Quality by Design Framework Applied to GMMA Purification.

IF 5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Carlo Giannelli, Francesca Necchi, Elena Palmieri, Davide Oldrini, Beatrice Ricchetti, Maria M Papathanasiou, Zoltan Kis, Cleo Kontoravdi, Cristiana Campa, Francesca Micoli
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引用次数: 0

Abstract

In recent years, Generalized Modules for Membrane Antigens (GMMA) have received increased attention as an innovative vaccine platform against bacterial pathogens, particularly attractive for low- and middle-income countries because of manufacturing simplicity. The assessment of critical quality attributes (CQAs), product-process interactions, identification of appropriate in process analytical methods, and process modeling is part of a robust quality by design (QbD) framework to support further development and control of manufacturing processes. QbD implementation in the context of the GMMA platform will ensure robust manufacturing of batches with desired characteristics, facilitating technical transfer to local manufacturers, regulatory approval, and commercialization of vaccines based on this technology. Here, we summarize the methodology suggested, applied to a first step of GMMA manufacturing process.

质量源于设计框架应用于 GMMA 净化。
近年来,膜抗原通用模块(GMMA)作为抗击细菌病原体的创新疫苗平台受到越来越多的关注,由于其制造简单,对中低收入国家尤其具有吸引力。对关键质量属性 (CQA)、产品与工艺之间的相互作用进行评估,确定适当的工艺分析方法,并建立工艺模型,这些都是强有力的质量设计 (QbD) 框架的一部分,可为进一步开发和控制生产工艺提供支持。在 GMMA 平台的背景下实施 QbD 将确保批量生产具有所需特性的稳健产品,从而促进向本地制造商的技术转移、监管审批以及基于该技术的疫苗商业化。在此,我们总结了应用于 GMMA 生产流程第一步的建议方法。
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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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