A chemiluminescence reagent free method for the determination of captopril in medicine and urine samples by using trivalent silver
A novel flow-injection chemiluminescence (FI-CL) method free of CL reagent was developed for the determination of captopril based on its enhancing effect on the CL derived from diperiodatoargentate(III)-sulfuric acid system. Compared with the conventional CL system,the CL system based on trivalent s...
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Published in: | Journal of pharmaceutical analysis Vol. 7; no. 4; pp. 252 - 257 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
China
Elsevier B.V
01-08-2017
Xi'an Jiaotong University, Journal of Pharmaceutical Analysis School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China Xi'an Jiaotong University Elsevier |
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Online Access: | Get full text |
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Summary: | A novel flow-injection chemiluminescence (FI-CL) method free of CL reagent was developed for the determination of captopril based on its enhancing effect on the CL derived from diperiodatoargentate(III)-sulfuric acid system. Compared with the conventional CL system,the CL system based on trivalent silver was characterized of good selectivity for the absence of CL reagent. The CL mechanism was discussed through CL spectra and UV–vis absorption spectra. The conditions of the FI-CL system were investigated and optimized.Under the optimal conditions, the relative CL intensity was linear with the captopril concentration in the range of 0.3–15.0 μg/mL. The detection limit for captopril was 0.05μg/mL, and the relative standard deviation(n=11) was 2.0% for 5.0 μg/mL captopril. The proposed method was applied to the analysis of captopril in tablet and human urine with the recoveries of 83.1%–112.5%, and the relative standard deviations of 0.5%–4.4%. The results obtained by the proposed method agreed well with those obtained from HPLC method. The proposed method is fast, convenient, and cost-effective for the determination of captopril in medicine and biological samples. |
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Bibliography: | 61-1484/R ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Zhaofu Fu and Wanting Huang contributed equally to this work. |
ISSN: | 2095-1779 2214-0883 |
DOI: | 10.1016/j.jpha.2017.05.005 |