Ettore Coni's research while affiliated with Istituto Superiore di Sanità and other places

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Publications (55)


Contamination of some foodstuffs marketed in Italy by fatty acid esters of monochloropropanediols and glycidol
  • Article

February 2020

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35 Reads

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17 Citations

Eleonora Di Campi

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Mauro Di Pasquale

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Ettore Coni

Fatty acid esters of 3-monochloropropanediol (3-MCPD), 2-MCPD and glycidol (Gly) are food-processing contaminants that cause concerns about possible adverse health effects. The present study evaluates the contamination levels of the three ester classes in 130 samples of foodstuffs marketed in Italy covering 10 food categories, namely margarines, oils, roasted coffee, breakfast cereals, salted crackers, cookies, infant biscuits, rusks, breads and potato crisps. The analytical method employed is a so-called indirect method that entails MCPD/glycidol cleavage from their esterified forms, cleanup, derivatisation and GC-MS analysis. The MCPDs and glycidol concentrations (from esters) were found to be equal or a little higher than the levels reported in previous studies conducted in other European countries and described in the literature. 3-MCPD was the predominant compound in all foodstuffs analysed with the exception for rusks where Gly levels were slightly higher. Considering the sum of MCPD and Gly esters, the most contaminated foodstuffs were seed oils, followed by margarines and cookies, whereas roasted coffee, bread, rusks, cornflakes and infant biscuits were less contaminated with MCPDs and Gly concentrations often below LOQ or LOD values. Refined olive oil, potato chips and salted crackers showed contamination levels intermediate between the two above groups. The results of this study also confirm that the use of palm oil as an ingredient or frying medium is an important cause of increase of the levels of MCPD and Gly esters, especially in salted crackers, rusks and potato crisps. Finally, the Italian intake of 3-MCPD due to the various foods analysed has been calculated and related to TDI. The MoE for Gly was also estimated.

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Development and pharmacokinetic evaluation of erythromycin lipidic formulations for oral administration in rainbow trout (Oncorhynchus mykiss)

March 2011

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140 Reads

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17 Citations

European Journal of Pharmaceutics and Biopharmaceutics

Francesca Serdoz

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[...]

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Enrico Pellegrini

The aim of this work was to enhance the bioavailability of erythromycin base when administered orally in rainbow trout (Oncorhynchus mykiss). Since erythromycin is normally given in the form of medicated feed, in this study three new types of feed formulation were developed. A self-emulsifying system and two types of double microemulsions (O/W/O) were prepared, characterized and adsorbed on a commercial extruded diet for fish. The emulsified systems were based on saturated polyglycolized glycerides and mono- and diglycerides of medium-chain fatty acids (as oily phase), Tween 80 (as surfactant) and, in the case of double microemulsions, distilled water. The systems differed in percentage composition and for the amount and position of erythromycin in different phases. The three medicated feed were then administered orally by means of a gastric probe to rainbow trout and their relative bioavailability was estimated in comparison with that obtained after oral administration of feed with erythromycin powder. For each medicated feed, 80 fish were tested. Finally, plasma profiles of erythromycin after single administration of medicated feeds were used to predict profiles obtainable by administering once-daily medicated feeds for 7 consecutive days. The results proved that the feeds containing microemulsified erythromycin provided largely superior oral bioavailability and the advantage of obtaining the same efficacy against bacterial infections with a much lower dose of drug.


Contamination of vegetable oils marketed in Italy by phthalic acid esters

February 2011

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332 Reads

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69 Citations

Food Control

More than 90% of the phthalic acid esters (PAEs) produced in Europe is used to plasticize polyvinyl chloride (PVC). Animal studies have shown that some PAEs can damage the liver and interfere with the endocrine system, whereas data on the toxic effects on humans are inconsistent. For the general population, the diet is believed to be the main source of PAEs. Food can be contaminated from environmental pollution, industrial food processing (PVC tubing) and certain storage containers. The present study evaluates the contamination levels of the four main PAEs named Di(2-ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP), diisobutyl phthalate (DIBP), diisononyl phthalate (DINP), in 172 samples of vegetable oils marketed in Italy. Diluted oils were directly analysed by GC–MS. PAEs concentrations in vegetable oils were lower than those reported in other studies. Olive-derived oils showed the highest levels. Considering their high consumption in Italy, this finding is significant and some hypotheses on environmental or technological causes have been made. In the case of extravirgin olive oil, the higher levels of PAEs can be ascribed to the absence of the refining process since it has been verified that this technological treatment partially decontaminates the final product while for olive and olive pomace oils, both refined oils, the reasons for a higher contamination are less clear. Probably, a different plant uptake of PAEs from the air, water and soil could give account of this finding. Finally, the percentage Italian intake of PAEs due to the various types of vegetable oils analysed has been calculated.


Depletion of Long-Acting Ampicillin in Goat Milk Following Intramuscular Administration

November 2010

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48 Reads

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7 Citations

Journal of Agricultural and Food Chemistry

Although goat milk production represents today a very small percentage of the world milk market, this percentage has been growing continuously during the past 20 years. Goat milk is the basic milk supply in many developing countries and provides tasteful derivative products in developed countries. Goats, as well as all milk-producing animals, can be affected by mastitis, but goats being considered a minor species, few drugs are specifically registered for these animals; most, at least for mastitis treatment, are usually tested and registered for use in cows. This situation leads often to the adoption for goat milk of withdrawal periods defined for cows even if these extrapolations prove almost never valid for goats. In the present study, the elimination of the β-lactam antibacterial agent ampicillin in goat milk was investigated. Ampicillin was chosen because it is one of the most common antibiotics used by goat farmers against mastitis due to the fact that it is well tolerated and has short elimination times in cows. Goats were treated with long-acting ampicillin at 15 mg (kg of body weight)(-1) by double intramuscular injection at 72 h interval. Milk was collected in a 12 h milking scheme. The method used to determine the levels of ampicillin in goat milk was based on a liquid-liquid extraction of this drug from the matrix, successive derivatization with formaldehyde, and final separation by HPLC with fluorescence detection. The results point out a slow depletion of ampicillin and, consequently, a withdrawal period (13 milkings) longer than that extrapolated and authorized for cows and sheep.


Monitoring of perfluorinated compounds in edible fish from the Mediterranean Sea

August 2009

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168 Reads

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112 Citations

Food Chemistry

Perfluorooctanoic acid (PFOA) and perfluorooctane sulphonate (PFOS) are environmental contaminants belonging to a chemical group known as perfluorinated compounds (PCFs). The United States Environmental Protection Agency (US EPA) considers both compounds to be carcinogenic. The goal of the present study was to evaluate the contamination levels of PFOS and PFOA in edible fish of the Mediterranean Sea. Twenty six fish muscles, 17 fish livers, five series of cephalopods (each composed of ten specimens) and thirteen series of bivalves (each composed of about 50 specimens) were used for the investigation. A fast sample treatment, followed by an LC–ESI–MS/MS method is described for the identification, and quantification of PFOA and PFOS in fish. The method was in-house-validated through the determination of precision, accuracy, specificity, calibration curve, decision limit (CCα), and detection capability (CCβ). The results showed PFOA and PFOS levels in fishes and molluscs lower than those reported for analogue matrices in different geographic areas. Therefore, our biomonitoring results did not show that the Mediterranean Sea had any particularly alarming pollution by PFCs, although it is located in a semi-closed basin with scarce water change. Nonetheless, a worrying element is that a few fish showed extremely high contamination by PFOA and PFOS. This finding needs further clarification in order to assess whether such unusual contamination is linked to “dot-like” pollutant release, which could explain the anomaly.


Climate change and food safety: An emerging issue with special focus on Europe

May 2009

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1,199 Reads

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589 Citations

Food and Chemical Toxicology

According to general consensus, the global climate is changing, which may also affect agricultural and livestock production. The potential impact of climate change on food security is a widely debated and investigated issue. Nonetheless, the specific impact on safety of food and feed for consumers has remained a less studied topic. This review therefore identifies the various food safety issues that are likely to be affected by changes in climate, particularly in Europe. Amongst the issues identified are mycotoxins formed on plant products in the field or during storage; residues of pesticides in plant products affected by changes in pest pressure; trace elements and/or heavy metals in plant products depending on changes in their abundance and availability in soils; polycyclic aromatic hydrocarbons in foods following changes in long-range atmospheric transport and deposition into the environment; marine biotoxins in seafood following production of phycotoxins by harmful algal blooms; and the presence of pathogenic bacteria in foods following more frequent extreme weather conditions, such as flooding and heat waves. Research topics that are amenable to further research are highlighted.


Contamination of Grape Seed Oil with Mineral Oil Paraffins

December 2008

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165 Reads

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31 Citations

Journal of Agricultural and Food Chemistry

The contamination of 11 commercial grape seed oils with paraffins of mineral oil origin was analyzed by online-coupled HPLC-HPLC-GC-FID and ranged from 43 to 247 mg kg(-1). The analysis of the marc and seeds indicated that the contamination is primarily from the peels. Since superficial extraction of the seeds with hexane removed most of the mineral paraffins, the contamination of the seeds is largely on the surface, perhaps transferred from the peels during storage of the marc. Mechanical purification of the seeds combined with washing with hexane reduced the contamination of the oil by a factor of about 10. The refining process removed 30% of the mineral paraffins, primarily the more volatile components. Oil obtained from the seeds of fresh grapes, including grapes not having undergone any phytochemical treatment, contained clearly less mineral paraffins (up to 14 mg kg(-1)), and the peels were less contaminated, suggesting an environmental background contamination. To this an additional contamination might be added by a treatment of the grapes used for wine making.


Coumarin and Cinnamaldehyde in Cinnamon Marketed in Italy: a Natural Chemical Hazard?
  • Article
  • Full-text available

December 2008

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2,368 Reads

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98 Citations

Food Additives & Contaminants Part A

Food Additives & Contaminants Part A

Some plants that are processed into foods often contain natural substances that may be hazardous to human health. One example is coumarin, which is known to cause liver and kidney damage in rats, mice and probably humans. The main source of coumarin in the diet is cinnamon. The name 'cinnamon' is correctly used to refer to Ceylon cinnamon, also known as 'true cinnamon'. However, other plant species are sometimes sold with the label of cinnamon. This is the case of Cinnamomun aromaticum (cassia). In recent years, due to its cheaper price, cassia is replacing true cinnamon in the European food market being largely used in the preparation of some kinds of sweets. Several European health agencies have recently warned against consuming high amounts of cassia due to its high content of coumarin. In this study, 34 samples of cinnamon and 50 samples of cinnamon-containing foodstuffs were collected from the Italian market. Quantitative determinations of coumarin and cinnamaldehyde were performed by high-performance liquid chromatography (HPLC) with diode array detector (DAD). The analytical method was in-house validated assessing recovery, repeatability, linearity, limit of detection (LOD) and limit of quantitation (LOQ). The results showed that about 51% of cinnamon samples consisted of cassia, 10% were probably a blend of cassia and Ceylon cinnamon, whereas only 39% were actually Ceylon cinnamon. As far as cinnamon-containing foods are concerned, the samples often exceeded the maximum level fixed in the European Flavourings Directive of 2 mg kg(-1).

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Bioaccumulation Potential of Dietary Arsenic, Cadmium, Lead, Mercury, and Selenium in Organs and Tissues of Rainbow Trout (Oncorhyncus mykiss) as a Function of Fish Growth

May 2008

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121 Reads

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96 Citations

Journal of Agricultural and Food Chemistry

The distribution and potential bioaccumulation of dietary arsenic, cadmium, lead, mercury, and selenium in organs and tissues of rainbow trout (Oncorhyncus mykiss Walbaum, 1792), a major aquaculture species, was studied in relation to fish growth over a period of >3 years. Fish were reared under normal farming conditions, that is, fed a standard fish food and exposed to negligible levels of waterborne trace elements. The age-related variations in the content of each trace element in gills, kidney, liver, muscle, and skin were studied through nonparametric regression analysis. A buildup of all elements in all tissues and organs was observed, but due to dilution with growth, the concentrations did not increase, except in a few cases such as cadmium and mercury in liver and kidney. In muscle tissue, the concentrations of mercury, lead, and selenium did not alter significantly with growth, whereas cadmium increased but remained at exceedingly low levels. The concentration of arsenic in muscle tissue peaked at 14 months and then decreased in adult specimens. Arsenic speciation by high-performance liquid chromatography--inductively coupled plasma mass spectrometry revealed that arsenic in muscle was almost exclusively present in the form of nontoxic arsenobetaine. Application of a mercury mass balance model gave predicted concentrations in agreement with measured ones and showed that in farmed rainbow trout the ratio of mercury concentrations in feed and in fish is about 1:1. Therefore, rainbow trout does not approach the limits established for human consumption even when reared with feed at the maximum permitted levels. These findings highlight the low bioaccumulation potential of toxic trace elements such as cadmium, lead, and mercury in rainbow trout following dietary exposure. On the other hand, selenium concentrations in muscle (about 0.2 microg g (-1) of fresh weight) show that rainbow trout may be a good source of this essential element.


An absorption study of dietary administered acrylamide in swine

August 2007

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18 Reads

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20 Citations

Food and Chemical Toxicology

Acrylamide is a food toxicant suspected to be carcinogenic to humans. It is formed in the heat processing of carbohydrate-rich food. A current issue in food safety is whether acrylamide actually represents a risk for human health. At present, available information is insufficient to reach any conclusions. Inter alias, a still unclear matter is the fraction of acrylamide ingested by food that is absorbed and metabolized. This study compared the in vivo relative absorption of acrylamide formed in cooked food with that of the pure compound dissolved in drinking water using the pig (25 Italian Large White females) as the animal model. Acrylamide intakes of about 0.8 and 8 microg kg(-1) pig body wt day(-1) equal to one and ten times, respectively, the maximum average acrylamide daily intake for humans from the diet (expressed on a body wt basis) in industrialized countries, were chosen for the study. Adducts with the N-terminal valine of haemoglobin formed by acrylamide and its epoxide metabolite glycidamide, were used as exposure markers. Analyses were carried out by gas chromatography/mass spectrometry following in-house method validation. Both for the low and the high dose regimen, the glycidamide adduct levels in swine globins were lower of the limit of quantification of the method. As concerns acrylamide adducts, it was found that the relative absorption of acrylamide from feed and water was the same and that there is a direct proportionality between the adduct concentration and acrylamide intake.


Citations (48)


... However, industrial processing, particularly hightemperature treatment during deodorisation, is the most important factor for the formation of undesirable process-induced chemical contaminants [4,5]. Apart from deodorisation, gas-frying, char grilling, and baking at approximately 200 C or higher also seem to result in the formation of MCPDEs and GEs in considerable amounts in edible oils and oil-based food products [6,7]. Studies have demonstrated that the formation of 2-and 3-MCPDE occurs during the chemical reactions of triacylglycerols (TAGs), some diacylglycerols (DAGs) and monoacylglycerols (MAGs) with reactive chlorine donors. ...

Reference:

Simultaneous determination of 24 congeners of 2- and 3‑monochloropropanediol esters and 7 congeners of glycidyl esters using direct multi-residue analytical LC-MS/MS methods in various food matrices
Contamination of some foodstuffs marketed in Italy by fatty acid esters of monochloropropanediols and glycidol
  • Citing Article
  • February 2020

... In particular, analyses were performed on pasture, bran, maize and water samples from wells placed in the geographical area of the farms. As described in previous studies, sampling and storage steps were optimized so as to reduce all possible contamination, loss or alteration that could negatively affect reliability of data (Coni et al., 1990a,b;Stacchini et al., 1992). Details on the experimental protocol adopted are reported elsewhere (Coni et al., 1994(Coni et al., , 1995. ...

ZEEMAN EFFECT IN THE DETERMINATION BY GFAAS OF TOXIC METALS (CADMIUM AND LEAD) IN FOODSTUFFS OF ANIMAL ORIGIN
  • Citing Chapter
  • December 1992

... Furthermore, there is a great diversity in reference values of trace elements in human biological material reported in the literature the past 2–3 decades. This is not solely due to technical progress, but also reflects inherent analytical difficulties associated with analysing a multitude of metals present at minute concentrations, and improvements in the preanalytical phase91011121314151617. Analysis of trace elements in biological fluids and tissues serves several purposes, including determination of the concentration and distribution of essential trace elements in normal and disease conditions, detection and allocation of potential toxic metals, and diagnosis of trace-element deficiency states and trace-element related diseases1819202122232425. ...

An experimental approach to the assessment of reference values for trace elements in human organs
  • Citing Article
  • January 1994

Trace Elements in Medicine

... For example in Morocco, Bouisfi found that his average is -0.521 °C [9], in Latvia the milk freezing point ranged from -0.640°C till -0.494°C [4], in Germany from -0.531°C till -0.468°C [3], in Poland -0.540°C and -0.570°C [10], in Estonia -0.550 °C and -0.497 °C [1], American researchers found that it ranged from -0.550°C till -0.512°C [11]. The mean milk freezing point in Italy is -0.528°C [12], in Netherlands -0.521°C [13], in Czech Republic -0.523°C [14], in Switzerland -0.526°C [15], in the UK -0.539°C is different too [16]. ...

A pilot survey on the freezing point of raw and heat-treated Italian milk
  • Citing Article
  • January 1997

Italian Journal of Food Science

... Inductively coupled plasma mass spectrometry is a powerful analytical technique for rapid multielemental analysis of biological samples, including milk, and has been shown to be a valuable method to assess the concentration of elements of nutritional interest (e.g. Fe, Cu, Zn, Se, I, Cr, Co) in both human milk and infant formulas [14][15][16][17][18]. Hyphenated techniques based on coupling on line size exclusion chromatography (SEC) with the ICP-MS are now established as the most realistic and potent analytical tools available for elemental speciation analysis [19][20][21][22]. ...

Speciation of trace elements in human milk by high performance liquid chromatography combined with inductively coupled plasma-mass spectrometry
  • Citing Article
  • March 1996

... Apart from the conventional biosensors, novel hybrid biosensors are developed for the determination of antibacterials. It combines the activities of microorganism with potentiometric measurements ( Pellegrini et al. 2005). Furthermore, bioluminescent bacteria have been used at the altar of biosensors ( Virolainen et al. 2008). ...

Reference:

Antibacterials
Advantages and limitations of a novel hybrid biosensor for detecting toxic compounds in food
  • Citing Article
  • October 2005

International Journal of Environmental Analytical Chemistry

... Triton X-100 solvent was scrapped because ICP OES nebulisation was not good, also provided problematic due to foam. In this respect, dairy products analysis by direct nebulisation of aqueous solutions has been reported to be compromised by poor accuracy attributed both aerosol droplet size and fatty acid content, resulting incomplete elemental quantification (Coni, Stacchini, Caroli, & Falconieri, 1990;Emmett, 1988). ...

Analytical approach to obtaining reference values for minor and trace elements in human milk
  • Citing Article
  • September 1990

Journal of Analytical Atomic Spectrometry

... The performances of ICPOES and NAA were examined for their suitability in determining Al, Cd, Cr, Cu, Mg, Mn, V, and Zn in human lung tissue. (145) For ICPOES, samples were pretreated by ashing and the residue dissolved in nitric acid. Both ICPOES and NAA gave reliable results, although Al, Cd, and V were troublesome. ...

Critical comparison of performances of inductively coupled plasma atomic emission spectrometry and neutron activation analysis for the determination of elements in human lungs
  • Citing Article
  • October 1989

Journal of Analytical Atomic Spectrometry

... The evaluation of inhibition after 2 h showed that Qs and TCs were detectable at 25 µg/L. The biosensor was reportedly not sensitive to any of the other antibiotics studied (β-Ls, macrolides, sulfonamides and aminoglycosides) [166]. Ferrini et al. presented a hybrid biosensor in which the microbiological screening of antibacterials was combined with electrochemical detection using Bacillus stearothermophilus var. ...

Electrochemical sensor for the detection and presumptive identification of quinolone and tetracycline residues in milk
  • Citing Article
  • August 2004

Analytica Chimica Acta

... To test the interference of other competing metals on Zn-induced zinquin fluorescence, equimolar Zn-zinquin solution (25 µmol/L) was incubated in the absence or presence of Mg (24 µg/ mL), Ca (100 µg/mL), Fe (2 µg/mL), Cu (1 µg/mL), Mn (0.01 µg/mL), Co (0.0005 µg/mL), Cd (0.005 µg/mL), Ba (0.06 µg/mL), and the fluorescence intensity at 490 nm emission wavelength was recorded by exciting the solution at 365 nm. These metal concentrations used were chosen based on their reported upper limits in the human serum/plasma [18][19][20][21]. The excitation and emission slit widths were set at 5 nm and all the spectra were recorded at a controlled temperature of 25 ± 2 °C. ...

The Assessment of Reference Values for Elements in Human Biological Tissues and Fluids: A Systematic Review