TY - JOUR
T1 - 3D-liquid chromatography as a complex mixture characterization tool for knowledge-based downstream process development.
AU - Hanke, A.T.
AU - Tsintavi, E.
AU - Del Pilar Ramirez Vazquez, M.
AU - van der Wielen, L.A.M.
AU - Verhaert, P.D.E.M.
AU - van de Sandt, E.J.A.X.
AU - Eppink, M.H.M.
AU - Ottens, M.
PY - 2016
Y1 - 2016
N2 - Knowledge-based development of chromatographic separation processes requires efficient techniques to determine the physicochemical properties of the product and the impurities to be removed. These characterization techniques are usually divided into approaches that determine molecular properties, such as charge, hydrophobicity and size, or molecular interactions with auxiliary materials, commonly in the form of adsorption isotherms. In this study we demonstrate the application of a three-dimensional liquid chromatography approach to a clarified cell homogenate containing a therapeutic enzyme. Each separation dimension determines a molecular property relevant to the chromatographic behaviour of each component. Matching of the peaks across the different separation dimensions and against a high-resolution reference chromatogram allows to assign the determined parameters to pseudo-components, allowing to determine the most promising technique for the removal of each impurity. More detailed process design using mechanistic models requires isotherm parameters. For this purpose, the second dimension consists of multiple linear gradient separations on columns in a high-throughput screening compatible format, that allow regression of isotherm parameters with an average standard error of 8%.
AB - Knowledge-based development of chromatographic separation processes requires efficient techniques to determine the physicochemical properties of the product and the impurities to be removed. These characterization techniques are usually divided into approaches that determine molecular properties, such as charge, hydrophobicity and size, or molecular interactions with auxiliary materials, commonly in the form of adsorption isotherms. In this study we demonstrate the application of a three-dimensional liquid chromatography approach to a clarified cell homogenate containing a therapeutic enzyme. Each separation dimension determines a molecular property relevant to the chromatographic behaviour of each component. Matching of the peaks across the different separation dimensions and against a high-resolution reference chromatogram allows to assign the determined parameters to pseudo-components, allowing to determine the most promising technique for the removal of each impurity. More detailed process design using mechanistic models requires isotherm parameters. For this purpose, the second dimension consists of multiple linear gradient separations on columns in a high-throughput screening compatible format, that allow regression of isotherm parameters with an average standard error of 8%.
KW - feedstock characterization
KW - host cell proteins
KW - multi-dimensional chromatography
KW - process development
U2 - 10.1002/btpr.2320
DO - 10.1002/btpr.2320
M3 - Article
SN - 1520-6033
VL - 32
SP - 1283
EP - 1291
JO - Biotechnology Progress
JF - Biotechnology Progress
IS - 5
ER -