1. Introduction
Color is one of the most important organoleptic characteristics of food products since it is one of the parameters that gives the consumer an idea about the food’s acceptability, its composition, flavor and/or freshness
[1]. According to the Food and Drug Administration (FDA), a food colorant is “any dye, pigment, or substance which when added or applied to a food, drug or cosmetic, or the human body, is capable (alone or through reactions with other substances) of imparting colour”
[2].
Colorants are added to food products for different reasons such as restoring the original color lost due to the influence of exposure to light, temperature variations, moisture and/or storage conditions; enhancing the natural color or adding color to colorless products
[2,3][2][3].
Color additives can be classified as subject to certification and exempt from certification. First are colorants that are obtained synthetically, while second comprise colorants that are obtained from vegetables, minerals, or animals; therefore, this classification is the same as artificial and natural colorants. Another way of categorizing them is as straight colors, lakes, and mixtures. Straight colors refer to colorants that have not been mixed or chemically reacted with any other substance (e.g., FD&C Blue No. 1). Lakes for food use refers to straight colors that have been chemically reacted with precipitants and substrates such as aluminum cation as the precipitant and aluminum hydroxide as the substratum (e.g., Blue 1 Lake). Finally, mixtures are colorants generated by mixing a color additive with one or more color additives or non-colored diluents without chemical reaction
[2,4][2][4].
Currently, artificial food colorants are widely use by the food industry, among others, in children’s products, since they have high intensity, stability, uniformity of color, and are cheap. However, their use has been controversial since 1976 when Feingold
[5] reported a quick improvement in the behavior of children with attention deficit and hyperactivity disorder (ADHD) due to the elimination of the intake of artificial food colorants (mostly azo colorants) and flavorings. Since then, several studies have been published, the most well-known being the one provided by McCann
[6], who evidenced the increase in the incidence of ADHD including inattention, impulsivity, and overactivity not only in children with extreme hyperactivity, but also in the general child population due to the consumption of artificial food colors (AFCs) and other additives such as sodium benzoate preservative (E 211). It is important to mention that a few studies regarding the effect of artificial food colorants in adults have been completed, such as that of Murdoch et al.
[7], who evidenced a significant increase in the histamine levels of adults after the consumption of 150 mg of tartrazine; Di Lorenzo et al.
[8], who evidenced symptoms of allergy in patients with chronic urticaria to different additives including tartrazine and erythrosine, in response to mixture of additives; Pestana et al.
[9], who did not find evidence of statistical differences between the reaction to tartrazine and the placebo in 26 adults with allergic pathologies such as rhinitis, asthma or urticaria; and Park et al.
[10], who tested a mix of seven food additives that included amaranth, erythrosine, tartrazine and sunset yellow FCF in 54 adults with allergic diseases evidencing that there were no significant differences in the reactions to the mix of additives and the placebo. However, the vast majority of studies on the effect of artificial food colorants have been carried out on children as they are more affected than the rest of the population, mainly due to the lack of control in their diet and to the fact that they are highly attracted by colors and present a higher consumption of processed sweet products such as candies or ice creams
[11].
Consequently, the responsible entities, EFSA (European Food Safety Agency) in the European Union and the FDA (Food and Drug Administration) in the United States of America, have carried out different reviews of the available studies in order to evaluate the safety of azo colorants, among other additives. On one hand, the most important communications have been the evaluation carried out in 2009 in the European Union by the EFSA where only a decrease in the acceptable daily intakes (ADI; the amount of the substances that a person can consume daily without risk) of three of these problematic colorants (quinoline yellow, E104; sunset yellow FCF, E110; and Ponceau 4R, E124) was established
[12,13,14][12][13][14]; and the statement release in 2013 by EFSA, where it was assured that a revaluation from the ADI of any of the azo colorants was not necessary and it was recommended that new tests should be carried out related to genotoxicity
[15]. On the other hand, in 2011, the Food Advisory Committee from the FDA from the United States concluded that a relationship between children’s consumption of AFCs and behavioral effects had not been established
[16].
However, the scientific community has continued working to establish the possible harmful effects of AFCs, having evidenced so far the potential of azo colorant to alter the normal functioning of the kidneys and liver, generation of reactive oxygen species, induction of hypersensitivity
[11], proinflammatory responses
[17] and, principally, an effect on ADHD
[18]. In addition, in recent years, the use of AFCs in the food industry has exponentially increased, to the point that in some categories, mainly in children’s products such as cakes, chips, chocolates, ice creams, drinks, etc., all products contain at least one AFC, and it should be noted that there have even been cases where the product exceeded the allowed level
[18,19,20][18][19][20]. On the whole, the different results have evidenced that is highly possible that many children may be consuming higher amounts of AFCs than previously thought
[21].
As a result of all the evidence regarding the problems that AFCs can generate, as well as the growing interest of the general population in healthier and more natural food, it has been necessary to provide a revaluation of the AFCs ADI, or the approval of their use, and at the same time, to acknowledge the development of natural colorants that can be used instead of AFCs obtaining the same or even better results in the final product.
2. Principal Colorant Compounds Found in Natural Matrices
Among the compounds present in plants that show coloring properties, there are four main groups, anthocyanins, which have the widest range of colors presenting hues from blue to red; betalains, for which the color could be red-violet, yellow-orange color, and mainly pink; carotenoids, which can range from red to yellow; and chlorophylls, which are mostly green but also can present blue tones. All these compounds, in addition to their colorant capacity, exhibit different bioactive properties evidencing health benefits with their consumption
[22].
2.1. Anthocyanins
Anthocyanins are pigments, for which the color can vary from blue to red. They derive from flavonoids and their base structure is an anthocyanidin which is constituted by two hexanes linked by three carbon atoms that form an oxygenated heterocycle; this structure presents a positive charge and is also known as a flavylium ion. When this anthocyanidin is in its glycosylated form, linked to a sugar, it is known as an anthocyanin (
Figure 1) and this sugar can be bonded in different positions, mainly position C3 or C5 of the first ring. In addition, anthocyanin can be hydroxylated and/or methoxylated in different positions. This chemical structure of conjugated double bonds provides them with strong colors as well as high antioxidant properties through the scavenging of free radicals
[23,24,25][23][24][25].
Figure 1.
Principal colorant compounds found in natural sources.
More than 700 different anthocyanins have been reported
[26[26][27],
27], which are differentiated from each other via the number and position of the hydroxy and methoxy substitutions, and the type and position of the sugar linked to the anthocyanidin
[24,28][24][28]. These variations provide them with different colors, stability, bioavailability, and health effects
[24,29][24][29].
Twenty-seven anthocyanidins have been observed in nature; however, cyanidin, delphinidin, pelargonidin, peonidin, malvidin, and petunidin represent 90% (50%, 12%, 12%, 12%, 7%, and 7%, respectively) of the anthocyanidins found in plants, being cyanidine-3-glucoside which is the predominant anthocyanin. The main edible sources of anthocyanins are berry fruits, including blueberry (
Vaccinium corymbosum L.), bilberry (
Vaccinium myrtillus L.), and strawberry (
Fragaria vesca L.), among others. In addition, they can also be found in other foods, such as red sweet potato (
Ipomoea batatas L.) and purple corn (
Zea mays L.)
[28]. Furthermore, different possible health benefits have been related to anthocyanins, such as possessing anti-inflammatory, anticancerogenic, antimutagenic and cardioprotective effects, being regulators of total cholesterol, LDL, HDL, and triglyceride levels, anticoagulants, and providing help in the prevention of neurological and cognitive alterations
[24].
Anthocyanins are one of the biggest types of natural pigment; hence, they have been highly studied for the generation of natural colorants, as an alternative to artificial one. Nevertheless, one of the biggest problems to overcome is the low stability that anthocyanins present, since they can be affected by light, temperature, pH, metal ions, enzymes, oxygen, and co-pigments
[30].
2.2. Betalains
Betalains are water soluble nitrogen-containing pigments with a core protonated structure commonly known as betalamic acid [4-(2-oxoethylidene)-1,2,3,4-tetrahydropyridine-2,6-dicarboxylic acid that can be found as betacyanins or betaxanthins, which have a pink–violet and yellow–orange color, respectively. Up to now, 75 different betalains have been identified, wherein, 51 of them are betacyanins. Therefore, betacyanins are the most commonly found. These pigments belong to 17 families of the order
Caryophyllales. They are present in fruits, flowers, leaves, and roots, with betanin being the most common structure. On the other hand, betaxanthins can also be found in tubers, but not as much in leaves, with proline-betaxanthin being the most common
[31,32][31][32]. The main edible sources of betalains are red beet roots (
Beta vulgaris L.), amaranth (
Amaranthus sp.) cacti (
Opuntia sp.) fruits, and dragon fruit (
Hylocereus sp.), among others. Different bioactivities have been related to betalains such as antioxidant, antibacterial, antifungal, antiprotozoal, and anticancer properties. Some of these effects, particularly the antioxidant properties, are related to the chemical structure of betalains, as they have a phenolic group and a cyclic amine, which are excellent electron donors and exhibit antiradical activities
[32].
Betalains are also characterized by their reduced stability, as these pigments are thermolabile and affected by light, high water activity, pH under 3 or above 7 and oxygen. For these reasons, recent research has focused on the preservation of the chemical structure and the functionality of betalains, by using different techniques such as complex formation, copigmentation and encapsulation
[33].
2.3. Carotenoids
Carotenoids are lipophilic pigments that go from yellow to red. They are composed of a C
40 skeleton which contains polyene groups with end groups at both ends of the chain (
Figure 1). Carotenoids can be classified in two categories according to their composition, namely carotenes and xanthophylls. Carotenes are hydrocarbons and include α-carotene, ß-carotene or lycopene. Xanthophylls contain functional groups with oxygen and include lutein, zeaxanthin or astaxanthin. These pigments can be found in different natural sources such as fruits, seed, roots and flowers, fulfilling functions as antioxidants, color attractants or hormone plant precursors. About 50 different carotenoids have been described in common human foods, including tomatoes (
Solanum lycopersicum L.), persimmon (
Diospyros kaki L.) and Gac fruit (
Momordica cochinchinensis Spreng.), these being some of the most representative sources. Regarding their beneficial effect on human health, some beneficial properties have been related in relation to ocular, cardiovascular and fatty liver diseases, liver fibrosis and cancer. The majority of these potential health benefits have been attributed to the anti-inflammatory and immunomodulatory activity, and the regulation of cell cycle/apoptosis exhibited by these molecules
[34,35][34][35].
Regarding the stability of these pigments, carotenoids are susceptible to various degradation and isomerization reactions, as was mentioned, above which cause their discoloration and can lead to a decrease and thus reduction in their biological activity. In particular, the stability of carotenoids is mainly affected by thermal processes, as well as by the presence of oxygen or light
[36].
2.4. Chlorophylls
Chlorophylls are green natural colorants present in a wide number of green fruits and vegetables. Spinach, alfalfa, grass and nettles are natural sources of chlorophylls. These pigments are constituted of a porphyrin ring with a magnesium atom as the central metal (chlorophyll a and b) or without a central metal (e.g., phaeophytin a and b, pheophorbide a and pyropheophytin a), with an isocyclic five-membered ring and a chain of propionic acid esterified with phytol (
Figure 1). To date, there are more than 100 chlorophylls or chlorophyll derivatives reported, with chlorophylls a and b being the most common in plants, which are found in a 3:1 proportion, respectively
[37,38,39][37][38][39]. Chlorophylls present a significant antioxidant activity through chelation of reactive ions and scavenging of free radicals preventing DNA damage and lipid peroxidation, as well as antimutagenic and antigenotoxic activity through the prevention of mutagen migration and its coupling to DNA by the formation of a chlorophyll–mutagen complex which facilitates the degradation of the mutagen
[37,40][37][40].
Chlorophylls are highly sensitive pigments that could be degraded by several factors, such as oxygen, light, heat, acids, and enzymes, causing a color change from green to brown, mostly due to the substitution of the central magnesium ion by two hydrogens, losing the green color characteristic of the presence of the magnesium ion
[37,41][37][41].
3. Source of Natural Colorants as a Potential Replacers of Artificial Food Colorants
Currently, the European Food Safety Authority (EFSA) and the Food and Drugs Administration (FDA) have approved the use of different extracts from plants as colorants, as can be seen in
Table 1, with the principal colorant compounds, anthocyanins, carotenoids, and chlorophylls being present, so there is a wide variety of colors. However, some of them are limited in their use to exact types of products, e.g., butter pea flower extract, which in the United States can only be used in beverages, juices, ice cream and candies, or copper complex of chlorophylls, which can only be used in citrus-based dry beverage mixes. Moreover, there is a bigger problem with these natural colorants than the restrictions of use to specific products, their low stability and therefore the small range of use, as these natural colorants can be affected by pH, temperature and light, among others, that make their use difficult in variety of products.
Table 1. Natural food colorants with approved use in Europe and United States, by EFSA and FDA, respectively [42,43]. Natural food colorants with approved use in Europe and United States, by EFSA and FDA, respectively [42][43].
Color
|
Origin
|
Scientific Name
|
Chemical Compound
|
Isolation
|
E Number
|
Different studies report the novel use of natural food colorants in food product formulations in order to replace the use of synthetic ones. In this sense,
Table 2 shows the most recent studies in this field.
Table 2. Recent studies of natural food colorants incorporated in different food matrices.
Food Color
|
Natural Colorant
|
Food Matrix
|
Natural Sources
|
Main Food Characteristics: Color and Stability
|
|
CFR Section
|
Reference |
|
Blue
|
Butterfly pea flower extract
|
Red-purple
|
Anthocyanins
|
Clitoria ternatea L.
|
Anthocyanins
|
|
Yogurt
Aqueous extraction
|
Black rice bran extract
|
Pink color with 0.2% (L*: 80.20,
NA
|
C*: 9.67, h: 18.34) and purplish pink with 0.6%, the highest percentage added (L*: 68.42, C
73.69
|
*: 15.23, h: 8.73) |
|
| [ | 109 | ][44]
|
Blue-green
|
Spirulina extract
|
Yogurt
|
Red onion by-products
|
Arthrospira platensis
|
Time zero: 0.05 mg cya-3-gluE/g (L*: 75.27, a*: 11.20, b*: 9.55)
After 4 weeks of storage 0.039 mg cya-3-gluE/g (L*: 75.19, a*: 11.35, b
Phycocyanins
|
|
NA
|
73.530
|
*: 9.75) |
|
| [53][45]
|
Green
|
Edible plant material, grass, lucerne and nettle extract
|
Gramineae,
|
Yogurt
|
Eggplant
| Medicago sativa |
Color parameters of the yogurt with 1% of encapsulated extract: L*: 83.74, a*: 3.96 b*: 8.18. L., Urtica dioica L.
|
Chlorophylls
|
|
[159][46Solvent extraction
|
]
E140i
Cl natural green 3; magnesium chlorophyll; magnesium phaeophytin
|
|
|
Green-blue
|
Edible plant material, grass, lucerne and nettle extract
|
Gramineae,
Medicago sativa L., Urtica dioica L.
|
b*: −0.78.
Chlorophyllins
|
[160][47]
Solvent extract and saponification
|
E140ii
Cl natural green 5; sodium chlorophyllin; potassium chlorophyllin
|
|
Bakery products
|
Onion skin
|
Color parameters of the extracts: L*: 22.56, a*: 20.84, |
|
Green-blue
|
Edible plant material, grass, lucerne and nettle extract
|
Marmalade
|
| Gramineae, |
Black carrot
Medicago sativa L., Urtica dioica L.
|
|
Thermal processing caused a loss of anthocyanins (79.2–89.5%)
Copper complex of chlorophylls
|
[161][48]
Solvent extraction and addition of a salt of copper
|
E141i
Cl natural green 3; copper chlorophyll; copper phaeophytin
|
|
Green-blue
|
EU: Edible plant material, grass, lucerne and nettle.
US: alfalfa extract
|
US: Medicago sativa L.
|
Red beer
|
Eggplant peel extract
|
| Copper complex of chlorophylls
|
Color parameters: L*: 74.67, a*: 9.86, b*: 21.76
|
[162][49]
Solvent extract, saponification, and addition of a salt of copper
|
E141 (ii)
CI Natural Green 5; Sodium Copper Chlorophyllin; Potassium Copper Chlorophyllin
|
73.125
|
Yellow
|
Carotenoids
(lycopene)
|
Turmeric extract
|
|
Butter
Curcuma longa L.
|
Tomato skin
Curcumin
|
|
Extract concentration: 20 mg/kg
Color parameters, at initial time: L*: 48.78, a*: 2.36, b*: 14.17
Color parameters at 4 months of storage at 4–6 °C: L*: 48.37, a*: 2.25, b
Solvent extraction
|
*: 14.18
E100
Cl natural yellow 3, turmeric yellow, diferoyl methane
|
73.600
|
|
| [ | 163 | ][50]
|
|
Turmeric oleoresin
|
Curcuma longa |
Mayonnaise
| L. |
|
|
Tomato skin
|
Extract concentration: 50 mg/kg
Color parameters, at initial time: L*: 55.82, a*: 10.32, b*: 19.95
Curcumin
|
Extraction with exact solvents
|
Color parameters at 4 months of storage at 4–6 °C:
NA
|
73.615
|
L | *: 53.66, | a *: 9.64, b*: 19.10
|
[163] |
Yellow-orange
|
Edible plants, carrots, vegetable oils, grass, alfalfa, and nettle extract
|
Daucus carota L.
|
Carotenoid—Beta-carotene
|
Solvent extraction
|
E160a (ii)
Cl food orange 5
|
73.95
|
[ | 50 | ] |
|
Ice cream
|
Tomato skin
|
Extract concentration: 70 mg/kg
Color parameters, at initial time: L*: 84.41, a*: 11.56, b*: 28.59
Color parameters at 4 months of storage at −25 °C: 83.97, a*: 11.16, b*: 21.29
|
[163][50]
|
Yellow-orange
|
Algae extract
|
Dunaliella salina Teod.
|
Carotenoid—Beta-carotene
|
Essential oil extraction |
Ice cream
|
|
|
Tomato peel
|
The ice cream prepared with 3% of extract obtained the highest score in all the parameters of the sensorial analysis
|
[E160a (iv)
Cl Food orange 5
|
|
91 | ] | [ | 51]
|
Yellow-brown
|
Edible fruits and plants, grass, lucerne and African marigold extract
|
African marigold: Tagetes erecta L.
|
Carotenoids–Lutein
|
Solvent extraction
|
E161b |
Pink
|
Betalains
|
Gummy candies
|
| Lutein; mixed carotenoids; xanthophylls |
|
|
| Cactus ( | Opuntia ficus-indica | L. Mill.) fruit pulp
|
High stability of the color in the gummy candies were observed after 30 days of storage al 4 °C
|
[164][52]
|
Red-brown
|
Yogurt
|
Annatto tree seeds outer coating extract
|
Pitaya
Bixa orellana L.
|
The yogurts with 0.5% and 2% of the colorant were statistically similar to the commercial yogurts with beetroot and carmine colorants, respectively
Carotenoid–bixin
|
|
[98][53]Solvent extraction
|
E160b (i)
Annatto; bixin; norbixin; Cl natural orange 4
|
73.30
|
|
Annatto tree seeds outer coating extract
|
|
Cookies
|
Gomphrena globose L. | Bixa orellana L.
|
|
Color parameters of samples with the lyophilized extract: L*: 56.3, a*: 22.1, b*: 8.0
Carotenoid–bixin
|
Color parameters of samples with the spray dried extract: L
Alkali extraction
|
E160b (ii)
Cl natural orange 4
|
|
*: 56.0, | a | *: 25.5, b*: 4.3
|
[165][54]
|
|
Annatto tree seeds outer coating extract
|
Bixa orellana L.
|
Carotenoid–bixin
|
Ice cream
|
Gomphrena globose L.
|
Color parameters: L*: 86, a*: 8, b*: 2.4
|
[166][55] |
Vegetal oil extraction
|
E160b (ii)
Cl natural orange 4
|
|
Yellow-orange
|
Carrot oil
|
Daucus carota L.
|
Carotenoid
|
Tagliatelle pasta |
| Solvent extraction |
|
|
Flowers of Amaranthus caudatus
|
Color parameters: L*: 62, a*: 17, b*: 8
NA
|
[166][55]
73.300
|
Yellow-orange
|
Dried stigma powder
|
|
Meringue cookies
| Crocus sativus | L.
|
Carotenoid–crocin
|
Dry grinding
|
NA
|
Red-fleshed pitaya peels
|
Color parameters: L*: 79.6, a*: 14.5, b*: 1.24
|
[166][55]
73.500
|
Red
|
Ground dried paprika
|
Capsicum annuum L.
|
Carotenoid–capsanthin and capsorubin
|
Dry grinding |
Yellow-Orange
|
Carotenoids
|
|
|
Dough biscuits
| NA
|
|
Mango peel
|
Color parameters of product with 20% of mango peel: 73.340
|
L | *: 52.90, | a | *: 7.71, | b*: 22.02
|
[167][56]
|
Red
|
Paprika oleoresin
|
Macaroni
|
Mango peel
|
Capsicum annuum L.
|
|
-
Carotenoid–capsanthin and capsorubin
|
[167][56
Solvent extraction
|
E160c
|
73.345
|
] |
|
Red
|
Red tomatoes extract
|
Lycopersicon esculentum L.
|
Green
|
Chlorophylls
|
| Lycopene
|
Syrup
Solvent extraction
|
|
Centella asiatica L.
|
The syrups with the extracts treated with zinc and copper were stable and presented minimum change in color, mostly an increase in the h* value.
E160d (ii)
Natural yellow 27
|
[148][57
73.585
|
] |
|
|
Red beets roots extract
|
Beta vulgaris L. var. Rubra
|
Betalaine
|
Pressing, aqueous extraction or dehydrating
|
Bread
|
Centella asiatica L.
|
The bread with the extract treated with zinc presented a yellow–green color, while the one with the extract treated with copper presented a green color. All of them changed significantly after 7 days
|
| E162 |
Beet red
|
[
73.40
|
148 | ] | [ | 57]
|
Red-purple
|
Grape or black carrot extract
|
|
White chocolate
| Vitis vinifera | L.,
Daucus carota L.
|
|
Nannochloropsis oculata D.J. HibberdAnthocyanin
|
Aqueous extraction
|
163
|
73.169 |
Samples with the encapsulated extract presented a higher quantity of chlorophylls. However, the samples with free extract presented a better stability of the color along the 28 days
|
| [ | 168 | ][58]
|
|
Grape skin extract
|
Chewing gum
|
Isochrysis galbana Pascher
|
Vitis vinifera L.
|
Samples showed a decrease in hardness as well as in the cohesiveness, which is advantageous for a chewing gum
Anthocyanin–enocianina
|
[169][59]
Aqueous extraction
|
163
|
73.170
|
E number: European number; CFR: Code of Federal Regulations; NA: not approved.
4. Incorporation of Natural Food Colorants in Food Matrix
|
Yogurt |
|
|
Spirulina |
|
|
The preparation with 0.25% showed the best acceptability in the sensory analysis |
|
|
[ |
170 |
] |
[ |
60 |
] |
|
Blue
|
Anthocyanins
|
Cooked rice
|
Butterfly pea flowers
|
The incorporation of 0.6% of extract resulted in better acceptance by consumers
|
[154][61]
|
L*: lightness; a*: red/green coordinate; b*: yellow/blue coordinate; h: hue; C*: chroma.