The oxidation of FFA is responsible for the formation of a large number of volatile compounds, loss of positive attributes, such as “freshness”, and formation of an attribute called “staleness” (Frankel, 2005). Several studies, through

evaluation of the volatile composition and sensory analysis, have focused on the shelf life of roasted coffee under various conditions of temperature, atmosphere and moisture. Data have shown that all these variables influenced the acceptability of stored roasted coffee (Manzocco & Lagazio, 2009; Ross, Pecka, & Weller, 2006; Toci, 2010). The interest on shelf life of roasted and ground coffee is especially important to consumers. However, the assessment of shelf life requires the exact definition of the criteria to determine the end of the product’s life. It has been speculated that hydrolysis of TAG results in release of free fatty Buparlisib acids, which are oxidized to produce, as mentioned above, off-flavors in coffee (Spadone, Takeoka, & Liardon, 1990; Speer, Sehat, & Montag, 1993). Nevertheless, studies on degradation of lipids in roasted coffee are scarce. The aim of the present study was to investigate potential changes in the content and composition of fatty acids contained in TAG and FFA fractions of roasted C. arabica

during storage under different temperature and atmospheric conditions. Excellent cup quality seeds of Brazilian C. arabica from Minas Gerais, classified as “strictly soft”, were used. One hundred grams of the seeds were roasted in a spouted bed roaster (IRoast, Gurnee, AZD4547 research buy IL, USA), reaching a maximum temperature of 221 °C. They were roasted for 5.5 min and 7.5 min to give light-medium and dark-medium color degrees, respectively, according to the Roast Color Classification System (AGTRON – SCAA, USA, 1995). All samples were ground to Methamphetamine pass a 500 μm sieve. Coffee storage was carried out by placing 2 g aliquots of each sample in 7 mL amber vials and storing them for 1–6

months, under controlled conditions of temperature (5 and 30 °C) and atmosphere (ambient air and N2). Storage was performed in triplicate. Total lipids contents were determined according to the method number 15.028 established by AOAC (1984). Total lipids were extracted in triplicate from 2.0 g of coffee samples with 40 mL of organic solvents (isopropanol:chloform, 1:1 mL/mL), by thoroughly mixing with an Ultra Turrax mixer (IKA; Germany) for 1 min at 14,000 rpm. The extract was transferred quantitatively into an extraction tube with 14 mL chloroform:methanol (2:1 mL/mL), followed by addition of 4.6 mL of KCl (8.8 g/L) (Kaluzny, Duncan, Merritt, & Eppse, 1985). Subsequently, the tube was centrifuged for 10 min at 224× g. The bottom fraction containing coffee lipids was collected and stored at −20 °C until the next analytical step of lipid class separation.