1. Introduction
Globally, maize (
Zea mays, L.), also known as corn, contributes significantly to human and animal diets and thus plays a pivotal role in food security [
1]. Food security is defined as a situation that exists when all people, at all times, have physical, social, and economic access to sufficient, safe, and nutritious food that meets their dietary needs and food preferences for an active and healthy life [
2]. Therefore, household food security exists when food is available, accessible, and affordable to households [
3]. However, household food insecurity is the leading cause of malnutrition and is directly or indirectly caused by inadequate food consumption and poor diet quality [
4].
Consuming a consistently diversified diet poses a challenge, as most African populations consume monotonous starchy staples coupled with a limited intake of animal products, fruit, and vegetables [
5]. A diversified diet consists of protein sources, such as beans, peas, fish, meat, and milk, as well as fruits and vegetables, which are abundant in vitamins and minerals, along with carbohydrates from cereals, which can effectively mitigate the challenges associated with malnutrition [
6]. Bouis (2003) emphasised that addressing malnutrition involves consuming non-staple foods, particularly animal products, which are abundant in bioavailable micronutrients [
7]. However, due to financial constraints, many households in developing countries need help to consume a nutritionally balanced diet [
7]. Lower-income groups are especially susceptible to malnutrition-related diseases and deaths due to the inaccessibility of affordable, nutrient-dense foods [
8]. Drammeh et al. (2019) further indicate that inadequate nutrition can impair physical and mental development and reduce productivity among children under the age of five and throughout their lives [
4].
South Africa is generally considered food secure because when the agricultural sector cannot produce sufficient staple crops, they can be imported [
9]. However, researchers believe that this is not true at the household level [
10,
11]. Inequality faced by South African citizens due to Apartheid has resulted in high levels of unemployment and poverty among non-white South Africans. Adverse conditions existed throughout the regime, from its inception (1948) to its eventual dismantling in 1994 [
12]. Inequality persists in South Africa, and according to StatsSA (2021), approximately 20% of South African households had inadequate access to food in 2017, and more black and coloured households face food insecurity when compared to white households [
13].
And yet, South Africa is well known for its reputable maize production. Approximately eight million tonnes of maize grain are produced annually in South Africa, with the Free State, North West, Mpumalanga, and KwaZulu-Natal being the major maize-producing provinces. Collectively, these provinces account for about 83% of the total national production of maize [
13]. It serves as a staple for most of the population and is a significant component of animal feed [
13]. Maize and maize-based products are consumed by approximately 67% to 83% of the population. The daily consumption averages between 476 g and 690 g per person [
14].
Thus, the significance of maize in the food industry cannot be understated, as maize meal products are consumed almost exclusively as pap (gruel cooked from maize meal and water) [
15]. Govender (2014) identified the consumption of pap as a significant problem, as it does not provide enough nutrients to nourish the body [
16]. Many people highly prefer to consume pap, particularly in lower-income and rural communities [
17]. This predominant reliance on maize and maize-based dishes (pap) without diversification in the diet exaggerates the issues of food and nutrition insecurity [
6]. Diets often need to be more balanced in the supply of essential nutrients [
6]. Maize is very high in carbohydrates but lacks several essential nutrients, such as the amino acids tryptophan and lysine [
18].
It is also partly due to the presence of resistant starch phytate in maize, which acts as an anti-nutritional factor by binding to essential nutrients present in maize, consequently hindering the availability for digestion and absorption in the body [
19]. Furthermore, conventional processing techniques involve the removal of the pericarp and germ, leading to the loss of critical nutrients, such as fibre, lipids, minerals, vitamins, and essential amino acids [
20].
Given the difficulties in achieving a diversified diet among most populations in developing countries, countries such as South Africa, Zimbabwe, Nigeria, Malawi, Uganda, and Kenya have implemented mandatory food fortification. These countries fortify essential commodities, such as salt, bread, maize meal, wheat flour, and infant formulas with various vitamins and minerals [
21]. However, food fortification presents its own set of limitations, such as mineral toxicity, due to inefficient monitoring systems by processors [
21,
22]. In addition, extra costs are incurred by the processor, which are included in the price of the final product [
23]. Therefore, fortified foods are more costly than unfortified foods. Furthermore, relying on fortified foods to address nutrient deficiencies has limited coverage in rural areas, as most rural populations depend on home-based food products that are not fortified [
22]. Despite government efforts, South Africa was listed as one of the 20 countries with severe child food poverty, meaning that children are fed only two or fewer food groups per day [
24].
There is a need for cost-effective alternative processing techniques for maize that can improve the nutrient composition of maize-based products, particularly considering their reliance on this staple food. An old but practical approach to processing maize that has the potential to increase its nutritional value without specialised equipment is nixtamalisation, which is a traditional processing technique used in Mexico, but not widely recognised in Africa [
25].
Nixtamalisation is not only a well-known industrial processing method but can be practised by any consumer who has access to whole-dried maize kernels and basic kitchen utensils. It is a process that could play an important role in decreasing food insecurity and malnutrition in poorer rural communities [
26].
The nixtamalisation process involves cooking maize kernels in an alkaline-aqueous solution of calcium hydroxide (slaked lime), followed by soaking for between eight and 24 h. After that, the soaked kernels are thoroughly rinsed to remove pericarp and residual alkali, known as nejayote [
27]. After rinsing, maize is called nixtamal, which can be ground to form a pliable dough, known as masa, or dried and ground into maize meal or flour [
28]. The process has many nutritional benefits that the maize kernel lacks, such as increased niacin bioavailability, which decreases the risk of pellagra; higher calcium intake as a result of the steeping process with calcium hydroxide; increased dietary fibre by elevating the content of resistant starch; a significant reduction in mycotoxin levels; and diminished levels of phytic acid, which inhibits the bioavailability of calcium, iron, and zinc [
29,
30]. Additionally, nixtamalisation increases the essential amino acids lysine and tryptophane [
31]. Therefore, combining this method with conventional processing techniques in Africa increases the nutrient content and reduces mycotoxin contamination, which is still a serious concern and poses a barrier to achieving food and nutrition security [
25,
32,
33].
It is unclear why nixtamalisation as a food processing technique has not been introduced in South Africa when it holds so many advantages for the consumer. It is widely known that maize is often grown in backyards and community plots as part of or in addition to vegetable gardens. Using nixtamalisation, home-grown dried whole maize kernels could be converted into safe and delicious meals in homes using basic equipment, as it is widely and effectively practised in Mexico by rural women [
34].
However, it needs to be determined if consumers would accept nixtamalised maize products that could be produced from home-grown whole-dried maize kernels and if the nutritional value would be comparable to commercial products. The aim of this study was to develop a consumer-acceptable nixtamalised maize product by employing consumer-led methods that could be produced in a household kitchen from whole-dried maize kernels.
To achieve this goal, nixtamalised maize was used to develop three well known and traditionally accepted products: vegetarian nixtamalised maize-based nuggets, burgers, and chips. To involve consumers in product development, consumer panels participated in sensory evaluations using the overall acceptability (hedonic scaling) and just-about-right (JAR) scales. Using a rigorous approach, the products were tested against similar products to provide reference products for comparison [
35]. The best product was developed further and reformulated to achieve a commercial quality product that could be produced at home using dried maize kernels.
A survey was conducted to assess the acceptability of the four attributes (appearance, aroma, taste, and texture) as well as the willingness to repeat consumption, purchase, and recommend the products. The last section included questions to assess the conditions under which nixtamalised products would be consumed and purchased. Lastly, the nutrient content was determined and compared to the nutrient content of similar products.
2. Materials and Methods
2.1. Sample Preparation
The maize used in this study was received as dry white maize kernels from a farm near the small town of Hoopstad in the Lejweleputswa district of the Free State Province. The kernels were stored in airtight containers in a refrigerator at 4 °C in the Food Laboratory at the University of the Free State (UFS), Bloemfontein. White maize is the most commonly cultivated maize for human consumption in South Africa [
36].
2.2. Description of Products
Nuggets are battered and breaded products that are popular in American fast-food restaurants. The most common nugget type is chicken nuggets, which are chicken breasts coated in a batter, rolled in breadcrumbs and fried in oil until cooked through [
37]. As products are benchmarked against similar products in sensory testing, the maize nugget was tested in combination with two other vegetarian nuggets: chickpea [
38] and potato [
39].
Characteristically, burgers are meat products made from ground beef that may or may not contain additional ingredients [
40]. The vegetarian maize burger was benchmarked using two vegetarian burger samples: a black bean [
41] and a chickpea [
42].
Chips (crisps) are thin slices of potatoes that are deep-fried until they are crunchy and flavoured with seasoning. These chips are commonly eaten as snacks [
43]. Additionally, a wide variety of chips are available in the market. The benefits of chips produced from maize instead of potatoes are the vitamin and mineral contents. However, three maize chip samples were tested and formulated similarly using different cooking methods: one sample was deep-fried in oil, and two samples were air-fried at different temperatures and intervals. The chips were deep-fried because of the distinctive taste and texture qualities they impart to fried food [
44]. However, deep-fried foods often contain high-fat content, comprising almost as much as 35–44% of the total product by weight [
45]. Hence, the two samples were air-fried to provide a healthier option for health-conscious consumers. Air frying uses hot air to cook food, eliminating the need for excessive amounts of oil [
46]. Consumers are becoming increasingly aware of the advantages of low-fat and fat-free products that do not require deep-frying [
45]. This cooking method results in a reduced fat content of up to 80%, providing a healthier option for health-conscious consumers who still want to enjoy snack food [
47]. It was further noted that lower oil content, such as crust formation, palatability, and appearance, may influence many sensory properties [
45].
2.3. Nixtamalisation
The traditional nixtamalisation process was employed in this study since it is a simple and economical method practised in a home kitchen using basic kitchen equipment. Dry maize kernels were used as they are a very economical product that households can easily access.
Nixtamalisation was carried out in a 7-step process [
33,
48,
49]. The ingredients used were six cups (1080 g) of whole dry maize kernels, 4.5 litres of water, and 4.5 teaspoons (10.4 g) of slaked lime. The ingredients were added to a stainless-steel pot and brought to a boil for 10 min until the pericarp loosened. After that, the maize kernels were left to soak overnight. The following day, the maize kernels were rubbed between gloved hands to remove the pericarp. The maize was transferred to a colander and rinsed under cold running water until the water was clear. The maize is now called nixtamal. The nixtamal was placed in a Kenwood Everyday Food Processor (FDP03.A0W) and finely ground to produce masa. The masa was spread evenly on baking sheets, lined with baking paper, and placed in an oven set at 100 °C, with the door slightly open, for 120 min. After that, the dried masa was then ground into a fine powder in a Nutribullet 600 W High-Speed Blender. The fine powder was sieved (0.8 mm) to remove unrefined particles. This process resulted in the production of masa flour. One cup (250 mL) of masa flour weighed an average of 165 g. This masa flour was used in the formulation of all the products.
To summarise, maize nuggets were evaluated with potato and chickpea nuggets, maize burgers with black bean and chickpea burgers, and maize chips were prepared in three ways (air-fried 1, air-fried two, and deep-fried). The formulations of the nixtamalised maize-based nuggets, burgers, original chips, and flavoured chips are regarded as the intellectual property of the UFS and are, therefore, not published.
2.4. Population Sampling and Panel Description
The target population was consumers; thus, naïve consumers who participated in the sensory evaluations were students and staff between 18 and 65 years of age from the University of the Free State on the Bloemfontein campus. The demographics of the four panels are shown in
Table 1. It was affective testing that took place in the institution’s sensory laboratory, in a central location (CLT). Posters that advertised the tasting panel were designed to recruit consumers who regularly ate maize. The panels comprised volunteers who completed a consent form containing information on the study’s purpose and details concerning potential product allergens. Participation was anonymous, and no one with related food allergies was part of the study.
Four sensory panels were conducted [panel 1: nuggets,
n = 79 (65 women and 14 men); panel 2: burgers,
n = 83 (69 women and 14 men); panel 3: chips,
n = 74 (61 women and 13 men); and panel 4: flavoured chips,
n = 99 (83 women, 14 men, and two others). Before each panel, the panellists were trained to rank products using the overall liking and JAR method. The nuggets and burgers were prepared two hours before sensory tasting. Before transferring to the tasting trays, all samples were cut into 3 cm × 3 cm cubes and served warm in small tasting bowls covered with aluminium foil. For the chip panels, the chips were prepared a maximum of five days ahead, and three chips measuring 4 cm in diameter were used at each tasting. The panellists could not identify the samples as they were three-digit numerical codes. The samples were served on a white polystyrene tray under white light to each panel member seated in individual sensory booths, with no means to identify the samples. Room temperature water, ranging from 20 to 22 °C, was provided to cleanse the pallet between each sample [
50] and a spitting cup for the less-than-satisfactory samples. The respondents received a small reward for participating in the study.
2.5. Sensory Analysis
2.5.1. Consumer Liking Rating (Hedonic Evaluation)
Firstly, the products were evaluated using a consumer liking rating using the overall liking 9-point hedonic scale [
51]. The most widely used scale for measuring food acceptability is the overall liking, a nine-point hedonic scale. It was administered at the same time as the JAR scaling task. The nine-point hedonic scale used in the consumer’s overall liking task consists of nine categories: 1 (dislike extremely), 2 (dislike very much), 3 (dislike moderately), 4 (dislike slightly), 5 (neither like nor dislike), 6 (like slightly), 7 (like moderately), 8 (like very much), and 9 (like extremely). The panellists were asked to taste the sample and rank it on a nine-point scale by marking one of the categories [
52].
2.5.2. Just-about-Right Evaluation
Secondly, the panellists were expected to complete the JAR scales, as shown in
Table 2, for four attributes, namely aroma, appearance, taste, and mouthfeel [
52]. The JAR scale is a bipolar assessment with two opposite reference points labelled “not enough” and “too much”, while the midpoint is labelled “just-about-right” (JAR), which the respondents used to rate the samples on the five-point scale [
53]. The respondents were asked to tick a box on a five-point JAR scale on a ballot sheet (much too low, somewhat not enough, just-about-right, somewhat too much, and much too high). Each sample was evaluated for four attributes: appearance, aroma, mouthfeel, and taste. The analysis of the JAR scales treats all attributes as independent of one another. It is possible for the adaptation of one attribute to have a positive effect on other attributes, thereby eliminating the need to make changes to all attributes [
54]. The JAR scale results in the study were obtained by counting the number of panel members who selected each category and calculating the corresponding percentage for each category. The scores for “much too low” and “somewhat too low” were combined and denoted “not enough”. Similarly, scores for “somewhat too high” and “much too high”) were combined and denoted “too much” [
55]. The scores were combined to streamline the results; instead of displaying five results for the JAR scale, only three were presented [
55]. The benchmark for good performance was set at 75% JAR for each attribute [
35].
2.5.3. Penalty Analysis
Data from JAR and consumers’ overall liking tasks were needed to determine the penalty analysis [
56]. The penalty shows the link between the results of the consumers’ liking scores and the JAR scores. It indicates that respondents who were unsatisfied with the JAR test were also unsatisfied with the consumer’s overall liking task and vice versa [
56]. It identifies an improvement opportunity that may bring the product closer to the ideal and shows the strength of prioritising improvement among attributes [
35]. Penalty analysis is inconsequential (N/A) when the non-JAR score is less than 20.0, therefore indicating that less than 20% of respondents scored the attribute “not enough” or “too much” [
35]. The penalty analysis has two results that give the product developer an indication of the attributes that have the greatest potential and could be improved. The mean drop is a measure of the impact of the “not enough” and “too much” scores (thus, each attribute has two mean drop penalties). The higher the mean drop, the greater the negative effect and 1.0 was considered the threshold. The penalty value also accounts for the number of respondents who gave the same score. It is used to determine whether changing a particular attribute through reformulation would impact the ranking of the attribute. An upper benchmark of 1.0 for the penalty was set as a threshold before an attribute should be improved or reformulation is necessary. The
p-value for the penalty is calculated using ANOVA. It compares the JAR level’s mean with that of the other levels’ mean. This is equivalent to testing whether the penalty is significantly different from 0 or not.
2.6. Survey
After evaluating the products, the panel members were asked to complete a survey. It was requested that panel members complete the questionnaire only once. Thus, the questionnaire was never completed more than once by the same panel members, even though the same panel members might have taken part in more than one panel (n = 186) (145 women, 32 men, one other, and 8 chose not to disclose gender).
The questionnaire was designed to conduct exploratory quantitative research. The respondents were asked to respond in terms of their overall perception of nixtamalised maize products rather than for one specific product. Each respondent was allocated 15 min to taste the products before completing the questionnaire, which took approximately five minutes.
Section one of the questionnaire contained questions to determine the demographic profile of the respondents regarding age and gender. Section two included questions to assess the acceptability of the four attributes (appearance, aroma, taste, and texture) and questions to determine the willingness to repeat consumption, purchase, and recommendation of the products. The last section included questions to assess the conditions under which nixtamalised products would be consumed and purchased.
All internal consistency estimates, as determined by Cronbach’s alpha coefficient, exceeded 0.80, rendering the data reliable, and confirming that the individual items of a construct were consistently measured within the same construct or concept.
2.7. Determination of the Nutrient Content
As the chutney-flavoured chips were considered the most successful product, three batches were produced, analysed (in triplicate) for nutrient content, and compared to two commercial maize chips. The gross energy values of the chip were measured in megajoules (MJ) using a bomb calorimeter and converted to kJ/100 g [
57].
2.7.1. Determination of the Crude Protein Content
For crude protein determination, the Dumas method of combustion (ASM 056) [
58] with a LECO FP 2000 machine (LECO Corporation, St. Joseph, MI, USA) was utilised [
59]. The analysis was carried out by weighing 1 g of oven-dried sample and placing it directly into a reusable boat, which was then placed in the purge chamber of a horizontal furnace. The sample was combusted in the presence of oxygen at a temperature of 950 °C to determine its nitrogen content. The crude protein of the chips (g/100 g DM) was calculated by multiplying the nitrogen content (g/100 g DM) by a factor of 6.25 [
60].
2.7.2. Determination of the Fibre Content
The acid detergent fibre (ADF) method (ASM 059) was used to determine the fibre content present in the chips [
58,
61]. It involved dissolving 20 g N-cetyl-N, N, N-trimethyl ammonium bromide (C19H42BrN) in 1 litre (L) 1 N sulphuric acid (28 mL 98% sulphuric acid filled up to 1 L with distilled water) in glass pill vials. It was dried overnight in an oven at 100 °C for 24 h, placed in a desiccator for 30 min to reach room temperature, placed in a hot extraction unit, and cooled in a condenser. One hundred millilitres of acid detergent solution (ADS) was added to the samples and then heated on an element for 60 min. The samples were filtered, washed three times with hot distilled water, and rinsed twice with acetone. Afterwards, the samples were oven-dried overnight at 100 °C and cooled in a desiccator for 30 min. Afterwards, the samples were placed in a muffle furnace at 550 °C for four hours and then cooled for 30 min. The remaining ash was used to determine the fibre content [
61].
The neural detergent fibre (NDF) was determined by the procedure outlined by Van Soest, Robertson and Lewis (1991) [
62]. The sample preparation and analysis involved multiple steps, including oven drying at 55 °C, grinding, and 0.5 g of the sample placed in a 600 mL Berzelius beaker. Approximately 45 mL of NDF solution was added to a digestion burette and heated. The sample was mixed and then weighed into a plastic weigh pan. After gentle boiling, the sample was poured into a burette and refluxing was continued for 60 min. Afterwards, 2 mL of amylase solution was added, and the burette sides were rinsed. Glass crucibles were hotly weighed before filtration, and the samples were filtered using a vacuum. Acetone was added, and the samples were rinsed before being placed in a 105 °C oven overnight. The samples were weighed using crucibles the following day.
2.7.3. Determination of the Fat Content
Total lipids from the maize chips were quantitatively extracted [
63] using chloroform and methanol in a ratio of 2:1. An antioxidant, butylated hydroxytoluene, was added at a concentration of 0.001% to the chloroform−methanol mixture. A rotary evaporator dried the fat extracts under vacuum overnight at 50 °C using phosphorus pentoxide as a moisture adsorbent. Total extractable fat was determined gravimetrically from the extracted fat and expressed as percentage fat (
w/
w) per 100 g of the samples. The fat extracted from the maize chips was stored in a polytope (glass vial, with a push-in top) under a nitrogen blanket and frozen at −20 °C, pending the fatty acid analyses.
A lipid aliquot (25 mg) was transferred to a Teflon-lined screw-top test tube using a disposable glass Pasteur pipette to analyse the fatty acids. Fatty acids (FAs) were trans-esterified to form methyl esters, using 0.5 N sodium hydroxide in methanol and 14% boron trifluoride in methanol [
64]. Analysis was performed using an initial isothermic period (40 °C for 2 min). After that, the temperature was increased from 4 °C/min to 230 °C. Finally, an isothermic period of 230 °C for 10 min followed. Fatty acid methyl ester (FAME) n-hexane (1 μL) was injected into the column using a Varian CP 8400 Autosampler. The injection port and detector were both maintained at 250 °C. Hydrogen, at 45 pounds per square inch (psi), functioned as the carrier gas, while nitrogen was employed as the makeup gas. Galaxy Chromatography Software (Galaxie CDS) was used to record the chromatograms.
Fatty acid methyl ester samples were identified by comparing the retention times of FAME peaks from the samples with those of standards obtained from Supelco (Supelco 37 Component Fame Mix 47885-U; Sigma-Aldrich Aston Manor, Pretoria, South Africa). All other reagents and solvents were of analytical grade and were obtained from Merck Chemicals (Pty Ltd., Halfway House, Johannesburg, South Africa). Fatty acids were expressed as a percentage of the total of all FAs present in the sample. The saturated fatty acid (SFA) percentage of the two commercialised chips was calculated as follows:
The following FA combinations were calculated: omega-3 (n-3) FAs, omega-6 (n-6) FAs, total SFAs, total monounsaturated fatty acids (MUFAs), polyunsaturated fatty acids (PUFAs), PUFA/SFA ratio (P/S), and n-6/n-3 ratio.
2.7.4. Determination of the Mineral Content
A spectroscopic analysis of the chips’ mineral content was conducted using atomic absorption flame spectroscopy for calcium and magnesium [
48,
65] and flame emission spectroscopy for sodium and potassium [
66]. Firstly, the calcium and magnesium contents of the samples were determined by the dry ashing AOAC method 927.02. The remaining calcium and magnesium quantities were analysed using a double-beam atomic absorption spectrometer, specifically the Analyst 300 Perkin Elmer model. A calcium standard with a concentration of 1000 parts per million (ppm) was used to generate a calibration curve. The spectrometer was operated with 12 psi of dry air and 70 psi of acetylene, using a 422.7 nanometer (nm) flame, a ten milliampere (mA) lamp current, and a 0.7 nm slit width. The average of the calcium and magnesium contents were recorded for each sample.
Secondly, flame emission spectroscopy for sodium and potassium was conducted by preparing standard sodium and potassium solutions using their respective salts. These solutions were then aspirated into a flame, atomised, and excited by the flame’s heat. The excited atoms emitted characteristic wavelengths of light, which were measured by a detector and converted into a signal. The intensity of the signal was proportional to the concentration of the element in the sample. Calibration curves were constructed using standard solutions of known concentrations, and the concentrations of sodium and potassium in the samples were determined by comparison with the calibration curves. The intensity of the light emitted by the flame was measured and used to determine the concentrations of sodium and potassium in the sample.
Lastly, phosphorus was examined using the AOAC method 931.01 [
67]. This involved burning 1-g samples in porcelain crucibles for 6 h at 500 °C in a Carbolite C.E. furnace and then dissolving the ash in 100 mL volumetric flasks with distilled deionised water and a small amount of concentrated hydrochloric acid. The amount of phosphorus in the solution was determined using colorimetric measurements with a Spectronic 20 instrument (Milton Roy Co., Cambridge, UK).
2.8. Statistical Analysis
The sensory and nutrient data were analysed using ‘R’, R libraries—Performance Analytics for correlations, and an Excel add-on: Sensory Analysis with XLSTAT [
68].
An analysis of variance (ANOVA) was utilised to examine whether there were any differences in means among the different samples. The Tukey-HSD post-hoc test was employed to identify specific significant differences between the samples, and these differences were then denoted in the tables using superscripts.
The survey data were captured on the EvaSys© V8.2 software and imported into the XLSTAT sensory analysis package for Excel (Microsoft 365) [
68]. The frequencies of each question and their possible answers were calculated. Furthermore, the data was analysed descriptively using the SPSS (Statistical Package for the Social Sciences) version 28 package. A reliability analysis was performed by calculating Cronbach’s alpha for the questionnaire.
4. Conclusions
An acceptable, nutritious, and consumer-acceptable nixtamalised maize-based product was developed by employing consumer-led methods that could be produced in a home-based environment. It received favourable sensory evaluations, and panel members were willing to consume, purchase, and prepare them.
A number of limitations have to be considered. The products were unique, and the formulations could not be published; the panels comprised a limited number of consumers (less than 100) due to limited space. The panel members were screened for being regular users of maize products and pre-trained to perform the tasks satisfactorily. However, other populations may respond differently, and the results cannot be widely applied.
Although the current study shows encouraging results, the researcher recommends that further research on a larger scale is warranted. Further studies are required to fully elucidate the potential impact of nixtamalisation on the nutritional value of maize products and to assess the feasibility of entrepreneurial action and scaling up nixtamalisation processes for commercial production.
Undoubtedly, the potential impact of this study on the future prospects of maize and maize products in South Africa cannot be overstated, particularly with respect to addressing food security and malnutrition among low-income populations. Given these factors, the current research presents a significant milestone in achieving the full potential of nixtamalisation as a means of adding value to maize-based products in South Africa.