An evaluation of the acidogenic potential of maltodextrins in vivo
Introduction
In nature, starch exists as long chain polymers of anhydroglucose units. These polymers can be hydrolysed into products with chain lengths varying from the monomer d-glucose to products with many linked glucose units (such as maltose, maltotriose and higher saccharides). Maltodextrins are carbohydrates derived from maize starch and are a group of oligosaccharides (long chain polysaccharides) composed of glucose, three units and above in length. They are obtained by acidic and/or enzymatic hydrolysis of corn starch, with subsequent drying to make free flowing powders [1]. They usually contain glucose, maltose, maltotriose and higher polymers of glucose, depending on the degree and method of hydrolysis. Therefore, maltodextrins are also called glucose polymers. Glucose polymers are virtually tasteless and odourless and their exact composition determines their sweetening power, as the sweetness increases with an increased concentration of low molecular weight saccharides [1]. Maltodextrins are increasingly being used in the food industry especially in baby drinks and baby dried food as an alternative carbohydrate. However, there are few data in the dental literature on the effect of these carbohydrates on pH of dental plaque in vivo. A study carried out by Moynihan et al. [2] investigated the acidogenicity of glucose polymers as 10% solutions in water, in cow's milk, or in a solution of milk substitute (calogen). They reported that glucose polymers caused a decrease in plaque pH but to a significantly lesser extent than 10% sucrose, and also the glucose polymers were equally acidogenic when given in water, milk or calogen. Another study [3] studied the effects on plaque pH in vivo of sucralose (alone or bulked with maltodextrin or with maltodextrin/dextrose) in iced tea. They found that tea with sucralose/maltodextrin and tea with sucralose/maltodextrin/dextrose did not differ from each other and both produced smaller pH drops compared with tea, which contained sucrose. In these studies, maltodextrins were not tested separately, therefore, direct comparisons between maltodextrin and other solutions were not available.
As far as the authors are aware there are no studies that have specifically investigated the acidogenicity of different types of maltodextrins, which are most commonly used in commercial products. It is essential to have information on their acidogenic potential so that advice can be given to health professionals, parents and patients on their safety and the safest mode of their use. The aims of this study were to investigate the ability of three different maltodextrin solutions to depress plaque pH in vivo, and to assess the acidogenic potential of three commercially available drink formulations for children containing maltodextrins using the plaque harvesting technique.
Section snippets
Test solutions
Three different maltodextrins that are commonly used in food and drink preparations were chosen for the study. The concentration of the maltodextrins is defined as DE, i.e. the dextrose equivalents. The three test products were:
- 1.
Maltodextrin DE=5.5;
- 2.
Maltodextrin DE=14.0;
- 3.
Maltodextrin DE=18.5.
The test maltodextrins were prepared as 10% (w/v) solutions with distilled water.
Three commercially available drinks used by infants and children were also studied. These were:
- 1.
Lemon Barley and Camomile sugar
Results
The results will be discussed separately for the three-maltodextrin solutions and commercial drinks for infants and children containing maltodextrins as carbohydrate.
Discussion
The only way to determine the true cariogenicity of a food is by determining the extent of tooth decay associated with a given food in humans. Since such experiments are not ethically acceptable and probably impractical, scientists must depend on standardised indirect methods for assessing food cariogenicity [9]. Measurements of plaque acidity, particularly as changes in pH, form a very important group of tests for assessing the foods acidogenicity and hence their possible cariogenicity [10].
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