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J Chromatogr A ; 1262: 122-9, 2012 Nov 02.
Article in English | MEDLINE | ID: mdl-22999205

ABSTRACT

A methodology based on on-line coupling of size exclusion chromatography (SEC) with mixed-mode liquid chromatography (LC) has been developed. The method allows for simultaneous measurement of a wide range of components in biopharmaceutical drug products. These components include the active pharmaceutical ingredient (protein) and various kinds of excipients such as cations, anions, nonionic hydrophobic surfactant and hydrophilic sugars. Dual short SEC columns are used to separate small molecule excipients from large protein molecules. The separated protein is quantified using a UV detector at 280 nm. The isolated excipients are switched, online, to the Trinity P1 mixed-mode column for separation, and detected by an evaporative light scattering detector (ELSD). Using a stationary phase with 1.7 µm particles in SEC allows for the use of volatile buffers for both SEC and mix-mode separation. This facilitates the detection of different excipients by ELSD and provides potential for online characterization of the protein with mass spectrometry (MS). The method has been applied to quantitate protein and excipients in different biopharmaceutical drug products including monoclonal antibodies (mAb), antibody drug conjugates (ADC) and vaccines.


Subject(s)
Antibodies, Monoclonal/analysis , Chromatography, Gel/methods , Chromatography, High Pressure Liquid/methods , Pharmaceutical Preparations/analysis , Acetonitriles/chemistry , Antibodies, Monoclonal/chemistry , Antibodies, Monoclonal/isolation & purification , Excipients/analysis , Excipients/chemistry , Excipients/isolation & purification , Hydrogen-Ion Concentration , Linear Models , Mass Spectrometry , Pharmaceutical Preparations/chemistry , Pharmaceutical Preparations/isolation & purification , Reproducibility of Results , Sensitivity and Specificity , Spectrophotometry, Ultraviolet , Vaccines/analysis , Vaccines/chemistry , Vaccines/isolation & purification
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