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Migration of plastic additives and non-intentionally added substances from packaging into edible oils and beverages: A combined GC–MS and hydrolysis–capillary electrophoresis approach

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dc.contributor.author STURZA, Rodica
dc.contributor.author DRAGANCEA, Veronica
dc.contributor.author GHENDOV-MOSANU, Aliona
dc.contributor.author NISTOR, Ileana-Denisa
dc.contributor.author MIRILA, Diana-Carmen
dc.contributor.author LAZACOVICI, Dmitri
dc.date.accessioned 2026-07-15T19:08:43Z
dc.date.available 2026-07-15T19:08:43Z
dc.date.issued 2026
dc.identifier.citation STURZA, Rodica; Veronica DRAGANCEA; Aliona GHENDOV-MOSANU; Ileana-Denisa NISTOR; Diana-Carmen MIRILA and Dmitri LAZACOVICI. Migration of plastic additives and non-intentionally added substances from packaging into edible oils and beverages: A combined GC–MS and hydrolysis–capillary electrophoresis approach. Polymers. 2026, vol. 18, nr. 8, art. nr. 965. ISSN 2073-4360. en_US
dc.identifier.issn 2073-4360
dc.identifier.uri https://www.doi.org/10.3390/polym18080965
dc.identifier.uri https://repository.utm.md/handle/5014/36844
dc.description Access full text: https://www.doi.org/10.3390/polym18080965 en_US
dc.description.abstract The present study aimed to investigate the migration of potentially hazardous compounds from plastic food packaging into edible oils, bottled water and soft drinks available on the market in the Republic of Moldova. GC–MS screening was applied to identify plastic additives and unintentionally added substances (NIAS). The influence of key extraction parameters, including solvent type, extraction time, pH, alcohol content and sugar concentration, was systematically investigated. The optimized procedure demonstrated satisfactory analytical performances, with recoveries ranging from 81 to 96%, repeatability below 5% and detection limits between 0.006 and 0.01 mg/L. To allow a comprehensive assessment of total phthalate contamination, an additional analytical approach based on the hydrolysis of phthalate esters and the determination of o-phthalic acid using capillary electrophoresis with spectrophotometric detection was proposed. The method showed a linearity range of 0.1–5.0 mg/L and a limit of quantification of 0.07 mg/L. The combined chromatographic and hydrolysis-capillary electrophoresis approaches provide a reliable tool for the integrated determination and evaluation of phthalate residues in aqueous-alcoholic systems and beverages, accessible to laboratories performing food quality control. en_US
dc.language.iso en en_US
dc.publisher Multidisciplinary Digital Publishing Institute (MDPI) en_US
dc.rights Attribution-NonCommercial-NoDerivs 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/us/ *
dc.subject phthalate esters en_US
dc.subject aqueous-alcoholic matrices en_US
dc.subject capillary electrophoresis en_US
dc.subject hydrolysis method en_US
dc.subject beverage contamination en_US
dc.title Migration of plastic additives and non-intentionally added substances from packaging into edible oils and beverages: A combined GC–MS and hydrolysis–capillary electrophoresis approach en_US
dc.type Article en_US


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