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Published on: April 23, 2019
Rapid inexpensive assay method for verapamil by spectrophotometric sequential injection analysis
Abubakr M Idris1, Atta E E Ibrahim, Abdalla M Abulkibash
1Department of Chemistry, College of Science, King Faisal University, Hofuf, Saudi Arabia. abubakridris@hotmail.com
A new, rapid, and eco-friendly sequential injection analysis (SIA) method using fiber optic spectrophotometry was developed for verapamil assay. This validated technique offers significant reagent savings and environmental benefits for pharmaceutical analysis.
Area of Science:
- Analytical Chemistry
- Spectrophotometry
- Pharmaceutical Analysis
Background:
- Verapamil is a crucial cardiovascular drug.
- Accurate quantification of verapamil in pharmaceutical formulations is essential for quality control.
- Existing analytical methods may have limitations in speed, cost, or environmental impact.
Purpose of the Study:
- To develop and validate a novel, rapid, and environmentally friendly analytical method for verapamil determination.
- To optimize the method using a 2(3) full-factorial design.
- To assess the method's selectivity and accuracy in pharmaceutical samples.
Main Methods:
- Sequential Injection Analysis (SIA) coupled with miniaturized fiber optic spectrophotometry.
- Spectrophotometric detection of verapamil-induced reduction of acidified permanganate at 546 nm.
- Optimization using a 2(3) full-factorial design to evaluate critical parameters.
Main Results:
- The method achieved high sample throughput (10.6 samples/h) with minimal reagent and sample consumption (190 µl).
- Demonstrated excellent environmental safety with low waste production (2140 µl).
- Showed high selectivity in the presence of common pharmaceutical excipients, with recovery rates between 98.8-103.0%.
Conclusions:
- The developed SIA method is rapid, cost-effective, and environmentally benign for verapamil assay.
- The method is selective and accurate, suitable for routine quality control of verapamil in pharmaceutical formulations.
- Results are comparable to the British Pharmacopoeia method, indicating its reliability.
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