Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, Colorado 80303, United States.
Ursa Analytics, Inc., Denver, Colorado 80212, United States.
ACS Appl Bio Mater. 2021 Sep 20;4(9):6946-6953. doi: 10.1021/acsabm.1c00622. Epub 2021 Aug 13.
This work reports the ability of hydrogel coatings to protect therapeutic proteins from cavitation-induced aggregation caused by mechanical stress. Here, we show that polyacrylamide hydrogel coatings on container surfaces suppress mechanical shock-induced cavitation and the associated aggregation of intravenous immunoglobulin (IVIg). First, crosslinked polyacrylamide hydrogels were grown on the surfaces of borosilicate glass vials. Treatment with ultrasound showed that these hydrogel surfaces suppressed cavitation events to levels below those found for unfunctionalized borosilicate glass. Next, IVIg solutions were loaded into these vials and subjected to tumbling, horizontal shaking, and drop testing. Aggregation was quantified by bisANS fluorescence staining and particle counting by flow imaging microscopy (FIM). In all cases, the presence of polyacrylamide hydrogels on the vial surfaces reduced the amount of IVIg aggregation and the number of particulates. In addition, the polyacrylamide appeared to have a protective effect that prevented additional aggregates from forming at extended tumbling times. Finally, drop test studies showed that the polyacrylamide coatings suppressed detectable cavitation. This work reveals how even a simple hydrogel vial coating can have a profound effect on stabilizing protein therapeutics.
这项工作报告了水凝胶涂层保护治疗性蛋白质免受机械应力引起的空化诱导聚集的能力。在这里,我们表明容器表面上的聚丙烯酰胺水凝胶涂层可以抑制机械冲击引起的空化以及相关的静脉注射免疫球蛋白(IVIg)聚集。首先,将交联的聚丙烯酰胺水凝胶生长在硼硅酸盐玻璃小瓶的表面上。超声处理表明,这些水凝胶表面抑制空化事件的程度低于未功能化的硼硅酸盐玻璃。接下来,将 IVIg 溶液装入这些小瓶中,并进行翻滚、水平晃动和滴注测试。通过双 ANS 荧光染色和流动成像显微镜(FIM)的颗粒计数来定量聚集体。在所有情况下,小瓶表面上存在聚丙烯酰胺水凝胶都减少了 IVIg 聚集的量和颗粒的数量。此外,聚丙烯酰胺似乎具有保护作用,可以防止在延长的翻滚时间内形成更多的聚集体。最后,滴注测试研究表明,聚丙烯酰胺涂层抑制了可检测到的空化。这项工作揭示了即使是简单的水凝胶小瓶涂层也可以对稳定蛋白质治疗剂产生深远的影响。