Abstract
A quick overview of published methods for analyzing compounds in complex biological samples reveals that the most difficult step is the clean-up or extraction of a required compound from the matrix. The strategy required to analyze exogenous compounds in biological fluids depends greatly upon the nature of the compound and upon the biomatrix. Coupled-column separation using restricted-access media as the first dimension in order to exclude macromolecules and retain micromolecules has been successfully used for a number of biological fluids. This paper presents the history of the development of restricted-access media supports and of their application to the direct injection of biological fluid samples in high-performance liquid chromatography.
Abbreviations
- ADS:
-
alkyl-diol-silica phase
- BSA:
-
Bovine Albumin Serum
- HAS:
-
Human Serum Albumin
- ISPBA:
-
internal surface phenylboronic acid
- ISRP:
-
internal surface reversed phase
- MFP:
-
mixed function phase
- SHP:
-
shielded hydrophobic phase
- SPS:
-
semipermeable surface
- XDS:
-
exchange diol silica
- CMC:
-
chiral multidimensional chromatography
- MC:
-
multidimensional chromatography
- SC:
-
single-column
- AD:
-
amperometric detector
- DAD:
-
diode-array detector
- FD:
-
fluorescence detection
- MS:
-
mass spectrometry detection
- UV:
-
ultraviolet detection
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Cassiano, N.M., Lima, V.V., Oliveira, R.V. et al. Development of restricted-access media supports and their application to the direct analysis of biological fluid samples via high-performance liquid chromatography. Anal Bioanal Chem 384, 1462–1469 (2006). https://doi.org/10.1007/s00216-005-0253-9
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DOI: https://doi.org/10.1007/s00216-005-0253-9