Abstract
An antibody-based solid-phase extraction method for filtered 384-well
plates was developed for a medical drug candidate having two
enantiomeric forms in order to demonstrate the potential of the use of
recombinant antibody fragments as specific and efficient immunosorbents.
An immobilization method using a six-histidine tag of the antibody
fragment and mild oxidation was applied in order to immobilize antibody
fragments in an oriented and kinetically stable way that ensured high
capacity of the antibody support. Phosphate buffer or plasma spiked with
enantiomers were used as samples. Selective solid-phase extraction was
followed by liquid chromatography−mass spectrometry analysis. Average
recoveries for buffer and plasma samples ranged from 79 to 122% and 80
to 108%, respectively. Good linearity was observed in the concentration
range of 30−3000 ng/mL of the enantiomer.
Original language | English |
---|---|
Pages (from-to) | 3038 - 3044 |
Number of pages | 7 |
Journal | Analytical Chemistry |
Volume | 77 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2005 |
MoE publication type | A1 Journal article-refereed |
Keywords
- antibodies
- antibody fragments
- solid-phase extraction
- drug candidates
- pharmaceutical compounds