The samples were transmethylated Ivacaftor nmr based on the methodology of Hartmann and Lago (1973), which consists of saponification

and conversion of fatty acid methyl esters. Three repetitions of each fatty acid were used and fatty acid profile was determined in a Varian CP-338 GC gas chromatograph fitted with a DB-WAX 25 m × 0.25 mm × 0.25 μm column (J&W Scientific), at the Chemistry Department of UFMG. Hydrogen was used as the carrier gas at a velocity of 40 cm/s. The initial column temperature of 50 °C was maintained for 2 min, increased at a rate of 4 °C/min until reaching 220 °C and kept at this temperature for more than 25 min. The temperature was 260 °C in both injection port (split of 1/50) and detector. The assays used 2 μl of sample and Sigma 189–19 as the standard fatty acid mixture. The identification of fatty acids was by comparison of retention times of methyl esters of standards with the sample and the measurement made by standardization. Statistical analysis was performed MK-1775 mouse using the SAS program version 6 software package and the means were compared by SNK test at 5% significance level. The results were analysed with the SAS version 6 software package (SAS Institute INC, North Caroline, USA, 1997). The means were compared by SNK test at 5% significance level. Mean temperature in the tanks was 28.23 ± 0.63 °C, pH was 7.25 ± 0.58 and dissolved oxygen was 5.23 ± 0.85 mg l−1.

These values meet the optimal conditions for tilapia growth according to Navarro et al. (2010b). The fatty acid profile in Nile tilapia carcasses was different among treatments with different vitamin E supplementation.

Fish receiving 100 or 150 mg vitamin E/kg diet had the highest levels of omega-3 and omega-6 PUFAs, as indicated by the higher levels of linoleic (18:2, ω-6) and linolenic (18:3, ω-3) acid in the carcass (Table 1). Maintaining high levels of PUFA is associated to the presence of vitamin E, which is added to diets not only to improve nutritional properties, but also to combat and neutralise free radicals before they oxidise these fats in cell membranes (Pita, Piber Neto, GNA12 Nakaoka, & Mendonça Junior, 2004). The vitamin E to promote the protection of PUFAs in fish meat, contributing to product quality and preservation during processing (Gonçalves et al., 2010). Nile tilapias receiving supplementation of 100 and 150 mg of vitamin E/kg diet had higher PUFA levels compared to saturated fatty acids (SFA), but this was not observed with other supplementation levels (Table 1). Due to this fatty acid balance, carcasses had lower SFA deposition and higher meat quality. A number of studies have shown a direct association between SFA consumption and blood cholesterol levels (HMSO Nutritional aspects of cardiovascular disease. Report on health & Department of, 1994). Palmitic acid (16:0) was the main SFA in the Nile tilapia carcasses tested (Table 1).