𝔖 Bobbio Scriptorium
✦   LIBER   ✦

On-line monitoring of monoclonal antibody formation in high density perfusion culture using FIA

✍ Scribed by Christel Fenge; Elisabeth Fraune; Ruth Freitag; Thomas Scheper; Karl Schügerl


Publisher
Springer
Year
1991
Tongue
English
Weight
615 KB
Volume
6
Category
Article
ISSN
0920-9069

No coin nor oath required. For personal study only.

✦ Synopsis


An automated flow injection system for on-line analysis of proteins in real fermentation fluids was developed by combining the principles of stopped-flow, merging zones flow injection analysis (FIA) with antigen-antibody reactions. IgG in the sample reacted with its corresponding antibody (a-IgG) in the reagent solution. Formation of insoluble immunocomplexes resulted in an increase of the turbidity which was determined photometrically. This system was used to monitor monoclonal antibody production in high cell density perfusion culture of hybridoma cells. Perfusion was performed with a newly developed static filtration unit equipped with hydrophilic microporous tubular membranes. Different sampling devices were tested to obtain a cell-free sample stream for on-line product analysis of high molecular weight (e.g., monoclonal antibodies) and low molecular weight (e.g., glucose, lactate) medium components. In fermentation fluids a good correlation (coefficient: 0.996) between the FIA method and an ELISA test was demonstrated. In a high density perfusion cultivation process mAb formation was successfully monitored on-line over a period of 400 h using a reliable sampling system. Glucose and lactate were measured over the same period of time using a commercially available automatic analyser based on immobilized enzyme technology.


📜 SIMILAR VOLUMES


On-line monitoring of glucose in mammali
✍ Keith B. Male; P. Octavian Gartu; A. Amine Kamen; John H. T. Luong 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 200 KB 👁 2 views

A flow injection analysis (FIA) biosensor system has been developed for on-line determination of glucose during mammalian cell cultivation. The culture sample was peristaltically withdrawn from the bioreactor and after cell separation by a steam sterilizable ceramic microfilter, the filtrate was con