Abstract
The performance of an existing enzyme immunoassay (EIA) with monoclonal antibodies (mAb) for the determination of terbutryn was improved by the application of a new enzyme tracer. For this purpose the triazine derivative 6‐chloro‐2‐(tert‐butylamino)‐1,3,5‐triazine‐4‐(6‐aminohexane carboxylic acid) was coupled to horseradish peroxidase (HRP). The competitive EIA on microwell plates made it possible to determine terbutryn in the range from 0.05 to 1 μg/L with a 50% B/B0 value of the test at 0.2 μg/L. The application of the EIA to determine terbutryn in spiked surface waters provided good recoveries of terbutryn without matrix effects.
| Original language | English |
|---|---|
| Pages (from-to) | 312-315 |
| Number of pages | 4 |
| Journal | Acta Hydrochimica et Hydrobiologica |
| Volume | 21 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1993 |
Keywords
- ELISA
- Enzyme Tracer
- Monoclonal Antibodies
- s‐Triazine
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