Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Giacomo Dugo is active.

Publication


Featured researches published by Giacomo Dugo.


Journal of Agricultural and Food Chemistry | 2008

Release of Protein, Lipid, and Vitamin E from Almond Seeds during Digestion

Giuseppina Mandalari; Richard M. Faulks; Gillian T. Rich; Vincenzo Lo Turco; David R. Picout; Rosario B. Lo Curto; Giuseppe Bisignano; Paola Dugo; Giacomo Dugo; Keith W. Waldron; Peter R. Ellis; Martin S. J. Wickham

The evaluation of the bioaccessibility of almond nutrients is incomplete. However, it may have implications for the prevention and management of obesity and cardiovascular disease. This study quantified the release of lipid, protein, and vitamin E from almonds during digestion and determined the role played by cell walls in the bioaccessibility of intracellular nutrients. Natural almonds (NA), blanched almonds (BA), finely ground almonds (FG), and defatted finely ground almonds (DG) were digested in vitro under simulated gastric and gastric followed by duodenal conditions. FG were the most digestible with 39, 45, and 44% of lipid, vitamin E, and protein released after duodenal digestion, respectively. Consistent with longer residence time in the gut, preliminary in vivo studies showed higher percentages of nutrient release, and microscopic examination of digested almond tissue demonstrated cell wall swelling. Bioaccessibility is improved by increased residence time in the gut and is regulated by almond cell walls.


Food Chemistry | 2013

Characterization of 12 Capsicum varieties by evaluation of their carotenoid profile and pungency determination.

Daniele Giuffrida; Paola Dugo; Germana Torre; Chiara Bignardi; Antonella Cavazza; Claudio Corradini; Giacomo Dugo

In this research 12 different varieties of Capsicum cultivars belonging to three species (Capsicum chinense, Capsicum annuum, Capsicum frutescens) and of various colour, shape, and dimension have been characterised by their carotenoids and capsaicinoids content. The berries were cultivated in the region Emilia-Romagna, in Northern Italy. The native carotenoid composition was directly investigated by an HPLC-DAD-APCI-MS methodology, for the first time. In total, 52 carotenoids have been identified and considerable variation in carotenoid composition was observed among the various cultivars investigated. Among the cultivars with red colour, some Habanero, Naga morich and Sinpezon showed an high β-carotene content, whereas Serrano, Tabasco and Jalapeno showed an high capsanthin content and the absence of β-carotene. Habanero golden and Scotch Bonnet showed a high lutein, α-carotene and β-carotene amounts, and Habanero orange was rich in antheraxanthin, capsanthin and zeaxanthin. Cis-cryptocapsin was present in high amount in Habanero chocolate. The qualitative and quantitative determination of the capsaicinoids, alkaloids responsible for the pungency level, has also been estimated by a validated chromatographic procedure (HPLC-DAD) after a preliminary drying step and an opportune extraction procedure. Results have also been expressed in Scoville units. Dry matter and water activity have also been established on the fresh berries. The dried peppers of each variety were then submitted to the evaluation of the total nitrogen content, measured by a Dumas system, permitting to provide information on the protein content that was found to be in the range between 7 and 16%.


Analytica Chimica Acta | 2002

Gas chromatographic–tandem mass spectrometric identification of phenolic compounds in Sicilian olive oils

Marcello Saitta; Simona Lo Curto; Francesco Salvo; Giuseppa Di Bella; Giacomo Dugo

Phenolic compounds in Sicilian olive oils were analyzed by GC–MS and GC–MS/MS after extraction with methanol:water 80:20 and derivatization with bis(trimethylsilyl)trifluoracetamide and trimethylchlorosilane (BSTFA:TMCS 99:1). Numerous compounds were detected and 23 were identified. Tyrosol, hydroxytyrosol and the decarbomethoxy ligstroside and oleuropein aglycons in the dialdehydic forms were the most abundant compounds. 4-(Acetoxyethyl)-1-hydroxybenzene, 3,4-dihydroxyphenylacetaldehyde, syringaldehyde and the cis form of ferulic acid were identified: these compounds were not found in olive oils before. The presence of the dialdehydic form of elenolic acid (without carbomethoxy group) linked to 3-methoxy-4-hydroxyphenylethanol was hypothesized. There were quantitative differences in oils from the varieties Nocellara del Belice, Santagatese and Cerasuola; these differences could depend on the olive varieties and ripeness.


Journal of Chromatography A | 2008

Serial coupled columns reversed-phase separations in high-performance liquid chromatography Tool for analysis of complex real samples

Miguel Herrero; Francesco Cacciola; Paola Donato; Daniele Giuffrida; Giacomo Dugo; Paola Dugo; Luigi Mondello

High-performance liquid chromatography is considered as the selected analytical tool for a huge number of applications, including the carotenoid analysis. However, due to the great complexity of some natural samples containing this kind of compounds, conventional LC could not have enough separation power. In this work, serial connection of several columns is proposed as an alternative to LC and also to comprehensive two-dimensional LC for the analysis of carotenoids from complex real matrices. Different parameters regarding these separation procedures are studied and discussed, such as the stationary phase used or the application of high separation temperatures. The applicability of connecting two C30 columns to significantly increase the separation power, resolution and peak capacity for the analysis of carotenoids has been demonstrated for the first time. In fact, a peak capacity of 79 was obtained when using two C30 serial coupled columns, compared to 61 achieved using a single column. Similar improvements were also observed for the other serial couplings studied. The present methodology could be applied to the analysis of carotenoids in a great variety of samples. To the best of our knowledge, this is the first development carried out to study natural products such as carotenoids using columns coupled in series.


Food Additives & Contaminants Part B-surveillance | 2015

Trace elements in Thunnus thynnus from Mediterranean Sea and benefit–risk assessment for consumers

Giuseppa Di Bella; Angela Giorgia Potortì; Vincenzo Lo Turco; Daniel Giuseppe Bua; Patrizia Licata; Nicola Cicero; Giacomo Dugo

Trace elemental levels were determined by inductively coupled plasma-mass spectrometry in muscle, eggs and sperm of 23 Thunnus thynnus fishes collected from May to August 2013 in the Mediterranean Sea. Zn, Mn, Fe, Cu, Cr, Ni and Se content was compared with Recommended Daily Allowances. Cd, Hg and Pb concentrations were below the maximum limits fixed by the European Legislation. Tuna food safety was evaluated considering Tolerable Weekly Intake (TWI) or Provisional Tolerable Weekly Intake for As, Hg, Cd and Pb. Only BMDL01 data for As and Pb were calculated as established by the Joint FAO/WHO Expert Committed on Food Additives. The daily consumption of fresh tuna ensures a good intake of these elements. None of the tested samples surpassed the European maximum limits. Cd, Hg and Pb remained within safety margins, while As is slightly higher than the provisional TWI.


Journal of Separation Science | 2008

Analysis of native carotenoid composition in orange juice using C30 columns in tandem

Paola Dugo; Miguel Herrero; Daniele Giuffrida; Carla Ragonese; Giacomo Dugo; Luigi Mondello

In the present contribution, a novel analytical approach based on using serial coupled conventional LC columns is proposed to the study of the native carotenoid composition of orange juice. The great difficulties that are found when analyzing complex carotenoid samples, due to the high natural variability of these compounds as well as to the presence of carotenoid esters are well documented. To overcome some of these limitations, we have developed a methodology including the study of both the saponified and the intact sample by means of two different LC-DAD/APCI-MS methods. The increase in the resolution and separation power obtained when using two serial coupled C(30) columns is demonstrated, and significant increases in peak capacity have been achieved. By using this new methodology, 44 different carotenoids have been tentatively identified. Among them, several violaxanthin diesters have been directly identified in orange juice for the first time. The main carotenoids in orange juice were violaxanthin, lutein, luteoxanthin, 9-cis-antheraxanthin, and beta-cryptoxanthin. Some of them were found in both their free and esterified forms. To the best of our knowledge, this is the first application of serial couplings of C(30) columns for the identification of the native carotenoid composition of natural matrices.


Natural Product Research | 2014

Statistical characterisation of heavy metal contents in Paracentrotus lividus from Mediterranean Sea

Andrea Salvo; Angela Giorgia Potortì; Nicola Cicero; Maurizio Bruno; Vincenzo Lo Turco; Giuseppa Di Bella; Giacomo Dugo

This work focuses on the estimation of Hg, As, Cr, Ni, Cu, V, Cd and Pb by inductively coupled plasma mass spectrometry in 135 adult specimens of Paracentrotus lividus collected in different coastal areas of Sicily (Gela, Punta Secca, Ragusa (RG), Siracusa, Priolo, Catania, Messina, Milazzo, Brolo and Filicudi), in order to monitor the Mediterranean marine ecosystem by use of sea urchin as bioindicator. Moreover, the paper deals with the statistical classification of the tested samples according to the sampling area based on metal concentrations. The descriptive statistics findings were obtained and, a starting multivariate matrix was built. Data-sets were subjected to Kruskal–Wallis test to verify the significance of differences in metal concentrations, and then a factor analysis with principal components extraction was performed to try to differentiate urchin samples collected in different areas. The results showed that P. lividus is a suitable organism to be used as bioindicator.


Hrc-journal of High Resolution Chromatography | 1999

Multidimensional capillary GC-GC for the analysis of real complex samples. Part IV. Enantiomeric distribution of monoterpene hydrocarbons and monoterpene alcohols of lemon oils

Luigi Mondello; Maurizio Catalfamo; Antonella Cotroneo; Giovanni Dugo; Giacomo Dugo; Harold M. McNair

This paper describes a fully automated, multidimensional, double-oven GC-GC system, developed in our laboratory. The system is based on the use of mechanical valves which allow the multitransfer of different fractions during the same GC analysis and the use of the two GC independently when the multitransfer options is not used. Pneumatic and electronic circuits permit maintenance of constant retention times in the pre-column, even for the components eluted after numerous transfers. The system has been used for the determination of the enantiomeric distribution of β-pinene, sabinene, limonene, linalol, terpinen-4-ol, and α-terpineol in lemon oils. The results obtained allowed the characterization of cold-pressed lemon oils.


Natural Product Research | 2016

Toxic and essential metals determination in commercial seafood: Paracentrotus lividus by ICP-MS

Andrea Salvo; Nicola Cicero; Rossella Vadalà; Antonio Francesco Mottese; Daniel Giuseppe Bua; Domenico Mallamace; Carlo Giannetto; Giacomo Dugo

Toxic and essential metals content was determined by inductively coupled plasma mass spectrometry in commercial sea urchins samples from the Mediterranean Sea and Pacific Ocean. Results show that Chilean samples have the highest values of Cd, As, Ni, Cr and V; Spanish samples have the maximum Hg content while Sicilian samples have the lowest content of toxic metals. The toxic metal traces were compared with the limits of European Community (EC) No. 1881/2006 for bivalve molluscs. All samples exceed Pb and Cd limit levels; regarding Hg levels, only Sicilian and Sardinian samples have Hg content below the EC limits. The dietary intake of toxic and essential elements was evaluated for an adult. Furthermore, our study highlights a correlation between the toxic elements content and the marine environmental conditions of the places of origin even though only the generic FAO fishing area is specified.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 2009

Analysis of furan in coffee of different provenance by head-space solid phase microextraction gas chromatography-mass spectrometry: effect of brewing procedures.

Lara La Pera; Alfredo Liberatore; Giuseppe Avellone; Serena Fanara; Giacomo Dugo; Pasquale Agozzino

A simple, sensitive and accurate method for the analysis of furan in roasted coffee has been used based on headspace–solid-phase micro-extraction (HS–SPME) coupled to gas chromatography–mass spectrometry (GC–MS). The extraction was performed using 75-µm carboxen/polydimethylsiloxane fiber. Ionic strength, extraction time and temperature, and desorption time were assessed as the most important parameters affecting the HS–SPME procedure and d 4-furan was used as the internal standard. The linearity range was in the range 0.0075–0.486 ng g−1; the LOD and LOQ calculated using the signal-to-noise ratio approach were 0.002 and 0.006 ng g−1, respectively. The inter- and intra-day precision was 8 and 10%, respectively. The concentration of furan found in batches of roasted coffee powder different producing countries ranged from 57.3 to 587.3 ng g−1. The mean reduction in furan levels observed when brewing coffee by either infusion, using a moka pot or an expresso machine was 57, 67.5 and 63.3%, respectively.

Collaboration


Dive into the Giacomo Dugo's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge