Determination of releasing plasticizers from dental floss using ultrasound-assisted extraction-dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detector

被引:2
作者
Farajzadeh, Mir Ali [1 ,2 ]
Fathipour, Zahra [1 ]
Aghdam, Mehri Bakhshizadeh [1 ]
Mogaddam, Mohammad Reza Afshar [3 ,4 ]
机构
[1] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[2] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkiye
[3] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
基金
美国国家科学基金会;
关键词
Dispersive liquid-liquid microextraction; Phthalate esters; Dental floss; Gas chromatography; PHASE MICROEXTRACTION; PHTHALATE-ESTERS; MEDIA;
D O I
10.1016/j.microc.2023.109363
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Recently, the wide existence of phthalate esters in healthcare products has attracted great attention from scientists due to their negative effects on human health. As a result, the current study was carried out to determine the presence of some plasticizers in dental floss such as di-n-butyl phthalate, diethyl phthalate, di-2-ethylhexyl phthalate, di-iso-butyl phthalate, and bis-2-ethylhexyl adipate. The studied analytes were extracted from dental floss by an ultrasound-assisted extraction procedure and then enriched by a dispersive liquid-liquid microextraction method. For this purpose, a piece of dental floss was immersed in acetonitrile under sonication to extract the analytes. Then, the acetonitrile phase containing the extracted analytes was mixed with a proper extraction solvent at mu L-level and injected into sodium chloride solution. The extracted analytes were determined by gas chromatography-flame ionization detector and gas chromatography-mass spectrometry. Under the best extraction conditions, limits of detection and quantification were found in the ranges 0.20-0.33 and 0.67-1.1 mu g/L in solution and 0.06-0.10 and 0.19-0.33 mu g g-1 in dental floss, respectively. Relative standard deviations were in the ranges 4.0-6.5% and 5.1-7.9% for intra-day and inter-day precisions for five replicates at 60 mu g/L of each analyte. Enrichment factors and extraction recoveries of the analytes ranged from 350 to 460 and 70-92%, respectively.
引用
收藏
页数:9
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