Abstract
Micronutrient deficiency is an important cause of growth stunting. To avoid micronutrient deficiency, the World Health Organization recommends complementary feeding with animal‐source foods. However, animal‐source foods are not readily available in many parts of the Democratic Republic of Congo (DRC). In such areas, caterpillars are a staple in adult diets and may be suitable for complementary feeding for infants and young children. We developed a cereal made from dried caterpillars and other locally available ingredients (ground corn, palm oil, sugar and salt), measured its macro‐ and micronutrient contents and evaluated for microbiologic contamination. Maternal and infant acceptability was evaluated among 20 mothers and their 8–10‐month‐old infants. Mothers were instructed in the preparation of the cereal and asked to evaluate the cereal in five domains using a Likert scale. Mothers fed their infants a 30‐g portion daily for 1 week. Infant acceptability was based on cereal consumption and the occurrence of adverse events. The caterpillar cereal contained 132 kcal, 6.9‐g protein, 3.8‐mg iron and 3.8‐mg zinc per 30 g and was free from microbiologic contamination. Mothers’ median ratings for cereal characteristics were (5 = like very much): overall impression = 4, taste = 5, smell = 4, texture = 4, colour = 5, and consistency = 4. All infants consumed more than 75% of the daily portions, with five infants consuming 100%. No serious adverse events were reported. We conclude that a cereal made from locally available caterpillars has appropriate macro‐ and micronutrient contents for complementary feeding, and is acceptable to mothers and infants in the DRC.
Keywords: complementary feeding, micronutrient malnutrition, growth, stunting, international child health nutrition, low‐income countries
Introduction
In children under 5 years of age, malnutrition is responsible for 2.1 million deaths annually and 91 million disability‐adjusted life years (Black et al. 2008). Growth stunting, defined as height‐for‐age Z‐score two standard deviations or more below appropriate World Health Organization (WHO) standards, is a consequence of long‐term malnutrition and has been associated with multiple negative health outcomes, including increased mortality, poor cognitive and school performance, delayed motor development, impaired physical performance, reduced income in adulthood, lower birthweight in offspring and maternal complications during pregnancy (Barker et al. 2005; Phuka et al. 2009). If stunting from malnutrition is not reversed by the age of 2 years, the adverse effects are likely to be permanent (Dewey & Adu‐Afarwuah 2008). The prevalence of stunting varies around the globe, but low‐income countries (LICs) are disproportionately affected. In the Democratic Republic of Congo (DRC), the stunting prevalence in children under 5 years of age is 46% (DHS 2007).
Children from 3 to 36 months are particularly vulnerable to insults affecting linear growth, especially after the period of exclusive breastfeeding when complementary foods are introduced into the diet (Frongillo 1999). Malnutrition from inadequate complementary feeding is a serious problem in many LICs where complementary foods consist of starch‐based cereals or gruel that may provide sufficient energy but inadequate protein and micronutrients (Dewey 2003). Micronutrient deficiencies, most notably zinc deficiency, are associated with stunting of growth and other serious health consequences including anaemia and a greater susceptibility to infection (Bhutta et al. 2008).
Authoritative guidelines on ideal complementary feeding recommend the daily consumption of animal‐source foods in order to achieve adequate intakes of deficient nutrients, specifically iron and zinc, which are not achievable with plant‐based diets alone (WHO 1998; Dewey 2003; Hambidge & Krebs 2007). Unfortunately, animal‐source foods are not affordable in many areas of the DRC. However, insects have played a critical role in the diet of many people in Central Africa, with 70% of the adult population of Kinshasa, the capital of the DRC, consuming insects (Balinga et al. 2004; Latham 2005). Dried caterpillars have a protein and micronutrient content similar to beef (Kodondi et al. 1987; Latham 2005). Therefore, we speculated that dried caterpillars may be an alternative to meat as a source of protein and micronutrients. The overall goal of this project is to test the nutrient content, safety and acceptability of a nutrient‐rich complementary food.
Problems with behavioural and social compliance to feeding interventions limit the efficacy of food supplementation (Lartey et al. 1999; Bhandari et al. 2001; Mamiro et al. 2004). Feeding programs have had limited success if little attention was paid to socio‐cultural influences on infant feeding, including maternal attitude (Bentley et al. 1991). Both maternal and infant acceptability of food sources are important indicators of compliance with a feeding intervention, and lack of compliance has resulted in erroneous conclusions about the potential benefits of previous dietary interventions (Paul et al. 2008). Therefore, one of the aims of this project was to test the acceptability of the caterpillar cereal. In this paper, we report the results of the biochemical and microbiologic analyses of a cereal made from caterpillars and the investigation of maternal and infant acceptability of the cereal.
Key messages
Locally available, micronutrient‐rich complementary foods are needed in low‐income countries like the Democratic Republic of Congo.
Cereal made from locally available caterpillars has an appropriate macro‐ and micronutrient content for infant and young child complementary feeding.
Based on a small cohort, caterpillar cereal appears to be acceptable to mothers and infants.
A study to investigate whether consuming this cereal may improve stunting of linear growth is warranted.
Materials and methods
Cereal development
We developed a cereal made from dried caterpillars, ground corn, sugar, salt and palm oil. We chose these ingredients based on the nutritional requirements of young children, the dietary habits of the population and the availability of these products in the local markets of the DRC. We chose corn because it constitutes a basic food source for many populations in the DRC, and its use in infant food is common throughout the country. We chose palm oil because it is a rich source of lipids and contributes β‐carotene, a precursor of vitamin A. We added small amounts of sugar and salt for palatability. We produced cereal in accordance with the international standards on the formulation of foods intended for infants and children up to 2 years of age outlined in the Codex Alimentarius (World Health Organization, Food and Agriculture Organization of the United Nations 1979, 2006).
To make the cereal, we processed each component separately and then mixed them together to create the final product.
Caterpillar flour: The caterpillars were initially washed and soaked in water for 30 min then dried in the sun. Dried caterpillars were crushed in a grinding mill and filtered to a flour of fine granularity and uniform consistency.
Corn flour: Dried kernels were initially filtered in a sleeve with broad mesh to remove foreign material from the corn. Twice, the kernels were soaked in water at room temperature and rinsed. The kernels were dried in the sun, crushed in a grinding mill, and filtered to a flour of fine granularity and uniform consistency.
Palm oil: Oil required no processing before mixing.
Sugar and salt: Each ingredient was crushed separately to obtain a fine powder.
We mixed caterpillar flour, corn flour, salt and sugar in a basin. The proportion of caterpillar flour to corn flour was 1:1. We chose this proportion such that the cereal would provide the recommended daily intake of zinc. We added palm oil to the mixture and dried the final mixture in an oven at 60°C for 24 h. Single feeding portions (30 g) of the cereal were sealed in plastic sachets. We assured hygienic production of cereal by cleansing all equipment prior to the cereal production, assuring hygiene of all personnel including hand washing, and requiring the use of masks and hair coverings during cereal production.
Chemical and microbiologic testing
We performed chemical analyses on samples of the cereal. We conducted all analyses at the Research Institute in Sciences and Health in Kinshasa. To measure water content, we dried the cereal at a temperature between 100 and 105°C followed by cooling in a desiccating chamber. We periodically performed weights until a stable weight was achieved. We calculated water content from the difference in weights before and after desiccation. We used the Kjeldahl method for analysis of protein content (Jones & Benton 1992) by digesting the cereal in sulphuric acid at a high temperature using potassium sulphate and cupric sulphate as catalysts. We added concentrated alkali (sodium hydroxide) to the digest to convert ammonium to free ammonia that was distilled, collected and titrated in the presence of an acidic solution. We calculated the percentage of nitrogen from milliequivalents of ammonia per grams of sample by multiplying using a standard conversion factor then converted to crude protein content by using a second standardised conversion factor. We used the Soxhlet method to determine lipid content in which lipids were extracted from the cereal using an organic solvent by backward flow under refrigeration. We placed the product in a drying oven to evaporate the organic solvent and then weighed it. We used spectrophotometry to determine the content of iron and zinc (Pinta 1973).
We performed microbiologic analyses by measuring the total organism count, and testing for the presence of Enterobacteria, Staphylococcus aureus, Salmonella, Shigella, yeast and fungus. We plated a sample on each of the following culture mediums: MacConkey, cellulose with blood, Hektoen and Mannitol salt culture, and the media were incubated at 37°C for 24 h. We suspended any recovered colonies in mediums for identification including: citrate of Simmons, Kliger and Mannitol. After incubation, we isolated fungus on Sabouraud cellulose agar. We identified all organisms based on colony morphology. We used chromatography to test for the presence of aflatoxin according to the method of the Association of Official Analytical Chemists (AOAC 1984).
Maternal and infant acceptability
We recruited a convenience sample of five mother–infant dyads from breastfed infants presenting to health centres in each of four communities in the rural Equateur province of the DRC. We enrolled healthy male and female infants between the ages of 8 and 10 months and their mothers. We excluded infants with intercurrent illness that may have interfered with oral intake, infants of multiple gestation, infants with congenital anomalies, and infants who were receiving free or subsidised complementary foods.
We provided each mother with a sachet containing a 30‐g portion of caterpillar cereal. We instructed mothers to cook the cereal in 100 mL of boiling water to a puree consistency (a consistency that does not fall readily off a spoon), allow the cereal to cool and then consume immediately. To assess maternal acceptability, we asked mothers to rate five features of the prepared cereal: smell, taste, texture, colour and consistency. Their responses were ranked on a 5‐point Likert scale from ‘dislike very much’ (score of 1) to ‘like very much’ (score of 5). We defined maternal acceptability as a median score for each feature of the cereal of 3 or greater and the upper limit of the lowest quartile of equal to or greater than 2.
To assess infant acceptability, we supplied each mother with seven sachets of cereal containing 30 g of dry cereal each, and instructed her to prepare and feed her infant one sachet daily. Study personnel visited the home three times during the week to reinforce preparation instructions, observe feedings and monitor for signs or symptoms of feeding intolerance. We advised mothers to save all unconsumed cereal. On the eighth day of the trial, study personnel collected all unconsumed cereal from the preceding 4 days and surveyed mothers about their infants’ health and feeding status during the trial. Study personnel estimated the amount of cereal remaining from each daily portion. We based cereal consumption on the amount the infant consumed during the last 4 days of the trial. We defined infant acceptability as 100% of infants consuming greater than or equal to 75% of the cereal allotment during the last 4 days of the trial and all infants being free from adverse symptoms attributable to cereal consumption.
The Institutional Review Boards at the University of North Carolina at Chapel Hill and Kinshasa School of Public Health approved this study. The trial was registered through clinicaltrials.gov (NCT01258647).
Results
Chemical and microbiologic testing
A 30‐g portion of the cereal contained 6.9 g of protein, 6.3 g of fat, and 12.0 g of carbohydrate, and yielded 132 kcal. A 30‐g portion also contained 3.8 mg of iron and 3.8 mg of zinc (Table 1). The cereal was free from Salmonella, Shigella, Enterobacteria, Staphylococcus aureus, yeast or fungus (Table 2). Aflatoxin was not present.
Table 1.
Macronutrients | Micronutrients | ||
---|---|---|---|
Energy (kcal) | ≈ 132 | Iron (mg) | 3.8 |
Protein (g) | 6.9 | Zinc (mg) | 3.8 |
Fat (g) | 6.3 | Magnesium (mg) | 9.4 |
Carbohydrate (g) | 12.0 | Copper (mg) | 3.7 |
Table 2.
Enrichment media | Quantifying media | Result |
---|---|---|
Peptone water | Blood agar (total organism count) | Negative |
MacConkey agar (Enterobacteria) | Negative | |
Mannitol salt agar (Staphylococcus aureus) | Negative | |
Sabouraud agar (yeast and fungus) | Negative | |
Selenite | Blood agar (total organism count) | Negative |
Hektoen (Salmonella) | Negative | |
Salmonella Shigella agar | Negative | |
Thioglycolate | Blood agar (total organism count) | Negative |
MacConkey agar (Enterobacteria) | Negative | |
Mannitol salt agar (Staphylococcus aureus) | Negative | |
Sabouraud agar (yeast and fungus) | Negative |
Maternal and infant acceptability
Twenty maternal–infant dyads were enrolled in the study to determine acceptability. One dyad voluntarily withdrew after enrolment. On a 5‐point Likert scale, all women rated the cereal as either 4 or 5 for overall impression and consistency. For taste, smell and texture: 18 mothers rated the cereal as either 4 or 5 and 1 mother rated the cereal as 3. For colour: 18 mothers rated the cereal as either 4 or 5 and 1 mother rated the cereal as 2 (Table 3). All mothers stated that they believed other mothers would be willing to participate in a 1‐year‐long feeding trial with caterpillar cereal.
Table 3.
Cereal characteristics | Maternal Opinion, n * | ||||
---|---|---|---|---|---|
Dislike very much | Neutral | Like very much | |||
1 | 2 | 3 | 4 | 5 | |
Overall impression | 0 | 0 | 0 | 11 | 8 |
Taste | 0 | 0 | 1 | 6 | 12 |
Smell | 0 | 0 | 1 | 9 | 9 |
Texture | 0 | 0 | 1 | 12 | 6 |
Colour | 0 | 1 | 0 | 7 | 11 |
Consistency | 0 | 0 | 0 | 10 | 9 |
*n refers to the number of women who ranked the cereal in each domain.
All participating infants consumed more than 75% of the daily cereal portions during the last 4 days of the trial. Five infants (26%) consumed 100% of the cereal. One infant experienced vomiting during the first day of the study and continued the trial without further symptoms. No other adverse feeding events were reported.
Discussion
Lutter & Dewey (2003) have proposed an ideal composition for fortified complementary foods. They recommend quantities of macronutrients in complementary foods for 6–11‐month‐old infants that include 3–4.5 g of protein and 4.8 g of fat. A 30‐g portion of our caterpillar cereal provides their recommended daily requirements for protein and fat. If 30 g of cereal was the sole source of complementary food, it would likely be deficient in energy (65% of the energy for 6–8 months old, 43% of the energy for 9–11 months old) (Lutter & Dewey 2003). However, it appears to be a satisfactory supplement to breast milk and existing complementary foods that provide adequate energy in the form of carbohydrates.
Lutter and Dewey recommend a daily intake of 11 mg of non‐haem iron for 6–11‐month‐old infants. This amount is suggested under the assumption that the bioavailability of elemental iron in ingested non‐haem iron is approximately 10% (Lutter & Dewey 2003). Less dietary iron is necessary from animal‐source foods that have haem‐associated iron because approximately 30% is bioavailable (Carpenter & Mahoney 1992). Haem proteins in non‐insect animals are usually found in muscles in the form of myoglobin and haemoglobin, but haem is also found in cytochrome and catalases (Locke & Nichol 1992). The primary source of haem iron in caterpillars is in cytochromes, and we presume that its bioavailability is similar to the haem iron of myoglobin and haemoglobin (Locke & Nichol 1992; Chapman 1998). Insects also have iron bound to the non‐haem molecules, ferritin and holoferritin. Iron associated with these proteins is typically in the ferrous state, which increases its bioavailability, and iron bound to these proteins appears to be more bioavailable than iron in the form of reduced salts. Therefore, it is likely that the bioavailability of iron in caterpillars is similar to beef, and that the content of iron in our cereal will be sufficient to meet the requirements of infants.
Zinc is critical for cellular growth, and its deficiency is associated with stunting. Our cereal contains 3.8 mg of zinc in a daily portion, which approaches the recommended daily intake of 4–5 mg of zinc in complementary feeding products for infants (Rosado 2003). Although there are no specific quantitative data for the appropriate daily requirements of B vitamins for infants, caterpillars contain riboflavin, niacin, pantothenic acid, pyridoxine, biotin, folic acid and cobalamins (Kodondi et al. 1987).
Human sensory testing of complementary feeding products predicts the acceptability of the introduction of the product's use within target populations (Mensa‐Wilmot et al. 2001). Sensory evaluation of the food product including smell, taste, and colour, as well as consumption of food products during pilot testing has been described as indicators of positive acceptability (Phuka et al. 2011). We chose to evaluate both maternal acceptability and infant consumption of cereal to provide an appropriate socio‐cultural framework for the introduction of this complementary food into infants’ diets. Previous studies on acceptability have focused on comparing two food products to each other (Paul et al. 2008; Aaron et al. 2011). Because this cereal is a novel product made from locally available ingredients, we deemed a study comparing caterpillar cereal to a fortified cereal product which was not locally available to be unreasonable. Based on our strategy of evaluation, caterpillar cereal was found to be acceptable to mothers and infants.
Although our data suggest a high level of maternal acceptability, we acknowledge that one of our a priori criteria for acceptability was not sufficiently stringent. Using our pre‐defined criteria, it would have been possible for a neutral opinion about the cereal to classify the cereal as acceptable. Therefore, we recommend that future studies of this nature utilise a more favourable response for the assignment of maternal acceptability.
Caterpillar cereal appears to be a promising alternative for animal‐source foods for complementary feeding; however, we recognise some limitations to this intervention. Although caterpillar cereal is designed to be easily integrated into existing food practices by using it as an additive to the usual diet of children, the volume of cereal that we used may be a challenge for infants at 6–8 months of age to consume. Although we recognise the importance of responsive feeding, mothers were not given guidance on responsive feeding techniques in the course of this study. We speculate that counselling on responsive feeding might have increased the number of children who consumed 100% of the daily cereal portion. Furthermore, although the iron content of caterpillars is haem associated, it is not clear if the absorption of this micronutrient will be sufficient to prevent iron deficiency. We described the short‐term microbiological and chemical profile of this cereal that was produced at the University of Kinshasa. Understanding the long‐term stability and production at external sites needs to be assessed.
Using locally available food products, we have developed a caterpillar‐based cereal that has the appropriate macro‐ and micronutrient contents for infant complementary feeding. This cereal is acceptable to both mothers and infants in a rural area of the DRC. Because the ingredients are locally available and the production of this cereal is simple, this cereal is likely to be a sustainable alternative animal‐source food for complementary feeding. However, this cereal will need to be tested in an efficacy trial to determine if it will have positive effects on micronutrient deficiencies and linear growth.
Source of funding
This project has been funded by Bill & Melinda Gates Foundation to FHI 360, through the Alive & Thrive Small Grants Program managed by UC Davis.
Conflicts of interest
The authors declare that they have no conflicts of interest.
Contributions
MB, AL, KK and JG analysed and interpreted the data. MB and CB wrote the initial draft of the manuscript. AV, MEB, CE, AT and CB assisted in the interpretation of results. All co‐authors participated in manuscript preparation and critically reviewed all sections of the text for important intellectual content.
Bauserman, M. , Lokangaka, A. , Kodondi, K.‐K. , Gado, J. , Viera, A. J. , Bentley, M. E. , Engmann, C. , Tshefu, A. , and Bose, C. (2015) Caterpillar cereal as a potential complementary feeding product for infants and young children: nutritional content and acceptability. Matern Child Nutr, 11: 214–220. doi: 10.1111/mcn.12037.
References
- Aaron G.J., Lo N.B., Hess S.Y., Guiro A.T., Wade S., Ndiaye N.F. et al (2011) Acceptability of complementary foods and breads prepared from zinc‐fortified cereal flours among young children and adults in Senegal. Journal of Food Science 76, S56–S62. [DOI] [PubMed] [Google Scholar]
- AOAC (Association of Official Analytical Chemists) (1984) Official Methods of Analysis of the Association of Official Analytical Chemists. 14th edn, pp 477–489. Association of Official Analytical Chemists: Arlington, VA. [Google Scholar]
- Balinga M., Monzambe Mapunzu P., Mussa J.‐P. & N'gasse G. (2004) Contribution des insectes de la foret a la securite alimentaire. L'exemple des chenilles d'Afrique Centrale. In: Div. de l' 'Economique et des Produits Forestiers. Rome, Italy; 107. [Google Scholar]
- Barker D.J., Osmond C., Forsen T.J., Kajantie E. & Eriksson J.G. (2005) Trajectories of growth among children who have coronary events as adults. The New England Journal of Medicine 353, 1802–1809. [DOI] [PubMed] [Google Scholar]
- Bentley M.E., Dickin K.L., Mebrahtu S., Kayode B., Oni G.A., Verzosa C.C. et al (1991) Development of a nutritionally adequate and culturally appropriate weaning food in Kwara State, Nigeria: an interdisciplinary approach. Social Science and Medicine 33, 1103–1111. [DOI] [PubMed] [Google Scholar]
- Bhandari N., Bahl R., Nayyar B., Khokhar P., Rohde J.E. & Bhan M.K. (2001) Food supplementation with encouragement to feed it to infants from 4 to 12 months of age has a small impact on weight gain. The Journal of Nutrition 131, 1946–1951. [DOI] [PubMed] [Google Scholar]
- Bhutta Z.A., Ahmed T., Black R.E., Cousens S., Dewey K., Giugliani E. et al (2008) What works? Interventions for maternal and child undernutrition and survival. Lancet 371, 417–440. [DOI] [PubMed] [Google Scholar]
- Black R.E., Allen L.H., Bhutta Z.A., de Caulfield L.E., Onis M., Ezzati M. et al (2008) Maternal and child undernutrition: global and regional exposures and health consequences. Lancet 371, 243–260. [DOI] [PubMed] [Google Scholar]
- Carpenter C.E. & Mahoney A.W. (1992) Contributions of heme and nonheme iron to human nutrition. Critical Reviews in Food Science and Nutrition 31, 333–367. [DOI] [PubMed] [Google Scholar]
- Chapman R.F. (1998) The Insects: Structure and Function. 4th edn, Cambridge University Press: Cambridge, UK; New York. [Google Scholar]
- Demographic and Health Survey (DHS) (2007) Democratic Republic of the Congo. In: Ministry of Planning and Macro International Inc, Calverton, Marylan: d. [Google Scholar]
- Dewey K. (2003) Guiding Principles for Complementary Feeding of the Breastfed Child. Pan American Health Organization. World Health Organization: Washington DC. [Google Scholar]
- Dewey K.G. & Adu‐Afarwuah S. (2008) Systematic review of the efficacy and effectiveness of complementary feeding interventions in developing countries. Maternal and Child Nutrition 4 (Suppl. 1), 24–85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frongillo E.A. Jr (1999) Symposium: causes and etiology of stunting. Introduction. The Journal of Nutrition 129, 529S–530S. [DOI] [PubMed] [Google Scholar]
- Hambidge K.M. & Krebs N.F. (2007) Zinc deficiency: a special challenge. The Journal of Nutrition 137, 1101–1105. [DOI] [PubMed] [Google Scholar]
- Jones J. & Benton J. (1992) A Kjeldahl Method of Nitrogen Determination. Micro‐Macro Publishing, Inc: Athens, GA. [Google Scholar]
- Kodondi K.K., Leclercq M. & Gaudin‐Harding F. (1987) Vitamin estimations of three edible species of Attacidae caterpillars from Zaire. International Journal for Vitamin and Nutrition Research 57, 333–334. [PubMed] [Google Scholar]
- Lartey A., Manu A., Brown K.H., Peerson J.M. & Dewey K.G. (1999) A randomized, community‐based trial of the effects of improved, centrally processed complementary foods on growth and micronutrient status of Ghanaian infants from 6 to 12 mo of age. The American Journal of Clinical Nutrition 70, 391–404. [DOI] [PubMed] [Google Scholar]
- Latham P. (2005) Edible Caterpilars and Their Food Plants in Bas‐Congo Province, Democratic Republic Of Congo, 2nd edn. United Kingdom Department for International Development: Canterbury. [Google Scholar]
- Locke M. & Nichol H. (1992) Iron economy in insects – transport, metabolism, and storage. Annual Review of Entomology 37, 195–215. [Google Scholar]
- Lutter C.K. & Dewey K.G. (2003) Proposed nutrient composition for fortified complementary foods. The Journal of Nutrition 133, 3011S–3020S. [DOI] [PubMed] [Google Scholar]
- Mamiro P.S., van Kolsteren P.W., Camp J.H., Roberfroid D.A., Tatala S. & Opsomer A.S. (2004) Processed complementary food does not improve growth or hemoglobin status of rural Tanzanian infants from 6–12 months of age in Kilosa district, Tanzania. The Journal of Nutrition 134, 1084–1090. [DOI] [PubMed] [Google Scholar]
- Mensa‐Wilmot Y., Phillips R.D. & Sefa‐Dedeh S. (2001) Acceptability of extrusion cooked cereal/legume weaning food supplements to Ghanaian mothers. International Journal of Food Sciences and Nutrition 52, 83–90. [PubMed] [Google Scholar]
- Paul K.H., Dickin K.L., Ali N.S., Monterrosa E.C. & Stoltzfus R.J. (2008) Soy‐ and rice‐based processed complementary food increases nutrient intakes in infants and is equally acceptable with or without added milk powder. The Journal of Nutrition 138, 1963–1968. [DOI] [PubMed] [Google Scholar]
- Phuka J., Ashorn U., Ashorn P., Zeilani M., Cheung Y.B., Dewey K.G. et al (2011) Acceptability of three novel lipid‐based nutrient supplements among Malawian infants and their caregivers. Maternal and Child Nutrition 7, 368–377. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Phuka J.C., Maleta K., Thakwalakwa C., Cheung Y.B., Briend A., Manary M.J. & Ashorn P. (2009) Postintervention growth of Malawian children who received 12‐mo dietary complementation with a lipid‐based nutrient supplement or maize‐soy flour. The American Journal of Clinical Nutrition 89, 382–390. [DOI] [PubMed] [Google Scholar]
- Pinta M. (1973) Reference methods for the determination of mineral elements in plant material. Determination of Ca, Mg, Fe, Mn, Zn, Cu by atomic absorption. Oleagineux 28, 87–92. [Google Scholar]
- Rosado J.L. (2003) Zinc and copper: proposed fortification levels and recommended zinc compounds. The Journal of Nutrition 133, 2985S–2989S. [DOI] [PubMed] [Google Scholar]
- World Health Organization (1998) Complementary Feeding of Young Children in Developing Countries: A Review of Current Scientific Knowledge. World Health Organization: Geneva. [Google Scholar]
- World Health Organization, Food and Agriculture Organization of the United Nations (1979) Recommended International Code of Hygienic Practice for Foods for Infants and Children. CAC/RCP 21‐1979. In: Commission CA, ed. Rome, Italy.
- World Health Organization, Food and Agriculture Organization of the United Nations (2006) Codex Standard for Processed Cereal‐Based Foods for Infants and Young Children. Codex Stan 074‐1981, Rev. 1‐2006. In: Commission CA, ed. Rome, Italy.