Streamlining viral safety in AAV manufacturing: simultaneous cell lysis and viral inactivation using biodegradable detergents

IF 3.8 3区 医学 Q2 CHEMISTRY, MEDICINAL Journal of pharmaceutical sciences Pub Date : 2025-03-17 DOI:10.1016/j.xphs.2025.103761
Tuhidul Islam, Jungmin Oh, Lori Fortin, Courtney Connors, Nandkumar Deorkar
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Abstract

Ensuring viral safety in biopharmaceutical production is vital for global regulatory standards adherence and safeguarding patients. This study evaluates the efficacy of newly developed biodegradable detergent formulations, designed to comply with regulatory requirements, for inactivating enveloped viruses during the cell lysis step of adeno-associated virus (AAV) production. Virus clearance (VC) studies showed robust inactivation kinetics against Xenotropic Murine Leukemia Virus (XMuLV), achieving a log reduction value (LRV) of ≥5.34 within 30 to 120 min. Comparative testing in crude cell lysate and PBS buffer showed consistent viral inactivation across different matrices, highlighting the versatility of the detergent formulations. Importantly, the detergent composition preserved AAV capsid integrity, and subsequent purification steps, including affinity and ion-exchange chromatography, effectively removed residual detergent. Overall, this study demonstrates the potential of biodegradable detergents to simultaneously facilitate cell lysis and viral inactivation in AAV manufacturing, offering a sustainable alternative that aligns with industry standards.
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简化AAV生产中的病毒安全性:使用可生物降解的洗涤剂同时进行细胞裂解和病毒灭活。
确保生物制药生产中的病毒安全性对于遵守全球监管标准和保护患者至关重要。本研究评估了新开发的符合法规要求的生物可降解洗涤剂配方,用于在腺相关病毒(AAV)生产的细胞裂解阶段灭活包膜病毒。病毒清除(VC)研究显示了对异嗜性小鼠白血病病毒(XMuLV)的强大失活动力学,在30至120分钟内实现对数降低值(LRV)≥5.34。在粗细胞裂解液和PBS缓冲液中进行的对比测试显示,不同基质的病毒灭活效果一致,突出了洗涤剂配方的多功能性。重要的是,洗涤剂组合物保持了AAV衣壳的完整性,随后的纯化步骤,包括亲和和离子交换色谱,有效地去除了残留的洗涤剂。总的来说,这项研究证明了生物可降解洗涤剂在AAV制造中同时促进细胞裂解和病毒灭活的潜力,提供了符合行业标准的可持续替代方案。
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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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