Suppr超能文献

体积排阻色谱法与多角度光散射在临床前阶段基因治疗方案分析开发中的应用。

Application of Size Exclusion Chromatography with Multiangle Light Scattering in the Analytical Development of a Preclinical Stage Gene Therapy Program.

机构信息

Analytical Development and Quality Control, StrideBio, Research Triangle Park, North Carolina, USA.

AjaxBio, LLC, Holly Springs, North Carolina, USA.

出版信息

Hum Gene Ther. 2023 Apr;34(7-8):325-338. doi: 10.1089/hum.2022.218.

Abstract

To provide safe recombinant adeno-associated viruses (rAAV) to patients, scalable manufacturing processes are required. However, these processes may introduce impurities that impact the performance and quality of the final drug product. Empty rAAV capsids are product-related impurities. Regulatory guidance requires that accurate analytical methods be implemented early in product development to measure the level of empty capsids. A process confirmation vector, produced from 200 L production, was used to develop and optimize a size exclusion chromatography with UV and multiangle light scattering (SEC-MALS) method. Vector produced from a 500 L production was used to assess the full-to-empty ratio using the following analytical methods: sedimentation velocity analytical ultracentrifugation (SV-AUC), droplet digital PCR (ddPCR) with capsid enzyme-linked immunosorbent assay (ELISA), bulk absorbance at 260/280 nm, cryogenic electron microscopy, and SEC-MALS. This test article was used for a 30-day, non-Good Laboratory Practices animal study that assessed biodistribution of the product (STRX-330). SEC-MALS outperformed the other methods and correlated well with SV-AUC values of full-to-empty particles. In addition, SEC-MALS agreed with ddPCR and ELISA measurements for vector genomes/mL and capsid particles/mL, respectively. SEC-MALS was linear, accurate, and precise while achieving chromatography quality control (QC) recommendations. Compared to other stability-indicating assays, SEC-MALS performed similarly to ddPCR, capsid ELISA, and infectivity assays in accelerated stress studies. In response to alkaline, but not acidic stress, SEC-MALS indicated distinct changes in the DNA content of the monomer Adeno-associated viruses (AAV) peak for STRX-330, which was supported by ddPCR data. Conversely, acidic treatment resulted in more aggregated vector, but did not impact the DNA content. This work indicates that SEC-MALS is a valuable analytical tool in the analytical development and QC testing of AAV. In addition, this work suggests that SEC-MALS can provide fundamental understanding of AAV in response to environmental stress. This may impact steps of the manufacturing process to minimize conditions that reduce performance.

摘要

为了向患者提供安全的重组腺相关病毒(rAAV),需要可扩展的制造工艺。然而,这些工艺可能会引入杂质,从而影响最终药物产品的性能和质量。空 rAAV 衣壳是与产品相关的杂质。监管指南要求在产品开发的早期实施准确的分析方法,以测量空衣壳的水平。使用来自 200L 生产的过程确认载体来开发和优化尺寸排阻色谱法与紫外和多角度光散射(SEC-MALS)方法。使用来自 500L 生产的载体来使用以下分析方法评估全空比:沉降速度分析超速离心(SV-AUC)、带有衣壳酶联免疫吸附测定(ELISA)的液滴数字 PCR(ddPCR)、260/280nm 的总吸光度、低温电子显微镜和 SEC-MALS。该测试品用于为期 30 天的非良好实验室规范动物研究,评估产品(STRX-330)的生物分布。SEC-MALS 优于其他方法,并且与全空颗粒的 SV-AUC 值相关性良好。此外,SEC-MALS 与 ddPCR 和 ELISA 分别一致,用于测量载体基因组/mL 和衣壳颗粒/mL。SEC-MALS 呈线性、准确且精密,同时达到色谱质量控制(QC)建议。与其他稳定性指示测定相比,在加速应激研究中,SEC-MALS 与 ddPCR、衣壳 ELISA 和感染性测定的性能相似。对碱性但不对酸性应激的响应,SEC-MALS 表明 STRX-330 的单体腺相关病毒(AAV)峰的 DNA 含量发生了明显变化,ddPCR 数据对此提供了支持。相反,酸性处理导致更多的载体聚集,但不影响 DNA 含量。这项工作表明,SEC-MALS 是 AAV 分析开发和 QC 测试中的有价值的分析工具。此外,这项工作表明,SEC-MALS 可以提供对 AAV 对环境应激的基本理解。这可能会影响制造工艺的步骤,以尽量减少降低性能的条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1c5/10125404/cc2d1c7e513a/hum.2022.218_figure1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验