The application of forward osmosis for producing highly concentrated biotherapeutics

IF 9 1区 工程技术 Q1 ENGINEERING, CHEMICAL Journal of Membrane Science Pub Date : 2025-04-01 Epub Date: 2025-02-11 DOI:10.1016/j.memsci.2025.123839
Vasudev Tangry, William Haddad, Ali Behboudi, Andrew L. Zydney
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Abstract

Forward osmosis (FO) has primarily been explored for applications in water desalination. While FO has also shown potential in concentrating dairy products, little to no attention has been paid to its potential in concentrating biotherapeutics, particularly to the very high concentrations needed for many monoclonal antibody products that are delivered by subcutaneous injection. This study demonstrates the feasibility of using FO as an alternative to ultrafiltration (UF) to achieve highly concentrated protein formulations using human Immunoglobin G (hIgG) as a model protein. The permeate flux in FO, using 1 M NaCl as the draw solution, decreased with increasing hIgG concentration due primarily to concentration polarization effects that are strongly influenced by the increase in feed viscosity for the concentrated hIgG solution. The importance of the hIgG viscosity on the FO performance was demonstrated by performing experiments with concentrated polyethylene glycol solutions and through mathematical modeling that accounts for the effects of both external and internal concentration polarization on FO performance. Batch concentration experiments with FO achieved final hIgG concentrations greater than 290 g/L compared to a maximum achievable concentration in UF of approximately 150 g/L. These results clearly demonstrate the potential of using FO, with high osmotic pressure draw solutions, to achieve highly concentrated formulations of therapeutic proteins that are beyond the capability of current UF processes.

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正向渗透在生产高浓度生物治疗药物中的应用
正向渗透(FO)技术在海水淡化中的应用已得到初步探索。虽然FO也显示出浓缩乳制品的潜力,但很少或根本没有注意到它在浓缩生物治疗药物方面的潜力,特别是许多单克隆抗体产品需要非常高的浓度,这些产品需要皮下注射。本研究证明了使用鱼油作为超滤(UF)的替代品,以人类免疫球蛋白G (hIgG)作为模型蛋白,实现高浓度蛋白质配方的可行性。以1 M NaCl为萃取液时,FO的渗透通量随着hIgG浓度的增加而减小,这主要是由于浓度极化效应,而浓度极化效应受浓缩后的hIgG溶液的进料粘度的增加的强烈影响。通过对浓聚乙二醇溶液进行实验,并通过数学建模证明了hIgG粘度对FO性能的重要性,该模型考虑了外部和内部浓度极化对FO性能的影响。与UF的最大可达到浓度约为150 g/L相比,FO的批量浓缩实验获得的最终hIgG浓度大于290 g/L。这些结果清楚地表明,使用高渗透压提取溶液的FO,可以实现目前超滤工艺无法实现的治疗性蛋白的高浓度配方。
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来源期刊
Journal of Membrane Science
Journal of Membrane Science 工程技术-高分子科学
CiteScore
17.10
自引率
17.90%
发文量
1031
审稿时长
2.5 months
期刊介绍: The Journal of Membrane Science is a publication that focuses on membrane systems and is aimed at academic and industrial chemists, chemical engineers, materials scientists, and membranologists. It publishes original research and reviews on various aspects of membrane transport, membrane formation/structure, fouling, module/process design, and processes/applications. The journal primarily focuses on the structure, function, and performance of non-biological membranes but also includes papers that relate to biological membranes. The Journal of Membrane Science publishes Full Text Papers, State-of-the-Art Reviews, Letters to the Editor, and Perspectives.
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