{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T17:26:06Z","timestamp":1790702766974,"version":"4.1.0"},"reference-count":39,"publisher":"Wiley","issue":"18","license":[{"start":{"date-parts":[[2013,8,12]],"date-time":"2013-08-12T00:00:00Z","timestamp":1376265600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Separation Science"],"published-print":{"date-parts":[[2013,9]]},"abstract":"<jats:p>The enantioselectivity of proton pump inhibitors, namely, omeprazole, lansoprazole, rabeprazole, pantoprazole, tenatoprazole, and ilaprazole were studied using new generation chiral packing materials: <jats:styled-content style=\"fixed-case\">CHIRALPAK IA<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">CHIRALPAK IB<\/jats:styled-content>, and <jats:styled-content style=\"fixed-case\">CHIRALPAK IC<\/jats:styled-content>. Two versatile techniques, <jats:styled-content style=\"fixed-case\">HPLC<\/jats:styled-content> and supercritical fluid chromatography (<jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content>) were used in this study. <jats:styled-content style=\"fixed-case\">CHIRALPAK IC<\/jats:styled-content> has shown superior selectivity under both <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content> conditions, whereas <jats:styled-content style=\"fixed-case\">CHIRALPAK IA<\/jats:styled-content> has shown good selectivity in <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content> when compared to <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content> under primary screening conditions. The chiral recognition ability in <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content> modes were found to be in the order <jats:styled-content style=\"fixed-case\">CHIRALPAK IC<\/jats:styled-content> &gt; <jats:styled-content style=\"fixed-case\">CHIRALPAK IA<\/jats:styled-content> &gt; <jats:styled-content style=\"fixed-case\">CHIRALPAK IB<\/jats:styled-content>. In addition to diode array detection, chiral detection was carried out using a laser polarimeter and the elution orders were found to be the same in both <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content> elution modes. Mobile phase modifiers and column temperature effects were also studied. In <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content>, modifiers (cosolvent) elution strength was found to be in the order ethanol &gt; methanol &gt; 2\u2010propanol &gt; acetonitrile. In both <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SFC<\/jats:styled-content>, a decrease in retention and increase in resolution with an increase in temperature was noticed for all the proton pump inhibitors.<\/jats:p>","DOI":"10.1002\/jssc.201300419","type":"journal-article","created":{"date-parts":[[2013,7,16]],"date-time":"2013-07-16T05:10:51Z","timestamp":1373951451000},"page":"3004-3010","source":"Crossref","is-referenced-by-count":23,"title":["Enantiomeric separation of proton pump inhibitors on new generation chiral columns using <scp>LC<\/scp> and supercritical fluid chromatography"],"prefix":"10.1002","volume":"36","author":[{"given":"Lakshmi Narayana","family":"Chennuru","sequence":"first","affiliation":[{"name":"Daicel Chiral Technologies (India) Pvt. 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