Evaluation of the Design, Development, and Performance of a Mass-Flow Based, Open-Source Buffer Manufacturing System.

Q3 Medicine
Natraj Ram, Jeff Johnson, Hiren Ardeshna, Joseph Camire, Ryan Campbell, Doan Chau, Sam Gardner, Kevin Gibson, Joey Norikane, Paul Randolph, Kelly Smith, Katherine Stafford, Rachel Swamy, Shana Usery, Kelvin H Lee
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引用次数: 1

Abstract

Buffer solutions are a critical component of the manufacturing process for therapeutic proteins and other biomolecules. The traditional way to make and use buffers is space and resource intensive, creating operational bottlenecks that impact efficiencies and costs. Here we describe a full-scale, current Good Manufacturing Practices (cGMP) capable buffer stock blending system that has an open-source, configurable design and that overcomes the challenges of traditional buffer preparation. The system comprises simplified control and operation using mass flow to provide on-demand supply of buffer solutions. The system also has self-cleaning capability and is amenable to be operated as a closed system. The data will demonstrate the excellent performance and capabilities of the system as well as illustrate its potential transformative impact on biomanufacturing.

基于质量流的开源缓冲器制造系统的设计、开发和性能评估。
缓冲溶液是治疗性蛋白质和其他生物分子制造过程的关键组成部分。制作和使用缓冲器的传统方法是空间和资源密集型的,产生了影响效率和成本的操作瓶颈。在这里,我们描述了一个全面的,符合现行良好生产规范(cGMP)的缓冲料混合系统,该系统具有开源,可配置的设计,克服了传统缓冲制剂的挑战。该系统包括简化的控制和使用质量流的操作,以提供按需供应的缓冲溶液。该系统还具有自清洁能力,可作为封闭系统运行。数据将展示该系统的卓越性能和能力,并说明其对生物制造的潜在变革性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
34
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