Cell confluency analysis on microcarriers by micro-flow imaging

被引:0
作者
Christopher J. Farrell
Stephanie M. Cicalese
Harrison B. Davis
Belma Dogdas
Tosha Shah
Tim Culp
Van M. Hoang
机构
[1] Merck & Co.,Vaccine Analytical Development
[2] Inc.,Vaccine Drug Product Development
[3] Eurofins Lancaster Laboratories Professional Scientific Services,Applied Mathematics and Modeling
[4] Merck & Co.,undefined
[5] Inc.,undefined
[6] Merck & Co.,undefined
[7] Inc.,undefined
来源
Cytotechnology | 2016年 / 68卷
关键词
Microcarriers; Micro-flow Imaging; Confluency; Mammalian cell culture;
D O I
暂无
中图分类号
学科分类号
摘要
The productivity of cell culture-derived vaccines grown in anchorage-dependent animal cells is limited by bioreactor surface area. One way to increase the available surface area is by growing cells as monolayers on small spheres called microcarriers, which are approximately 100–250 μm in diameter. In order for microcarrier-based cell culture to be a success, it is important to understand the kinetics of cell growth on the microcarriers. Micro-flow imaging (MFI) is a simple and powerful technique that captures images and analyzes samples as they are drawn through a precision flow cell. In addition to providing size distribution and defect frequency data to compare microcarrier lots, MFI was used to generate hundreds of images to determine cell coverage and confluency on microcarriers. Same-day manual classification of these images provided upstream cell culture teams with actionable data that informed in-process decision making (e.g. time of infection). Additionally, an automated cell coverage algorithm was developed to increase the speed and throughput of the analyses.
引用
收藏
页码:2469 / 2478
页数:9
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