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J Dent Res 83(7): 578-582, 2004
© 2004 International and American Associations for Dental Research


RESEARCH REPORT
Clinical

Particle Size Distribution of Food Boluses after Mastication of Six Natural Foods

M.-A. Peyron, A. Mishellany, and A. Woda*

Institut National de la Recherche Agronomique, Theix, Station de Recherches sur la Viande, Saint-Genès-Champanelle, France; and GEDIDO, Groupe d’Etude sur les Déficiences Incapacités et Désavantages en santé orale, Faculté Dentaire, 11 Bd C De Gaulle, 63000 Clermont-Ferrand, France;

* corresponding author, alain.woda{at}u-clermont1.fr


   ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
There is a large variability between and among individuals in the physiology of mastication, but it is not known whether this produces a similar variability in the particle sizes of food boluses at the end of the chewing process. Food boluses obtained just before swallowing were analyzed in ten subjects (aged 36.7 ± 9.5 yrs) with normal dentition. Food samples of 3 nuts (peanut, almond, pistachio) and 3 vegetables (cauliflower, radish, and carrot) were chewed and expectorated after self-estimated complete mastication. Measurements with sieving and laser diffraction methods indicated that particles were much larger in vegetables than in nuts. Particle size distributions were similar among nuts and among vegetables. Surprisingly, no inter-individual variability was observed in the particle distributions for the 6 foods, although several sequence variables differed markedly. A need for a bolus to be prepared with a precisely determined texture before it can be swallowed may explain the inter-subject variability of the masticatory function.

KEY WORDS: mastication • food bolus • particle size • swallowing


   INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The primary role of mastication is to transform a mouthful of food into a bolus ready for swallowing (Lillford, 1991; Prinz and Lucas, 1995). The subject achieves this by reducing the food to small particles and by lubricating it with saliva and any liquid released from the food itself. A cohesive mixture is formed in the food bolus from liquid-coated particles that cohere by viscous adhesion. The resulting entity can flow smoothly down the pharyngeal walls during deglutition (Lucas and Luke, 1986; Prinz and Lucas, 1995) and prevents stray particles from entering the trachea (Prinz and Lucas, 1995; Alexander, 1999). Exactly how particle size reduction triggers swallowing is unclear. The process has been claimed to depend on food type (Prim and Lucas, 1997; Hoebler et al., 1998, 2000) and on bolus size (Lucas and Luke, 1984; Buschang et al., 1997). We tested the hypothesis that particle size is an important triggering factor for deglutition, and thus there is no difference in particle size between and among individuals.

In this study, we determined the particle size distribution of the boluses collected before swallowing to test for variability between and among individuals. Six different natural foods—3 nuts and 3 fresh raw vegetables—were chewed by ten healthy adults. We used two methods, sieving and laser diffraction, to measure the particle sizes in the food boluses after mastication.


   MATERIALS & METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Ten subjects with a healthy dentition (six females, four males, aged 36.7 ± 9.5 yrs) were selected on the basis of strict dental criteria (Lassauzay et al., 2000). Informed consent was obtained according to the guidelines of the ethical committee of the Université d’Auvergne. Two groups of foods were studied. The first included peanuts, almonds, and pistachios (dry nuts, 9% water) and the second carrots, radishes, and cauliflower (raw vegetables, 87% water). Portions consisted of 5 peanuts, 4 pistachios, or 3 almonds (2.5 to 4 g) and cylindrical samples (1 cm height, 2 cm diameter, 3.5 to 4.5 g) prepared from raw vegetables. Each subject attended 6 sessions, one per test food, spaced 1 wk apart and scheduled between 1 and 2 hrs after a meal. Each session consisted of 4 sequences for training and 4 sequences to measure particle sizes. The first 2 samples were chewed and swallowed, and the following 2 were chewed and expectorated just before the subject felt the need to swallow. After each sequence, the subject rinsed his/her mouth with water (26 g), and the result was added to the expectorated boluses. During these 4 masticatory sequences, the experimenter watched the subjects to time the sequences (T) and counted the cycles (N) to calculate masticatory frequency (T/N). The subjects then performed 2 further sequences to give expectorated boluses designated Sieve-Bolus1 and Sieve-Bolus2. Finally, while chewing the last 2 samples, the subjects were stopped by the experimenter after N/2 cycles (Sieve-Bolus3) and N/4 cycles (Sieve-Bolus4). For measurement by laser diffraction, 2 boluses (Laser-Bolus1 and Laser-Bolus2) resulting from complete mastication were collected in a second session.

For particle size measurements by the sieving method, the expectorated boluses were washed on the 0.4-mm sieve for 1 min in running water and dried (40°C, 1 hr). The boluses were then poured through a stack of 7 sieves with apertures of 4, 2.5, 2, 1.4, 1, 0.8, and 0.4 mm (Saulas, Paisy Cosdon, France). The fractions retained on each of the 7 sieves were weighed, and the weights were expressed as a percentage of the weight of the mouthful before mastication. We achieved particle size measurements of Laser-Bolus1 and Laser-Bolus2 by laser light diffraction using a Mastersizer S (Malvern Instruments Ltd, Malvern, UK) equipped with a 1000-mm lens, allowing for analysis of particles between 5 and 2000 µm. Particles larger than 2 mm were eliminated from Laser-Bolus1 and 2 by means of a 2-mm sieve. This method expressed size distributions as a percentage of the total volume occupied in the laser chamber by the particles. The volume was converted to weight with the use of volumetric mass and expressed as cumulative values. The 5-µm- to 2-mm-diameter range of particle sizes was divided into 17 classes for analysis.

Statistical analyses were performed by SAS®. The distribution was normal in all cases, and a one-way or two-way analysis of variance was performed. When ANOVA indicated a significant difference, a Student Newman-Keuls test was carried out for the comparison of means (risk at 5%).


   RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Sieving: Sieve and Bolus Type (Sieve-Boluses1 to 4) as Factors, Weight as Measured Variable
The weights of all foods collected after mastication represented only a fraction of the initial mouthful. Approximately 40% of the initial weight was recovered for Sieve-Boluses1 and 2, and 60% and 80% for Sieve-Boluses3 and 4, respectively (TableGo). A two-way ANOVA [boluses (Sieve-Boluses1 and 2) and sieves (n = 7) as factors] was performed for each of the 6 foods. It indicated, for each of the 6 foods, that: (1) the total weights of Sieve-Boluses1 and 2 were similar (p > 0.05); (2) the weight collected in the 7 sieves varied significantly (22 ≤ F ≤ 41, p < 0.001); and (3) there was no significant difference in the distribution of particles among the sieves between Sieve-Boluses1 and 2, since no interaction between bolus and sieve factors was observed (p > 0.05). The reduction of the number of masticatory cycles to one-half (Sieve-Bolus3) and one-quarter (Sieve-Bolus4) induced a corresponding increase in the total weight of the bolus (16 ≤ F ≤ 33, p < 0.001, TableGo), together with a different distribution of particle sizes in favor of the largest ones (Fig. 1Go).


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Table. Weight of the Food Boluses Expectorated after a Complete Masticatory Sequence (Sieve-Boluses1 and 2), Half a Sequence (Sieve-Bolus3), or a Quarter Sequence (SieveBolus4)
 


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Figure 1. Mean distribution of the particles (% of the initial weight among the sieves). The particle distributions in the boluses obtained after a complete chewing sequence (Sieve-Bolus1, n = 20), a half of a sequence (Sieve-Bolus3, n = 10), and one-quarter of a sequence (SieveBolus4, n = 10) differentiate the dry foods (A,B,C) from the vegetables (D,E,F).

 
Sieving: Subject as Factor, Weight as Measured Variable
No inter-individual variability was noted in any of the 24 one-way ANOVAs (6 foods x Sieve-Boluses1 to 4; 0.29 < p < 1). Distribution of the particle size across sieves was also similar for all subjects, regardless of the nature of the chewed food (0.5 < p < 0.69 for 6 two-way ANOVAs, with subject and sieve as factors). This was in contrast to the inter-subject variability of every time-related parameter. For example, sequence duration differed across the 10 subjects (range, 6.5–42.4 sec), depending on the food (6 one-way ANOVAs with subject as factor and sequence duration as measured variable). Masticatory frequency also differed across the 10 subjects, ranging from 1.53 ± 0.23 to 1.92 ± 0.27 Hz (p < 0.001 for 24 one-way ANOVAs with subject as factor). Masticatory frequency varied neither with food (p > 0.05 for the 6 one-way ANOVAs) nor with the type of bolus (p > 0.05 for the 4 one-way ANOVAs).

Sieving: Food Type and Sieve as Factors and Weight as Measured Variable
The distribution of the particles within the sieves depended on the type of food. A two-way ANOVA (with food and sieve as factors) was performed for each of the 4 Sieve-Boluses. They indicated no difference among the foods, differences among the 7 sieves (p < 0.0001), and, most importantly, an interaction between these two factors, indicating that the distribution of particle sizes among the sieves depended on the food (p < 0.0001). This effect appeared to vary greatly with food group (Fig. 1Go). Comminution of nuts gave a 1.4-mm peak in the size distribution, whereas the vegetables showed a peak at 2.5 mm. Particle size distribution, however, was not identical in the 3 nuts (food effect, p = 0.0012; sieve effect, p < 0.001; and interaction, p = 0.004, two-way ANOVA). This food effect was due to the almonds. In contrast, the vegetables presented similar particle size distributions (sieve effect, p < 0.001; no food effect and no interaction, p > 0.05).

Laser Diffraction
Particle diameters were not distributed at random (p < 0.001), and both total weights and the diameter distribution did not differ between Laser-Boluses1 and 2 (two-way ANOVA for each food, with bolus type and diameter class as factors). Again, no significant difference between and among subjects was noted (12 one-way ANOVAs, Laser-Boluses1 and 2 x 6 foods, p > 0.05). As observed with sieving, particles were not evenly distributed in the diameter classes (p < 0.001 for diameter class). No difference was observed between the total weight of the boluses (p > 0.05 for food type), and particle diameter distributions differed between and among foods (p < 0.001 for interaction, two-way ANOVA, Fig. 2Go).



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Figure 2. Laser diffraction analysis of expectorated boluses obtained for the different foods (Laser-Bolus1). Means (± SD) of the cumulative mass of particles are presented for each of the 17 diameter classes of particles. Means are expressed as the percentage of the total mass analyzed by laser diffraction (n = 20).

 
Full-spectrum Representation of Particle Size Distribution
The sieve method analyzed the bolus particle sizes above 0.4 mm, whereas the laser diffraction method could be used only for particles below 2 mm. This defines three measurement intervals (5 µm < size < 0.4 mm; 0.4 mm < size < 2 mm, size > 2 mm). The full distributions were calculated for the 6 foods by two equations with two unknowns for the percentages measured with sieving and laser diffraction methods (Fig. 3Go). In doing this, we assumed that the particle size distributions were representative of the collected bolus in both methods.



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Figure 3. Particle size distribution of food (% of the total weight before mastication). The values of this composite diagram were calculated from results obtained with laser diffraction and sieving methods.

 

   DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The results of this study show; (1) that, after complete mastication, the weight of the food boluses was only 40% of the initial weight of the food sample; (2) that particle size distributions depended on food type, a large difference between nuts and vegetables being observed, whereas strong similarity was found within each of these two groups; (3) that there was little or no variability between and among individuals in particle size; and (4) that different methods are needed to characterize the particle size distribution more accurately.

Weight of Food Boluses before Being Swallowed
The boluses collected after complete mastication had lost nearly 60% of the initial weight of the food samples, for all foods or subjects. The amount of loss might be different in normal, not expectorated, boluses. However, intermediate swallowing probably accounts for this marked loss of particles. The weight loss may result from the transportation of bolus fractions, but also from the liquid content liberated by the food and loaded with soluble nutrients. According to several authors, intermediate swallows, which occur in nearly 80% of masticatory sequences, are characterized by several transportations of food fractions to the oropharynx, operated by tongue-palate contact during protraction of the tongue and hyoid (Palmer et al., 1992; Hiiemae et al., 1996; Hiiemae and Palmer, 1999).

Particle Size Distribution Depends on Food Type
The 6 foods analyzed in this study resulted in two particle size distributions. Raw vegetables were transformed into boluses made up of particles larger than 2 mm, and nuts gave a bolus which contained 90% of particles smaller than 2 mm (Fig. 3Go). A special food index based on mechanical properties of a large array of foods was shown to correlate with the breakdown properties observed after a single stroke (Agrawal et al., 1997). It is also correlated with the electromyographic activities recorded during mastication of the same product (Agrawal et al., 1998). This food index, which takes into account important characteristics such as water and fiber content, separated nuts from raw vegetables and reflects the differences in particle size distribution observed in this study.

Analysis of our data shows that deglutition is triggered in spite of very different particle size distributions. Thus, other parameters must be at work to inform the swallowing center of the need to operate. Prinz and Lucas (1997) have proposed that particle size reduction by increasing the surface tension, insalivation, by adding viscosity within the bolus and optimal duration for preparing the bolus inside the mouth are the main factors that determine the rheological properties of the bolus. The perception of the resulting bolus cohesion and plasticity may, in turn, be the key factor to triggering a safe swallow.

Significance of the Small Inter-individual Variability in Bolus Composition
Variability between and among subjects is a major characteristic of the physiology of human mastication. This variability has been observed, for example, in cycle shape, amplitude of muscular contraction, duration of masticatory sequences, number of masticatory cycles, and masticatory frequency (Pröschel and Hoffmann, 1988; Lassauzay et al., 2000) and was confirmed in this study. It could not be eliminated by the use of strict dental criteria or rheological control of the food (Lassauzay et al., 2000; Peyron et al., 2002). The most striking result of the present study is that the size distribution of bolus particle for a given food type was similar in the 10 subjects. This means that the requirements that the food bolus must meet before it is ready to be swallowed are similar for everyone. These requirements may strongly depend, for each food type, on a certain bolus particle size. Until the mandatory particle size is reached, swallowing may be inhibited and chewing prolonged. The wide inter-individual variability displayed by electromyographic activity and masticatory kinematics (Pröschel and Hoffmann, 1988; Lassauzay et al., 2000) may therefore be explained by the individuals’ need to adapt their chewing strategy to their personal anatomical features and acquired sensori-motor patterns and conditionings. Several properties other than particle size—for example, lubrication, plasticity, or modification of the structure of meat—may also be included in the required properties of the pre-swallow bolus (Hutchings and Lillford, 1988; Lillford, 1991; Prinz and Lucas, 1995; Alexander, 1999; Mioche et al., 2002).

The Rationale for the Use of Different Methods
Several methods can be used to measure particle size, including microscopy and image analysis, sedimentation analysis, diffusion of light, sieving, and laser diffraction (Shi et al., 1990; Mahmood et al., 1992; Van Der Bilt et al., 1993; Hoebler et al., 1998, 2000). Sieving and laser diffraction were chosen here because their combined use widens the range of analysis from 5 µm to 4 mm. Laser diffraction appeared to be the most suitable method for measuring the granularity of dry and brittle foods, since these foods contain a high percentage of particles under 400 µm. Food boluses of raw vegetables made up of larger particles can also be characterized by sieving. Other kinds of foods would certainly need other approaches. For example, some foods break not into regular spherical particles but into fibrous spines. Hence, examining particle shapes with image analysis might be the best method (Shi et al., 1990; Hoebler et al., 1998 , 2000). In other cases, the observation of either the softening or the dissolution of the bolus rather than its breakdown might be appropriate.


   ACKNOWLEDGMENTS
 
We thank the Laboratoire Régional des Ponts et Chaussées de Clermont-Ferrand for technical help, and INRA and Université d’Auvergne for funding.

Received February 14, 2003; Last revision November 11, 2003; Accepted April 16, 2004


   REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS & METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Agrawal KR, Lucas PW, Prinz JF, Bruce IC (1997). Mechanical properties of foods responsible for resisting food breakdown in the human mouth. Arch Oral Biol 42:1–9.[ISI][Medline]

Agrawal KR, Lucas PW, Bruce IC, Prinz JF (1998). Food properties that influence neuromuscular activity during human mastication. J Dent Res 77:1931–1938.[Abstract/Free Full Text]

Alexander RM (1999). Engineering approaches to chewing and digestion. Sci Progress 82:171–184.

Buschang PH, Throckmorton GS, Travers KH, Johnson G (1997). The effects of bolus size and chewing rate on masticatory performance with artificial test foods. J Oral Rehabil 24:522–526.[ISI][Medline]

Hiiemae K, Palmer JB (1999). Food transport and bolus formation during complete feeding sequences on foods of different initial consistency. Dysphagia 14:31–42.[ISI][Medline]

Hiiemae K, Heath MR, Heath G, Kazazoglu E, Murray J, Sapper D, et al. (1996). Natural bites, food consistency and feeding behaviour in man. Arch Oral Biol 41:175–189.[ISI][Medline]

Hoebler C, Karinthi A, Devaux MF, Guillon F, Gallant DJG, Bouchet B, et al. (1998). Physical and chemical transformations of cereal food during oral digestion in human subjects. Br J Nutr 80:429–436.[ISI][Medline]

Hoebler C, Devaux MF, Karinthi A, Belleville C, Barry JL (2000). Particle size of solid food after human mastication and in vitro simulation of oral breakdown. Int J Food Sci Nutr 51:353–366.[ISI][Medline]

Hutchings JB, Lillford PJ (1988). The perception of food texture—the philosophy of the breakdown path. J Texture Stud 19:103–115.

Lassauzay C, Peyron MA, Albuisson E, Dransfield E, Woda A (2000). Variability of the masticatory process during chewing of elastic model foods. Eur J Oral Sci 108:484–492.[ISI][Medline]

Lillford PJ (1991). Texture and acceptability of human foods. In: Feeding and the texture of food. Vincent JFV, Lillford PJ, editors. Cambridge: Cambridge University Press, pp. 231–243.

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This Article
Right arrow Abstract Freely available
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Services
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Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
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Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (15)
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Right arrow Articles by Peyron, M.-A.
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