Determination of Paclitaxel and Related Taxanes in Bulk Drug and Injectable Dosage Forms by Reversed Phase Liquid Chromatography
Baseline separation of 15 taxanes including paclitaxel (Taxol) was achieved on pentafluorophenyl (PFP) HPLC columns. Methods using aqueous acetonitrile gradients on each of two commercial PFP columns were developed that are suitable for the determination of potency, content uniformity, and degradati...
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Veröffentlicht in: | Analytical chemistry (Washington) 1997-06, Vol.69 (11), p.2008-2016 |
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creator | Shao, Lillian Kuangjing Locke, David C |
description | Baseline separation of 15 taxanes including paclitaxel (Taxol) was achieved on pentafluorophenyl (PFP) HPLC columns. Methods using aqueous acetonitrile gradients on each of two commercial PFP columns were developed that are suitable for the determination of potency, content uniformity, and degradation profile of the paclitaxel bulk drug and injectable dosage form. The elution order is apparently related to molecular size, the number of acetylated hydroxyl groups, and the substitution of a xylosyl group at the 7-position. The resolution of several of the taxanes is a sensitive function of the starting eluent composition and the programming rate, which requires optimization of the methods on both columns. Retention of 10 of the taxanes was studied over the temperature range from 30 to 70 °C, and enthalpies of transfer, ΔH°, were determined. Conversion of a hydroxy group to an acetyl group, which can interact more strongly with the fluorines on the PFP, has a large effect on the ΔH°, as does the addition of a xylosyl derivative to the 7-hydroxy. The methods developed for the injectable drug form allow good resolution of the taxanes from the excipient Cremophor EL, a polyethoxylated castor oil used with ethanol to solubilize the paclitaxel. The methods for the bulk drug were fully validated in terms of accuracy, precision, specificity including forced degradation, limits of detection and quantitation, and linearity and range. |
doi_str_mv | 10.1021/ac961312g |
format | Article |
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Methods using aqueous acetonitrile gradients on each of two commercial PFP columns were developed that are suitable for the determination of potency, content uniformity, and degradation profile of the paclitaxel bulk drug and injectable dosage form. The elution order is apparently related to molecular size, the number of acetylated hydroxyl groups, and the substitution of a xylosyl group at the 7-position. The resolution of several of the taxanes is a sensitive function of the starting eluent composition and the programming rate, which requires optimization of the methods on both columns. Retention of 10 of the taxanes was studied over the temperature range from 30 to 70 °C, and enthalpies of transfer, ΔH°, were determined. Conversion of a hydroxy group to an acetyl group, which can interact more strongly with the fluorines on the PFP, has a large effect on the ΔH°, as does the addition of a xylosyl derivative to the 7-hydroxy. The methods developed for the injectable drug form allow good resolution of the taxanes from the excipient Cremophor EL, a polyethoxylated castor oil used with ethanol to solubilize the paclitaxel. The methods for the bulk drug were fully validated in terms of accuracy, precision, specificity including forced degradation, limits of detection and quantitation, and linearity and range.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac961312g</identifier><identifier>PMID: 9183174</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Analysis ; Antineoplastic Agents, Phytogenic - analysis ; Antineoplastic Agents, Phytogenic - metabolism ; Biological and medical sciences ; Bridged-Ring Compounds - analysis ; Bridged-Ring Compounds - chemistry ; Bridged-Ring Compounds - isolation & purification ; Bridged-Ring Compounds - metabolism ; Chromatography, High Pressure Liquid ; Dosage Forms ; Fluorobenzenes - chemistry ; General pharmacology ; Medical sciences ; Paclitaxel - analogs & derivatives ; Paclitaxel - analysis ; Paclitaxel - metabolism ; Pharmacology. Drug treatments ; Phenols - chemistry ; Reference Standards ; Reproducibility of Results ; Taxoids ; Thermodynamics</subject><ispartof>Analytical chemistry (Washington), 1997-06, Vol.69 (11), p.2008-2016</ispartof><rights>Copyright © 1997 American Chemical Society</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a443t-436c6e83675b17d0470d433032fdacfceae94c643c09631275b0ca182fcaa61c3</citedby><cites>FETCH-LOGICAL-a443t-436c6e83675b17d0470d433032fdacfceae94c643c09631275b0ca182fcaa61c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ac961312g$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ac961312g$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2685960$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9183174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shao, Lillian Kuangjing</creatorcontrib><creatorcontrib>Locke, David C</creatorcontrib><title>Determination of Paclitaxel and Related Taxanes in Bulk Drug and Injectable Dosage Forms by Reversed Phase Liquid Chromatography</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>Baseline separation of 15 taxanes including paclitaxel (Taxol) was achieved on pentafluorophenyl (PFP) HPLC columns. Methods using aqueous acetonitrile gradients on each of two commercial PFP columns were developed that are suitable for the determination of potency, content uniformity, and degradation profile of the paclitaxel bulk drug and injectable dosage form. The elution order is apparently related to molecular size, the number of acetylated hydroxyl groups, and the substitution of a xylosyl group at the 7-position. The resolution of several of the taxanes is a sensitive function of the starting eluent composition and the programming rate, which requires optimization of the methods on both columns. Retention of 10 of the taxanes was studied over the temperature range from 30 to 70 °C, and enthalpies of transfer, ΔH°, were determined. Conversion of a hydroxy group to an acetyl group, which can interact more strongly with the fluorines on the PFP, has a large effect on the ΔH°, as does the addition of a xylosyl derivative to the 7-hydroxy. The methods developed for the injectable drug form allow good resolution of the taxanes from the excipient Cremophor EL, a polyethoxylated castor oil used with ethanol to solubilize the paclitaxel. The methods for the bulk drug were fully validated in terms of accuracy, precision, specificity including forced degradation, limits of detection and quantitation, and linearity and range.</description><subject>Analysis</subject><subject>Antineoplastic Agents, Phytogenic - analysis</subject><subject>Antineoplastic Agents, Phytogenic - metabolism</subject><subject>Biological and medical sciences</subject><subject>Bridged-Ring Compounds - analysis</subject><subject>Bridged-Ring Compounds - chemistry</subject><subject>Bridged-Ring Compounds - isolation & purification</subject><subject>Bridged-Ring Compounds - metabolism</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Dosage Forms</subject><subject>Fluorobenzenes - chemistry</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Paclitaxel - analogs & derivatives</subject><subject>Paclitaxel - analysis</subject><subject>Paclitaxel - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenols - chemistry</subject><subject>Reference Standards</subject><subject>Reproducibility of Results</subject><subject>Taxoids</subject><subject>Thermodynamics</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E2P0zAQBmALgZbuwoEfgOQDIHEI-CNxkuPSbmGlSlRLOVtTZ9K6m8Rd20HtjZ-OoVVPnHx4nxmNX0LecPaJM8E_g6kVl1xsnpEJLwTLVFWJ52TCGJOZKBl7Sa5D2DHGOePqilzVvJK8zCfk9wwj-t4OEK0bqGvpEkxnIxywozA09AE7iNjQFRxgwEDtQL-M3SOd-XHzD9wPOzQR1h3SmQuwQTp3vg90fUyzv9CHNLzcQkC6sE-jbeh0610P0W087LfHV-RFC13A1-f3hvyc362m37LF96_309tFBnkuY5ZLZRRWUpXFmpcNy0vW5FIyKdoGTGsQsM6NyqVhtUpNJMYM8Eq0BkBxI2_Ih9PevXdPI4aoexsMdl36lRuDLmuWCymqBD-eoPEuBI-t3nvbgz9qzvTftvWl7WTfnpeO6x6bizzXm_J35xyCga71MBgbLkyoqqgVSyw7MRsiHi4x-EetSlkWerX8oVfzQkhePGie_PuTBxP0zo1-SM3957w_SneiCA</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>Shao, Lillian Kuangjing</creator><creator>Locke, David C</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19970601</creationdate><title>Determination of Paclitaxel and Related Taxanes in Bulk Drug and Injectable Dosage Forms by Reversed Phase Liquid Chromatography</title><author>Shao, Lillian Kuangjing ; Locke, David C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a443t-436c6e83675b17d0470d433032fdacfceae94c643c09631275b0ca182fcaa61c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Analysis</topic><topic>Antineoplastic Agents, Phytogenic - analysis</topic><topic>Antineoplastic Agents, Phytogenic - metabolism</topic><topic>Biological and medical sciences</topic><topic>Bridged-Ring Compounds - analysis</topic><topic>Bridged-Ring Compounds - chemistry</topic><topic>Bridged-Ring Compounds - isolation & purification</topic><topic>Bridged-Ring Compounds - metabolism</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Dosage Forms</topic><topic>Fluorobenzenes - chemistry</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Paclitaxel - analogs & derivatives</topic><topic>Paclitaxel - analysis</topic><topic>Paclitaxel - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenols - chemistry</topic><topic>Reference Standards</topic><topic>Reproducibility of Results</topic><topic>Taxoids</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shao, Lillian Kuangjing</creatorcontrib><creatorcontrib>Locke, David C</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shao, Lillian Kuangjing</au><au>Locke, David C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of Paclitaxel and Related Taxanes in Bulk Drug and Injectable Dosage Forms by Reversed Phase Liquid Chromatography</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>69</volume><issue>11</issue><spage>2008</spage><epage>2016</epage><pages>2008-2016</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>Baseline separation of 15 taxanes including paclitaxel (Taxol) was achieved on pentafluorophenyl (PFP) HPLC columns. Methods using aqueous acetonitrile gradients on each of two commercial PFP columns were developed that are suitable for the determination of potency, content uniformity, and degradation profile of the paclitaxel bulk drug and injectable dosage form. The elution order is apparently related to molecular size, the number of acetylated hydroxyl groups, and the substitution of a xylosyl group at the 7-position. The resolution of several of the taxanes is a sensitive function of the starting eluent composition and the programming rate, which requires optimization of the methods on both columns. Retention of 10 of the taxanes was studied over the temperature range from 30 to 70 °C, and enthalpies of transfer, ΔH°, were determined. Conversion of a hydroxy group to an acetyl group, which can interact more strongly with the fluorines on the PFP, has a large effect on the ΔH°, as does the addition of a xylosyl derivative to the 7-hydroxy. The methods developed for the injectable drug form allow good resolution of the taxanes from the excipient Cremophor EL, a polyethoxylated castor oil used with ethanol to solubilize the paclitaxel. The methods for the bulk drug were fully validated in terms of accuracy, precision, specificity including forced degradation, limits of detection and quantitation, and linearity and range.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>9183174</pmid><doi>10.1021/ac961312g</doi><tpages>9</tpages></addata></record> |
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subjects | Analysis Antineoplastic Agents, Phytogenic - analysis Antineoplastic Agents, Phytogenic - metabolism Biological and medical sciences Bridged-Ring Compounds - analysis Bridged-Ring Compounds - chemistry Bridged-Ring Compounds - isolation & purification Bridged-Ring Compounds - metabolism Chromatography, High Pressure Liquid Dosage Forms Fluorobenzenes - chemistry General pharmacology Medical sciences Paclitaxel - analogs & derivatives Paclitaxel - analysis Paclitaxel - metabolism Pharmacology. Drug treatments Phenols - chemistry Reference Standards Reproducibility of Results Taxoids Thermodynamics |
title | Determination of Paclitaxel and Related Taxanes in Bulk Drug and Injectable Dosage Forms by Reversed Phase Liquid Chromatography |
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