Ultrasonic processing can suit a number of potential applications in the dairy industry. However, the impact of ultrasound treatment on milk stability during storage has not been fully explored under wider ranges of frequencies, specific energies and temperature applications. The effect of ultrasonication on lipid oxidation was investigated in various types of milk. Four batches of raw milk (up to 2L) were sonicated at various frequencies (20, 400, 1000, 1600 and 2000kHz), using different temperatures (4, 20, 45 and 63°C), sonication times and ultrasound energy inputs up to 409kJ/kg. Pasteurized skim milk was also sonicated at low and high frequency for comparison. In selected experiments, non-sonicated and sonicated samples were stored at 4°C and were drawn periodically up to 14days for SPME-GCMS analysis. The cavitational yield, characterized in all systems in water, was highest between 400kHz and 1000kHz. Volatile compounds from milk lipid oxidation were detected and exceeded their odor threshold values at 400kHz and 1000kHz at specific energies greater than 271kJ/kg in raw milk. However, no oxidative volatile compounds were detected below 230kJ/kg in batch systems at the tested frequencies under refrigerated conditions. Skim milk showed a lower energy threshold for oxidative volatile formation. The same oxidative volatiles were detected after various passes of milk through a 0.3L flow cell enclosing a 20kHz horn and operating above 90kJ/kg. This study showed that lipid oxidation in milk can be controlled by decreasing the sonication time and the temperature in the system depending on the fat content in the sample among other factors.
Ultrasound (US) has been suggested for many whey processing applications. This study examined the effects of ultrasound treatment on the oxidation of lipids in Cheddar cheese whey. Freshly pasteurized whey (0.86 L) was ultrasonicated in a contained environment at the same range of frequencies and energies for 10 and 30 min at 37°C. The US reactor used was characterized by measuring the generation of free radicals in deionized water at different frequencies (20-2000 kHz) and specific energies (8.0-390 kJ/kg). Polar lipid (PL), free and bound fatty acids and lipid oxidation derived compounds were identified and quantified before and after US processing using high performance liquid chromatography equipped with an evaporative light scattering detector (HPLC-ELSD), methylation followed by gas chromatography flame ionized detector (GC-FID) and solid phase micro-extraction gas chromatography mass spectrometry (SPME-GCMS), respectively. The highest concentration of hydroxyl radical formation in the sonicated whey was found between 400 and 1000 kHz. There were no changes in phospholipid composition after US processing at 20, 400, 1000 and 2000 kHz compared to non-sonicated samples. Lipid oxidation volatile compounds were detected in both non-sonicated and sonicated whey. Lipid oxidation was not promoted at any tested frequency or specific energy. Free fatty acid concentration was not affected by US treatment per se. Results revealed that US can be utilized in whey processing applications with no negative impact on whey lipid chemistry.
Summary
This study describes the preparation and characterisation of nanoparticles with gelatin as the wall matrix to encapsulate Moringa oleifera (MO) extract using an electrospraying technique. The electrospraying conditions for voltage, flow rate and emitter/collector distance were 20 kV, 0.5 mL h−1 and 10 cm, respectively. Nanoparticles with encapsulated MO extract (1–5%, w/w) were successfully produced and characterised in relation to spectroscopic, morphological and thermal properties. Increasing amounts of MO extract resulted in a significant decrease in the nanocapsule size (ranging from 140 and 179 nm) produced. Spectroscopic analysis indicated no chemical interactions between core and wall materials. The encapsulation efficiency (EE) of MO extract‐loaded nanocapsules obtained was 83.0 ± 4.0%. Surface analysis showed that roughness decreased from 91 nm (empty beads) to 57.5 nm with addition of 3% MO extract. The thermal stability of encapsulated nanoparticles slightly increased and the glass transition temperature (Tg) disappeared due to increase in crystallinity.
Pressurised liquid extraction (PLE) of antioxidant compounds from bitter gourd fruits (Momordica charantia) in aqueous ethanolic solvent was investigated using response surface methodology at laboratory scale to understand key impact of extraction variables. Extraction efficiency was optimised by measuring the yield of extraction, total phenolic content (TPC), total flavonoid content (TFC), ferric reducing/ antioxidant power assay (FRAP) and radical scavenging activity (RSA). The optimal extraction conditions were reached at 80% ethanol concentration, 10-min extraction time and at 160°C. Under these extraction conditions, values of TPC (5.40 AE 0.30 g GAE per 100 g), TFC (1.50 AE 0.10 g QE per 100 g), FRAP (778.55 AE 10 lmol eq Fe (II) g À1 ), yield (178.50 AE 5.50 mg g À1 dc) and RSA (75.50 AE 4.50%) were achieved. Furthermore, statistical analysis revealed that antioxidative attributes of bitter gourd extract were strongly and positively correlated with extraction temperature and ethanol concentration rather than processing time. This study illustrated that PLE has the potential to extract antioxidant compounds from tropical fruit vegetables in an accelerated manner. Furthermore, influential parameters affecting the process could be optimised for further industrial intake. PLE of BG fruit antioxidative compounds Z. A. Syahariza et al. Subscripts: 1 = ethanol concentration; 2 = temperature; 3 = time. CV%, coefficient of variance [%]; Adequ. precision, adequate precision; P lf -value, probability of F value for the lack of fit; P m -value, probability of F value for the model. n.s. nonsignificant at P > 0.05. *P < 0.001, **P < 0.01, ***P < 0.05. PLE of BG fruit antioxidative compounds Z. A. Syahariza et al. † Prediction interval; ‡ Values are averages of triplicate analysis AE SD of three individual runs.
Fat from freshly pasteurized liquid whey was partially separated by gravity for 5, 10, and 30min, with and without simultaneous application of ultrasound. Ultrasound treatments were carried out at 400 and 1,000 kHz at different specific energy inputs (23-390 kJ/kg). The fat-enriched top layers (L1) and the fat-depleted bottom layers (L2) were separately removed and freeze-dried. Nonsonicated and sonicated L2 powders were stored for 14d at ambient temperature to assess their oxidative stability. Creaming was enhanced at both frequencies and fat separation increased with higher ultrasonic energy, extended sonication, or both. The oxidative volatile compound content decreased in defatted whey powders below published odor detection threshold values for all cases. Sonication had a minor influence on the partitioning of phospholipids with fat separation. The current study suggested that ultrasonication at high frequency enhanced fat separation from freshly pasteurized whey while improving whey powder oxidative stability.
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