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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >The influence of size, structure and hydrophilicity of model surfactants on the adsorption of lysozyme to oil-water interface-Interfacial shear measurements
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The influence of size, structure and hydrophilicity of model surfactants on the adsorption of lysozyme to oil-water interface-Interfacial shear measurements

机译:模型表面活性剂的大小,结构和亲水性对溶菌酶在油水界面上的吸附的影响-界面剪切测量

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The flexibility and aggregation of proteins can cause adsorption to oil-water interfaces and thereby create challenges during formulation and processing. Protein adsorption is a complex process and the presence of surfactants further complicates the system, in which additional parameters need to be considered. The purpose of this study is to scrutinize the influence of surfactants on protein adsorption to interfaces, using lysozyme as a model protein and sorbitan monooleate 80 (S80), polysorbate 80 (T80), polyethylene-block-poly(ethylene glycol) (PE-PEG) and polyglycerol polyricinoleate (PG-PR) as model surfactants. Rheological properties, measured using a TA AR-G2 rheometer equipped with a double wall ring (DWR) geometry, were used to compare the efficacy of the surfactant in hindering lysozyme adsorption. The system consists of a ring and a Delrin? trough with a circular channel (interfacial area=1882.6mm~2). Oscillatory shear measurements were conducted at a constant frequency of 0.1Hz, a temperature of 25°C, and with strain set to 1%.The adsorption of lysozyme to the oil-water interface results in the formation of a viscoelastic film. This can be prevented by addition of surfactants, in a manner depending on the concentration and the type of surfactant. The more hydrophilic surfactants are more effective in hindering lysozyme adsorption to oil-water interfaces. Additionally, the larger surfactants are more persistent in preventing film formation, whereas the smaller ones eventually give space for the lysozyme on the interface. The addition of a mixture of two different surfactants was only beneficial when the two hydrophilic surfactants were mixed, in which case a delay in the multilayer formation was detected.The method is able to detect the interfacial adsorption of lysozyme and thus the hindering of film formation by model surfactants. It can therefore aid in processing of any delivery systems for proteins in which the protein is introduced to oil-water interfaces.
机译:蛋白质的柔韧性和聚集会导致吸附到油水界面,从而在配制和加工过程中带来挑战。蛋白质吸附是一个复杂的过程,表面活性剂的存在使系统更加复杂,其中需要考虑其他参数。这项研究的目的是使用溶菌酶作为模型蛋白和脱水山梨糖醇单油酸酯80(S80),聚山梨酸酯80(T80),聚乙烯嵌段-聚乙二醇(PE- PEG)和聚甘油聚蓖麻油酸酯(PG-PR)作为模型表面活性剂。使用配备有双壁环(DWR)几何形状的TA AR-G2流变仪测量的流变性质用于比较表面活性剂在阻碍溶菌酶吸附方面的功效。该系统包括一个环和一个Delrin?槽内有圆形槽(界面面积= 1882.6mm〜2)。振荡剪切测量是在0.1Hz的恒定频率,25°C的温度下进行的,应变设置为1%。溶菌酶在油水界面上的吸附会形成粘弹性膜。可以通过根据表面活性剂的浓度和类型的方式添加表面活性剂来防止这种情况。亲水性更高的表面活性剂在阻碍溶菌酶吸附到油水界面方面更有效。另外,较大的表面活性剂在防止膜形成方面更具持久性,而较小的表面活性剂最终在界面上为溶菌酶提供了空间。仅当两种亲水性表面活性剂混合时才添加两种不同表面活性剂的混合物才是有益的,在这种情况下,可以检测到多层形成的延迟。该方法能够检测溶菌酶的界面吸附并因此阻止膜形成通过模型表面活性剂。因此,它可以帮助处理任何将蛋白质引入油-水界面的蛋白质递送系统。

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