Abstract
Iron deficiency (ID) and ID with anaemia (IDA) are serious global health problems that disproportionately affect women aged 15–49 years. Although food fortification is one of the most effective and sustainable ways to combat nutritional deficiencies, iron remains one of the most difficult micronutrients to fortify, given its tendency to react strongly with food constituents. Therefore, it is important to assess the sensory properties of foods fortified with iron to determine the acceptability and palatability in target populations. We aimed to determine the palatability and acceptability of a novel iron and zinc‐enriched powder fortified in tap water by conducting sensory evaluations in 35 women of reproductive age using a 9‐point hedonic scale, where participants rated the sensory properties of six samples containing different amounts of the active or placebo powder. We found significant differences between samples reconstituted at 1, 2, and 3 g/L for sensory properties, including overall taste. Participants were found to be more willing to drink the mineral‐enriched powder when prepared at the lowest concentration (1 g/L) compared to higher concentrations. Our results provide important insight into the sensory qualities of a novel formulation of an iron and zinc‐enriched powder for at‐home fortification and indicate consumer acceptability in reproductive‐aged women, a key group at risk for ID/IDA. If found to improve iron status, novel treatments like this product will contribute to global efforts to develop safe, acceptable and sustainable interventions for ID and IDA.
Keywords: anaemia, iron deficiency, malnutrition, maternal health, micronutrients, reproductive health, women
In this study, we investigate the sensory qualities of a novel fortification system involving an iron and zinc‐enriched powder for the treatment and prevention of iron deficiency (ID) and ID anaemia (IDA) in women of reproductive age. We found that this intervention, compared to placebo, only minimally affects sensory qualities (colour, odour and taste properties) and is acceptable and palatable to women of reproductive age when prepared in tap water at a concentration of 1 g/L. This study helps to fill gaps in our understanding of consumer preferences in one of the populations most at risk for ID/IDA and in need of acceptable and sustainable treatments for these conditions.

Key messages
There is a need to develop effective and acceptable treatments for ID/IDA in women of reproductive age, a population most at risk for these conditions.
Fortification is one of the most sustainable approaches to combat nutritional deficiencies.
Iron is one of the most difficult micronutrients to fortify, as it can result in unacceptable sensory changes that lead to poor long‐term adherence and decreased treatment efficacy.
This study provides novel insights into the sensory perceptions of an iron fortification system in reproductive aged women, and can support global efforts towards developing acceptable treatments for ID/IDA in women.
1. INTRODUCTION
Iron and zinc are two of the most common mineral deficiencies worldwide (Miller, 2013; Wirth et al., 2018). These deficiencies are often caused by inadequate dietary intakes of these minerals and can result in serious adverse health problems if left untreated (Benson et al., 2021; Institute, 2016). Both iron and zinc are important for proper immune function and disease resistance (Cherayil, 2010; Wessels et al., 2017). Iron and zinc deficiencies often occur simultaneously as these nutrients are frequently found in many of the same foods, and their absorption in the body is affected by many of the same dietary ligands (Sandstead, 2000). Notably, zinc also serves as an important catalyst in iron metabolism, meaning that low dietary intake of zinc can contribute to the development of iron deficiency (ID) (Abdo et al., 2019; Kondaiah et al., 2019).
ID affects approximately 20−25% of the population and 52% of pregnant people (Petry et al., 2016; Turawa et al., 2021; Whitney et al., 2021). Women of reproductive age (15−49 years) have an increased risk of developing ID due to their increased physiologic demand for iron as a result of menstruation and pregnancy (Benson et al., 2021; Lu et al., 2019). ID results in fatigue, weakness, cognitive dysfunction, and decreased immunity, which ultimately affects quality of life (Benson et al., 2021; Lu et al., 2019; Miller, 2013; Mirza et al., 2018). If left untreated, ID can develop into ID anaemia (IDA), which is the most common form of anaemia globally (Turawa et al., 2021). IDA exacerbates the symptoms of ID while introducing additional health risks, such as cardiac complications (Abu‐Ouf & Jan, 2015) due to reduced erythropoiesis, which, in pregnant people, threatens maternal health and birth outcomes (Means, 2020; Milman, 2019; Mirza et al., 2018). Currently, IDA is a serious public health problem affecting one in three women aged 15−49 worldwide, and 10% of women aged 15−49 in Canada (Cooper et al., 2012; Di Cesare et al., 2021; Ltd, 2021; Turawa et al., 2021). Therefore, there is an urgent need to ensure adequate iron status in women of reproductive age to prevent adverse health problems and ultimately promote healthy pregnancies.
According to the Canadian Clinical Guidelines for Family Medicine, (Committee CGaPA, 2019) the first‐line treatment for ID and IDA in most patients is oral iron‐replacement therapy, in addition to dietary modifications (Baird‐Gunning & Bromley, 2016; Committee CGaPA, 2019). Current interventions include supplementation with iron salts (such as ferrous gluconate, ferrous fumarate, and ferrous sulphate) and other at‐home fortification systems (Mansour et al., 2021; Stoffel et al., 2020; Waller et al., 2020). However, many of these interventions have only been moderately successful due to low long‐term (more than 18‐months) compliance (less than 50%), which decreases the overall effectiveness of the intervention (DeMaeyer et al., 1989; Mirkovic et al., 2016; Ranganathan et al., 2016).
Low compliance rates with current treatments are mainly attributed to unpleasant side effects, including nausea and constipation (associated with iron supplementation) (Peña‐Rosas et al., 2015; Pereira et al., 2014; Souza et al., 2009). Iron fortification is more gentle on the digestive system than supplementation with iron salts, (Cancelo‐Hidalgo et al., 2013; Pereira et al., 2014) resulting in fewer side effects (such as nausea, flatulence, abdominal pain, constipation, and black or tarry stools) (Cancelo‐Hidalgo et al., 2013; Ojukwu et al., 2009; Peña‐Rosas et al., 2015; Pereira et al., 2014). However, fortification with iron has historically been known to affect various sensory modalities (taste, colour and odour) when reconstituted in food and drink, causing poor palatability, and ultimately resulting in low consumer compliance rates (DeMaeyer et al., 1989; Hurrell, 2021).
To more effectively prevent and treat ID and IDA in women of reproductive age, new interventions with improved consumer adherence are required. Such interventions would contribute to sustainable solutions to address these conditions and improve the health of populations globally. To meet this need, we investigated the palatability and acceptability of an iron and zinc‐enriched powder composed of a novel formulation of electrolytic ferrous iron with a small particle size (<20 µm) and zinc sulphate monohydrate that can be reconstituted in tap water for at‐home fortification. The main purpose of this intervention is to address ID, however, the formulation of the enriched powder also contains zinc, given that low baseline zinc levels can negatively affect iron absorption (Kondaiah et al., 2019). Further, iron and zinc deficiencies often occur simultaneously due to these minerals being frequently found in many of the same foods and populations who are affected by malnutrition may not be consuming adequate amounts of foods containing these minerals (Ishfaq et al., 2021; Lim et al., 2013). To establish regulatory guidelines for this product, it is important to demonstrate that fortification with the mineral‐enriched powder is palatable to end‐users when reconstituted in tap water. This powder has been designed to only minimally affect the sensory properties of the water (odour, colour, and taste), to circumvent the problem of poor palatability. An at‐home fortification system for iron that is palatable would suggest good consumer acceptability and may ultimately contribute to higher compliance rates (Asibey‐Berko et al., 2007; Hurrell, 1997, 2021; Hurrell et al., 2018; Lester et al., 2022; Waller et al., 2020). Therefore, the objectives of our study were to determine whether the mineral‐enriched powder affects sensory perceptions (odour, colour and taste) when reconstituted in tap water and if the reconstituted solution is palatable and acceptable to women of reproductive age.
2. METHODS
2.1. Study design and population
This study aimed to determine the palatability and acceptability of an iron and zinc micronutrient‐enriched powder compared to a placebo powder. The study was conducted as a single‐blinded study, where only the researcher knew which samples contained the intervention and which samples contained the placebo, and their concentrations, between November 2021 and March 2022 in Ottawa, Ontario, Canada. Participants were biologically female women of reproductive age (18−35 years), a target consumer population for this intervention. All participants were recruited locally from a university campus. This study was approved by the Office of Research Ethics at Carleton University (CUREB‐B Protocol #116204).
Interested participants met virtually with a member of the research team for a 5‐minute phone or Zoom call to discuss the objectives of the study and to review the screening criteria. Eligible participants were those who were: women of the biological female sex (assigned at birth), between 18 and 35 years old, and not currently taking any mineral supplements. Only participants who were not taking any supplements containing minerals were included in this study because some nutritional supplements contain iron, chromium, calcium and zinc, which can cause temporary changes in taste perception (Delompré et al., 2019; Nguyen & Tadi, 2021).
Fifty‐two participants were screened for this study. Of these, 35 were deemed eligible and agreed to participate in the study (Figure 1).
Figure 1.

Participant recruitment and enrolment flow‐chart.
2.2. Study products
This study sought to evaluate the palatability and acceptability of three different concentrations of a mineral‐enriched powder dissolved in water, compared to a placebo. Participants evaluated a total of six samples, three samples containing the intervention and three containing a placebo. The three samples containing the intervention were grouped as the ‘active samples’. These samples were labelled S1, S2, S3 and contained 1, 2 and 3 g/L of the mineral‐enriched powder, respectively. The three placebo samples were labelled S4, S5, S6 and contained 1, 2, and 3 g/L of the placebo powder, respectively.
The iron and zinc‐enriched powder has been developed using a fine‐grade electrolytic iron powder that has been approved for use and regularly incorporated into breakfast cereals worldwide. The zinc is derived from zinc sulphate monohydrate and is approved for supplementation. These minerals are included in a proprietary mixture of food stabilisers (primarily vegetable‐derived gums) and a milled vinegar, adapted by the manufacturer (Gum Products International [GPI] Inc.). The placebo powder was composed of the same proprietary mixture as the active powder, only without the added iron and zinc. All constituents of the mixture are designated by Health Canada as ‘safe for human consumption’ and meet the international Food Codex standards for food additives (CODEX, 2021). The levels of iron and zinc in the formulation are at levels similar to those used for routine fortification of staple products such as flour, corn flakes and other cereals, and well below the levels where toxicity would be a concern.
2.3. Evaluation of palatability and acceptability of study products
Eligible individuals were invited to individually participate in a 20−30‐min sensory evaluation session conducted in‐person. Only one participant and one member of the research team were present during each session. During the study, participants were presented with a total of six samples to evaluate: three samples containing the intervention and three samples containing the placebo. Each sample was prepared by dissolving different amount of either the mineral‐enriched powder or the placebo powder in 1 L of water.
Each participant was presented with the six samples to evaluate in a random order, given a score card, and provided with instructions on how to perform the sensory tests (for odour, colour and taste). The score cards were used to capture information about the palatability of the active and placebo preparations, using a 9‐point hedonic scale (Wichchukit & O'Mahony, 2015).
The 9‐point hedonic scale measures how much an individual likes or dislikes a food product (Wichchukit and O'Mahony, 2015). The scale ranges from 1 to 9, with a score of 9 meaning ‘like extremely’ and a score of 1 meaning ‘dislike extremely’. A score of 5 indicates a neutral response, meaning ‘neither like nor dislike’. These hedonic scores are interpreted to understand the palatability of the samples: A score of 5 indicates that the sensory property is palatable, a hedonic score of 7 or greater indicates that the sensory property is well liked (good acceptability by the consumer (Wichchukit & O'Mahony, 2015); Everitt, 2009; Singh‐Ackbarali & Maharaj, 2014) and a hedonic score of 4 or less indicates that the sensory property is disliked (and not acceptable to the consumer [Wichchukit & O'Mahony, 2015]; Everitt, 2009; Singh‐Ackbarali & Maharaj, 2014).
Participants were asked to use the 9‐point hedonic scale to evaluate the sensory properties of colour, odour, overall taste, and the 5 organoleptic properties of taste (sour, sweet, bitter, salty and umami) for each sample by recording their answers on the provided score card. Participants were also asked “would you be willing to drink this sample daily?” to determine the acceptability of the samples.
2.4. Statistical analysis
Within groups (active and placebo), hedonic scores for each sensory property (odour, colour, salty, sweet, bitter, sour, and umami) and overall taste were compared between concentrations (1, 2, and 3 g/L) using the Friedman's two‐way analysis of variance by ranks test. When there were significant differences found between the three groups, Wilcoxon signed‐rank tests were performed to determine individual differences between groups, and p values were adjusted for multiple comparisons with Bonferroni correction. Hedonic scores were also compared between groups (active vs. placebo) at each concentration using the Wilcoxon signed‐rank test and visualised in polar plots. Responses to the question “would you be willing to drink this sample daily?” (yes/no) were reported as the proportion of participants who answered ‘yes’ or ‘no’ to this question (95% confidence interval). Data were analysed using RStudio Statistical Software (v2022.02.1 + 461). Hedonic scores for the five organoleptic properties of taste are reported as medians and interquartile ranges and visualised using polar plots (RStudio version 2022.02.1 + 461). All values were considered to be statistically significant at p < 0.05.
2.5. Ethical Statement
This study was approved by Office of Research Ethics at Carleton University (CUREB‐B Protocol #116204).
3. RESULTS
3.1. Mineral‐enriched samples score higher than placebo samples on the hedonic scale
Overall, with increasing concentration of the active and placebo powders, hedonic scores decreased (Figure 2). At the lowest concentration (1 g/L), there were significant differences between the active intervention and placebo samples for the sensory properties of ‘colour’ (p < 0.001), ‘salty’ (p = 0.01), ‘sweet’ (p = 0.03) and ‘sour’ (p = 0.03) (Figure 2). Participants also rated the ‘overall taste’ of the active powder at 1 g/L (S1) higher than the placebo at 1 g/L (S4) (p = 0.01 Figure 2). At a concentration of 2 g/L, there were significant differences between the active intervention (S2) and the placebo samples (S5) for the sensory properties of ‘colour’ (p < 0.001), ‘salty’ (p = 0.002), ‘sweet’ (p = 0.02), ‘bitter’ (p = 0.004), ‘umami’ (p = 0.04) and ‘sour’ (p = 0.002) and in the ‘overall taste’ (p < 0.001, Figure 2). At a concentration of 3 g/L, there were significant differences between the active intervention (S3) and placebo samples (S6) for the sensory properties of ‘colour’ (p < 0.001), ‘odour’ (p = 0.006), ‘salty’ (p < 0.001), ‘bitter’ (p = 0.03), ‘umami’ (p = 0.02), and ‘sour’ (p = 0.01), and in the ‘overall taste’ (p < 0.001, Figure 2).
Figure 2.

Participant evaluations for seven sensory properties (colour, odour, salty, sweet, bitter, sour, umami) and overall taste for active and placebo solutions at three concentrations. Sensory evaluations were reported using a numeric 9‐point hedonic scale. (a) Hedonic ratings of 1 g/L active and placebo solutions, (b) Hedonic ratings of 2 g/L active and placebo solutions, (c) Hedonic ratings of 3 g/L active and placebo solutions. A hedonic score of 7 or greater indicates the sample will likely have good consumer acceptability. A score of 5 or greater indicates the overall taste of the sample (or sensory property) is palatable. S1, S2 and S3 (blue) = active solutions containing the mineral‐enriched powder at concentrations of 1, 2 and 3 g/L, respectively. S4, S5 and S6 (pink) = placebo solutions containing the control powder at concentrations of 1, 2 and 3 g/L, respectively. *indicates a significant difference between a sensory property in the active vs placebo solution (Wilcoxon signed‐rank test, p < 0.05).
3.2. Favourable sensory perceptions decrease with increasing concentration of mineral‐enriched samples and placebo samples
To determine which concentrations of the active and placebo preparations were more palatable and liked, sensory properties were evaluated across the concentrations within each group (active and placebo). For the active preparations (S1, S2 and S3), there were significant differences across concentrations in participants' reporting of all sensory properties other than ‘umami’ (p < 0.05, Table 1). The 1 g/L (S1) active sample received the highest hedonic scores for each sensory property compared to the active samples at 2 or 3 g/L (Table 1).
Table 1.
Sensory properties and overall taste for active and placebo powders across concentrations.
| Active solutions | ||||
|---|---|---|---|---|
| Sensory property of samples | S1 (1 g/L) (N = 35) | S2 (2g/L) (N = 35) | S3 (3 g/L) (N = 35) | p Value |
| Odour | 8 (6−9)a | 8 (5−9)a,b | 6 (4−8)c | p < 0.05 |
| Colour | 9 (8−9)a | 9 (8−9)a,b | 8 (7−9)c | p < 0.05 |
| Salty | 8 (6−9)a | 5 (3−8)b | 4 (3−6)c | p < 0.05 |
| Sweet | 8 (7−9)a | 7 (6−9)a,b | 6 (4−9)c | p = 0.003 |
| Bitter | 8 (5−9)a | 5 (4−8)b | 4 (3−6)c | p < 0.05 |
| Umami | 9 (6−9) | 8 (5−9) | 8 (4−9) | p = 0.169 |
| Sour | 9 (8−9)a | 6 (4−9)b | 4 (3−5)c | p < 0.05 |
| Placebo solutions | ||||
|---|---|---|---|---|
| Sensory Property of samples | S4 (1 g/L) (N = 35) | S5 (2g/L) (N = 35) | S6 (3 g/L) (N = 35) | p Value |
| Odour | 8 (5−9)a | 6 (4−8)a | 4 (3−6)b | p < 0.05 |
| Colour | 8 (7−9)a | 6 (4−8)b | 4 (3−7)c | p < 0.05 |
| Salty | 6 (4−7)a | 4 (2−5)b | 2 (2−4)c | p < 0.05 |
| Sweet | 7 (6−9) a | 6 (4‐7)b | 6 (3−8)b | p = 0.003 |
| Bitter | 7 (4−9)a | 4 (2−5)b | 3 (2−5)b | p < 0.05 |
| Umami | 7 (4−9) | 5 (4−7) | 4 (2−6) | p = 0.07 |
| Sour | 7 (4−9)a | 4 (3−5)b | 3 (1−4)c | p < 0.05 |
Note: Hedonic scores of participants' (N = 35) evaluation of each sensory property compared within groups for active samples (S1, S2 and S3) and placebo samples (S4, S5 and S6) at concentrations of 1L, 2 and 3 g/L. Hedonic scores range from 1−9, where a score of 1 = Disliked extremely, 9 = Liked extremely, and 5 = Neither like nor dislike. Data are median (IQR). Groups with different letters (a, b, c) are significantly different (p < 0.05) (Friedmans two‐way analysis of variance by ranks test and Wilcoxon signed‐rank test with Bonferroni correction for multiple comparisons, p < 0.05).
Abbreviation: IQR, interquartile ranges.
Notably, the median hedonic score for the ‘overall taste’ of the active sample at 1 g/L (S1) was also significantly higher when compared to the median hedonic scores for ‘overall taste’ in both the active sample at 2 g/L (S2) (p < 0.05, [1.00−2.99]) and the active sample at 3 g/L (S3) (p < 0.001, [3.49−4.50], Figure 3). Further, to better understand the distribution of scores from participants, the proportion of participants who disliked (hedonic scores 1−4), were neutral towards (hedonic score of 5), or liked (hedonic scores of 6−9) the ‘overall taste’ of each active sample were determined (Table 2). In total, 82% of participants indicated that they liked the overall taste of sample S1, 57% indicated that they liked sample S2, and only 6% indicated that they liked sample S3 (Table 2).
Figure 3.

Participant evaluation of the overall taste for active and placebo solutions. S1, S2 and S3 (blue) = active solutions containing the mineral‐enriched powder at concentrations of 1, 2, and 3 g/L, respectively. S4, S5 and S6 (pink) = placebo solutions containing the control powder at concentrations of 1, 2 and 3 g/L, respectively. Data are median and IQR. Within panels, groups with different letters are significantly different (Wilcoxon signed‐rank test with Bonferroni correction for multiple comparisons, p < 0.05). IQR, interquartile ranges.
Table 2.
Proportion of participant scores for ‘overall taste’ of active and placebo samples.
| Hedonic scores for participant liking | Proportion of participants (n) | ||
|---|---|---|---|
| Active Samples | S1 | S2 | S3 |
| Dislike (Score 1−4) | 9% (3) | 34% (12) | 74% (26) |
| Neutral (Score 5) | 9% (3) | 9% (3) | 11% (4) |
| Like (Score 6−9) | 82% (29) | 57% (20) | 15% (5) |
| Placebo Samples | S4 | S5 | S6 |
|---|---|---|---|
| Dislike (Score 1−4) | 29% (10) | 74% (26) | 94% (33) |
| Neutral (Score 5) | 11% (4) | 3% (1) | 0% (0) |
| Like (Score 6−9) | 60% (21) | 23% (8) | 6% (2) |
Note: Participants' (N = 35) ‘overall liking’ of each sample (S1−S6) using 9‐point hedonic scale. Hedonic scores range from 1‐9, where a score of 1 = Disliked extremely, 9 = Liked extremely, and 5 = Neither like nor dislike. Active samples S1, S2 and S3 contain the mineral‐enriched powder at concentrations of 1, 2 and 3 g/L, respectively. Placebo samples S4, S5 and S6 contain the placebo powder at concentrations of 1, 2 and 3 g/L, respectively. Proportion reporting overall disliking of each active and placebo sample include participants who gave hedonic scores between 1−4. Proportion reporting of overall liking of each active and placebo sample include participants who gave the samples hedonic scores between 6−9.
For the placebo preparations (S4, S5 and S6), there were significant differences across concentrations in participants' reporting of six out of the seven sensory properties (‘odour’, ‘colour’, ‘salty’, ‘sweet’, ‘bitter’ and ‘sour’, p < 0.001, Table 1). The placebo sample at 1 g/L (S4) received the highest hedonic scores for each sensory property compared to samples at 2 or 3 g/L (Table 1).
Notably, the median hedonic score for the ‘overall taste’ of the placebo sample at 1 g/L (S4) was significantly higher when compared to the median hedonic score for both the placebo sample at 2 g/L (S5) (p < 0.001, [1.50−3.50]) and at 3 g/L (S6) (p < 0.001, [3.00−4.99]) (Figure 3). The proportion of participants who disliked, were neutral towards, or liked the ‘overall’ taste of each placebo sample was also determined (Table 2). In total, 60% of participants indicated that they liked the overall taste of S1, 23% indicated that they liked S2, and only 6% indicated that they liked S3 (Table 2).
3.3. Acceptability was higher at lower sample concentrations
Acceptability of the samples was assessed by comparing participant responses within active and placebo groups to the question “would you be willing to drink this sample daily?”. For both the active and placebo samples, the proportion of participants willing to drink the sample daily decreased as the concentration increased. Among the active samples, the proportion of participants who were willing to drink the active sample with the lowest concentration at 1 g/L (S1) daily was 97% (85−99%), whereas 74% were willing to drink the sample daily when prepared at 2 g/L (S2) (58−86%), and only 46% were willing to drink the sample daily when prepared at 3 g/L (S3) (30−62%) (Figure 4).
Figure 4.

Proportion of participant responses to the question of ‘would you be willing to drink this sample daily?’ for each sample (S1−S6). A. Active samples (S1, S2 and S3), containing the mineral‐enriched powder. B. Placebo samples (S4, S5 and S6), containing the placebo powder. Participants who responded ‘yes’ (green bars) and ‘no’ (grey bars) at each concentration to samples within active and placebo groups.
Among the placebo samples, the proportion of participants willing to drink the sample with the lowest concentration at 1 g/L (S4) daily was 69% (52−81%), whereas 40% were willing to drink the placebo sample daily when prepared at 2 g/L (S5) (26−56%), and only 14% were willing to drink the sample daily when prepared at 3 g/L (S6) (6−29%) (Figure 4).
4. DISCUSSION
ID and IDA remain serious global health concerns and current interventions, including iron fortification and supplementation, vary in their effectiveness as treatments for these conditions, in part due to unpleasant sensory changes or adverse side effects (Hurrell et al., 2002). Here we conducted a palatability and acceptability study to analyse sensory properties of fortified beverages containing different concentrations of either a mineral‐enriched or a placebo powder. We found that the addition of either powder to tap water resulted in sensory changes, and that both the mineral‐enriched powder and placebo were most palatable and acceptable to participants when reconstituted at a concentration of 1 g/L (compared to 2 or 3 g/L). Our study suggests that interventional products to combat ID and IDA can be formulated with improved consumer acceptability, which may help increase adherence when treating these conditions in women of reproductive age.
We demonstrate that fortification with a mineral‐enriched powder containing electrolytic iron did not result in unpleasant sensory changes when reconstituted in tap water at the lowest concentration (1 g/L). An inverse relationship was observed between the concentration of iron and hedonic scores for almost every sensory category, in both treatment and placebo groups. Specifically, the ‘odour’, ‘colour’ and ‘overall taste’ (and thus, palatability) were the sensory properties most significantly affected by increased concentration. While to our knowledge there are no other studies that specifically investigate sensory changes to tap water fortified with electrolytic iron, our finding is consistent with results from similar studies involving other iron fortification systems (Dutra‐de‐Oliveira & de Almeida, 2002; Dutra‐de‐Oliveira et al., 2011; Kisinski et al., 2011; Siddique & Park, 2019; Theuer, 2008). A series of studies that assessed the use of water fortified with ferrous sulphate for the prevention of IDA in children in Brazil found that 20 mg doses of iron were associated with more unfavourable sensory changes in the colour and taste of tap water; however, this was not observed when the water was fortified with lower amounts (10 mg) of iron (Dutra‐de‐Oliveira et al., 2011; Galloway & McGuire, 1994; Hirve et al., 2007). These findings suggest that fortification of tap water with lower iron dosages will be more favourable and palatable. Similarly, an investigation of the sensory properties (colour, odour, and taste) in cheese fortified with different amounts of ferrous sulphate (either 0.016, 0.822 or 0.932 mg of Fe/g of cheese) reported that the samples with the lowest amount of iron (0.016 mg) had the most favourable sensory properties across every category (Siddique & Park, 2019). Together, these findings demonstrate that fortification with lower doses of iron is consistently associated with improved palatability and that favourability is important to consider in terms of consumer uptake and adherence, as the acceptability of commercial iron fortification programmes can be negatively affected by unfavourable sensory changes to food vehicles, leading to poor adherence (Asibey‐Berko et al., 2007; Dutra‐de‐Oliveira et al., 2011; Preedy et al., 2013; Waller et al., 2020).
To investigate the acceptability of this mineral‐enriched powder, we assessed the willingness of participants to drink the samples daily and found an inverse relationship between acceptability and sample concentration. In general, participants reported they would be less willing to drink the samples as the concentration of the active or placebo powder increased. This further suggests that our mineral‐enriched powder will be more acceptable to the target population when reconstituted at lower concentrations, which may thus increase adherence to a treatment regimen using an iron fortified beverage (Vecchiato et al., 2021). Although there are very few studies that investigate the acceptability of iron fortification systems in women of reproductive age, there have been several efficacy studies conducted in different populations that have reported participant adherence and acceptability as part of their secondary outcomes (Christofides et al., 2006; Dutra‐de‐Oliveira & de Almeida, 2002; Dutra‐de‐Oliveira et al., 2011; Hirve et al., 2007). Two research groups conducted randomised controlled trials in different paediatric populations to investigate the efficacy of food fortification using a micronutrient powder (‘Sprinkles’) containing either 12.5, 20 or 30 mg of ferrous fumarate compared to supplementation with oral iron drops (‘DROPS’) containing either 12.5 (Christofides et al., 2006) or 20 (Hirve et al., 2007) mg of ferrous sulphate (Christofides et al., 2006; Hirve et al., 2007). Both studies found that the serum ferritin levels in all participants increased after 8 weeks of treatment, with no significant differences between groups; however, they did report that participant adherence to the consumption regimen varied significantly between treatment groups. Specifically, both studies found that participants randomised to low dose Sprinkles (12.5 mg of ferrous fumarate) had significantly better adherence rates than participants randomised to higher dose Sprinkles (20 or 30 mg of ferrous fumarate) or DROPS (Christofides et al., 2006; Hirve et al., 2007). These findings demonstrate that food fortification with low doses of iron can be both effective and acceptable to consumers, further supporting our results.
A strength of our study includes that the tested home‐beverage fortification system used a mineral‐enriched powder containing electrolytic iron, a relatively inert form of iron known to have sensory‐related advantages over other common iron fortificants (Kondaiah et al., 2019; Siddique & Park, 2019; Stoffel et al., 2020; SUSTAIN, 2001; Vatandoust & Diosady, 2022). While we recognise the importance of bioavailability when selecting an iron compound, the size of the iron particle is also an important consideration, as a smaller particle size helps to increase bioabsorption (Hurrell et al., 2002; Nathan, 1999). The particle size of the electrolytic iron used in this study is very small (less than <20 µm) allowing us to focus on the sensory perceptions of this intervention in the current study in an effort to determine consumer acceptability. The World Health Organisation also regards food fortification as one of the safest, most effective, and most affordable ways to administer dietary iron in deficient populations (Allen et al., 2006; Christofides et al., 2006). However, iron is one of the most difficult micronutrients with which to fortify the diet, as it is known to interact strongly with many food constituents, resulting in unfavourable sensory changes to the colour, odour, and taste of fortified foods (Hurrell, 2021; Hurrell et al., 2018; WHO, 2006). Water soluble forms of iron (such as ferrous sulphate, ferrous gluconate, and ferrous fumarate) are most commonly used for oral iron replacement therapy given their high bioavailability; however, fortification with these iron compounds is frequently limited by their strong interactions with many foods (Hurrell, 1997; SUSTAIN, 2001; WHO, 2006). In contrast, fortification with electrolytic iron has been widely studied in many foods and has been consistently associated with significantly fewer organoleptic changes compared to water‐soluble forms of iron fortified in the same foods (Hackl et al., 2019; Kiskini et al., 2011; Theuer, 2008; Ziegler et al., 2011). Researchers have even recommended that cereal staples be fortified with electrolytic iron when other water‐soluble forms of iron result in unfavourable sensory changes (Hurrell et al., 2002; Richins et al., 2008; SUSTAIN, 2001). Given that the sensory perceptions of food can influence the likelihood of consumption, (Delompré et al., 2019; Siddique & Park, 2019) fortification with electrolytic iron can overcome the sensory barriers faced by treatment interventions involving water‐soluble iron compounds, thus contributing to greater palatability and long‐term consumer adherence (Allen et al., 2006; Hurrell et al., 2002; Hurrell, 2021; Vatandoust & Diosady, 2022). Further, electrolytic iron is more cost‐effective than ferrous sulphate (the current leading compound in oral iron replacement therapy (Hurrell et al., 2002)) which is advantageous, as economic feasibility is an important feature of sustainable treatments for micronutrient deficiencies (Hurrell et al., 2002; Swain et al., 2007). An additional strength of our study includes that we are one of the first to report on the palatability and acceptability of a fortification system involving electrolytic iron in women of reproductive age. Women are one of the most vulnerable populations at risk for ID and IDA, (Milman, 2019; Mirza et al., 2018; Swareldhab et al., 2021; Turawa et al., 2021) and thus there is a great need for palatable interventions that are accepted by this population for regular consumption to effectively treat these conditions (Vecchiato et al., 2021).
The generalisability of our results is limited by the small sample size and the subjective nature of the data collected. However, our approach used the 9‐point hedonic scale, a validated methodological tool that has been used to assess the acceptability of foods and beverages for over 40 years (Munoz & King, 2007; Gambaro & McSweeney, 2020; Johnson; Wang et al., 2022). Further, the known organoleptic changes to food and beverages due to iron make the application of this scale an appropriate methodologic approach for our study (Allen et al., 2006; Bovell‐Benjamin and Guinard, 2010; Huma et al., 2007; Hurrell, 2021; Swain et al., 2007).
We found that electrolytic iron fortification in tap water is palatable, acceptable, and favourable to women of reproductive age. These findings provide important preliminary data on the sensory perceptions of this preparation in one of the most vulnerable populations at risk for ID and IDA. Successful fortification systems consist of foods or beverages that are already common in the diet and can be effectively incorporated into an individual's daily routine (Allen et al., 2006; Olson et al., 2021). Evaluating consumer preferences for fortified foods and beverages, including palatability and acceptability, is also critical to inform the formulation or consumption regimen of these products, (Bovell‐Benjamin & Guinard, 2003; Everitt, 2009; Sutrisna et al., 2017) which will influence intervention success. Our findings suggest that electrolytic iron fortification of tap water could improve consumer consumption and adherence, and if efficacious in improving iron status, may ultimately help to strengthen global efforts to combat ID and IDA among women of reproductive age.
AUTHOR CONTRIBUTIONS
Clara H. Miller performed the research. Kristin L. Connor and Hauna Sheyholislami designed the research study. Clara H. Miller analysed the data. Clara H. Miller, Jessie L. Burns and Kristin L. Connor wrote the paper. All authors, Clara H. Miller, Kristin L. Connor, Hauna Sheyholislami and Jessie L. Burns have read and approved the final manuscript.
CONFLICT OF INTEREST STATEMENT
The authors declare no conflict of interest.
ACKNOWLEDGEMENTS
We would also like to acknowledge and thank the individuals who generously volunteered their time and data for the purposes of this study. Gum Products International Inc. (GPI) provided the proprietary food stabiliser in the mineral‐enriched powder. This study was funded by Lucky Iron Fish Enterprises (LIFe) and the National Research Council of Canada Industrial Research Assistance Programme (NRC IRAP).
Miller, C. H. , Sheyholislami, H. , Burns, J. L. , & Connor, K. L. (2024). Sensory evaluations of a novel iron and zinc‐enriched powder for the potential treatment and prevention of iron deficiency in women of reproductive age. Maternal & Child Nutrition, 20, e13575. 10.1111/mcn.13575
DATA AVAILABILITY STATEMENT
The findings of this study are supported by data that can be obtained upon request from the corresponding author. Data are not publicly available due to privacy restrictions.
REFERENCES
- Abu‐Ouf, N. M. , & Jan, M. M. (2015). The impact of maternal iron deficiency and iron deficiency anemia on child's health. Saudi Medical Journal, 36(2), 146–149. 10.15537/smj.2015.2.10289 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Allen, L. , De‐Benoist, B. , Dary, O. , Hurrell, R. , Allen Ld‐B, B. , Dary, O. , & Hurrell, R. (Eds.). (2006). Guidelines on food fortification with micronutrients (p. 331). The World Health Organization. https://apps.who.int/iris/bitstream/handle/10665/43412/9241594012_eng.pdf [Google Scholar]
- Asibey‐Berko, E. , Zlotkin, S. H. , Yeung, G. S. , Nti‐Nimako, W. , Ahunu, B. , Kyei‐Faried, S. , Johnston, J. L. , Tondeur, M. C. , & Mannar, V. (2008). Dual fortification of salt with iron and iodine in women and children in rural Ghana. East African Medical Journal, 84(10), 473–480. 10.4314/eamj.v84i10.9565 [DOI] [PubMed] [Google Scholar]
- Baird‐Gunning, J. , & Bromley, J. (2016). Correcting iron deficiency. Australian Prescriber, 39(6), 193–199. 10.18773/austprescr.2016.069 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benson, C. S. , Shah, A. , Stanworth, S. J. , Frise, C. J. , Spiby, H. , Lax, S. J. , Murray, J. , & Klein, A. A. (2021). The effect of iron deficiency and anaemia on women's health. Anaesthesia, 76(Suppl. 4), 84–95. 10.1111/anae.15405 [DOI] [PubMed] [Google Scholar]
- Bovell‐Benjamin, A. C. , & Guinard, J. X. (2003). Novel approaches and application of contemporary sensory evaluation practices in iron fortification programs. Critical Reviews in Food Science and Nutrition, 43(4), 379–400. 10.1080/10408690390826563 [DOI] [PubMed] [Google Scholar]
- Cancelo‐Hidalgo, M. J. , Castelo‐Branco, C. , Palacios, S. , Haya‐Palazuelos, J. , Ciria‐Recasens, M. , Manasanch, J. , & Pérez‐Edo, L. (2013). Tolerability of different oral iron supplements: A systematic review. Current Medical Research and Opinion, 29(4), 291–303. 10.1185/03007995.2012.761599 [DOI] [PubMed] [Google Scholar]
- Di Cesare, M. G. S. , Osendarp, S. , & Mozaffarian, D. (2021). 2021 Global Nutrition Report: The state of global nutrition. https://globalnutritionreport.org/reports/2021-global-nutrition-report/
- Cherayil, B. J. (2010). Iron and immunity: Immunological consequences of iron deficiency and overload. Archivum Immunologiae et Therapiae Experimentalis, 58(6), 407–415. 10.1007/s00005-010-0095-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christofides, A. , Asante, K. P. , Schauer, C. , Sharieff, W. , Owusu‐Agyei, S. , & Zlotkin, S. (2006). Multi‐micronutrient sprinkles including a low dose of iron provided as microencapsulated ferrous fumarate improves haematologic indices in anaemic children: A randomized clinical trial. Maternal and Child Nutrition, 2(3), 169–180. 10.1111/j.1740-8709.2006.00060.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- CODEX . (1995. −2021). General standards for food additives. CODEX Alimentarius International Food Standards.
- Committee CGaPA . (2019). Iron Deficiency—Diagnosis and management. 1–17. https://www2.gov.bc.ca/assets/gov/health/practitioner-pro/bc-guidelines/full_guideline_-_iron_deficiency.pdfhttps://www2.gov.bc.ca/gov/content/health/practitioner-professional-resources/bc-guidelines/iron-deficiency
- Cooper, M. , Greene‐Finestone, L. , Lowell, H. , Levesque, J. , & Robinson, S. (2012). Iron sufficiency of Canadians. Health Reports, 23(4), 41–48. [PubMed] [Google Scholar]
- Delompré, T. , Guichard, E. , Briand, L. , & Salles, C. (2019). Taste perception of nutrients found in nutritional supplements: A review. Nutrients, 11(9), 2050. 10.3390/nu11092050 [DOI] [PMC free article] [PubMed] [Google Scholar]
- DeMaeyer, E. M. , Dallman, P. , Gurney, J. M. , Hallberg, L. , & Sood, S. K. (1989). Preventing and controlling iron deficiency anaemia through primary health care: A guide for health administrators and programme managers.
- Dutra‐de‐Oliveira, J. E. , & de Almeida, C. A. N. (2002). Domestic drinking water‐‐an effective way to prevent anemia among low socioeconomic families in Brazil. Food and Nutrition Bulletin, 23(Suppl 3), 213–216. [PubMed] [Google Scholar]
- Dutra‐de‐Oliveira, J. E. , Marchini, J. S. , Lamounier, J. , & Almeida, C. A. N. (2011). Iron‐Fortified drinking water studies for the prevention of children's anemia in developing countries. Anemia, 2011, 1–5. 10.1155/2011/815194 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Everitt, M. (2009). Chapter 8—Consumer‐targeted sensory quality. global issues in food science and technology.
- Fathy Abdelhaleim, A. , Amer, A. Y. , & Abdo Soliman, J. S. (2019). Association of zinc deficiency with iron deficiency anemia and its symptoms: Results from a case‐control study. Cureus, 11(1), e3811. https://doi.org/10.7759/cureus.3811 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Galloway, R. , & McGuire, J. (1994). Determinants of compliance with iron supplementation: Supplies, side effects, or psychology? Social Science & Medicine, 39(3), 381–390. 10.1016/0277-9536(94)90135-x [DOI] [PubMed] [Google Scholar]
- Gambaro, A. , & McSweeney, M. B. (2020). Probiotic and prebiotics in foods: Challenges, innovations and advances, chapter 8. Advances in Food and Nutrition Research, 94, 295–337. [DOI] [PubMed] [Google Scholar]
- Hackl, L. S. , Abizari, A. R. , Speich, C. , Zungbey‐Garti, H. , Cercamondi, C. I. , Zeder, C. , Zimmermann, M. B. , & Moretti, D. (2019). Micronutrient‐fortified rice can be a significant source of dietary bioavailable iron in schoolchildren from rural Ghana. Science Advances, 5(3), eaau0790. 10.1126/sciadv.aau0790 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirve, S. , Bhave, S. , Bavdekar, A. , Naik, S. , Pandit, A. , Schauer, C. , Christofides, A. , Hyder, Z. , & Zlotkin, S. (2007). Low dose ‘sSprinkles’—An innovative approach to treat iron deficiency anemia in infants and young children. Indian Pediatrics, 44(2), 91–100. [PubMed] [Google Scholar]
- Huma, N. , Rehman, S. U. , Anjum, F. M. , Murtaza, M. A. , & Sheikh, M. A. (2007). Food fortification Strategy—Preventing iron deficiency anemia: A review. Critical Reviews in Food Science and Nutrition, 62(32), 269–265. 10.1080/10408390600698262 [DOI] [PubMed] [Google Scholar]
- Hurrell, R. , Bothwell, T. , Cook, J. D. , Dary, O. , Davidsson, L. , Fairweather‐Tait, S. , Hallberg, L. , Lynch, S. , Rosado, J. , Walter, T. , & Whittaker, P. (2002). The usefulness of elemental iron for cereal flour fortification: A sustain task force report. Nutrition Reviews, 60(12), 391–406. 10.1301/002966402320964061 [DOI] [PubMed] [Google Scholar]
- Hurrell, R. F. (1997). Preventing iron deficiency through food fortification. Nutrition Reviews, 55(6), 210–222. 10.1111/j.1753-4887.1997.tb01608.x [DOI] [PubMed] [Google Scholar]
- Hurrell, R. F. (2021). Iron fortification practices and implications for iron addition to salt. The Journal of Nutrition, 151(Suppl. 1), 3S–14S. 10.1093/jn/nxaa175 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hurrell, R. F. , Venkatesh Mannar, M. , & Hurrell, R (Eds.). (2018). Efficacy and Safety of Iron Fortification (1st ed., pp. 196–212). Academic Press. [Google Scholar]
- Institute, I. F. P. R. (2016). International Food Policy Research Institute. Global Nutrition Report: From Promise to Impact: Ending Malnutrition by 2030. 2016:182. https://www.ifpri.org/publication/global-nutrition-report-2016-promise-impact-ending-malnutrition-2030
- Ishfaq, M. , Wakeel, A. , Shahzad, M. N. , Kiran, A. , & Li, X. (2021). Severity of zinc and iron malnutrition linked to low intake through a staple crop: A case study in east‐central Pakistan. Environmental Geochemistry and Health, 43(10), 4219–4233. 10.1007/s10653-021-00912-3 [DOI] [PubMed] [Google Scholar]
- Johnson, M. The 9‐point hedonic scale. The Society of Sensory Professionals. https://www.sensorysociety.org/knowledge/sspwiki/Pages/The%209-point%20Hedonic%20Scale.aspx [Google Scholar]
- Kiskini, A. , Kapsokefalou, M. , Yanniotis, S. , & Mandala, I. (2011). Effect of iron fortification on physical and sensory quality of gluten‐free bread. Food and Bioprocess Technology, 5, 385–390. 10.1007/s11947-011-0651-2 [DOI] [Google Scholar]
- Kondaiah, P. , Yaduvanshi, P. S. , Sharp, P. A. , & Pullakhandam, R. (2019). Iron and zinc homeostasis and interactions: Does enteric zinc excretion Cross‐Talk with intestinal iron absorption? Nutrients, 11(8), 1885. 10.3390/nu11081885 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lester, S. , Kleijn, M. , Cornacchia, L. , Hewson, L. , Taylor, M. A. , & Fisk, I. (2022). Factors affecting adherence, intake, and perceived palatability of oral nutritional supplements: A literature review. The Journal of Nutrition, Health & Aging, 26, 663–674. [DOI] [PubMed] [Google Scholar]
- Lim, K. , Riddell, L. , Nowson, C. , Booth, A. , & Szymlek‐Gay, E. (2013). Iron and zinc nutrition in the economically‐developed world: A review. Nutrients, 5(8), 3184–3211. 10.3390/nu5083184 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ltd DIPR . (2021). Global Nutrition Report: The state of global nutrition. https://globalnutritionreport.org/reports/2021-global-nutrition-report/
- Lu, J. , Cai, J. , Ren, T. , Wu, J. , Mao, D. , Li, W. , Zhang, Y. , Piao, J. , Wang, J. , Yang, L. , Yang, X. , & Ma, Y. (2019). Physiological requirements for iron in women of reproductive age assessed by the stable isotope tracer technique. Nutrition & Metabolism, 16, 55. 10.1186/s12986-019-0384-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mansour, D. , Hofmann, A. , & Gemzell‐Danielsson, K. (2021). A review of clinical guidelines on the management of iron deficiency and Iron‐Deficiency anemia in women with heavy menstrual bleeding. Advances in Therapy, 38(1), 201–225. 10.1007/s12325-020-01564-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- Means, R. T. (2020). Iron deficiency and iron deficiency anemia: Implications and impact in pregnancy, fetal development, and early childhood parameters. Nutrients, 12(2), 447. 10.3390/nu12020447 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller, J. L. (2013). Iron deficiency anemia: A common and curable disease. Cold Spring Harbor Perspectives in Medicine, 3(7), a011866. 10.1101/cshperspect.a011866 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milman, N. T. (2019). Dietary iron intake in women of reproductive age in Europe: A review of 49 studies from 29 countries in the period 1993‐2015. Journal of Nutrition and Metabolism, 2019, 1–13. 10.1155/2019/7631306 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mirkovic, K. R. , Perrine, C. G. , Subedi, G. R. , Mebrahtu, S. , Dahal, P. , Staatz, C. , & Jefferds, M. E. D. (2016). Predictors of micronutrient powder intake adherence in a pilot programme in Nepal. Public Health Nutrition, 19(10), 1768–1776. 10.1017/S1368980015003572 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mirza, F. G. , Abdul‐Kadir, R. , Breymann, C. , Fraser, I. S. , & Taher, A. (2018). Impact and management of iron deficiency and iron deficiency anemia in women's health. Expert Review of Hematology, 11(9), 727–736. 10.1080/17474086.2018.1502081 [DOI] [PubMed] [Google Scholar]
- Munoz, A. M. , & King, S. C. (Eds.). (2007). International consumer product testing across cultures and countries. ASTM MNL 55 International. [Google Scholar]
- Nathan, R. (1999). Regulation of Fortified Foods to Address Micronutrient Malnutrition: Legislation, Regulations and Enforcement (Third). [Google Scholar]
- Nguyen, M. , & Tadi, P. Iron Supplementation . 2021. https://www.ncbi.nlm.nih.gov/books/NBK557376/ [PubMed]
- Ojukwu, J. U. , Okebe, J. U. , Yahav, D. , & Paul, M. (2009). Oral iron supplementation for preventing or treating anaemia among children in malaria‐endemic areas. Cochrane Database of Systematic Reviews, 2(2), CD006589. https://doi.org/10.1002/14651858.CD006589.pub3 [DOI] [PubMed] [Google Scholar]
- Olson, R. , Gavin‐Smith, B. , Ferraboschi, C. , & Kraemer, K. (2021). Food fortification: The advantages, disadvantages and lessons from. Nutrients, 13(4), 1118. 10.3390/nu13041118 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peña‐Rosas, J. P. , De‐Regil, L. M. , Garcia‐Casal, M. N. , & Dowswell, T. (2015). Daily oral iron supplementation during pregnancy. Cochrane Database of Systematic Reviews, 2015, CD004736. 10.1002/14651858.CD004736.pub5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pereira, D. I. , Couto Irving, S. S. , Lomer, M. C. , & Powell, J. J. (2014). A rapid, simple questionnaire to assess gastrointestinal symptoms after oral ferrous sulphate supplementation. BMC Gastroenterology, 14, 103. 10.1186/1471-230X-14-103 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Petry, N. , Olofin, I. , Hurrell, R. , Boy, E. , Wirth, J. , Moursi, M. , Donahue Angel, M. , & Rohner, F. (2016). The proportion of anemia associated with iron deficiency in low, medium, and high human development index countries: A systematic analysis of national surveys. Nutrients, 8(11), 693. 10.3390/nu8110693 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Preedy, V.R. , Srirajaskanthan, R. , Patel, V. B. , Preedy, V. R. S. , Rajaventhan, & Patel, V. B. (Eds.). (2013). Handbook of food fortification and health (Vol. 2013, 1 ed., p. 400). Human Press Springer Science+Business Media New York. https://link.springer.com/book/10.1007/978-1-4614-7076-2#bibliographic-information [Google Scholar]
- Ranganathan, P. , Pramesh, C. , & Aggarwal, R. (2016). Common pitfalls in statistical analysis: Intention‐to‐treat versus per‐protocol analysis. Perspectives in Clinical Research, 7(3), 144–146. 10.4103/2229-3485.184823 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richins, A. T. , Burton, K. E. , Pahulu, H. F. , Jefferies, L. , & Dunn, M. L. (2008). Effect of iron source on color and appearance of Micronutrient‐Fortified corn flour tortillas. Cereal Chemistry, 85(4), 561–565. 10.1094/CCHEM-85-4-0561 [DOI] [Google Scholar]
- Sandstead, H. H. (2000). Causes of iron and zinc deficiencies and their effects on brain. The Journal of Nutrition, 130(2), 347S–349S. 10.1093/jn/130.2.347S [DOI] [PubMed] [Google Scholar]
- Siddique, A. , & Park, Y. W. (2019). Effect of iron fortification on microstructural, textural, and sensory characteristics of caprine milk cheddar cheeses under different storage treatments. Journal of Dairy Science, 102(4), 2890–2902. 10.3168/jds.2018-15427 [DOI] [PubMed] [Google Scholar]
- Singh‐Ackbarali, D. , & Maharaj, R. (2014). Sensory evaluation as a tool in determining acceptability of innovative products developed by undergraduate students in food science and technology at the university of Trinidad and Tobago. Journal of Curriculum and Teaching, 3(1), 10–18. 10.5430/jct.v3n1p10 [DOI] [Google Scholar]
- Souza, A. I. , Batista Filho, M. , Bresani, C. C. , Ferreira, L. O. C. , & Figueiroa, J. N. (2009). Adherence and side effects of three ferrous sulfate treatment regimens on anemic pregnant women in clinical trials. Cadernos de Saúde Pública, 25(6), 1225–1233. 10.1590/s0102-311x2009000600005 [DOI] [PubMed] [Google Scholar]
- Stoffel, N. U. , von Siebenthal, H. K. , Moretti, D. , & Zimmermann, M. B. (2020). Oral iron supplementation in iron‐deficient women: How much and how often? Molecular Aspects of Medicine, 75, 100865. 10.1016/j.mam.2020.100865 [DOI] [PubMed] [Google Scholar]
- SUSTAIN . (2001). Guidelines for iron fortification of cereal food staples. https://www.yumpu.com/en/document/view/13268018/sustain-guidelines-for-iron-fortification-of-cereal-food-idpasorg/2
- Sutrisna, A. , Vossenaar, M. , Izwardy, D. , & Tumilowicz, A. (2017). Sensory evaluation of foods with added micronutrient powder (MNP) ‘taburia’ to assess acceptability among children aged 6–24 months and their caregivers in Indonesia. Nutrients, 9(9), 979. 10.3390/nu9090979 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Swain, J. H. , Johnson, L. K. , & Hunt, J. R. (2007). Electrolytic iron or ferrous sulfate increase body iron in women with moderate to low iron stores. The Journal of Nutrition, 137(3), 620–627. 10.1093/jn/137.3.620 [DOI] [PubMed] [Google Scholar]
- Swareldhab, E. S. , Al‐Jawaldeh, A. , Qureshi, A. B. , Ali, A. M. E. , Abu‐Manga, M. , Al‐Areeqi, M. , & Dureab, F. (2021). Assessment of micronutrient situation among Reproductive‐Age women (15‐49) and Under‐Five children in Sudan. Nutrients, 13(8), 2784. 10.3390/nu13082784 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Theuer, R. C. (2008). Iron‐Fortified infant cereals. Food Reviews International, 24(3), 277–310. 10.1080/87559120801926260 [DOI] [Google Scholar]
- Turawa, E. , Awotiwon, O. , Dhansay, M. A. , Cois, A. , Labadarios, D. , Bradshaw, D. , & Pillay‐van Wyk, V. (2021). Prevalence of anaemia, iron deficiency, and iron deficiency anaemia in women of reproductive age and children under 5 years of age in South Africa (1997‐2021): A systematic review. International Journal of Environmental Research and Public Health, 18(23), 12799. 10.3390/ijerph182312799 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vatandoust, A. , & Diosady, L. (2022). Iron compounds and their organoleptic properties in salt fortification with iron and iodine: An overview. Current Opinion in Food Science, 43, 232–236. 10.1016/j.cofs.2021.12.007 [DOI] [Google Scholar]
- Vecchiato, D. , Torquati, B. , Venanzi, S. , & Tempesta, T. (Sep 1s5 2021). The role of sensory perception in consumer demand for tinned meat: A contingent valuation study. Foods, 10(9), 2185. 10.3390/foods10092185 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waller, A. W. , Andrade, J. E. , & Mejia, L. A. (2020). Performance factors influencing efficacy and effectiveness of iron fortification programs of condiments for improving anemia prevalence and iron status in populations: A systematic review. Nutrients, 12(2), 275. 10.3390/nu12020275 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang, G. , Chen, Y. , Xia, Y. , Song, X. , & Ai, L. (2022). Characteristics of probiotic preparations and their applications. Foods, 11, 2472. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wessels, I. , Maywald, M. , & Rink, L. (2017). Zinc as a gatekeeper of immune function. Nutrients, 9(12), 1286. 10.3390/nu9121286 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Whitney, R. , Centrone, W. A. , Mamani, H. S. , Falkenstein, K. , Levine, R. S. , Harris, J. , Hazlitt, M. , & Lim, C. A. (2021). Impact of a collaborative childhood anaemia intervention programme in Peru. Tropical Medicine & International Health, 26(6), 680–686. 10.1111/tmi.13564 [DOI] [PubMed] [Google Scholar]
- WHO . (2006). PART III ‐ Fortificants: Physical characteristics, selection and use with specific food vehicles (p. 42). World Health Organization. https://cdn.who.int/media/docs/default-source/micronutrients/gff-part-3-en.pdf?sfvrsn=620a179c_2 [Google Scholar]
- Wichchukit, S. , & O'Mahony, M. (2015). The 9‐point hedonic scale and hedonic ranking in food science: Some reappraisals and alternatives. Journal of the Science of Food and Agriculture, 95(11), 2167–2178. 10.1002/jsfa.6993 [DOI] [PubMed] [Google Scholar]
- Wirth, J. , Rajabov, T. , Petry, N. , Woodruff, B. , Shafique, N. , Mustafa, R. , Tyler, V. , & Rohner, F. (2018). Micronutrient deficiencies, over‐ and undernutrition, and their contribution to anemia in Azerbaijani preschool children and non‐pregnant women of reproductive age. Nutrients, 10(10), 1483. 10.3390/nu10101483 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ziegler, E. E. , Fomon, S. J. , Nelson, S. E. , Jeter, J. M. , & Theuer, R. C. (2011). Dry cereals fortified with electrolytic iron or ferrous fumarate are equally effective in breast‐fed infants. The Journal of Nutrition, 141(2), 243–248. 10.3945/jn.110.127266 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The findings of this study are supported by data that can be obtained upon request from the corresponding author. Data are not publicly available due to privacy restrictions.
