Abstract
An acetonitrile-salt stacking method was established for the assay of lipoic acid (LA) in biological samples. Samples were deproteinized with acetonitrile at a final concentration of 60 % (v/v) and then injected hydrodynamically at 3.45 × 103 Pa for 180.0 s. The optimum background electrolyte was found to be 90.0 mmol L-1 pH 9.1 borate buffer. LA could be detected within 35 min at +7.0 kV with satisfactory repeatability (relative standard deviations, RSDs, of migration times and peak areas were both below 10 % for intraday and interday; n = 6/9) and a relatively low limit of detection of ca. 0.5 μmol L-1.
| Original language | English |
|---|---|
| Pages (from-to) | 145-150 |
| Number of pages | 6 |
| Journal | Chromatographia |
| Volume | 77 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - Jan 2014 |
Keywords
- Acetonitrile stacking
- Biological samples
- Capillary electrophoresis
- Lipoic acid