ABSTRACT
Endotoxin removal using detergent washes and extractions are well-established, efficient, and cost-effective methods; however, removing residual detergent post treatment has been shown to be a challenge. In this communication, we show a simple and fast method for determining the detergent concentration in a protein solution post treatment and highlight strategies for detergent removal to achieve levels below the critical micelle concentration (CMC), the minimum concentration at which detergent micelles form.
Subject(s)
Detergents/analysis , Endotoxins/chemistry , Endotoxins/isolation & purification , Octoxynol/analysis , Recombinant Proteins/chemistry , Recombinant Proteins/isolation & purification , Animals , CHO Cells , Cricetulus , Detergents/isolation & purification , Methods , Micelles , Octoxynol/isolation & purification , SolutionsABSTRACT
The removal of bacterial endotoxins from biological samples is critical to avoid the potentially fatal pyrogenic response possible when introduced to mammalian systems. Endotoxins have a variety of specific characteristics that can be exploited to target their isolation and subsequent removal, but one that has not been extensively characterized is their difference in size from that of monoclonal antibodies. Here, we present a study which utilizes gel filtration chromatography as a method for endotoxin removal from both aggregated and nonaggregated antibody preparations, outlining a mechanistically simple method for removal of this impurity.
Subject(s)
Antibodies, Monoclonal/chemistry , Chromatography, Gel/methods , Endotoxins/isolation & purification , Animals , Antibodies, Monoclonal/isolation & purification , CHO Cells , Cricetinae , Cricetulus , MicellesABSTRACT
The expanding use of monoclonal antibodies in the biopharmaceuticals industry has brought the need for new analytical tools. We have developed a coupled affinity and gel-filtration high-performance liquid chromatography method to simultaneously analyze titer and quality of monoclonal antibodies. Before this assay, available analytical methods for protein aggregation required highly purified proteins. This assay can qualitatively describe a protein from a clarified cell culture solution by trending protein aggregation over time while measuring protein titer. It can be used to assess proteins in both early- and late-stage culture due to its dynamic range and sensitivity. This assay is a sensitive technique that overcomes the time limitations of previous approaches. It provides an essential tool to accomplish process optimization.
