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首页> 外文期刊>Food Chemistry >Selenium release kinetics and mechanism from Cordyceps sinensis exopolysaccharide-selenium composite nanoparticles in simulated gastrointestinal conditions
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Selenium release kinetics and mechanism from Cordyceps sinensis exopolysaccharide-selenium composite nanoparticles in simulated gastrointestinal conditions

机译:硒释放动力学和机制来自冬虫夏草中的肠外二糖 - 硒复合纳米粒子在模拟胃肠环境中

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摘要

This work investigated selenium (Se) release kinetics and mechanism from exopolysaccharide-selenium nano particles (EPS-SeNPs, Se/EPS = 1/20, 1/1 and 4/3) in simulated gastric (SGF) and intestinal fluids (SIF) using kinetics models of Zero order, First order, Higuchi, Hixson-Crowell and Korsmeyer-Peppas. EPS-SeNPs showed an increase in size from 80?125 nm to 250?320 nm and more ambiguous boundary after gastrointestinal digestion. Se/EPS ratio and pH had significant influence on Se release. Se release kinetics from EPS-SeNPs (Se/EPS = 1/1 and 4/3 in SGF) followed a classical Fickian diffusion, in contrast to an erosion governed by macromolecular chains relaxation for Se/EPS = 1/20 in SIF. Se release from EPS-SeNPs (Se/EPS = 1/1 and 4/3 in SIF) was well fitted to Korsmeyer-Peppas model and followed a non-Fickian mechanism controlled by both diffusion and erosion. Additionally, EPS-SeNPs (Se/EPS = 1/20) showed a low Se release after SGF digestion, but a high release after SIF digestion, suggesting its application in controlled release of Se-enriched supplements for Se-deficiency treatment.
机译:这项工作研究了Selenium(Se)释放动力学和来自潜水糖 - 硒纳米颗粒(EPS-SENP,SE / EPS = 1/20,1 / 1和4/3)的释放动力学和机制在模拟胃(SGF)和肠液中(SIF)使用零阶的动力学模型,一阶,Higuchi,Hixson-Crowell和Korsmeyer-Peppas。 EPS-SENP显示大小从80?125nm至250?320nm和胃肠道消化后更加暧昧的边界。 SE / EPS比和pH对SE释放有重大影响。 SE释放来自EPS-SENP的动力学(SE / EPS = 1/1和4/3在SGF中)之后是一种经典的Fickian扩散,与SIF中SE / EPS = 1/20的大分子链弛豫的侵蚀相比。 SE从EPS-SENP(SE / EPS = 1/1和4/3中的SIF)释放到Korsmeyer-Peppas模型,并遵循由扩散和侵蚀控制的非Fickian机制。此外,EPS-SENP(SE / EPS = 1/20)在SGF消化后显示出低SE释放,但SIF消化后的高释放,表明其在富含SE缺乏治疗的SE-FICHED补充剂中的应用。

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