Determination of Four Priority Polycyclic Aromatic Hydrocarbons in Food Samples by Gas Chromatography - Mass Spectrometry (GC-MS) after Vortex Assisted Dispersive Liquid-Liquid Microextraction (DLLME)


Chormey D. S. , Tonbul G., Soylu G., Saygilar A., BAKIRDERE S.

ANALYTICAL LETTERS, 2021 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume:
  • Publication Date: 2021
  • Doi Number: 10.1080/00032719.2021.1922432
  • Journal Name: ANALYTICAL LETTERS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Chimica, Communication Abstracts, Food Science & Technology Abstracts, Metadex, Veterinary Science Database, Civil Engineering Abstracts
  • Keywords: Dispersive liquid-liquid microextraction (DLLME), gas chromatography, mass spectrometry (GC-MS), polycyclic aromatic hydrocarbons, QuEChERS
  • Yıldız Technical University Affiliated: Yes

Abstract

Dispersive liquid-liquid microextraction (DLLME) is a useful preconcentration technique but its direct application is limited to aqueous samples. Two pretreatment methods for solid samples, QuEChERS (quick easy cheap efficient rugged and safe) and a standard method, were used to isolate four polycyclic aromatic hydrocarbons (PAHs) from the sample matrix. However, since these methods result in analyte dilution, DLLME was used to augment them by concentrating the analytes from 8.0 mL of sample into 150 mu L of 1,2-dichloroethane. Under the optimum conditions, the instrumental detection limit was enhanced by approximately 100-fold for chrysene, benzo[a]pyrene, benz[a]anthracene, and benzo[k]fluoranthene with corresponding detection limits of 29, 29, 30, and 28 ng/L, respectively. The precision of the method based on inter-analyst and inter-day analysis yielded relative standard deviations less than 9.0 and 4.0%, respectively. The optimized method was applied to snail samples spiked at 5.0, 10, 20, and 50 ng/g and the recoveries were nearly 100%. Matrix matched standards were also used to determine the recoveries; the results did not vary significantly from the direct calibration recoveries.