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The Effects of Excipients on Protein Aggregation During Agitation: An Interfacial Shear Rheology Study

机译:赋形剂对搅拌过程中蛋白质聚集的影响:界面剪切流变学研究

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摘要

We investigated the effects of excipients in solutions of keratinocyte growth factor 2 (KGF-2) on protein aggregation during agitation as well as on interfacial shear rheology at the air-water interface. Samples were incubated with or without agitation, and in the presence or absence of the excipients heparin, sucrose or polysorbate 80 (PS80). The effect of excipients on the extent of protein aggregation was determined by UV spectroscopy and microflow imaging (MFI). Interfacial shear rheology was used to detect the gelation time and strength of protein gels at the air-water interface. During incubation, protein particles of size ≥ 1 μm and insoluble aggregates formed faster for KGF-2 solutions subjected to agitation. Addition of either heparin or sucrose promoted protein aggregation during agitation. In contrast, PS 80 substantially inhibited agitation-induced KGF-2 aggregation but facilitated protein particulate formation in quiescent solutions. The combination of PS 80 and heparin or sucrose completely prevented protein aggregation during both non-agitated and agitated incubations. Interfacial rheological measurements showed that KGF-2 in buffer alone formed an interfacial gel within a few minutes. In the presence of heparin, KGF-2 interfacial gels formed too quickly for gelation time to be determined. KGF-2 formed gels in about 10 minutes in the presence of sucrose. The presence of PS80 in the formulation inhibited gelation of KGF-2. Furthermore, the interfacial gels formed by the protein in the absence of PS80 were reversible when PS80 was added to the samples after gelation. Therefore, there is a correspondence between formulations that exhibited interfacial gelation and formulations that exhibited agitation-induced aggregation.
机译:我们研究了角化细胞生长因子2(KGF-2)溶液中赋形剂对搅拌过程中蛋白质聚集以及在空气-水界面的界面剪切流变学的影响。在存在或不存在赋形剂肝素,蔗糖或聚山梨酯80(PS80)的情况下,在有或没有搅拌的情况下孵育样品。通过紫外光谱和微流成像(MFI)确定了赋形剂对蛋白质聚集程度的影响。界面剪切流变学用于检测空气-水界面处的胶凝时间和蛋白质凝胶的强度。在孵育过程中,对于KGF-2溶液进行搅拌时,尺寸≥1μm的蛋白质颗粒和不溶性聚集体形成更快。肝素或蔗糖的添加促进了搅拌过程中的蛋白质聚集。相反,PS 80基本上抑制了搅拌诱导的KGF-2聚集,但促进了静态溶液中蛋白质颗粒的形成。 PS 80和肝素或蔗糖的组合完全防止了在非搅拌培养和搅拌培养中的蛋白质聚集。界面流变学测量表明,仅缓冲液中的KGF-2在几分钟内形成界面凝胶。在肝素的存在下,KGF-2界面凝胶形成太快,无法确定胶凝时间。 KGF-2在蔗糖存在下约10分钟内形成凝胶。制剂中PS80的存在抑制了KGF-2的胶凝。此外,当在凝胶化之后将PS80添加到样品中时,在不存在PS80的情况下由蛋白质形成的界面凝胶是可逆的。因此,表现出界面胶凝的制剂和表现出搅拌诱导的聚集的制剂之间存在对应关系。

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