Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, Copenhagen, Denmark.
Colloids Surf B Biointerfaces. 2011 Oct 1;87(1):96-102. doi: 10.1016/j.colsurfb.2011.05.007. Epub 2011 May 10.
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=1882.6 mm(2)). Oscillatory shear measurements were conducted at a constant frequency of 0.1 Hz, 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.
蛋白质的灵活性和聚集性可导致其吸附到油水界面,从而在制剂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进一步复杂化,需要考虑更多的参数。本研究的目的是研究表面活性剂对蛋白质在界面上吸附的影响,以溶菌酶为模型蛋白,山梨醇单油酸酯 80(S80)、聚山梨醇酯 80(T80)、聚乙二醇-聚氧丙烯(PE-PEG)和聚甘油蓖麻醇酸酯(PG-PR)为模型表面活性剂。使用配备双壁环(DWR)几何形状的 TA AR-G2 流变仪测量流变特性,以比较表面活性剂阻止溶菌酶吸附的效果。该系统由一个环和一个 Delrin®槽组成,其中有一个圆形通道(界面面积=1882.6mm²)。在 0.1Hz 的恒定频率、25°C 的温度和 1%的应变下进行振荡剪切测量。溶菌酶吸附到油水界面会导致形成粘弹性膜。通过添加表面活性剂可以阻止这种情况的发生,其效果取决于表面活性剂的浓度和类型。亲水性越强的表面活性剂越能有效地阻止溶菌酶吸附到油水界面。此外,较大的表面活性剂更能持久地防止形成薄膜,而较小的表面活性剂最终会在界面上为溶菌酶留出空间。当混合两种不同的亲水性表面活性剂时,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,检测到多层形成的延迟。该方法能够检测到溶菌酶在界面上的吸附,从而阻止模型表面活性剂形成薄膜。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输送系统。