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Development of solid-phase chemiluminescence immunoassays for digoxin comparing flow injection and sequential
D Dreveny1, J Michalowski, R Seidl
1Institute of Pharmaceutical Chemistry, Karl Franzens University, Graz, Austria.
The Analyst
|July 9, 1999
Summary
A new competitive solid-phase immunoassay for digoxin utilizes acridinium chemiluminescence. The sequential injection technique offers improved precision and faster assay times compared to flow injection analysis.
Area of Science:
- Analytical Chemistry
- Biochemistry
- Clinical Diagnostics
Background:
- Digoxin is a critical medication for heart conditions, requiring precise therapeutic drug monitoring.
- Existing immunoassays for digoxin may face limitations in speed, precision, or automation.
- Acridinium chemiluminescence offers high sensitivity for biomarker detection.
Purpose of the Study:
- To develop and compare two instrumental approaches for a competitive solid-phase immunoassay for digoxin.
- To evaluate the performance of a sequential injection technique against a flow injection analysis system.
- To optimize the assay for speed, precision, and sensitivity.
Main Methods:
- Development of a solid-phase immunoassay using immobilized antibodies in a flow cell.
- Comparison of a continuous flow injection analysis system with a novel sequential injection technique.
- Utilizing an acridinium chemiluminescence detection system for signal generation.
Main Results:
- The sequential injection technique demonstrated higher precision (2.16–5.5% RSD) compared to flow injection analysis.
- Total assay time, including regeneration, was under 8 minutes using the sequential injection method.
- Both techniques achieved a low femtomole detection limit for digoxin.
Conclusions:
- The sequential injection technique provides a precise, rapid, and sensitive method for digoxin quantification.
- This immunoassay system is suitable for high-throughput clinical diagnostics.
- The acridinium chemiluminescence system enhances the sensitivity of digoxin detection.