A cluster analysis of the relationship between sucking habits,consistency of food ingested,and taste sensitivity in children

As sucking habits and eating behavior may be interrelated and also associated with taste, body composition, and sociodemographic factors, the objective was to perform an exploratory analysis to identify groups of children with a high degree of association between intragroup subjects, providing explanation and interpretation of the data. The study initially included 352 prepubertal children (197 girls; 7‐ to 11‐year‐old), from whom information about sociodemographic characteristics, duration of breastfeeding, past bottle‐feeding and non‐nutritive sucking habits, taste sensitivity, body mass index (BMI), and consistency of food ingested were collected. Salivary concentrations of amylase and total protein were also determined. Data were submitted to cluster analysis (hierarchical analysis, K‐means, and silhouette plot), one‐way ANOVA and correlation tests. Cluster analysis included 159 children, generating three reliable and meaningful clusters: Cluster 1 (labeled “good tasters”), was characterized by older children and higher taste sensitivity; Cluster 2 (“softer food consistency”) by longer bottle‐feeding duration and children who eat food with lower consistency, and Cluster 3 (“breastfed”) by longer breastfeeding duration (silhouette coefficient = 0.61). Cluster 3 also showed the higher percentage of normal‐weight children, normal delivery, maternal schooling, and lower rate of past non‐nutritional sucking habit. No correlation was found between salivary amylase and total protein concentrations, taste sensitivity and BMI, although taste sensitivity showed to be higher among girls (p = 0.002; power = 88%). The study identified three clusters, highlighting the relationship between nutritional sucking habits, consistency of food ingested, and sociodemographic characteristics. Most importantly, a close relation between bottle‐feeding and consumption of soft food consistency was observed.     

Sensory and mass spectrometric analysis of the peptidic fraction lower than one thousand daltons in Manchego cheese

A total of 107 different peptides, all derived from α_S1-, α_S2-, and β-casein, were identified in different fractions of artisan or industrial Manchego cheese at 4 and 8 mo of ripening, and their sequences were examined. Most of these peptides are described for the first time in Manchego cheese. Taste characteristics (umami and bitter) were assigned based on their AA sequence and the position of these AA within the sequence. The umami taste was predominant in all fractions analyzed by the panelists, and the peptides EQEEL, QEEL, and EINEL, containing a high number of glutamic residues, were found within the fractions. However, in several fractions described as having umami characteristics, no peptides responsible for this taste were detected. Therefore, compounds other than peptides seem to be involved in the umami properties of water-soluble extracts lower than 1,000 Da of Manchego cheese.     

电感耦合等离子体质谱法测定固体饮料中有害元素的含量及其来源分析

目的利用电感耦合等离子体质谱法(inductively coupled plasma mass spectrometry,ICP-MS)对固体饮料中有害元素的含量进行全面的测定和分析,为固体饮料中污染物测定和判定能够提供更合理的参考依据。方法样品经硝酸消解赶酸后,采用ICP-MS对不同类型的固体饮料中的有害元素铅、砷、镉、铬、汞、铝、铜、镍、硼元素含量进行测定,并对其来源进行研究。结果固体饮料中有害元素含量表现为AlBCuNiCrAsPbCdHg。由于茶粉的添加,茶固体饮料中铝平均含量高达49.4 mg/kg;同时由于大豆粉的添加,蛋白固体饮料中硼、铜和镍平均含量高达3.86、2.87和1.43 mg/kg。而以添加剂为主要原辅料的风味固体饮料和其他类固体饮料中9种有害元素的平均含量均低于总体的平均值。结论固体饮料中由原辅料引入的有害元素污染风险较高,而由食品添加剂引入的有害元素污染风险较低。     

Effect of High Fat Diets on Body Mass,Oleylethanolamide Plasma Levels and Oxytocin Expression in Growing Rats

Obesity prevalence in developed countries has promoted the need to identify the mechanisms involved in control of feeding and energy balance. We have tested the hypothesis that different fats present in diet composition may contribute in body weight gain and body indexes by regulation of oxytocin gene (oxt) expression in hypothalamus and Oleylethanolamide (OEA) levels in plasma. Sprague–Dawley rats were fed two high fat diets, based on corn (HCO) and extra virgin olive oil (HOO) and results were compared to a low fat diet (LF). LC‐MS/MS analysis showed an increasing trend of OEA plasma levels in HOO group, although no significant differences were found. However, body weight gain of LF and HOO were similar and significantly lower than HCO. HCO rats also had higher Lee index than HOO. Rats fed HOO diet showed higher levels of hypothalamic oxt mRNA expression, which could indicate that oxytocin may be modulated by dietary lipids.     

Association between body composition of growing pigs determined by magnetic resonance imaging, deuterium dilution technique, and chemical analysis

Development of body composition of 440 growing pigs from a three generation full-sib design to identify quantitative trait loci (QTL) was determined by three different methods. Firstly, the non-invasive method deuterium dilution technique (DT), was applied to all pigs in the experiment at six weights 20, 30, 60, 90, 120 and 140kg. Secondly, at each weight class, eight pigs were slaughtered and their entire body chemically analysed (CA). Thirdly, magnetic resonance imaging (MRI) was applied on 16 live pigs at different weights. For the entire empty body (without content of the gastrointestinal tract and bladder), allometric prediction equations to predict body composition from empty body water content measured by DT were derived from chemically analysed serial slaughtered pigs. These equations showed high correlations of 0.92, 0.90 and 0.85 for the contents of body water, fat-free substance as well as protein in fat-free substance, respectively. For the soft tissue (empty body without bones and viscera), allometric prediction equation of body composition based on DT and CA showed correlations of 0.91, 0.88 and 0.82 for water content, fat-free substance, and protein content of fat free substance, respectively. Fat tissue content, fat tissue mass, and lean tissue mass measured by MRI showed allometric relationships to lipid content, lipid mass, and protein mass determined by DT with correlations of 0.98, 0.87, and 0.98, respectively. Lean (measured by MRI) and protein (determined by DT) content of soft tissue was best fitted by a linear-quadratic polynomial and resulted in a correlation of 0.86. Allometric coefficients for change of percentages of chemical components, water (b=-0.036) and protein (b=0.106) in fat-free substance of empty body during growth were similar to those in the literature indicating the consistency of accretion rates of chemical components of the fat-free substance in different studies. Means for protein- and lipid-deposition rates (determined by DT) as well as lean tissue- and fat tissue-deposition rates (measured by MRI) ranged from 95 to 154, 147 to 328, 373 to 420 and 129 to 254g in the different weight ranges. Variation between animals in protein (lean tissue) and lipid (fat tissue) deposition rate was large which can be exploited in order to identify QTL of these traits.     

Development of a novel solid-phase extraction,LC-MS/MS method for the analysis of ethyl carbamate in alcoholic beverages: application to South African wine and spirits

Ethyl carbamate (EC) is a known genotoxic carcinogen that is frequently present in alcoholic beverages and is therefore a public health concern. As a consequence, maximum concentration levels for EC in these commodities are legislated in several countries. Quantitative analytical methods are therefore essential to monitor EC levels in beverages. Most published analytical methods for the determination of EC in alcoholic beverages utilise elaborate sample pre-treatment procedures to obtain injectable samples, or yield low sensitivity, for example where direct injection is used. In addition, these procedures often require large volumes of toxic solvents and are not generally applicable to diverse alcoholic beverages. This paper describes a novel procedure for the determination of EC in wines, fortified wines and spirits. The procedure is based on reversed-phase solid-phase extraction (SPE) sample clean-up combined with normal-phase liquid chromatography-atmospheric pressure chemical ionisation tandem mass spectrometric (NP-LC-APCI-MS/MS) analysis. This method provides a rapid, robust and simple analytical procedure suitable for the analysis of a diverse range of alcoholic beverages. The accuracy of the method (expressed as average recovery from diverse matrices) is 94.5%, with limits of detection (LODs) ranging between 0.25 and 0.63?µg?l^?1 for different matrices. Benefits such as simplified sample preparation, low detection limits, low solvent consumption and good selectivity render the methodology ideally suited to study the occurrence of EC in diverse commodities. The method was applied to study the occurrence of EC in South African wines, fortified wines and spirits. South African wines, aged 1–9 years, contained 1.8–31?µg?l^?1 EC (RSD?=?69%, n?=?106), fortified wines aged 2–34 years contained 2.8–79?µg?l^?1 EC (RSD?=?89%, n?=?21), and brandies aged 3–20 years contained 4.4–95?µg?l^?1 EC (RSD?=?105%, n?=?26). Factors affecting the formation of EC in these commodities were investigated and storage temperature, alcohol content and pH were found to affect the rate of EC formation. Of these variables storage temperature has by far the greatest effect.     

Quantitative targeted and retrospective data analysis of relevant pesticides,antibiotics and mycotoxins in bakery products by liquid chromatography-single-stage Orbitrap mass spectrometry

In addition to ‘traditional’ multi-residue and multi-contaminant multiple reaction monitoring (MRM) mass spectrometric techniques devoted to quantifying a list of targeted compounds, the global food industry requires non-targeted methods capable of detecting other possible potentially hazardous compounds. Ultra-high-performance liquid chromatography combined with a single-stage Orbitrap high-resolution mass spectrometer (UHPLC-HRMS Exactive?-Orbitrap Technology) was successfully exploited for the complete selective and quantitative determination of 33 target compounds within three major cross categories (pesticides, antibiotics and mycotoxins) in bakery matrices (specifically milk, wheat flour and mini-cakes). Resolution was set at 50 000 full width at half maximum (FWHM) to achieve the right compromise between an adequate scan speed and selectivity, allowing for the limitations related to the necessary generic sample preparation approach. An exact mass with tolerance of 5 ppm and minimum peak threshold of 10 000 units were fixed as the main identification conditions, including retention time and isotopic pattern as additional criteria devoted to greatly reducing the risk of false-positive findings. The full validation for all the target analytes was performed: linearity, intermediate repeatability and recovery (28 analytes within 70–120%) were positively assessed; furthermore, limits of quantification between 5 and 100 µg kg^?1 (with most of the analytes having a limit of detection below 6 µg kg^?1) indicate good performance, which is compatible with almost all the regulatory needs. Naturally contaminated and fortified mini-cakes, prepared through combined use of industrial and pilot plant production lines, were analysed at two different concentration levels, obtaining good overall quantitative results and providing preliminary indications of the potential of full-scan HRMS cluster analysis. The effectiveness of this analytical approach was also tested in terms of the formulation of hypotheses for the identification of other analytes not initially targeted which can have toxicological implications (e.g. 3-acetyl-deoxynivalenol and deoxynivalenol-3-glucoside), opening a window on retrospective investigation perspectives in food safety laboratories.     

Structural analysis of enniatin H,I, and MK1688 and beauvericin by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and their production by Fusarium oxysporum KFCC 11363P

The molecular structures of enniatins H, I, and MK1688 and beauvericin were investigated by liquid chromatography-tandem mass spectrometry (LC-MS/MS). MS fragmentation occurred by loss of -CO after opening of the cyclic molecule to carbonyl carbon, and cleavage of the peptide and ester bonds in the molecular structure. Fusarium oxysporum KFCC 11363P was tested for its ability to produce beauvericin and enniatins H, I, and MK1688 on five cereal substrates: rice, barley, maize, wheat, and Indian millet kernels. Furthermore, optimal conditions for the production of the four mycotoxins by the Fusarium isolate were examined on maize at four temperatures (15, 20, 25, and 30°C) and at three moisture contents (10, 20, and 40%). Large amounts of beauvericin and enniatin H were present in maize cultures at 25°C (232.4 and 196.4 µg g^?1, respectively). Enniatins I and MK1688 were maximally formed at 20°C (221.5 and 180.2 µg g^?1, respectively). The optimal moisture contents for the production of enniatins H (196.4 µg g^?1) and MK1688 (165.6 µg g^?1), were 40%.     

Relationships between volatile production,fruit quality and sensory evaluation of Fuji apples stored in different atmospheres by means of multivariate analysis

Aroma compounds, quality parameters and sensory characteristics of Fuji apples were analysed after 3, 5 and 7 months of storage at 1 °C in normal air (AIR; 210 l m^?3 O₂/0.3 l m^?3 CO₂) and in controlled atmospheres with O₂/CO₂ ratios of 10 l m^?3/10 l m^?3 (ULO1), 10 l m^?3/20 l m^?3 (ULO2) and 30 l m^?3/20 l m^?3 (SCA). After storage the apples were kept at 20 °C for 1, 5 and 10 days. The components that contributed most to the characteristic aroma of Fuji apples were ethyl 2‐methylbutanoate, 2‐methylbutyl acetate and hexyl acetate. The highest aroma compound production was found in ULO1 fruits after 5 months of cold storage and 1 day of shelf‐life. After 3 and 5 months of storage, ULO1 fruits showed the highest firmness after both 1 day and 10 days at 20 °C. After 7 months of storage plus 1 day at 20 °C, ULO2 fruits showed higher titratable acidity and soluble solid content; fruit firmness was also maintained throughout the shelf‐life period. Generally, background and superficial colour were not influenced by storage conditions. A statistically significant correlation was found between aroma compounds, quality parameters and sensory evaluation. Copyright © 2003 Society of Chemical Industry     

近红外光谱应用于高粱中总淀粉、直链淀粉与支链淀粉的定量分析

酱香型白酒以高粱为主要原料发酵而成,高粱中的淀粉,尤其是支链淀粉的含量对于酱香型白酒的产品质量起着至关重要的作用,因此针对其总淀粉、直链淀粉与支链淀粉的检测手段研究也应受到人们高度的重视。傅里叶变换近红外光谱法因其准确性高、稳定性好以及快速无损检测等特点,在建立总淀粉、直链淀粉和支链淀粉同时定量分析模型方面得到了较为成功的应用。结果表明,总淀粉、直链淀粉以及支链淀粉的定量分析模型相关系数分别达到0.954 9、0.923 6和0.940 1,交互验证均方根误差分别为1.027 1、0.088 5和1.264 6。可见,基于近红外光谱技术的定量分析方法可适用于高粱中总淀粉、直链淀粉与支链淀粉的同时定量分析。     

Analysis of sudan I,sudan II,sudan III,and sudan IV in food by HPLC with electrochemical detection: Comparison of glassy carbon electrode with carbon nanotube-ionic liquid gel modified electrode

A method was developed for analyzing of sudan I, sudan II, sudan III, and sudan IV by high performance liquid chromatography coupled with an electrochemical detector. The electrochemical oxidation of each compound was investigated with a carbon nanotube-ionic liquid gel modified glassy carbon (MWNTs-IL-Gel/GC) electrode using cyclic voltammetry. The results were compared with those of glassy carbon electrodes. At the MWNTs-IL-Gel/GC electrode, highly reproducible, well-defined cyclic voltammograms for sudan oxidation were obtained. In the flow system, MWNTs-IL-Gel/GC exhibited highly reproducible and well-defined amperometric signals without peak tailing. In addition, the determination of sudan dyes by mean of isocratic reverse-phase HPLC, with amperometric detection at MWNTs-IL-Gel/GC and GC electrode, have been investigated. The chromatograms showed excellent separation. The detection limits ranged from 0.001 to 0.005 ppm. The method was sensitive, selective and could be applicable for the assay of sudan dyes in soft drink samples.