Optimization and Validation of a HS-SPME/GC–MS Method for the Analysis of Gluten-Free Bread Volatile Flavor Compounds
| Autor: | Saša Drakula, Duška Ćurić, Mirjana Hruškar, Nikolina Čukelj Mustač, Marina Krpan, Bojana Voučko, Dubravka Novotni |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Detection limit
Chromatography Extraction (chemistry) Repeatability Mass spectrometry Applied Microbiology and Biotechnology Analytical Chemistry chemistry.chemical_compound chemistry Standard addition Gluten-free · Bread crumb and crust · Volatile favor compounds · HS-SPME time and temperature · GC–MS · Method development Phenols Gas chromatography–mass spectrometry Safety Risk Reliability and Quality Safety Research Flavor Food Science |
| Zdroj: | Food Analytical Methods. 15:1155-1170 |
| ISSN: | 1936-976X 1936-9751 |
| Popis: | Flavor is one of the most important, but also the least researched parameter of bread quality. Numerous volatile compounds that contribute to the flavor profile of bread are usually extracted by the headspace solid-phase microextraction (HS- SPME) method. The development of a reliable and sensitive HS-SPME method requires the selection and optimization of all key extraction parameters as well as performance of a validation procedure. The aim of this study was to optimize the temperature and time of HS-SPME of volatile flavor compounds of gluten-free bread and to validate an optimized HS-SPME/gas chromatography-mass spectrometry (GC-MS) method for their quantification. This study included 62 volatile flavor compounds from the chemical classes of aldehydes, ketones, alcohols, acids, esters, aromatic hydrocarbons, phenols, sulfur compounds, pyrazines, pyrroles, and furans. The determined optimal conditions for extraction with carboxen/divinylbenzene/polydimethylsiloxane fiber were temperature 60 °C and time 60 min. Calibration was performed using a standard addition method. Linearity and precision were achieved within the examined method range for all compounds analyzed, with correlation coefficients r ≥ 0.999. The relative SDs of the determined method repeatability and intermediate precision ranged from 0.3 to 18.9% and from 2.4 to 31.2%, respectively. The obtained limits of detection and quantification differed significantly among the analyzed compounds and ranged from 49.0 pg/kg to 94.5 μg/kg and 163 pg/kg to 315 μg/kg, respectively. Based on the obtained results, the proposed optimized method can be successfully applied for the quantification of all the analyzed bread volatile flavor compounds. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink