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Indirect determination of captopril by AAS
M A El Reis1, F M Abou Attia, I M Kenawy
1National Organization for Drug Control and Research, Cairo, Egypt.
Journal of Pharmaceutical and Biomedical Analysis
|August 10, 2000
Summary
A new indirect method accurately determines captopril (KPL) in pharmaceuticals using atomic absorption spectrometry (AAS). This technique relies on KPL complexation with palladium (Pd(II)) and ion-exchange separation for precise quantification.
Area of Science:
- Analytical Chemistry
- Spectroscopy
- Pharmaceutical Analysis
Background:
- Captopril (KPL) is a widely used pharmaceutical agent.
- Accurate quantification of KPL in pharmaceutical preparations is crucial for quality control.
- Existing analytical methods may have limitations in sensitivity or specificity.
Purpose of the Study:
- To develop and validate a novel indirect method for captopril determination.
- To utilize atomic absorption spectrometry (AAS) for sensitive and accurate KPL quantification.
- To establish a reliable analytical procedure for pharmaceutical preparations containing captopril.
Main Methods:
- Indirect determination of captopril (KPL) via complexation with excess palladium (Pd(II)).
- Separation of unreacted Pd(II) using a cationic ion-exchange resin.
- Quantification of retained Pd(II)-KPL complex in the effluent by AAS.
- Characterization of the solid Pd(II)-KPL complex using elemental analysis, TG, conductance, IR, and 1H-NMR spectroscopy.
Main Results:
- A linear relationship was observed between absorbance and KPL concentration (correlation coefficient 0.9939).
- The method demonstrated adherence to Beer's law in the range of 1-40 microg/ml.
- The standard deviation was found to be 0.039 (n=5), indicating good precision.
- The Pd(II)-KPL complex was successfully synthesized and characterized.
Conclusions:
- The developed indirect AAS method provides a sensitive and accurate approach for captopril determination in pharmaceutical formulations.
- The ion-exchange separation step enhances the specificity and reliability of the assay.
- The method's validation through correlation coefficient and standard deviation supports its utility in pharmaceutical quality control.