A selective cation exchange chromatographic method, coupled to integrated pulsed amperometric detection, has been developed to quantify biogenic amines in fresh and processed meat. The method is based on gradient elution of aqueous methanesulfonic acid with post column addition of a strong base to obtain suitable conditions for amperometric detection. A potential wave-form able to keep long time performance of the Au electrode was set up. The analysis time is about 68 min. Amounts of tyramine, putrescine, cadaverine, histamine, agmatine, spermidine and spermine were measured, after extraction with perchloric acid. The method was used to determine analytes in fresh and processed meat. Analyte quantification was made with external calibration method after demonstration that matrix effects were not present. All analytes were identified in real samples except phenethylamine which is eluted in a zone of the chromatogram rich of interfering peaks. Repeatabilities, computed on their amounts in real samples, were better than 9% for all of them. Detection limits were computed according to the Hubaux–Vos method. The obtained values ranged between 0.70 and 2.12 mg/l corresponding to 7–21 mg/kg, low enough to determine all analytes in real matrices.

Determination of Biogenic Amines in Fresh and Processed Meat by Ion Chromatography and Integrated Pulsed Amperometric Detection on Au Electrode.

FAVARO, GABRIELLA;PASTORE, PAOLO;
2007

Abstract

A selective cation exchange chromatographic method, coupled to integrated pulsed amperometric detection, has been developed to quantify biogenic amines in fresh and processed meat. The method is based on gradient elution of aqueous methanesulfonic acid with post column addition of a strong base to obtain suitable conditions for amperometric detection. A potential wave-form able to keep long time performance of the Au electrode was set up. The analysis time is about 68 min. Amounts of tyramine, putrescine, cadaverine, histamine, agmatine, spermidine and spermine were measured, after extraction with perchloric acid. The method was used to determine analytes in fresh and processed meat. Analyte quantification was made with external calibration method after demonstration that matrix effects were not present. All analytes were identified in real samples except phenethylamine which is eluted in a zone of the chromatogram rich of interfering peaks. Repeatabilities, computed on their amounts in real samples, were better than 9% for all of them. Detection limits were computed according to the Hubaux–Vos method. The obtained values ranged between 0.70 and 2.12 mg/l corresponding to 7–21 mg/kg, low enough to determine all analytes in real matrices.
2007
File in questo prodotto:
File Dimensione Formato  
Food Chemistry 105 (2007) 1652–1658.pdf

Accesso riservato

Tipologia: Published (Publisher's Version of Record)
Licenza: Accesso privato - non pubblico
Dimensione 171.25 kB
Formato Adobe PDF
171.25 kB Adobe PDF Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/1775832
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 77
  • ???jsp.display-item.citation.isi??? 71
  • OpenAlex 83
social impact