Giuseppe Cinelli

Prof. Giuseppe Cinelli

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 December 2011 in Analytical and Bioanalytical Chemistry
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Journal Article
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MRMario Vincenzo Russo
Mario Vincenzo Russo
INIvan Notardonato
Ivan Notardonato
GCGiuseppe Cinelli
Giuseppe Cinelli
Pasquale AvinoPasquale Avino
Pasquale Avino

1 December 2017 in Journal of Water Process Engineering
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Journal Article
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GCGiuseppe Cinelli
Giuseppe Cinelli
FCFrancesca Cuomo
Francesca Cuomo
LALuigi Ambrosone
Luigi Ambrosone
MCMatilde Colella
Matilde Colella
ACAndrea Ceglie
Andrea Ceglie
Francesco LopezFrancesco Lopez
Francesco Lopez

1 August 2018 in Colloids and Surfaces B: Biointerfaces
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Journal Article
Closed access
LPLuisa Perugini
Luisa Perugini
GCGiuseppe Cinelli
Giuseppe Cinelli
MCMartina Cofelice
Martina Cofelice
ACAndrea Ceglie
Andrea Ceglie
Francesco LopezFrancesco Lopez
Francesco Lopez
FCFrancesca Cuomo
Francesca Cuomo


20 November 2013 in Analytical Methods
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Journal Article
Closed access
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GCGiuseppe Cinelli
Giuseppe Cinelli
Pasquale AvinoPasquale Avino
Pasquale Avino
INIvan Notardonato
Ivan Notardonato
MRMario Vincenzo Russo
Mario Vincenzo Russo
A low solvent consumption method for the sensitive determination of organophosphorus (OP) and triazine (TR) pesticides in wine samples is studied. The pesticides were extracted by ultrasound vortex assisted dispersive liquid–liquid microextraction (USVADLLME): 10 mL of sample, 1 mL of NaH2PO4 1 M, 10 μL tolidin in ethanol (internal standard) and 250 μL of C2H4Cl2 (extraction solvent) were vortexed for 30 s (any dispersive solvent was used) and the solution was kept in an ultrasound bath: the extraction was performed at 40 kHz of ultrasound frequency and 110 W for 10 min at room temperature. The determination was performed by means of gas chromatography equipped with nitrogen–phosphorus detector (GC-NPD). The enrichment factors of the analytes ranged from 210 to 232 fold and the recovery ranged from 92.0% to 103.4% (with a Relative Standard Deviation, RSD, below 7.5%). After centrifugation, the bottom phase of the chlorinated solvent was separated from the liquid hydro-alcoholic matrix, dried with anhydrous Na2SO4 and injected into the GC-NPD system. The efficiency of the liquid-phase micro-extraction process was slightly affected by the characteristics of wine samples, therefore the analytical characteristics of the method were evaluated in the linear range 0.01–10 ng mL−1. The correlation coefficients (R2) of each pesticide are above 0.963. The Limits of Detection (LOD) in GC-NPD vary between 0.007 ng mL−1 and 0.07 ng mL−1 (RSD ≤ 9.0) whereas the Limits of Quantification (LOQ) range between 0.024 ng mL−1 and 0.225 ng mL−1 (RSD ≤ 6.9); the intra-day and inter-day repeatabilities, calculated as RSD in the real matrix, are below 6.7% and 8.8%, respectively. Particular attention was devoted to comparing this methodology with other similar analytical methodologies: LODs and RSDs were studied and commented upon. It should be underlined that the good sensibility and high versatility of this methodology allow investigation of organophosphorus and triazine pesticides. At the end, the applicability of the method was demonstrated using commercial wine samples.