A new headspace-GC-sniffing method is proposed. Using a recently
developed headspace cell, the
vapor phase is collected under conditions that mimic well those of an
aroma above a food. Data
treatment is based on detection frequency, rather than on perceived
intensity or successive dilutions
as used in other approaches. Repeatability appears satisfactory,
and independent panels are even
able to generate similar aromagrams, without training prior to the
analysis. Using a minimum of
six assessors, this technique seems to be more reliable than classical
ones. To compare detection
frequencies between two aromagrams, an estimation of the least
significant difference is given. A
theoretical justification of this approach is suggested, on the basis
of determination of detection
thresholds.
Keywords: Headspace-GC-sniffing; impact odorants; detection
frequency
The MNA is a practical, noninvasive, and cost-effective instrument allowing for rapid nutritional evaluation and effective intervention in frail older persons.
A quick headspace GC method for quantification of volatiles was developed, involving only minor sample preparation. Yogurt flavor compounds could be quantified in the micrograms per kilogram to milligrams per kilogram range without any difficulty, despite the complex matrix. Volatiles of traditional acidic and mild, less acidic yogurts were compared, and important differences were found for acetaldehyde, 2,3-butanedione, and 2,3-pentanedione. Concentrations of 2,3-butanedione and 2,3-pentanedione increased 2-3-fold in mild, less acidic yogurts compared to traditional acidic ones. This is due to accumulation of the precursors of the diketones, 2-acetolactate and 2-acetohydroxybutyrate, during fermentation in mild, less acidic yogurt. These precursors are subsequently converted to the corresponding diketones during storage. On the contrary, acetaldehyde formation was reduced in the mild yogurt, due to growth differences between the lactic acid bacteria used for fermentation of the milk. The quantitative results presented in this study validate previous GC sniffing conclusions (Ott et al. J. Agric. Food Chem. 1997, 45, 850-858), showing that yogurt aroma is the superposition of impact flavor compounds generated by fermentation on milk compounds.
The sensory properties of traditional acidic and mild, less acidic yogurts were characterized by a trained panel using a descriptive approach. Many of the descriptive attributes varied almost linearly with pH, showing either a positive or negative correlation with increasing acidity. The panel was very sensitive to acidity differences, as demonstrated by the linear relationship between acidity perception and pH. Important flavor differences were found between the two classes of yogurt. They were mainly due to differences in acidity and not to different concentrations of the three impact aroma compounds, acetaldehyde, 2,3-butanedione, and 2, 3-pentanedione. This emphasizes the importance of acidity in yogurt flavor. Deodorization and impact aroma compound addition had much less influence on yogurt flavor than pH variations.
Objective: To evaluate the effects of nutrient intake and vitamin D status on markers of type I collagen formation and degradation in adolescent boys and girls. Design: Cross-sectional study. Setting: Canton of Vaud, West Switzerland. Subjects: A total of 92 boys and 104 girls, aged 11-16 y. Data were collected on height, weight, pubertal status (self-assessment of Tanner stage), nutrient intake (3-day dietary record) and fasting serum concentration of 25-hydroxyvitamin D (25OHD), and markers of collagen formation (P1NP) and degradation (serum C-terminal telopeptides: S-CTX). Results: Tanner stage was a significant determinant of P1NP in boys and girls and S-CTX in girls. Of the nutrients examined, only the ratio of calcium to phosphorus (Ca/P) was positively associated with P1NP in boys, after adjustment for pubertal status. 25OHD decreased significantly at each Tanner stage in boys. Overall, 15% of boys and 17% of girls were identified as being vitamin D insufficient (serum 25OHD o30 nmol/l), with the highest proportion of insufficiency at Tanner stage 4-5 (29%) in boys and at Tanner stage 3 (24%) in girls. A significant association was not found between 25OHD and either bone turnover marker, nor was 25OHD insufficiency associated with higher concentrations of the bone turnover markers. Conclusions: The marked effects of puberty on bone metabolism may have obscured any possible effects of diet and vitamin D status on markers of bone metabolism. The mechanistic basis for the positive association between dietary Ca/P ratio and P1NP in boys is not clear and may be attributable to a higher Ca intake per se, a critical balance between Ca and P intake or higher dairy product consumption. A higher incidence of vitamin D insufficiency in older adolescents may reflect a more sedentary lifestyle or increased utilisation of 25OHD, and suggests that further research is needed to define their requirements.
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