<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tran-Lam TT</submitter><funding>VAST.TĐ.TP/16-18</funding><pagination>E69</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6316763</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(4)</volume><pubmed_abstract>A novel method was developed for the sensitive, cheap and fast quantitation of 10 phthalates in non-alcoholic beverages by liquid⁻liquid extraction (LLE) combined with gas chromatography tandem mass spectrometry (GC-MS/MS). The best results were obtained when &lt;i>n&lt;/i>-hexane was used as extraction solvent. A central composite design (CCD) was applied to select the most appreciated operating condition. The method performance was evaluated according to the SANTE/11945/2015 guidelines and was linear in the 0.1 to 200 µg/L range for 10 phthalate compounds, with &lt;i>r&lt;/i>² > 0.996 and individual residuals &lt;15%. Repeatability (RSD&lt;sub>r&lt;/sub>), within-laboratory reproducibility (RSD&lt;sub>wr&lt;/sub>), and the trueness range were from 2.7 to 9.1%, from 3.4 to 14.3% and from 91.5 to 118.1%, respectivel</pubmed_abstract><journal>Toxics</journal><pubmed_title>Optimization of Sample Preparation for Detection of 10 Phthalates in Non-Alcoholic Beverages in Northern Vietnam.</pubmed_title><pmcid>PMC6316763</pmcid><funding_grant_id>VAST.TĐ.TP.03/16-18</funding_grant_id><pubmed_authors>Nguyen DT</pubmed_authors><pubmed_authors>Ma HK</pubmed_authors><pubmed_authors>Le GT</pubmed_authors><pubmed_authors>Tran-Lam TT</pubmed_authors><pubmed_authors>Pham TQ</pubmed_authors><pubmed_authors>Dao YH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of Sample Preparation for Detection of 10 Phthalates in Non-Alcoholic Beverages in Northern Vietnam.</name><description>A novel method was developed for the sensitive, cheap and fast quantitation of 10 phthalates in non-alcoholic beverages by liquid⁻liquid extraction (LLE) combined with gas chromatography tandem mass spectrometry (GC-MS/MS). The best results were obtained when &lt;i>n&lt;/i>-hexane was used as extraction solvent. A central composite design (CCD) was applied to select the most appreciated operating condition. The method performance was evaluated according to the SANTE/11945/2015 guidelines and was linear in the 0.1 to 200 µg/L range for 10 phthalate compounds, with &lt;i>r&lt;/i>² > 0.996 and individual residuals &lt;15%. Repeatability (RSD&lt;sub>r&lt;/sub>), within-laboratory reproducibility (RSD&lt;sub>wr&lt;/sub>), and the trueness range were from 2.7 to 9.1%, from 3.4 to 14.3% and from 91.5 to 118.1%, respectivel</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2026-07-16T16:37:14.153Z</modification><creation>2019-03-26T22:36:08Z</creation></dates><accession>S-EPMC6316763</accession><cross_references><pubmed>30463241</pubmed><doi>10.3390/toxics6040069</doi></cross_references></HashMap>