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通过蛋白质释放和消化测定藻酸盐、壳聚糖和聚乙二醇作为胶体药物递送物质的潜力。

Potential of alginate, chitosan and polyethylene glycol as substances for colloidal drug delivery as determined by protein release and digestion.

作者信息

Just Philip N, Slater Matthew J

机构信息

Sustainable Bioeconomy, Alfred-Wegener-Institute, Helmholtz Centre for Polar and Marine Research, 27570, Bremerhaven, Germany.

出版信息

Vet Anim Sci. 2024 Jan 18;23:100335. doi: 10.1016/j.vas.2024.100335. eCollection 2024 Mar.

Abstract

Colloidal encapsulations can be applied as protective matrices in aquaculture feeds. They promise an ideal approach to protect bioactive substances such as oral vaccines, pre- or probiotics against degradation due to acidic environments or untimely lixiviation. Alginate, chitosan and polyethylene glycol (PEG) are substances frequently applied in encapsulations as protective matrices. However, essential information on their direct and comparable characteristics and their effects on digestion speeds after oral application in aquaculture are lacking. The current study evaluated in vitro release and retention profiles of a model protein bovine serum albumin (BSA) after encapsulation with four experimental formulations of protective matrices: ALG - alginate; AC -alginate and chitosan, AP - alginate and PEG and APC - alginate, PEG and chitosan. The iron marked treatment diets were fed to juvenile rainbow trout and digestion speed was investigated using radiographic imaging. Digestion speeds did not differ significantly between treatments, with all test diets reaching the anterior fish intestine 10 h after feeding. The BSA retention under low pH was highest for the alginate-chitosan PM (84.7 ± 5.8 %). The inclusion of PEG reduced the retention rate in low pH but significantly increased the absolute BSA release. An oil coating significantly reduced the BSA release during the initial burst for the alginate, alginate-PEG and alginate-chitosan-PEG treatments and significantly reduced retention potential under neutral pH conditions. The feeding simulation trial showed that an oil-coated diet containing alginate-chitosan as a protective matrix can be used to protect the model protein during feeding (release to the water) and against the harmful milieu of the fish stomach. Different combinations of the investigated encapsulation substances can be used to achieve optimal encapsulation and protective characteristics depending on the application objective.

摘要

胶体包封可作为水产养殖饲料中的保护基质。它们有望成为一种理想的方法,用于保护生物活性物质,如口服疫苗、益生元或益生菌,防止其因酸性环境或过早浸出而降解。海藻酸盐、壳聚糖和聚乙二醇(PEG)是常用于包封作为保护基质的物质。然而,缺乏关于它们直接和可比特性以及口服应用于水产养殖后对消化速度影响的基本信息。本研究评估了用四种实验性保护基质配方包封后模型蛋白牛血清白蛋白(BSA)的体外释放和保留情况:ALG - 海藻酸盐;AC - 海藻酸盐和壳聚糖;AP - 海藻酸盐和PEG;APC - 海藻酸盐、PEG和壳聚糖。将铁标记的处理饲料投喂给幼年虹鳟鱼,并使用放射成像研究消化速度。各处理之间的消化速度没有显著差异,所有试验饲料在投喂后10小时到达鱼的前肠。在低pH值下,海藻酸盐 - 壳聚糖保护基质的BSA保留率最高(84.7±5.8%)。加入PEG降低了低pH值下的保留率,但显著增加了BSA的绝对释放量。油包衣显著降低了海藻酸盐、海藻酸盐 - PEG和海藻酸盐 - 壳聚糖 - PEG处理在初始爆发期的BSA释放,并显著降低了中性pH条件下的保留潜力。投喂模拟试验表明,含有海藻酸盐 - 壳聚糖作为保护基质的油包衣饲料可用于在投喂期间(释放到水中)保护模型蛋白,并抵御鱼胃的有害环境。根据应用目标,所研究的包封物质的不同组合可用于实现最佳的包封和保护特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/447c/10810738/823474f0005e/gr1.jpg

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