Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Rapid Identification of Pathogens01:25

Rapid Identification of Pathogens

MALDI-TOF MS has transformed clinical microbiology by offering a rapid and reliable method for pathogen identification. The traditional approach to microbial identification typically involves time-consuming culture techniques and biochemical tests, which can delay the initiation of appropriate antimicrobial therapy. MALDI-TOF MS avoids these delays by using characteristic ribosomal protein mass patterns of microbial cells, enabling accurate species-level identification within minutes.Principle...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Oncolytic virus-delivered GSDME: Unlocking pyroptosis to improve dendritic cell function and amplify cytotoxic T cell response.

Molecular therapy. Oncology·2026
Same author

Mechanistic deconvolution of BSA size variants by constrained Raman pseudo-Voigt hard modeling during anion-exchange chromatography.

Biotechnology progress·2026
Same author

Reply to comments on "Comprehensive stress study on recombinant adeno-associated virus vectors: Evaluating the capabilities of established analytical techniques".

Journal of pharmaceutical sciences·2026
Same author

An ex vivo permissivity assay to assess replication of the oncolytic virus VSV-GP in patient-derived tumor samples.

Oncogene·2026
Same author

Optimizing single molecule, real-time sequencing for enhanced characterization of adeno-associated viral vector genomes.

Molecular therapy. Advances·2026
Same author

Proof of concept for aqueous two-phase system-based extraction of cell-free DNA from plasma for liquid biopsy applications.

Scientific reports·2026

相关实验视频

Updated: Jul 4, 2026

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses
11:29

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses

Published on: December 3, 2011

12.2K

一种基于HPLC-SEC的囊性口腔炎病毒颗粒快速定量方法,以促进过程开发.

Adrian Schimek1, Judy K M Ng1, Ioannes Basbas1

  • 1ViraTherapeutics GmbH, Bundesstraße 27, 6063 Rum, Austria.

Molecular therapy. Methods & clinical development
|May 22, 2024
PubMed
概括

一种新的无标签方法使用尺寸排除色谱 (SEC) 和HPLC准确量化包裹病毒颗粒 (VPs). 这种高效的技术对于开发基于病毒的疗法和确保过程的一致性至关重要.

关键词:
在HPLC中使用HPLC.在VSV-GP中使用VSV.分析性的SEC证券交易所.膀性口腔炎病毒的病毒病毒颗粒量化定量化

更多相关视频

High-throughput Titration of Luciferase-expressing Recombinant Viruses
08:09

High-throughput Titration of Luciferase-expressing Recombinant Viruses

Published on: September 19, 2014

12.9K
Development and Validation of a Quantitative PCR Method for Equid Herpesvirus-2 Diagnostics in Respiratory Fluids
09:57

Development and Validation of a Quantitative PCR Method for Equid Herpesvirus-2 Diagnostics in Respiratory Fluids

Published on: March 17, 2016

28.3K

相关实验视频

Last Updated: Jul 4, 2026

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses
11:29

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses

Published on: December 3, 2011

12.2K
High-throughput Titration of Luciferase-expressing Recombinant Viruses
08:09

High-throughput Titration of Luciferase-expressing Recombinant Viruses

Published on: September 19, 2014

12.9K
Development and Validation of a Quantitative PCR Method for Equid Herpesvirus-2 Diagnostics in Respiratory Fluids
09:57

Development and Validation of a Quantitative PCR Method for Equid Herpesvirus-2 Diagnostics in Respiratory Fluids

Published on: March 17, 2016

28.3K

科学领域:

  • 生物技术是生物技术.
  • 分析化学 分析化学
  • 过程开发 过程开发

背景情况:

  • 准确的病毒粒子 (VP) 量化对于生产用于治疗应用的VP至关重要.
  • 目前的方法可能缺乏效率或需要标签,阻碍了过程开发.

研究的目的:

  • 开发和描述一种无标签的方法来量化包装VPs.
  • 为VP生产建立可靠的工艺性能指标.

主要方法:

  • 使用尺寸排除染色学 (SEC) 与高性能液态染色学 (HPLC) 相结合.
  • 采用紫外线 (UV) 检测用于量化和多角度光散射 (MALS) 进行表征.
  • 优化了移动阶段,并使用牛血清白蛋白 (BSA) 来稳定样本,实现>97%的回收.

主要成果:

  • 证明了高精度,<1%的可重复性和<3%的中间精度变化.
  • 建立了一个广泛的线性范围 (7.08 × 10^8至1.72 × 10^11 VP/mL),LOD为7.72 × 10^7 VP/mL,LLOQ为4.20 × 10^8 VP/mL.
  • 已验证的适用于加工中的样品.

结论:

  • 开发的SEC-HPLC方法为VP量化提供了一个精确,高效和无标签的方法.
  • 该方法支持基于病毒的疗法的过程开发,包括瘤性病毒疗法,疫苗开发和基因疗法.
  • 测试的速度和最小的实践时间使同一天的结果更容易用于过程监测.