Sensitive assay for carvedilol in tablets and spiked human plasma using a flow-injection chemiluminometric method
A simple and sensitive chemiluminometric method using flow injection (FI) is developed for the determination of carvedilol, based on the reaction of carvedilol with tris (2, 2'-bipyridyl) ruthenium (II), and KMnO4 in sulfuric acid medium. Under the optimum conditions; the chemiluminescence (CL)...
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Veröffentlicht in: | International journal of biomedical science 2007-06, Vol.3 (2), p.131-136 |
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description | A simple and sensitive chemiluminometric method using flow injection (FI) is developed for the determination of carvedilol, based on the reaction of carvedilol with tris (2, 2'-bipyridyl) ruthenium (II), and KMnO4 in sulfuric acid medium. Under the optimum conditions; the chemiluminescence (CL) intensity is a linear function of carvedilol concentration over the range of 0.04-1.0 µg ml(-1) (9.8 × 10(-8) - 2.5 × 10(-6) mol L(-1)) with a detection limit (S/N=3) of 0.025 µgml(-1) (6.2 × 10(-8) mol L(-1)). The relative standard deviation of the proposed method calculated from 10 replicate injections of 0.4 µg ml(-1) carvedilol is 0.95%. The sample throughput is 90 samples h(-1). The method is applied successfully to the determination of carvedilol in tablets dosage form and spiked human plasma. |
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Under the optimum conditions; the chemiluminescence (CL) intensity is a linear function of carvedilol concentration over the range of 0.04-1.0 µg ml(-1) (9.8 × 10(-8) - 2.5 × 10(-6) mol L(-1)) with a detection limit (S/N=3) of 0.025 µgml(-1) (6.2 × 10(-8) mol L(-1)). The relative standard deviation of the proposed method calculated from 10 replicate injections of 0.4 µg ml(-1) carvedilol is 0.95%. The sample throughput is 90 samples h(-1). The method is applied successfully to the determination of carvedilol in tablets dosage form and spiked human plasma.</description><identifier>ISSN: 1550-9702</identifier><identifier>EISSN: 1555-2810</identifier><identifier>PMID: 23675035</identifier><language>eng</language><publisher>United States: Master Publishing Group</publisher><ispartof>International journal of biomedical science, 2007-06, Vol.3 (2), p.131-136</ispartof><rights>Nawal Al Arfaj Licensee Master Publishing Group 2007 Nawal Al Arfaj</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614627/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614627/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23675035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arfaj, Nawal Al</creatorcontrib><creatorcontrib>Abdine, Heba H</creatorcontrib><creatorcontrib>Sultan, Maha A</creatorcontrib><title>Sensitive assay for carvedilol in tablets and spiked human plasma using a flow-injection chemiluminometric method</title><title>International journal of biomedical science</title><addtitle>Int J Biomed Sci</addtitle><description>A simple and sensitive chemiluminometric method using flow injection (FI) is developed for the determination of carvedilol, based on the reaction of carvedilol with tris (2, 2'-bipyridyl) ruthenium (II), and KMnO4 in sulfuric acid medium. Under the optimum conditions; the chemiluminescence (CL) intensity is a linear function of carvedilol concentration over the range of 0.04-1.0 µg ml(-1) (9.8 × 10(-8) - 2.5 × 10(-6) mol L(-1)) with a detection limit (S/N=3) of 0.025 µgml(-1) (6.2 × 10(-8) mol L(-1)). The relative standard deviation of the proposed method calculated from 10 replicate injections of 0.4 µg ml(-1) carvedilol is 0.95%. The sample throughput is 90 samples h(-1). 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Under the optimum conditions; the chemiluminescence (CL) intensity is a linear function of carvedilol concentration over the range of 0.04-1.0 µg ml(-1) (9.8 × 10(-8) - 2.5 × 10(-6) mol L(-1)) with a detection limit (S/N=3) of 0.025 µgml(-1) (6.2 × 10(-8) mol L(-1)). The relative standard deviation of the proposed method calculated from 10 replicate injections of 0.4 µg ml(-1) carvedilol is 0.95%. The sample throughput is 90 samples h(-1). The method is applied successfully to the determination of carvedilol in tablets dosage form and spiked human plasma.</abstract><cop>United States</cop><pub>Master Publishing Group</pub><pmid>23675035</pmid><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | Sensitive assay for carvedilol in tablets and spiked human plasma using a flow-injection chemiluminometric method |
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