Extraction and reliable determination of acrylamide from thermally processed foods using ionic liquid-based ultrasound-assisted selective microextraction combined with spectrophotometry


ALTUNAY N., ELİK A., GÜRKAN R.

FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, cilt.35, sa.2, ss.222-232, 2018 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 35 Sayı: 2
  • Basım Tarihi: 2018
  • Doi Numarası: 10.1080/19440049.2017.1394585
  • Dergi Adı: FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.222-232
  • Anahtar Kelimeler: Acrylamide, thermally processed foods, microextraction, spectrophotometry, TANDEM MASS-SPECTROMETRY, CEREAL-BASED FOODS, ELECTRON-CAPTURE DETECTOR, SOLID-PHASE EXTRACTION, GAS-CHROMATOGRAPHY, POTATO-CHIPS, BABY FOODS, SAMPLES, STATE, CHEMISTRY
  • Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

Acrylamide (AAm) is a carcinogenic chemical that can form in thermally processed foods by the Maillard reaction of glucose with asparagine. AAm can easily be formed especially in frequently consumed chips and cereal-based foods depending on processing conditions. Considering these properties of AAm, a new, simple and green method is proposed for the extraction of AAm from thermally processed food samples. In this study, an ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, [Bmim][BF4]) as extractant was used in the presence of a cationic phenazine group dye, 3,7-diamino-5-phenylphenazinium chloride (PSH+, phenosafranine) at pH 7.5 for the extraction of AAm as an ion-pair complex from selected samples. Under optimum conditions, the analytical features obtained for the proposed method were as follows; linear working range, the limits of detection (LOD, 3S(b)/m) and quantification (LOQ, 10S(b)/m), preconcentration factor, sensitivity enhancement factor, sample volume and recovery% were 2.2-350 mu g kg(-1), 0.7 mu g kg(-1), 2.3 mu g kg(-1), 120, 95, 60 mL and 94.1-102.7%, respectively. The validity of the method was tested by analysis of two certified reference materials (CRMs) and intra-day and inter-day precision studies. Finally, the method was successfully applied to the determination of AAm levels in thermally processed foods using the standard addition method.