Process Analytical Technology (PAT) for Continuous Purification of mRNA via Precipitation and Tangential Flow Filtration

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Rajan R. Bhawnani, Maria del Carme Pons Royo, Rohan Kadambi, Andrew Hatas, Steve Burcat, Tyler Arnold, Hasan Al‐Mahayni, Richard D. Braatz, Allan S. Myerson
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引用次数: 0

Abstract

Continuous downstream processing of messenger ribonucleic acid (mRNA) therapeutics requires purification strategies that are scalable, robust, and capable of removing product‐ and process‐related impurities from in vitro transcription mixtures. Precipitation‐based purification coupled with tangential flow filtration (TFF) has recently been demonstrated as a chromatography‐free route for continuous mRNA purification. However, implementation of this approach requires real‐time monitoring strategies that can distinguish the product‐rich precipitated phase from the impurity‐rich liquid phase, as well as phase‐dependent transport behavior across the integrated process. In this work, we develop a phase‐resolved process analytical technology (PAT) and residence time distribution (RTD) framework for continuous mRNA purification by PEG/NaCl precipitation and sequential TFF. Inline UV–Vis spectroscopy and LED‐based optical density measurements were used concurrently to separate nucleic‐acid absorbance from turbidity‐driven responses associated with suspended mRNA precipitates. RTD experiments with dissolved and precipitated tracers revealed phase‐dependent transport behavior in both the tubular precipitator and TFF module, which was quantified using axial dispersion and tanks‐in‐series models. During integrated operation, inline PAT captured startup, steady‐state, and washout behavior, while stable TMP indicated operation without observable membrane fouling. This work demonstrates that precipitation‐based continuous mRNA purification can be strengthened through phase‐resolved monitoring and RTD‐based process understanding, providing a framework for robust development of continuous downstream processes for nucleic acid therapeutics.
通过沉淀和切向流过滤连续纯化mRNA的过程分析技术(PAT)
信使核糖核酸(mRNA)疗法的连续下游处理需要可扩展的、强大的、能够从体外转录混合物中去除产品和过程相关杂质的纯化策略。基于沉淀的纯化结合切向流过滤(TFF)最近被证明是一种无色谱的连续mRNA纯化途径。然而,这种方法的实施需要实时监测策略,以区分富产物沉淀相和富杂质液相,以及在整个集成过程中依赖于相的传输行为。在这项工作中,我们开发了一种相分辨过程分析技术(PAT)和停留时间分布(RTD)框架,用于通过PEG/NaCl沉淀和顺序TFF连续纯化mRNA。同时使用内联UV-Vis光谱和基于LED的光密度测量来分离与悬浮mRNA沉淀相关的浊度驱动响应的核酸吸光度。溶解示踪剂和沉淀示踪剂的RTD实验揭示了管式沉淀器和TFF模块中相依赖的输运行为,并使用轴向分散和槽内串联模型对其进行了量化。在集成操作过程中,内联PAT捕获启动、稳态和冲洗行为,而稳定TMP表示操作过程中没有可观察到的膜污染。这项工作表明,基于沉淀的连续mRNA纯化可以通过相分辨监测和基于RTD的过程理解来加强,为核酸治疗的连续下游过程的稳健发展提供了框架。
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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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