LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation
The objective of the present investigation was to separate, identify and characterize the degradation products of hydrochlorothiazide under hydrolytic, oxidative, photolytic and thermal stress conditions as per the International Conference on Harmonization (ICH) guideline Q1A (R2). The drug degraded...
Gespeichert in:
Veröffentlicht in: | Journal of the Brazilian Chemical Society 2012-03, Vol.23 (3), p.445-452 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 452 |
---|---|
container_issue | 3 |
container_start_page | 445 |
container_title | Journal of the Brazilian Chemical Society |
container_volume | 23 |
creator | Mahajan, Anand Avinash Thaker, Anil Keshavlal Mohanraj, Krishnapriya |
description | The objective of the present investigation was to separate, identify and characterize the degradation products of hydrochlorothiazide under hydrolytic, oxidative, photolytic and thermal stress conditions as per the International Conference on Harmonization (ICH) guideline Q1A (R2). The drug degraded under acidic, basic, neutral and oxidative stress, while it was stable under photolytic and thermal stress conditions. Two degradation products were formed, which were separated by using HPLC on C18 column using isocratic elution program. A complete mass fragmentation pathway of the drug was first established with the help of LC-MS/MS studies. The stressed samples were subjected to LC-MS studies. The obtained mass spectral data were employed to characterize the degradation products and assign structures. The degradation products were identified as 4-amino-6-chloro-1,3-benzenedisulfonamide and 6-chloro-2-oxy-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide. |
doi_str_mv | 10.1590/S0103-50532012000300010 |
format | Article |
fullrecord | <record><control><sourceid>scielo_cross</sourceid><recordid>TN_cdi_scielo_journals_S0103_50532012000300010</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><scielo_id>S0103_50532012000300010</scielo_id><sourcerecordid>S0103_50532012000300010</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-5a9e3facc1305a1432e808fab95695290bf487a6e8f89a84b990eadb22d4204a3</originalsourceid><addsrcrecordid>eNp1kdtOwzAMhnMBEmPwDOQB6OY2zdZeoomT1ImLwXXl5kAzdc2UZELbO_GOZCtCSIgLy_Jv_58lm5CbFCYpL2G6ghRYwoGzDNIMAFiMFM7I6KdxQS69XwNkPA6NyGe1uKXVIlmupssV9WEnjfJUW0dDq6iRqg9GG4HB2J5iL6lo0aEIypnDIFpNpXp3KIdy66zcieCPeruXzoq2s86G1uAh4k4M5QM2nfHtJuKPgxsVsb3xwQiK24hA0dJgP9BJ_5t-Rc41dl5df-cxeXu4f108JdXL4_PirkoEy3lIOJaKaRQiZcAxzVmmCig0NiWflTwrodF5MceZKnRRYpE3ZQkKZZNlMs8gRzYmk4HrhVGdrdd25_q4sD4duP5z4GiYDwbhrPdO6XrrzAbdvk6hPr7mX-cXHiKFZQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>Mahajan, Anand Avinash ; Thaker, Anil Keshavlal ; Mohanraj, Krishnapriya</creator><creatorcontrib>Mahajan, Anand Avinash ; Thaker, Anil Keshavlal ; Mohanraj, Krishnapriya</creatorcontrib><description>The objective of the present investigation was to separate, identify and characterize the degradation products of hydrochlorothiazide under hydrolytic, oxidative, photolytic and thermal stress conditions as per the International Conference on Harmonization (ICH) guideline Q1A (R2). The drug degraded under acidic, basic, neutral and oxidative stress, while it was stable under photolytic and thermal stress conditions. Two degradation products were formed, which were separated by using HPLC on C18 column using isocratic elution program. A complete mass fragmentation pathway of the drug was first established with the help of LC-MS/MS studies. The stressed samples were subjected to LC-MS studies. The obtained mass spectral data were employed to characterize the degradation products and assign structures. The degradation products were identified as 4-amino-6-chloro-1,3-benzenedisulfonamide and 6-chloro-2-oxy-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide.</description><identifier>ISSN: 0103-5053</identifier><identifier>ISSN: 1678-4790</identifier><identifier>DOI: 10.1590/S0103-50532012000300010</identifier><language>eng</language><publisher>Sociedade Brasileira de Química</publisher><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><ispartof>Journal of the Brazilian Chemical Society, 2012-03, Vol.23 (3), p.445-452</ispartof><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-5a9e3facc1305a1432e808fab95695290bf487a6e8f89a84b990eadb22d4204a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids></links><search><creatorcontrib>Mahajan, Anand Avinash</creatorcontrib><creatorcontrib>Thaker, Anil Keshavlal</creatorcontrib><creatorcontrib>Mohanraj, Krishnapriya</creatorcontrib><title>LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation</title><title>Journal of the Brazilian Chemical Society</title><addtitle>J. Braz. Chem. Soc</addtitle><description>The objective of the present investigation was to separate, identify and characterize the degradation products of hydrochlorothiazide under hydrolytic, oxidative, photolytic and thermal stress conditions as per the International Conference on Harmonization (ICH) guideline Q1A (R2). The drug degraded under acidic, basic, neutral and oxidative stress, while it was stable under photolytic and thermal stress conditions. Two degradation products were formed, which were separated by using HPLC on C18 column using isocratic elution program. A complete mass fragmentation pathway of the drug was first established with the help of LC-MS/MS studies. The stressed samples were subjected to LC-MS studies. The obtained mass spectral data were employed to characterize the degradation products and assign structures. The degradation products were identified as 4-amino-6-chloro-1,3-benzenedisulfonamide and 6-chloro-2-oxy-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide.</description><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><issn>0103-5053</issn><issn>1678-4790</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kdtOwzAMhnMBEmPwDOQB6OY2zdZeoomT1ImLwXXl5kAzdc2UZELbO_GOZCtCSIgLy_Jv_58lm5CbFCYpL2G6ghRYwoGzDNIMAFiMFM7I6KdxQS69XwNkPA6NyGe1uKXVIlmupssV9WEnjfJUW0dDq6iRqg9GG4HB2J5iL6lo0aEIypnDIFpNpXp3KIdy66zcieCPeruXzoq2s86G1uAh4k4M5QM2nfHtJuKPgxsVsb3xwQiK24hA0dJgP9BJ_5t-Rc41dl5df-cxeXu4f108JdXL4_PirkoEy3lIOJaKaRQiZcAxzVmmCig0NiWflTwrodF5MceZKnRRYpE3ZQkKZZNlMs8gRzYmk4HrhVGdrdd25_q4sD4duP5z4GiYDwbhrPdO6XrrzAbdvk6hPr7mX-cXHiKFZQ</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Mahajan, Anand Avinash</creator><creator>Thaker, Anil Keshavlal</creator><creator>Mohanraj, Krishnapriya</creator><general>Sociedade Brasileira de Química</general><scope>AAYXX</scope><scope>CITATION</scope><scope>GPN</scope></search><sort><creationdate>20120301</creationdate><title>LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation</title><author>Mahajan, Anand Avinash ; Thaker, Anil Keshavlal ; Mohanraj, Krishnapriya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-5a9e3facc1305a1432e808fab95695290bf487a6e8f89a84b990eadb22d4204a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>CHEMISTRY, MULTIDISCIPLINARY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahajan, Anand Avinash</creatorcontrib><creatorcontrib>Thaker, Anil Keshavlal</creatorcontrib><creatorcontrib>Mohanraj, Krishnapriya</creatorcontrib><collection>CrossRef</collection><collection>SciELO</collection><jtitle>Journal of the Brazilian Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahajan, Anand Avinash</au><au>Thaker, Anil Keshavlal</au><au>Mohanraj, Krishnapriya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation</atitle><jtitle>Journal of the Brazilian Chemical Society</jtitle><addtitle>J. Braz. Chem. Soc</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>23</volume><issue>3</issue><spage>445</spage><epage>452</epage><pages>445-452</pages><issn>0103-5053</issn><issn>1678-4790</issn><abstract>The objective of the present investigation was to separate, identify and characterize the degradation products of hydrochlorothiazide under hydrolytic, oxidative, photolytic and thermal stress conditions as per the International Conference on Harmonization (ICH) guideline Q1A (R2). The drug degraded under acidic, basic, neutral and oxidative stress, while it was stable under photolytic and thermal stress conditions. Two degradation products were formed, which were separated by using HPLC on C18 column using isocratic elution program. A complete mass fragmentation pathway of the drug was first established with the help of LC-MS/MS studies. The stressed samples were subjected to LC-MS studies. The obtained mass spectral data were employed to characterize the degradation products and assign structures. The degradation products were identified as 4-amino-6-chloro-1,3-benzenedisulfonamide and 6-chloro-2-oxy-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide.</abstract><pub>Sociedade Brasileira de Química</pub><doi>10.1590/S0103-50532012000300010</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0103-5053 |
ispartof | Journal of the Brazilian Chemical Society, 2012-03, Vol.23 (3), p.445-452 |
issn | 0103-5053 1678-4790 |
language | eng |
recordid | cdi_scielo_journals_S0103_50532012000300010 |
source | EZB-FREE-00999 freely available EZB journals |
subjects | CHEMISTRY, MULTIDISCIPLINARY |
title | LC, LC-MS/MS studies for the identification and characterization of degradation products of hydrochlorothiazide and establishment of mechanistic approach towards degradation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T22%3A06%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-scielo_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=LC,%20LC-MS/MS%20studies%20for%20the%20identification%20and%20characterization%20of%20degradation%20products%20of%20hydrochlorothiazide%20and%20establishment%20of%20mechanistic%20approach%20towards%20degradation&rft.jtitle=Journal%20of%20the%20Brazilian%20Chemical%20Society&rft.au=Mahajan,%20Anand%20Avinash&rft.date=2012-03-01&rft.volume=23&rft.issue=3&rft.spage=445&rft.epage=452&rft.pages=445-452&rft.issn=0103-5053&rft_id=info:doi/10.1590/S0103-50532012000300010&rft_dat=%3Cscielo_cross%3ES0103_50532012000300010%3C/scielo_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_scielo_id=S0103_50532012000300010&rfr_iscdi=true |