Abstract
During coffee roasting, temperatures exceeding 200 °C induce chemical reactions such as the Maillard reaction, altering the beans’ chemical and sensory properties. This leads to positive and negative changes, including the formation of chemical process contaminants such as acrylamide. Acrylamide exposure involves risks to consumers, emphasizing the need for its control during food processing. Strategies to reduce acrylamide during coffee roasting involve managing precursor levels in the raw materials (reducing sugars and asparagine), adjusting processing conditions (time and temperature), and utilizing different roasting technologies. Additionally, alternative methods for eliminating acrylamide after roasting have been explored. However, there is limited information regarding the bioaccessibility of acrylamide in coffee, particularly in understanding the behavior of the contaminant once coffee is ingested. This aspect is crucial for accurately assessing the real risk associated with acrylamide exposure. In this context, the acrylamide bioaccessibility in different instant soluble coffees and coffee substitutes made from cereals and chicory were assessed. In addition, we further investigated the potential influence of mixing with milk. Following the in vitro digestion of the samples using the International Network of Food Digestibility and Gastrointestinal Health (INFOGEST) protocol, acrylamide bioaccessibility ranged between 73 and 90% (soluble coffees) and 78 and 99% (coffee substitutes). An increase in acrylamide bioaccessibility in instant chicory when samples were mixed with milk was observed but not in the remaining samples. These results underscore the importance of exploring the interactions between acrylamide and food matrix components, as they influence its availability during the digestive process and, consequently, the final risk of exposure to the contaminant.
Author Contributions
Conceptualization, M.M., C.D.-A. and F.J.M.; methodology, M.M. and C.D.-A.; software, M.M. and C.D.-A.; validation, M.M. and C.D.-A.; formal analysis, M.M. and C.D.-A.; investigation, M.M., C.D.-A. and F.J.M.; resources, M.M., C.D.-A. and F.J.M.; data curation, M.M. and C.D.-A.; writing—original draft preparation, M.M.; writing—review and editing, M.M., C.D.-A. and F.J.M.; visualization, M.M., C.D.-A. and F.J.M.; supervision, M.M., C.D.-A. and F.J.M.; project administration, M.M., C.D.-A. and F.J.M.; funding acquisition, M.M., C.D.-A. and F.J.M. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by the R&D project ACRINTAKE (RTI2018-094402-B-I00), financed by MCIN/AEI (https://doi.org/10.13039/501100011033) and Fondo Europeo de Desarrollo Regional (FEDER), a way to make Europe, and by the Community of Madrid and European funding from FSE and FEDER programs (project S2018/BAA-4393, AVANSECAL-II-CM) and CSIC (project 202070E193).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The data presented in this study are available from the authors.
Acknowledgments
Authors wish to thank I. Alvarez for the technical assistance with acrylamide analysis.
Conflicts of Interest
The authors declare no conflicts of interest.
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