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UV-SPECTROPHOTOMETRIC STABILITY INDICATING METHODS FOR THE QUANTITATIVE DETERMINATION OF CIMETIDINE, FAMOTIDINE, AND RANITIDINE HYDROCHLORIDE IN THE PRESENCE OF THEIR OXIDATIVE DERIVATIVES
Simple, sensitive and rapid spectrophotometric techniques have been established for the determination of cimetidine (I), famotidine (II) and ranitidine hydrochloride (III) in presence of their S-oxide derivatives in both raw materials and in pharmaceutical formulations. Hydrogen peroxide was used to...
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Published in: | Analytical letters 2002-06, Vol.35 (6), p.1055-1073 |
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container_start_page | 1055 |
container_title | Analytical letters |
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creator | Kelani, Khadiga M. Aziz, Azza M. Hegazy, Maha A. Abdel Fattah, Laila |
description | Simple, sensitive and rapid spectrophotometric techniques have been established for the determination of cimetidine (I), famotidine (II) and ranitidine hydrochloride (III) in presence of their S-oxide derivatives in both raw materials and in pharmaceutical formulations. Hydrogen peroxide was used to enhance the formation of S-oxide compounds (oxidative derivatives). The first derivative of the ratio spectra (
1
DD) technique has been applied for the determination of (I) and (II). While, direct zero order (
0
D), first derivative (
1
D) and the second derivative of the ratio spectra (
2
DD) have been carried out for the determination of drug (III). Linear calibration curves were obtained for determination of (I) and (II) by applying
1
DD at 220 and 230 nm in the concentration range of 2-20 and 4-40 µg mL
−1
with the mean percentage recoveries of 99.88 ± 0.943 (n = 10) and 99.88 ± 0.824% (n = 10) for (I) and (II), respectively. While for (III) linear calibration curves were obtained by applying
0
D,
1
D and
2
DD at 313, 334 and 255 nm, respectively. The concentration range was 2-20 µg mL
−1
with the corresponding mean percentage recoveries of 100.13 ± 0.464, 100.01 ± 0.428 and 99.94 ± 0.439 for (I), (II) and (III), respectively. The results obtained by the proposed methods were statistically analyzed and compared with those obtained by the official BP methods. |
doi_str_mv | 10.1081/AL-120004555 |
format | article |
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1
DD) technique has been applied for the determination of (I) and (II). While, direct zero order (
0
D), first derivative (
1
D) and the second derivative of the ratio spectra (
2
DD) have been carried out for the determination of drug (III). Linear calibration curves were obtained for determination of (I) and (II) by applying
1
DD at 220 and 230 nm in the concentration range of 2-20 and 4-40 µg mL
−1
with the mean percentage recoveries of 99.88 ± 0.943 (n = 10) and 99.88 ± 0.824% (n = 10) for (I) and (II), respectively. While for (III) linear calibration curves were obtained by applying
0
D,
1
D and
2
DD at 313, 334 and 255 nm, respectively. The concentration range was 2-20 µg mL
−1
with the corresponding mean percentage recoveries of 100.13 ± 0.464, 100.01 ± 0.428 and 99.94 ± 0.439 for (I), (II) and (III), respectively. The results obtained by the proposed methods were statistically analyzed and compared with those obtained by the official BP methods.</description><identifier>ISSN: 0003-2719</identifier><identifier>EISSN: 1532-236X</identifier><identifier>DOI: 10.1081/AL-120004555</identifier><identifier>CODEN: ANALBP</identifier><language>eng</language><publisher>Philadelphia, PA: Taylor & Francis Group</publisher><subject>Analysis ; Biological and medical sciences ; Cimetidine ; Famotidine ; General pharmacology ; Medical sciences ; Pharmacology. Drug treatments ; Ranitidine hydrochloride ; Stability indicating method; Derivative of the ratio spectra ; UV-Spectrophotometry</subject><ispartof>Analytical letters, 2002-06, Vol.35 (6), p.1055-1073</ispartof><rights>Copyright Taylor & Francis Group, LLC 2002</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-e3e308708c29aca4f6979939fde42af78c47a4c4180b3994bb49ac4b39c2aa223</citedby><cites>FETCH-LOGICAL-c311t-e3e308708c29aca4f6979939fde42af78c47a4c4180b3994bb49ac4b39c2aa223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13760015$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelani, Khadiga M.</creatorcontrib><creatorcontrib>Aziz, Azza M.</creatorcontrib><creatorcontrib>Hegazy, Maha A.</creatorcontrib><creatorcontrib>Abdel Fattah, Laila</creatorcontrib><title>UV-SPECTROPHOTOMETRIC STABILITY INDICATING METHODS FOR THE QUANTITATIVE DETERMINATION OF CIMETIDINE, FAMOTIDINE, AND RANITIDINE HYDROCHLORIDE IN THE PRESENCE OF THEIR OXIDATIVE DERIVATIVES</title><title>Analytical letters</title><description>Simple, sensitive and rapid spectrophotometric techniques have been established for the determination of cimetidine (I), famotidine (II) and ranitidine hydrochloride (III) in presence of their S-oxide derivatives in both raw materials and in pharmaceutical formulations. Hydrogen peroxide was used to enhance the formation of S-oxide compounds (oxidative derivatives). The first derivative of the ratio spectra (
1
DD) technique has been applied for the determination of (I) and (II). While, direct zero order (
0
D), first derivative (
1
D) and the second derivative of the ratio spectra (
2
DD) have been carried out for the determination of drug (III). Linear calibration curves were obtained for determination of (I) and (II) by applying
1
DD at 220 and 230 nm in the concentration range of 2-20 and 4-40 µg mL
−1
with the mean percentage recoveries of 99.88 ± 0.943 (n = 10) and 99.88 ± 0.824% (n = 10) for (I) and (II), respectively. While for (III) linear calibration curves were obtained by applying
0
D,
1
D and
2
DD at 313, 334 and 255 nm, respectively. The concentration range was 2-20 µg mL
−1
with the corresponding mean percentage recoveries of 100.13 ± 0.464, 100.01 ± 0.428 and 99.94 ± 0.439 for (I), (II) and (III), respectively. The results obtained by the proposed methods were statistically analyzed and compared with those obtained by the official BP methods.</description><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Cimetidine</subject><subject>Famotidine</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Ranitidine hydrochloride</subject><subject>Stability indicating method; Derivative of the ratio spectra</subject><subject>UV-Spectrophotometry</subject><issn>0003-2719</issn><issn>1532-236X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNptUMlOwzAUtBBIlOXGB_jCjYC3NskxJG5jKbWL41ZwilyTSEVdUFIJ9d_4OFxK4cLJM-_Nm7EGgBuM7jGK8ENSBJgghFi_3z8BPdynJCB08HwKen5KAxLi-BxcdN0bQphEBPfA53QWlBOeGq0muTJqzI0WKSxN8igKYV6gkJlIEyPkCPpdrrISDpWGJufwaZpII4xfzjjMuOF6LKRnSkI1hKnwepEJye_gMBmrI05kBnUixYHD_CXTKs0LpUXGfdq380TzksuU7308FxqqZ5Edg7SYfcPyCpw1dtnV1z_vJZgOuUnzoFAj_-kicBTjbVDTmqIoRJEjsXWWNYM4jGMaN681I7YJI8dCyxzDEZrTOGbzOfM65rEj1hJCL8Hdwde1m65r66Z6bxcr2-4qjKp981VSVL_Ne_ntQf5uO2eXTWvXbtH93dBw4Pvf68KDbrFuNu3Kfmza5Wu1tbvlpj0e0X8TvgBCAodk</recordid><startdate>20020627</startdate><enddate>20020627</enddate><creator>Kelani, Khadiga M.</creator><creator>Aziz, Azza M.</creator><creator>Hegazy, Maha A.</creator><creator>Abdel Fattah, Laila</creator><general>Taylor & Francis Group</general><general>Taylor & Francis</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20020627</creationdate><title>UV-SPECTROPHOTOMETRIC STABILITY INDICATING METHODS FOR THE QUANTITATIVE DETERMINATION OF CIMETIDINE, FAMOTIDINE, AND RANITIDINE HYDROCHLORIDE IN THE PRESENCE OF THEIR OXIDATIVE DERIVATIVES</title><author>Kelani, Khadiga M. ; Aziz, Azza M. ; Hegazy, Maha A. ; Abdel Fattah, Laila</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-e3e308708c29aca4f6979939fde42af78c47a4c4180b3994bb49ac4b39c2aa223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Cimetidine</topic><topic>Famotidine</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Ranitidine hydrochloride</topic><topic>Stability indicating method; Derivative of the ratio spectra</topic><topic>UV-Spectrophotometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelani, Khadiga M.</creatorcontrib><creatorcontrib>Aziz, Azza M.</creatorcontrib><creatorcontrib>Hegazy, Maha A.</creatorcontrib><creatorcontrib>Abdel Fattah, Laila</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Analytical letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelani, Khadiga M.</au><au>Aziz, Azza M.</au><au>Hegazy, Maha A.</au><au>Abdel Fattah, Laila</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>UV-SPECTROPHOTOMETRIC STABILITY INDICATING METHODS FOR THE QUANTITATIVE DETERMINATION OF CIMETIDINE, FAMOTIDINE, AND RANITIDINE HYDROCHLORIDE IN THE PRESENCE OF THEIR OXIDATIVE DERIVATIVES</atitle><jtitle>Analytical letters</jtitle><date>2002-06-27</date><risdate>2002</risdate><volume>35</volume><issue>6</issue><spage>1055</spage><epage>1073</epage><pages>1055-1073</pages><issn>0003-2719</issn><eissn>1532-236X</eissn><coden>ANALBP</coden><abstract>Simple, sensitive and rapid spectrophotometric techniques have been established for the determination of cimetidine (I), famotidine (II) and ranitidine hydrochloride (III) in presence of their S-oxide derivatives in both raw materials and in pharmaceutical formulations. Hydrogen peroxide was used to enhance the formation of S-oxide compounds (oxidative derivatives). The first derivative of the ratio spectra (
1
DD) technique has been applied for the determination of (I) and (II). While, direct zero order (
0
D), first derivative (
1
D) and the second derivative of the ratio spectra (
2
DD) have been carried out for the determination of drug (III). Linear calibration curves were obtained for determination of (I) and (II) by applying
1
DD at 220 and 230 nm in the concentration range of 2-20 and 4-40 µg mL
−1
with the mean percentage recoveries of 99.88 ± 0.943 (n = 10) and 99.88 ± 0.824% (n = 10) for (I) and (II), respectively. While for (III) linear calibration curves were obtained by applying
0
D,
1
D and
2
DD at 313, 334 and 255 nm, respectively. The concentration range was 2-20 µg mL
−1
with the corresponding mean percentage recoveries of 100.13 ± 0.464, 100.01 ± 0.428 and 99.94 ± 0.439 for (I), (II) and (III), respectively. The results obtained by the proposed methods were statistically analyzed and compared with those obtained by the official BP methods.</abstract><cop>Philadelphia, PA</cop><pub>Taylor & Francis Group</pub><doi>10.1081/AL-120004555</doi><tpages>19</tpages></addata></record> |
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source | Taylor and Francis Science and Technology Collection |
subjects | Analysis Biological and medical sciences Cimetidine Famotidine General pharmacology Medical sciences Pharmacology. Drug treatments Ranitidine hydrochloride Stability indicating method Derivative of the ratio spectra UV-Spectrophotometry |
title | UV-SPECTROPHOTOMETRIC STABILITY INDICATING METHODS FOR THE QUANTITATIVE DETERMINATION OF CIMETIDINE, FAMOTIDINE, AND RANITIDINE HYDROCHLORIDE IN THE PRESENCE OF THEIR OXIDATIVE DERIVATIVES |
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