6533b828fe1ef96bd1288526
RESEARCH PRODUCT
Test procedures for obtaining representative extracts suitable for reliable in vitro toxicity assessment of paper and board intended for food contact.
E.l. BradleyA. StammatiM. Salkinoja-salonenM. AnderssonF. BertaudD. HoornstraF. ZuccoA. WeberL. TurcoH. TraussnigP. HakulinenD.r. SpeckA.j. Von WrightU. Honkalampi-hämäläinenJ. Mäki-paakkanenI. SeverinJ.-c. LhuguenotO. Dahlmansubject
PaperFood contact materialsHealth Toxicology and MutagenesisSample (material)[ SDV.TOX ] Life Sciences [q-bio]/ToxicologyTenax[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainIn Vitro TechniquesToxicologyPaper and boardMESH : Gas Chromatography-Mass Spectrometry01 natural sciencesMESH : Food PackagingGas Chromatography-Mass SpectrometryMESH : Toxicity Tests0404 agricultural biotechnologyToxicity TestsBioassayPaperboardMESH : WoodFood contactbusiness.industryTest procedures010401 analytical chemistryExtraction (chemistry)Food PackagingPublic Health Environmental and Occupational HealthLife Sciences04 agricultural and veterinary sciencesGeneral ChemistryGeneral MedicinePulp and paper industryToxicity assessmentWood040401 food science0104 chemical sciencesBiotechnologyMESH : PaperIn vitro testingExtraction proceduresFood contact materialsvisual_artvisual_art.visual_art_mediumEnvironmental sciencebusinessFood Sciencedescription
International audience; This paper describes the use of a suite of extraction procedures applicable to the assessment of the in vitro toxicity of paper/board samples intended for food-contact applications. The sample is extracted with ethanol, water, or exposed to modified polyphenylene oxide (Tenax) for fatty, non-fatty and dry food applications, respectively. The water extracts are directly suitable for safety assessment using in vitro bioassays. The ethanol extracts of the paper/board and of the exposed Tenax require pre-concentration to give acceptable sensitivity. This is because the in vitro bioassays can tolerate only a small percentage of added organic solvent before the solvent itself inhibits. The extraction procedures have been selected such that they mimic the foreseeable conditions of use with foods and that they are also fully compatible with the battery of in vitro biological assays for the safety assessment of the total migrate. The application of the extraction protocols is illustrated by the results for one of the many paper/board samples provided by the BIOSAFEPAPER project industrial platform members. The assessment indicated that this sample should not be considered as suitable for use with fatty foodstuffs but was suitable for dry and non-fatty foods. Information subsequently received from the manufacturer revealed that this was a non-food-grade product included in the project to test the capabilities of the bioassay procedures. The selection criteria for the test conditions and the suite of methods developed have been prepared in Comité Européen de Normalisation (CEN) format and is currently being progressed by CEN/TC172 as a European Standard.
year | journal | country | edition | language |
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2009-12-09 |