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Browsing by Subject "camelina oil"

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  • Salomaa, Sini (2014)
    The aim of this study was to investigate the effects of graded amounts of camelina oil on milk fatty acid composition in lactating cows fed diets based on a mixture of grass and red clover silages. The experiment was carried out at the University of Helsinki research farm in Viikki 30th January 2009 – 23th April 2009. Eight multiparous Finnish Ayrshire cows participated in this experiment and four of them were rumen fistulated. Experimental design used was 4 x 4 Latin square. Treatments consisted of concentrate supplements containing various levels of camelina oil (0%, 2%, 4% and 6% on air-dry basis). All concentrates contained camelina expeller (20% on air-dry basis). The cows were offered daily 12 kg of experimental concentrate and silage ad libitum. The experimental periods lasted for 21 days. The first 14 days were adaptation period and the last 7 days formed sampling period. Increase of camelina oil level in the diet linearly decreased forage and whole diet dry matter intake (P?0,002). Camelina oil level did not affect organic matter, NDF and nitrogen whole-tract digestibility (P>0,10). Milk yield and milk protein- and lactose content linearly decreased when camelina oil level increased (P<0,001). Camelina oil level did not affect milk fat yield (P>0,100). Milk fat content (P=0,014) linearly increased and protein content (P=0,032) and urea content (P<0,001) linearly decreased when camelina oil level increased. Camelina oil level did not affect milk lactose content (P>0,100). Increase of camelina oil level linearly worsened milk taste panel scores (P=0,018). Camelina oil level did not affect plasma metabolite concentrations except that of total free fatty acids that linearly increased with camelina oil supplementation (P<0,001). Effects of camelina oil supplementation on rumen pH and rumen fermentation pattern were numerically negligible. Increase of camelina oil level linearly decreased the concentration of saturated fatty acids in milk fat (P<0,001) and linearly increased those of monounsaturated (P<0,001) and polyunsaturated (P<0,002) fatty acids. Increase of camelina oil level linearly decreased the content of mammary de novo synthesised short- and medium-chain 6-14-carbon fatty acid in milk fat (P?0,028). Camelina oil level had no effect on alphalinolenic acid content in milk fat (P>0.100). Increase of camelina oil level linearly increased trans fatty acids and CLA content in milk fat (P?0,008). Camelina oil supplementation did not affect neither the milk fat content of the final product of ruminal biohydrogenation of 18-carbon unsaturates stearic acid nor that of oleic acid (P>0,10). This is possibly due to biohydrogenation not proceeding to the end, ceasing to the last step before stearic acid. Milk fat trans-11 18:1 and cis-9, trans-11 CLA contents linearly increased at remarkably high levels when camelina oil level in the diet increased (P?0,008). This is possibly due to incomplete ruminal biohydrogenation of 18-carbon unsaturated fatty acids. Camelina oil supplement improved milk fat composition by decreasing saturated and increasing the trans-11 18:1 and cis-9,trans-11 CLA content in milk. However, giving camelina oil at high levels decreased silage and whole diet dry matter intake and affected milk production negatively.
  • Moilanen, Henna (2020)
    Lipid oxidation presents one of the most important challenges for the processing and storage of edible oils by lowering the shelf life, nutritional value, and organoleptic properties of oils. Microencapsulation is a process where oil droplets are coated within a wall material matrix, and it offers a suitable solution to protect edible oils against oxidative deterioration. This study aimed at exploring the effects of wall material composition and relative humidity (RH) on the potential of microencapsulation to protect camelina and blackcurrant seed oils against lipid oxidation. Camelina and blackcurrant seed oils were emulsified using whey protein isolate (WPI) and maltodextrin (MD) as wall materials in 1:1, 1:3, and 1:9 ratio, and the total solids content and wall-to-oil ratio were kept constant. Microencapsulation was conducted by spray drying, and various parameters were analyzed, including emulsion viscosity, water sorption properties, and the surface oil content of microencapsulated powders. The powders were conditioned at 11% and 44% RHs at 21 °C, after which the sample vials were closed to maintain constant water content. The oxidative stability of the conditioned microencapsulated powders was analyzed over 10 weeks of accelerated storage conditions at 40 °C by measuring the volatile secondary lipid oxidation products every two weeks by headspace-solid phase-microextraction-gas chromatography-mass spectrometry method. The results showed that the best oxidative stability during the storage period was obtained by WPI-MD 1:1 ratio in both of the microencapsulated oils, even though this wall material composition resulted in the highest surface oil content and the lowest encapsulation efficiency. In blackcurrant seed oil powders, the water content obtained at 44% RH seemed to provide better protection against lipid oxidation than that of 11% RH. Regarding camelina oil powders, water content obtained in different RHs did not seem to affect the oxidative stability of the powders. However, based on the peak areas of volatile compounds detected at week 10, the water content obtained at 44% RH might provide better storage stability for camelina oil containing powders in long-term storage than that of 11% RH.