ, Holick MF, et al. Rationale and plan for vitamin D food fortification: A review and guidance paper. Frontiers in Endocrinology. 2018;9:1-16. DOI: 10.3389/fendo.2018.00373
  82. 82. Singh GM, Micha R, Khatibzadeh S, Shi P, Lim S, Rews KG, et al. Global, regional, and national consumption of sugar-sweetened beverages, fruit juices, and milk: A systematic assessment of beverage intake in 187 countries. PLoS One. 2015;10(8):1-20. DOI: 10.1371/journal.pone.0124845
  83. 83. Calvo MS, Whiting SJ, Barton CN. Vitamin D fortification in the United States and Canada: Current status and data needs. The American Journal of Clinical Nutrition. 2004;80:1710S-1716S. DOI: 10.1093/ajcn/80.6.1710S
  84. 84. El-Shibiny S, El-Gawad M, Assem FM, El-Sayed SM. The use of nano-sized eggshell powder for calcium fortification of cow’s and buffalo’s milk yogurts. Acta Scientiarum Polonorum. Technologia Alimentaria. 2018;17(1):37-49. DOI: 10.17306/J.AFS.0541
  85. 85. Curtis EM, Moon RJ, Dennison EM, Harvey NC, Cooper C. Recent advances in the pathogenesis and treatment of osteoporosis. Clinical Medicine. 2015;15(6):92-96. DOI: 10.7861/clinmedicine.15-6-s92
  86. 86. Meschino J. Calcium: Requirements, bioavailable forms, physiology and clinical aspects. Dynamic Chiropractic. 2002;20(18):1-12
  87. 87. Heaney RP, Rafferty K, Dowell MS, Bierman J. Calcium fortification systems differ in bioavailability. Journal of the American Dietetic Association. 2005;105(5):807-809. DOI: 10.1016/j.jada.2005.02.012
  88. 88. Fulgoni VL, Keast DR, Auestad N, Quann EE. Nutrients from dairy foods are difficult to replace in diets of Americans: Food pattern modeling and an analyses of the National Health and Nutrition Examination Survey 2003–2006. Nutrition Research. 2011;31(10):759-765. DOI: 10.1016/j.nutres.2011.09.017
  89. 89. Janve M, Singhal RS. Fortification of puffed rice extrudates and rice noodles with different calcium salts: Physicochemical properties and calcium bioaccessibility. Lebensmittel-Wissenschaft & Technologie. 2018;97:67-75. DOI: 10.1016/j.lwt.2018.06.030
  90. 90. Benjakul S, Karnjanapratum S. Characteristics and nutritional value of whole wheat cracker fortified with tuna bone bio-calcium powder. Food Chemistry. 2018;259:181-187. DOI: 10.1016/j.foodchem.2018.03.124
  91. 91. Agrahar-Murugkar D, Dwivedi S, Dixit-Bajpai P, Kumar M. Effect of natural fortification with calcium and protein rich ingredients on texture, nutritional quality and sensory acceptance of cookies. Nutrition & Food Science. 2018. DOI: 10.1108/nfs-02-2018-0041
  92. 92. Elshehy H, Agamy N, Ismail H. Effect of fortification of biscuits with flaxseed on omega 3 and calcium content of the products. Journal of High Institute of Public Health. 2018;48(2):58-66
  93. 93. Wojciechowska-Durczynska K, Lewinski A. Search for relevant indications for selenium supplementation in thyroid diseases. Neuroendocrinology Letters. 2017;38:237-241
  94. 94. Stuss M, Michalska-Kasiczak M, Sewerynek E. The role of selenium in thyroid gland pathophysiology. Endokrynologia Polska. 2017;68:440-454. DOI: 10.5603/EP.2017.0051
  95. 95. Gill H, Walker G. Selenium, immune function and resistance to viral infections. Nutrition and Dietetics. 2008;65:41-47. DOI: 10.1111/j.1747-0080.2008.00260.x
  96. 96. Rayman MP. Selenium in cancer prevention: A review of the evidence and mechanism of action. The Proceedings of the Nutrition Society. 2005;64:527-542. DOI: 10.1079/PNS2005467
  97. 97. Gao J, Liu Y, Huang Y, Lin ZQ, Banuelos GS, Lam MHW, et al. Daily selenium intake in a moderate selenium deficiency area of Suzhou, China. Food Chemistry. 2011;126:1088-1093. DOI: 10.1016/j.foodchem.2010.11.137
  98. 98. Fox TE, Fairweather-Tait S. Selenium. In: Hurrell RF, editor. The Mineral Fortification of Foods. Leatherhead, Surrey: Leatherhead Publishing; 1999. pp. 112-153
  99. 99. Cheng YY, Qian PC. The effect of selenium-fortified table salt in the prevention of Keshan disease on a population of 1.05 million. Biomedical and Environmental Sciences. 1990;3:422-428
  100. 100. Alsuhaibani AMA. Functional role of selenium-fortified yogurt against aflatoxin-contaminated nuts in rats. Agriculture & Food Security. 2018;7(1). DOI: 10.1186/s40066-018-0171-7
  101. 101. Dahl WJ, Whiting SJ, Healey A, Zello GA, Hildebrandt SL. Increased stool frequency occurs when finely processed pea hull fiber is added to usual foods consumed by elderly residents in long-term care. Journal of the American Dietetic Association. 2003;103(9):1199-1202. DOI: 10.1016/s0002-8223(03)00977-5
  102. 102. Besbes S, Attia H, Deroanne C, Makni S, Blecker C. Partial replacement of meat by pea fiber and wheat fiber: Effect on the chemical composition, cooking characteristics and sensory properties of beef burgers. Journal of Food Quality. 2008;31(4):480-489. DOI: 10.1111/j.1745-4557.2008.00213.x
  103. 103. Choi Y, Choi J, Han D, Kim H, Lee M, Lee E, et al. Effects of rice bran fiber on quality of low-fat tteokgalbi. Food Science and Biotechnology. 2008;17(5):959-964
  104. 104. Salazar P, Garcia ML, Selgas MD. Short-chain fructooligosaccharides as potential functional ingredient in dry fermented sausages with different fat levels. International Journal of Food Science and Technology. 2009;44(6):1100-1107. DOI: 10.1111/j.1365-2621.2009.01923.x
  105. 105. Yilmaz I, Gecgel U. Effect of inulin addition on physico-chemical and sensory characteristics of meatballs. Journal of Food Science and Technology-Mysore. 2009;46(5):473-476
  106. 106. Sayago-Ayerdi SG, Brenes A, Goni I. Effect of grape antioxidant dietary fiber on the lipid oxidation of raw and cooked chicken hamburgers. LWT- Food Science and Technology. 2009;42(5):971-976. DOI: 10.1016/j.lwt.2008.12.006
  107. 107. Pop F. Improvement of the nutritional value of pasta by the addition of wheat bran. Journal of Agroalimentary Processes and Technologies. 2017;23(4):245-249
  108. 108. Mudgil D, Barak S, Khatkar BS. Development of functional yoghurt via soluble fiber fortification utilizing enzymatically hydrolyzed guar gum. Food Bioscience. 2006;14:28-33. DOI: 10.1016/j.fbio.2016.02.003
  109. 109. Fürst P, Stehle P. What are the essential elements needed for the determination of amino acid requirements in humans? The Journal of Nutrition. 2004;134(6):1558S-1565S. DOI: 10.1093/jn/134.6.1558S
  110. 110. Nagy M, Semeniuc CA, Socaci SA, Pop CR, Rotar AM, Sălăgean CD, et al. Utilization of brewer’s spent grain and mushrooms in fortification of smoked sausages. Food Science and Technology. 2017;37(2):315-320. DOI: 10.1590/1678-457x.23816
  111. 111. Zhang W, Xiao S, Samaraweera H, Lee EJ, Ahn DU. Improving functional value of meat products. Meat Science. 2010;86(1):15-31. DOI: 10.1016/j.meatsci.2010.04.018
  112. 112. Simopoulos AP. Dossier: Polyunsaturated fatty acids in biology and diseases. The importance of the ratio of omega-6/omega-3 essential fatty acids. Biomedicine & Pharmacotherapy. 2002;56:365-379
  113. 113. Moldovan OP. Study quality parameters obtained from bakers flour fortified with legumes. PhD Thesis. USAMV-CN; 2016
  114. 114. Modoran C. Tehnologia produselor făinoase. Cluj-Napoca: Editura Academic Press; 2003
  115. 115. Bordei D. Tehnologia modernă a panificației. București: Editura AGIR; 2004
  116. 116. Păucean A, Man S. Tehnologia produselor vegetale. Cluj Napoca: Editura Academic Press; 2015
  117. 117. Modoran C. Tehnologia morăritului și a panificației. Cluj-Napoca: Editura Risoprint; 2007
  118. 118. Mureșan CC, Fӑrcaș A, Man S, Suharoschi R, Vlaic RA. Obtaining a functional product through the exploitation of mushroom flour in pasta. Bulletin UASVM Food Science and Technology. 2017;74:17-22. DOI: 10.15835/buasvmcn-fst:12641
  119. 119. Fărcaş AC, Socaci SA, Dulf FV, Tofană M, Mudura E, Diaconeasa Z. Volatile profile, fatty acids composition and total phenolics content of brewers’ spent grain by-product with potential use in the development of new functional foods. Journal of Cereal Science. 2015;64:34-42. DOI: 10.1016/j.jcs.2015.04.003
  120. 120. Man S, Păucean A, Muste S, Mureşan C, Frâncu AV. Chestnut flour addition influence on bread quality. Journal of Agroalimentary Processes and Technologies. 2012;18(2):150-154
  121. 121. Muresan C, Pop A, Man S, Socaci S, Fărcas A, Nagy M, et al. The influence of different proportions of spirulina (Arthrospira plantensis) on the quality of pasta. Journal of Agroalimentary Processes and Technologies. 2016;22(1):24-27
  122. 122. Khezri S, Mahmoudi R, Dehghan P. Fig juice fortified with inulin and Lactobacillus delbrueckii: A promising functional food. Applied Food Biotechnology. 2018;5(2):97-106. DOI: https://doi.org/10.22037/afb.v5i2.19844
  123. 123. Martínez-Bustos F, Cruz Sánchez A, Ortega-Martínez A, del C, Aguilar-Palazuelos E. Study of the functionality of nixtamalized maize flours and tortillas added with microcapsules of ferrous fumarate and folic acid. Cereal Chemistry. 2018;95:699-707. DOI: 10.1002/cche.10084
  124. 124. Popel S, Draganova E, Parşacova L, Colesnicenco A, Evtodienco L, Cropotova J. Fortifierea făinii de grâu cu suplimente de vitamine şi minerale. In: Papers of the Sibiu Alma Mater University Conference, FLftfa Editiom 24–26 March 2011. Sibiu

Written By

Vlaic Romina Alina, Mureşan Crina Carmen, Muste Sevastita, Mureşan Andruţa, Muresan Vlad, Suharoschi Ramona, Petruţ Georgiana and Mihai Mihaela

Submitted: 14 September 2018 Reviewed: 25 October 2018 Published: 18 January 2019