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The Halogen Bond between Amantadine and Iodine and Its Application in the Determination of Amantadine Hydrochloride in Pharmaceuticals
It is proposed that molecular iodine as a donor could form halogen bonding complexes with amantadine (AMD) and amantadine hydrochloride (AMD-HCl) in chloroform and the resultant charge transfer bands (CT band) would be located at 259 and 253 nm, respectively. The halogen bonding interaction was expl...
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Published in: | Analytical Sciences 2014/03/10, Vol.30(3), pp.365-370 |
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description | It is proposed that molecular iodine as a donor could form halogen bonding complexes with amantadine (AMD) and amantadine hydrochloride (AMD-HCl) in chloroform and the resultant charge transfer bands (CT band) would be located at 259 and 253 nm, respectively. The halogen bonding interaction was explored by UV absorption, Raman and X-ray crystallography, and a new bonding model named N+···Nlep bond in crystal was observed. The halogen bonding complexes were utilized in the development of simple and accurate spectrophotometry for the analysis of AMD/AMD-HCl. Compared with the traditional method based on the absorption of I3− at 290 and 365 nm, the new proposed spectrometry based on the CT band of halogen bonding complex was more sensitive and selective for the detection of AMD/AMD-HCl. Linear relationships with good correlation coefficients (>0.9994) were obtained between the absorbance and the AMD/AMD-HCl concentration in the range of 10 – 180 μg mL−1 for AMD-HCl and 0.2 – 13 μg mL−1 for AMD. The limit of detection (LOD) was 2.23 μg mL−1 and limit of quantification (LOQ) was 7.45 μg mL−1 for AMD-HCl. And because of the stronger bond constant between AMD and iodine than AMD-HCl, the method is more sensitive for AMD; the LOD was 0.02 μg mL−1 and LOQ was 0.08 μg mL−1 which was 100 times lower than that of AMD-HCl. |
doi_str_mv | 10.2116/analsci.30.365 |
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The halogen bonding interaction was explored by UV absorption, Raman and X-ray crystallography, and a new bonding model named N+···Nlep bond in crystal was observed. The halogen bonding complexes were utilized in the development of simple and accurate spectrophotometry for the analysis of AMD/AMD-HCl. Compared with the traditional method based on the absorption of I3− at 290 and 365 nm, the new proposed spectrometry based on the CT band of halogen bonding complex was more sensitive and selective for the detection of AMD/AMD-HCl. Linear relationships with good correlation coefficients (>0.9994) were obtained between the absorbance and the AMD/AMD-HCl concentration in the range of 10 – 180 μg mL−1 for AMD-HCl and 0.2 – 13 μg mL−1 for AMD. The limit of detection (LOD) was 2.23 μg mL−1 and limit of quantification (LOQ) was 7.45 μg mL−1 for AMD-HCl. And because of the stronger bond constant between AMD and iodine than AMD-HCl, the method is more sensitive for AMD; the LOD was 0.02 μg mL−1 and LOQ was 0.08 μg mL−1 which was 100 times lower than that of AMD-HCl.</description><identifier>ISSN: 0910-6340</identifier><identifier>EISSN: 1348-2246</identifier><identifier>DOI: 10.2116/analsci.30.365</identifier><identifier>PMID: 24614731</identifier><language>eng</language><publisher>Singapore: The Japan Society for Analytical Chemistry</publisher><subject>amantadine ; Amantadine - chemistry ; amantadine hydrochloride ; Analytical Chemistry ; charge transfer ; Chemistry ; Halogen bond ; iodine ; Iodine - chemistry ; N+···Nlep bond ; Pharmaceutical Preparations - analysis ; primary amine cation</subject><ispartof>Analytical Sciences, 2014/03/10, Vol.30(3), pp.365-370</ispartof><rights>2014 by The Japan Society for Analytical Chemistry</rights><rights>The Japan Society for Analytical Chemistry 2014</rights><rights>Copyright Japan Science and Technology Agency 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c679t-3bb2ee013865934c84a037e16b0edbe7a8baede977e7128bd0ba2d7d58070a343</citedby><cites>FETCH-LOGICAL-c679t-3bb2ee013865934c84a037e16b0edbe7a8baede977e7128bd0ba2d7d58070a343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1882,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24614731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YAN, Xiao Qing</creatorcontrib><creatorcontrib>WANG, Hui</creatorcontrib><creatorcontrib>CHEN, Wei Di</creatorcontrib><creatorcontrib>JIN, Wei Jun</creatorcontrib><title>The Halogen Bond between Amantadine and Iodine and Its Application in the Determination of Amantadine Hydrochloride in Pharmaceuticals</title><title>Analytical Sciences</title><addtitle>ANAL. SCI</addtitle><addtitle>Anal Sci</addtitle><description>It is proposed that molecular iodine as a donor could form halogen bonding complexes with amantadine (AMD) and amantadine hydrochloride (AMD-HCl) in chloroform and the resultant charge transfer bands (CT band) would be located at 259 and 253 nm, respectively. The halogen bonding interaction was explored by UV absorption, Raman and X-ray crystallography, and a new bonding model named N+···Nlep bond in crystal was observed. The halogen bonding complexes were utilized in the development of simple and accurate spectrophotometry for the analysis of AMD/AMD-HCl. Compared with the traditional method based on the absorption of I3− at 290 and 365 nm, the new proposed spectrometry based on the CT band of halogen bonding complex was more sensitive and selective for the detection of AMD/AMD-HCl. Linear relationships with good correlation coefficients (>0.9994) were obtained between the absorbance and the AMD/AMD-HCl concentration in the range of 10 – 180 μg mL−1 for AMD-HCl and 0.2 – 13 μg mL−1 for AMD. The limit of detection (LOD) was 2.23 μg mL−1 and limit of quantification (LOQ) was 7.45 μg mL−1 for AMD-HCl. And because of the stronger bond constant between AMD and iodine than AMD-HCl, the method is more sensitive for AMD; the LOD was 0.02 μg mL−1 and LOQ was 0.08 μg mL−1 which was 100 times lower than that of AMD-HCl.</description><subject>amantadine</subject><subject>Amantadine - chemistry</subject><subject>amantadine hydrochloride</subject><subject>Analytical Chemistry</subject><subject>charge transfer</subject><subject>Chemistry</subject><subject>Halogen bond</subject><subject>iodine</subject><subject>Iodine - chemistry</subject><subject>N+···Nlep bond</subject><subject>Pharmaceutical Preparations - analysis</subject><subject>primary amine cation</subject><issn>0910-6340</issn><issn>1348-2246</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kU-P0zAQxS0EYsvClSOKxIVLuv6TxMmxLAtdaSU4LGdrYk9bV4ldbEdovwCfe12llAWJk-2Z33sjzyPkLaNLzlhzBQ6GqO1S0KVo6mdkwUTVlpxXzXOyoB2jZSMqekFexbinlPGW85fkIrdZJQVbkF_3OyzWMPgtuuKjd6boMf3E_FiN4BIY67CAXL71f64pFqvDYbAakvWusK5I2eUTJgyjdXPRb546rB9M8Ho3-GANHgXfdhBG0Dil7DLE1-TFJh_45nReku-fb-6v1-Xd1y-316u7UjeyS6Xoe45ImWibuhOVbiugQiJreoqmRwltD2iwkxJl_mtvaA_cSFO3VFIQlbgkH2bfQ_A_JoxJjTZqHAZw6KeoWE3zoIZ3NKPv_0H3fgrHdWeKcVnXkh8NlzOlg48x4EYdgh0hPChG1TEhdUpICapyQlnw7mQ79SOaM_47kgxczUDMLbfF8GTu_yxXs2IfE2zxbAkhL3fAv_CT5tzTOQeFTjwCrXC2tA</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>YAN, Xiao Qing</creator><creator>WANG, Hui</creator><creator>CHEN, Wei Di</creator><creator>JIN, Wei Jun</creator><general>The Japan Society for Analytical Chemistry</general><general>Springer Nature Singapore</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>L7M</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2014</creationdate><title>The Halogen Bond between Amantadine and Iodine and Its Application in the Determination of Amantadine Hydrochloride in Pharmaceuticals</title><author>YAN, Xiao Qing ; WANG, Hui ; CHEN, Wei Di ; JIN, Wei Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c679t-3bb2ee013865934c84a037e16b0edbe7a8baede977e7128bd0ba2d7d58070a343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>amantadine</topic><topic>Amantadine - chemistry</topic><topic>amantadine hydrochloride</topic><topic>Analytical Chemistry</topic><topic>charge transfer</topic><topic>Chemistry</topic><topic>Halogen bond</topic><topic>iodine</topic><topic>Iodine - chemistry</topic><topic>N+···Nlep bond</topic><topic>Pharmaceutical Preparations - analysis</topic><topic>primary amine cation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YAN, Xiao Qing</creatorcontrib><creatorcontrib>WANG, Hui</creatorcontrib><creatorcontrib>CHEN, Wei Di</creatorcontrib><creatorcontrib>JIN, Wei Jun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YAN, Xiao Qing</au><au>WANG, Hui</au><au>CHEN, Wei Di</au><au>JIN, Wei Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Halogen Bond between Amantadine and Iodine and Its Application in the Determination of Amantadine Hydrochloride in Pharmaceuticals</atitle><jtitle>Analytical Sciences</jtitle><stitle>ANAL. SCI</stitle><addtitle>Anal Sci</addtitle><date>2014</date><risdate>2014</risdate><volume>30</volume><issue>3</issue><spage>365</spage><epage>370</epage><pages>365-370</pages><issn>0910-6340</issn><eissn>1348-2246</eissn><abstract>It is proposed that molecular iodine as a donor could form halogen bonding complexes with amantadine (AMD) and amantadine hydrochloride (AMD-HCl) in chloroform and the resultant charge transfer bands (CT band) would be located at 259 and 253 nm, respectively. The halogen bonding interaction was explored by UV absorption, Raman and X-ray crystallography, and a new bonding model named N+···Nlep bond in crystal was observed. The halogen bonding complexes were utilized in the development of simple and accurate spectrophotometry for the analysis of AMD/AMD-HCl. Compared with the traditional method based on the absorption of I3− at 290 and 365 nm, the new proposed spectrometry based on the CT band of halogen bonding complex was more sensitive and selective for the detection of AMD/AMD-HCl. Linear relationships with good correlation coefficients (>0.9994) were obtained between the absorbance and the AMD/AMD-HCl concentration in the range of 10 – 180 μg mL−1 for AMD-HCl and 0.2 – 13 μg mL−1 for AMD. The limit of detection (LOD) was 2.23 μg mL−1 and limit of quantification (LOQ) was 7.45 μg mL−1 for AMD-HCl. And because of the stronger bond constant between AMD and iodine than AMD-HCl, the method is more sensitive for AMD; the LOD was 0.02 μg mL−1 and LOQ was 0.08 μg mL−1 which was 100 times lower than that of AMD-HCl.</abstract><cop>Singapore</cop><pub>The Japan Society for Analytical Chemistry</pub><pmid>24614731</pmid><doi>10.2116/analsci.30.365</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | amantadine Amantadine - chemistry amantadine hydrochloride Analytical Chemistry charge transfer Chemistry Halogen bond iodine Iodine - chemistry N+···Nlep bond Pharmaceutical Preparations - analysis primary amine cation |
title | The Halogen Bond between Amantadine and Iodine and Its Application in the Determination of Amantadine Hydrochloride in Pharmaceuticals |
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