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    Contamination of vegetables oils with mineral oils [La contaminazione degli oli vegetali con oli minerali]

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    Mineral oils are complex mixtures of hydrocarbons (saturated and unsaturated) deriving from petroleum. Different products such as combustible oils, fuel oils, bases for lubricating oils, motor oils, hydraulic oils and purified mineral oils (food grade), are obtained from fractional distillation and further processing of petroleum. Toxicity of mineral oils depends on the molecular weight of the hydrocarbons and the refining degree. Raw mineral oils contain high amounts of aromatics and are classified as carcinogens to humans, meanwhile refined paraffins are responsible for adverse effects when administered to rats (F-344) at levels ranging from 0.01 to 20 mg/kg b.w. (Depending on the oil type and its viscosity). High contamination levels have been also found in human milk and adipose tissues. There are many possible sources of contamination for vegetable oils and we can not exclude a contribution by the environment. Among other possible sources we can remember: the lubricating oils used in the extraction plant, storage and transport in jute bags, transport in ship previously used to transport mineral oils, handling and storage of the raw matter (it is the case of pomace) under inappropriate conditions. Coupled LC-GC represents an optimal choice for determining the contamination: it allows to analyse a high number of samples per day, minimising sample preparation which is reduced to a simple sample dilution before injection. Except for extra virgin olive oils, which rarely result contaminated with levels above the detection limit, the different types of vegetable oils have a contamination level generally above 10 mg/kg. Among the different vegetable oils, pomace olive oils result to be the most contaminated (with amounts always higher than 100 mg/kg)

    A survey on the presence of free glutamic acid in foodstuffs, with and without added monosodium glutamate

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    A survey on free glutamic acid (Glu) content in a variety of foods (broths, soups, sauces and salad dressings), with and without added monosodium glutamate (MSG), was carried out. A simple procedure, involving a dilution step for liquid samples or homogenization with 0.1 N HCl for solid and slurry samples, followed by derivatization with o-phthaldialdehyde, HPLC separation on C18 column and spectrofluorometric detection, was employed to quantify Glu, as well as a number of other free amino acids and biogenic amines. Broths and soups with added MSG had Glu contents of 92.7–341 mg/100 g. The highest amounts of Glu in foods with no added MSG were found in products containing hydrolyzed proteins (up to 129 mg/100 g). None of the products ready for consumption exceeded the limit of 10 g/kg of food, established by the European Directive, 95/2/CE [European Parliament and Council Directive (1995). No. 95/2/ EC of 20 February 1995 on food additives other than colours and sweeteners. Official Journal, L061, 1–40]. Relatively high amounts of biogenic amines were found in marmite (77.3 mg/100 g of putrescine and 32.2 mg/100 g of tyramine) and soy sauce while broths and soups showed generally low amounts of biogenic amines, putrescine being the most represented. Ó 2007 Elsevier Ltd. All rights reserved

    Variety Differentiation of Virgin Olive Oil Based on n-Alkane profile

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    An on-line LC–GC method was used to assess the n-alkane composition of 40 olive oil samples obtained from three different cultivars from a restricted grove zone in Croatia. Olive samples were handpicked at three different ripening stages during four consecutive years. No significant differences were found in relation to the variable ‘‘period of harvesting’’, while the effects ‘‘variety’’ and ‘‘year’’ as well as their interaction caused significant differences for most of the n-alkane components (p60:05). Despite the influence of the production year, linear discriminant analysis based on the n-alkane components was able to correctly identify the variety of 97.5% of the samples

    Relative hopane content confirming the mineral origin of hydrocarbons contaminating foods and human milk

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    Hopanes, triterpenoid hydrocarbons formed under geological conditions, were analysed to confirm the mineral origin of the unresolved complex mixtures of hydrocarbons observed in the gas chromatography with flame ionization detection chromatograms of human milk and certain foodstuffs. The ‘relative hopane content’ (RHC) is introduced, i.e. it is the area ratio of the sum of the hopanes and the paraffins in the same segment of the chromatogram. The RHC in various mineral oil products (motor oils, hydraulic oils, lubricating oils, Vaseline) was 3.4%, with a relative standard deviation of 19%. The RHC determined in samples of vegetable oils, mussels and clams as well as of human milk containing an unresolved complex mixture of hydrocarbons was in the same range, confirming that these samples were contaminated by mineral oil material
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