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单克隆抗体在硅油-水界面发生凝胶化,随后界面凝胶破裂,导致聚集和颗粒形成。

Gelation of a monoclonal antibody at the silicone oil-water interface and subsequent rupture of the interfacial gel results in aggregation and particle formation.

作者信息

Mehta Shyam B, Lewus Rachael, Bee Jared S, Randolph Theodore W, Carpenter John F

机构信息

Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, 80045.

出版信息

J Pharm Sci. 2015 Apr;104(4):1282-90. doi: 10.1002/jps.24358. Epub 2015 Jan 30.

Abstract

The formation of viscoelastic gels by a monoclonal antibody (mAb) at the silicone oil-water interface was studied using interfacial shear rheology. At a concentration of 50 μg/mL, the mAb formed gels in less than 1 h, and the gelation time decreased with increasing protein concentration. To probe the effects of mechanical rupture of the interfacial gel layers, a layer of silicone oil was overlaid on the surface of aqueous solutions of mAb, and the interface was ruptured periodically with a needle. Rupture of the interfacial gel resulted in formation of subvisible particles and substantial losses of mAb monomer, which were detected by microflow imaging and quantified by size-exclusion chromatography, respectively. Resonance mass measurement showed that levels of both protein particles and silicone oil droplets increased as the gel was repeatedly ruptured with a needle. In contrast, in samples wherein the interfacial gels were not ruptured, much lower levels of aggregates and particles were detected. Addition of nonionic surfactants (polysorbate 20 or polysorbate 80) protected against aggregation and protein particle formation, with increased protection seen with increasing surfactant levels, and with the greatest inhibition observed in samples containing polysorbate 80.

摘要

利用界面剪切流变学研究了单克隆抗体(mAb)在硅油-水界面形成粘弹性凝胶的过程。在浓度为50μg/mL时,mAb在不到1小时内形成凝胶,且凝胶化时间随蛋白质浓度的增加而缩短。为了探究界面凝胶层机械破裂的影响,在mAb水溶液表面覆盖一层硅油,并用针定期破坏界面。界面凝胶的破裂导致亚可见颗粒的形成和mAb单体的大量损失,分别通过微流成像检测和尺寸排阻色谱定量。共振质量测量表明,随着凝胶被针反复破坏,蛋白质颗粒和硅油滴的水平均增加。相比之下,在未破坏界面凝胶的样品中,检测到的聚集体和颗粒水平要低得多。添加非离子表面活性剂(聚山梨酯20或聚山梨酯80)可防止聚集和蛋白质颗粒形成,随着表面活性剂水平的增加,保护作用增强,在含有聚山梨酯80的样品中观察到的抑制作用最大。

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