Lipid nanoparticles based on omega-3 fatty acids as effective carriers for lutein delivery. Preparation and in vitro characterization studies

This study aimed at exploring the behavior of fish oil enriched with ω-3 fatty acids in order to obtain stable lipid nanocarriers (NLCs) with improved characteristics as effective delivery systems for lutein. The particle size of optimized lutein-NLCs was below 200 nm. The less ordered arrangement of lipid core revealed by scanning calorimetry and the high entrapment efficiency of 88.5% clearly indicated the appropriate role of fish oil in obtaining effective lipid nanocarriers. The evaluation of in vitro antioxidant activity has demonstrated a significant blocking effect of NLCs, scavenging up to 98% oxygen free radicals. The in vitro release profile has shown that NLCs are able to ensure a better, in vitro sustained release of lutein as compared to conventional nanoemulsions.     

红外光谱技术在鱼产品质量检测与安全评估中的应用

近年来消费者对鱼产品的掺假问题愈发关注,从而针对鱼产品的质量评估的相关研究也逐渐增加。传统的鱼类成分分析和质量检测技术方法繁琐、费力、昂贵、费时,而光谱技术因其具有速度快、使用方便、样品制备最少或不需要样品制备,及避免样品破坏等优点而受到越来越多的关注。本文综述了以红外光谱技术为主的光谱技术,包括近红外光谱(near infrared spectroscopy,NIR)、中红外光谱(mid-infrared spectroscopy,MIR)等的在鱼产品的成分和其他质量特性监测中的应用,并对光谱技术的应用前景和发展方向进行了展望,以期为红外光谱技术在鱼类及鱼产品质量监测体系中推广应用提供指导,为解决鱼产品及相关行业的质量问题提供了一种新的途径。     

高效液相色谱法测定鱼油中的EPA乙酯和DHA乙酯

目的:建立高效液相色谱法分离测定鱼油制品中的二十碳五烯酸乙酯(EPA-EE)和二十二碳六烯酸乙酯(DHA-EE)的方法。方法:采用C18色谱柱(250mm×4.6mm),以乙腈-水(90∶10)溶液为流动相,流速为1.0mL.min-1,检测波长205nm。结果:EPA-乙酯和DHA-乙酯分别在0.00273.40μg和0.0031 3.92μg的范围内呈良好线性,线性回归方程分别为y=46014x+25975(R2=1)和y=27036x+53635(R2=0.9995),EPA乙酯和DHA乙酯平均回收率分别为99.45%和101.78%,相对标准偏差分别为1.84%和2.92%(n=5),鱼油中EPA-乙酯和DHA乙酯的含量分别为8.15%和59.6%。结论:本法简便、快速、重现性好,可用于油脂样品中EPA、DHA乙酯含量测定。     

Effect of concentration,pH and ionic strength on the kinetic self-assembly of acid-soluble collagen from walleye pollock (Theragra chalcogramma) skin

The effects of concentration, pH value and ionic strength on the kinetic self-assembly of acid-soluble collagen from walleye pollock (Theragra chalcogramma) skin were investigated. A two-phase kinetic process was provided which included the formation of nucleus center and nucleus growth, the first phase being the controlled step for collagen self-assembly. Collagen showed marked assembly behavior when concentration reaching and above 0.6 mg/mL, and higher concentration could accelerate collagen self-assembly. Rate constants of the first and second assembly phase both increased with pH to a maximum around pH 7.2 and then decreased, indicating that pH 7.2 was the optimum pH value for collagen self-assembly. The kinetics of collagen self-assembly could be modulated by NaCl concentration. The concentration of NaCl from 30 to 60 mM was more suitable to self-assemble for pollock skin collagen.     

Estimation of freezing storage time and quality changes in hake (Merluccius merluccius, L.) by low field NMR

The potential of low field NMR (LF NMR) as a fast monitoring technique to estimate the quality of hake (Merluccius merluccius) frozen stored at -10°C for up to 6months was evaluated. LF NMR clearly detected three populations of water: water strongly bound to macromolecules (T(2b)), trapped water (T(21)) and free water (T(22)). As storage time increased, and concomitant with an increase in the T(22) and a decrease in the T(21) water populations, the water holding capacity (WHC) and apparent viscosity values decreased and the shear strength increased, reflecting the characteristic loss of juiciness and tougher texture developed by hake during frozen storage. Two mathematical models were constructed: a simple regression using the biexponential analysis of the relaxation times (T(21), T(22)) and amplitudes (A(21), A(22)) and a partial least square regression (PLS) of CONTIN analysis. Both models seemed suitable to estimate the quality of the product.     

The effect of replacing dietary fish oil with canola oil on fatty acid composition and expression of desaturase and elongase genes in Jade Tiger hybrid abalone

This study investigates the effect of graded substitution of dietary fish oil (FO) with canola oil (CO) on fatty acid composition and expression of Δ-6 desaturase and elongase 2 genes in the muscle of Jade Tiger hybrid abalone. The control diet contained 1.5% FO supplement (0% CO). Four other diets contained FO/CO in ratios of 3:1 (CO 25%), 1:1 (CO 50%), 1:3 (CO 75%) and 100% CO. The result demonstrated that abalone fed the diets supplemented with 25% and 50% CO showed similarly high levels of total omega-3 polyunsaturated fatty acid (n-3 PUFA), eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3) (P < 0.05) as the 0% CO group. The highest levels of total PUFA and total monounsaturated fatty acids were found in the 100% CO group (P < 0.05). The results also showed that Δ-6 desaturase and elongase 2 gene expression was increased in a graded manner by increasing dietary CO (P < 0.05). It was concluded that replacement of FO by CO at the levels of 25-50% can improve the contents of health-benefiting EPA and DHA in abalone.     

Supercritical fluid extraction of fish oil from fish by-products: A comparison with other extraction methods

Fish and fish by-products are the main natural source of omega-3 polyunsaturated fatty acids, especially EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid), both of them with a great importance in the food and pharmaceutical industries. Comparing to conventional fish oil extraction processes such as cold extraction, wet reduction or enzymatic extraction, supercritical fluid extraction with carbon dioxide under moderate conditions (25 MPa and 313 K) may be useful for reducing fish oil oxidation, especially when fish oil is rich in omega-3 such as salmon oil, and the amount of certain impurities, such as some species of arsenic. Furthermore, taking profit of the advantages of supercritical carbon dioxide as extractive solvent, a coupled extraction-fractionation process is proposed as a way to remove free fatty acids and improve fish oil quality, alternatively to physical and chemical refining procedures.     

Giant Amazonian fish pirarucu (Arapaima gigas): Its viscera as a source of thermostable trypsin

A trypsin was purified from pyloric caeca of pirarucu (Arapaima gigas). The effect of metal ions and protease inhibitors on its activity and its physicochemical and kinetic properties, as well its N-terminal sequence, were determined. A single band (28.0 kDa) was observed by SDS–PAGE. Optimum pH and temperature were 9.0 and 65 °C, respectively. The enzyme was stable after incubation for 30 min in a wide pH range (6.0–11.5) and at 55 °C. The kinetic parameters K_m, k_cat and k_cat/K_m were 0.47 ± 0.042 mM, 1.33 s⁻¹ and 2.82 s⁻¹ mM⁻¹, respectively, using BApNA as substrate. This activity was shown to be very sensitive to some metal ions, such as Fe²⁺, Hg²⁺, Zn²⁺, Al³⁺, Pb²⁺, and was highly inhibited by trypsin inhibitors. The trypsin N-terminal sequence IVGGYECPRNSVPYQ was found. The features of this alkaline peptidase suggest that it may have potential for industrial applications (e.g. food and detergent industries).     

The choice of homogenisation equipment affects lipid oxidation in emulsions

Milk proteins are often used by the food industry because of their good emulsifying properties. In addition, they can also provide oxidative stability to foods. However, different milk proteins or protein components have been shown to differ in their antioxidative properties, and their localisation in emulsions has been shown to be affected by the emulsification conditions. The objective of this study was to investigate the influence of homogenisation equipment (microfluidizer vs. two-stage valve homogeniser) on lipid oxidation in 10% fish oil-in-water emulsions prepared with two different milk proteins. Emulsions were prepared at pH 7 with similar droplet sizes. Results showed that the oxidative stability of emulsions prepared with sodium caseinate was not influenced by the type of homogeniser used. In contrast, the type of homogenisation equipment significantly influenced lipid oxidation when whey protein was used as emulsifier, with the microfluidizer resulting in lower levels of oxidation.