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Developing membrane platform technology for manufacturing of clinical-grade bioproducts

Developing membrane platform technology for manufacturing of clinical-grade bioproducts
开发用于制造临床级生物产品的膜平台技术
批准号:
363823-2007
负责人:
Chou, Perry
金额:
$2.8万
依托单位:
依托单位国家:
加拿大
项目类别:
Collaborative Research and Development Grants
财政年份:
2009
资助国家:
加拿大
项目状态:
已结题
起止时间:
2009-01-01 至 2010-12-31

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中文摘要
翻译
生物制造过程通常包含三个主要组成部分,即上游菌株开发、中游细胞培养和下游纯化处理。分离或遗传构建具有增强的生产所需生物产物(核糖体或非核糖体)的能力的生物细胞。然后在生物反应器中进行繁殖。培养后,采用一系列下游加工步骤进行生物产品纯化。虽然生产菌株的构建通常被认为是成功的生物工艺开发的关键先决条件,但下游加工可能占整个生物工艺的大部分资本和运营成本。因此,开发有效的下游加工策略成为生物工程师的一项具有挑战性的任务。尼萨膜技术公司是一家加拿大公司,拥有一种新颖的专有膜基平台技术,在蛋白质纯化和其他生物和工业分离方面具有广泛的全球应用。通过建立可以补充纯聚合物膜相关技术限制的水凝胶技术,该公司迄今已开发出几种用于澄清(即微滤),色谱(即阴离子/阳离子交换)和浓缩(即超滤)步骤的水凝胶膜产品。这些产品具有特殊的功能,如高通量,高结合能力和高机械强度,基于这些功能,它们能够超越许多现有的商业产品。认识到缺乏实际应用于临床级生物制品生产的商业膜产品,该公司有兴趣通过瞄准生物制药和质粒DNA生产的全球市场来商业化其产品。为此,该公司将需要建立他们的平台技术作为一个上级替代传统的生物产品纯化。这是拟议项目的主要目标,尼萨和滑铁卢大学之间的合作。
英文摘要
Biomanufacturing processes often contain three major components, namely upstream strain development, midstream cell cultivation, and downstream purification processing. Biological cells with an enhanced ability for the production of desired bioproducts, either ribosomal or non-ribosomal, are isolated or genetically constructed. They are then cultivated in bioreactors for multiplication. Following cultivation, a series of downstream processing steps are adopted for bioproduct purification. While construction of production strains is generally recognized as a key prerequisite for successful bioprocess development, downstream processing could account for a big portion of the capital and operation costs of the overall bioprocess. Hence, developing strategies for effective downstream processing becomes a challenging task for bioengineers. Nysa Membrane Technologies, Inc. is a Canadian company in possession of a novel, proprietary membrane-based platform technology with broad global applications in protein purification and other biological and industrial separations. By establishing the hydrogel technologies which can complement technical limitations associated with pure polymeric membranes, the company has so far developed several hydrogel membrane products for clarification (i.e. microfiltration), chromatography (i.e. anion/cation exchange), and concentration (i.e. ultrafiltration) steps. These products have special features, such as high flux, high binding capacity, and high mechanical strength, based on which they are able to outperform many existing commercial products. Recognizing the lack of commercial membrane products practically applied for manufacturing of clinical-grade bioproducts, the company is interested in commercializing their products by targeting the global market in biopharmaceutical and plasmid DNA manufacturing. To this end, the company will need to establish their platform technology as a superior alternative to the conventional one for bioproduct purification. This is the primary goal of the proposed project, a collaborative work between Nysa and University of Waterloo.
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