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静脉输液器在线过滤器的蛋白质吸附。

Protein Adsorption to In-Line Filters of Intravenous Administration Sets.

机构信息

Technical Development NBE, Biologics Technical Development and Manufacturing, Novartis Pharma AG, Basel, Switzerland.

出版信息

J Pharm Sci. 2017 Oct;106(10):2959-2965. doi: 10.1016/j.xphs.2017.05.028. Epub 2017 May 27.

DOI:10.1016/j.xphs.2017.05.028
PMID:28559043
Abstract

Ensuring compatibility of administered therapeutic proteins with intravenous administration sets is an important regulatory requirement. A low-dose recovery during administration of low protein concentrations is among the commonly observed incompatibilities, and it is mainly due to adsorption to in-line filters. To better understand this phenomenon, we studied the adsorption of 4 different therapeutic proteins (2 IgG1s, 1 IgG4, and 1 Fc fusion protein) diluted to 0.01 mg/mL in 5% glucose (B. Braun EcoFlac; B. Braun Melsungen AG, Melsungen, Germany) or 0.9% sodium chloride (NaCl; Freeflex; Fresenius Kabi, Friedberg, Germany) solutions to 8 in-line filters (5 positively charged and 3 neutral filters made of different polymers and by different suppliers). The results show certain patterns of protein adsorption, which depend to a large extent on the dilution solution and filter material, and to a much lower extent on the proteins' biophysical properties. Investigation of the filter membranes' zeta potential showed a correlation between the observed adsorption pattern in 5% glucose solution and the filter's surface charge, with higher protein adsorption for the strongly negatively charged membranes. In 0.9% NaCl solution, the surface charges are masked, leading to different adsorption patterns. These results contribute to the general understanding of the protein adsorption to IV infusion filters and allow the design of more efficient compatibility studies.

摘要

确保给予的治疗性蛋白与静脉输液装置的兼容性是一个重要的监管要求。在低蛋白浓度给予期间的低剂量回收是常见的不相容性之一,这主要是由于吸附在线性过滤器上。为了更好地理解这一现象,我们研究了 4 种不同的治疗性蛋白(2 种 IgG1、1 种 IgG4 和 1 种 Fc 融合蛋白)在 5%葡萄糖(B. Braun EcoFlac;B. Braun Melsungen AG,Melsungen,德国)或 0.9%氯化钠(NaCl;Freeflex;Fresenius Kabi,Friedberg,德国)溶液中稀释至 0.01mg/mL 时对 8 个在线性过滤器(5 个带正电荷和 3 个由不同聚合物和不同供应商制成的中性过滤器)的吸附情况。结果显示出一定的蛋白吸附模式,这些模式在很大程度上取决于稀释溶液和过滤器材料,而在很大程度上与蛋白质的生物物理特性无关。对过滤器膜的 zeta 电位的研究表明,在 5%葡萄糖溶液中观察到的吸附模式与过滤器的表面电荷之间存在相关性,带强负电荷的膜吸附蛋白的能力更强。在 0.9%NaCl 溶液中,表面电荷被屏蔽,导致不同的吸附模式。这些结果有助于普遍了解蛋白对静脉输液过滤器的吸附,并允许设计更有效的相容性研究。

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