Importance of the ionization states of m-THPC for its HPLC fluorescence detection
An original, rapid and sensitive high‐performance liquid chromatographic (HPLC) method has been developed for the detection of 5, 10, 15, 20 tetra‐meso‐hydroxyphenylchlorine (m‐THPC), a photosensitizer used in the photodynamic therapy (PDT) of cancers. Chromatographic separation was carried out on a...
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Veröffentlicht in: | Luminescence (Chichester, England) England), 2001-03, Vol.16 (2), p.173-178 |
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creator | Desroches, M.-C. Bourdon, O. Morokro, Y. Chaminade, P. Blais, J. Prognon, P. Kasselouri, A. |
description | An original, rapid and sensitive high‐performance liquid chromatographic (HPLC) method has been developed for the detection of 5, 10, 15, 20 tetra‐meso‐hydroxyphenylchlorine (m‐THPC), a photosensitizer used in the photodynamic therapy (PDT) of cancers. Chromatographic separation was carried out on a C8 Zorbax® column (80 × 4 mm, 5 µm). The mobile phase was an ethanol/aqueous sulphuric acid, pH 2.0 (65/35 v/v), in an isocratic mode yielding to rapid analysis (3.1 min) with narrow peaks. As the fluorescence intensity was found to be highly pH‐dependent and to increase with pH values, a post‐column device prior to the fluorescence detection (λexc = 423 nm, λem = 650 nm) was used to allow the addition of a 0.05 mol/L Na2HPO4 solution to the mobile phase. Compared to standard conditions, a 300% increase of the fluorescence intensity was obtained for optimized operating conditions using experimental design. The validation of this analytical method showed that the response function was linear for concentrations up to 1000 µg/L (1.47 × 10−6 mol/L) with a detection limit of 188 pg (S/N = 3). Copyright © 2001 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/bio.639 |
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Chromatographic separation was carried out on a C8 Zorbax® column (80 × 4 mm, 5 µm). The mobile phase was an ethanol/aqueous sulphuric acid, pH 2.0 (65/35 v/v), in an isocratic mode yielding to rapid analysis (3.1 min) with narrow peaks. As the fluorescence intensity was found to be highly pH‐dependent and to increase with pH values, a post‐column device prior to the fluorescence detection (λexc = 423 nm, λem = 650 nm) was used to allow the addition of a 0.05 mol/L Na2HPO4 solution to the mobile phase. Compared to standard conditions, a 300% increase of the fluorescence intensity was obtained for optimized operating conditions using experimental design. The validation of this analytical method showed that the response function was linear for concentrations up to 1000 µg/L (1.47 × 10−6 mol/L) with a detection limit of 188 pg (S/N = 3). 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Chromatographic separation was carried out on a C8 Zorbax® column (80 × 4 mm, 5 µm). The mobile phase was an ethanol/aqueous sulphuric acid, pH 2.0 (65/35 v/v), in an isocratic mode yielding to rapid analysis (3.1 min) with narrow peaks. As the fluorescence intensity was found to be highly pH‐dependent and to increase with pH values, a post‐column device prior to the fluorescence detection (λexc = 423 nm, λem = 650 nm) was used to allow the addition of a 0.05 mol/L Na2HPO4 solution to the mobile phase. Compared to standard conditions, a 300% increase of the fluorescence intensity was obtained for optimized operating conditions using experimental design. The validation of this analytical method showed that the response function was linear for concentrations up to 1000 µg/L (1.47 × 10−6 mol/L) with a detection limit of 188 pg (S/N = 3). Copyright © 2001 John Wiley & Sons, Ltd.</description><subject>Chromatography, High Pressure Liquid - methods</subject><subject>fluorescence</subject><subject>HPLC</subject><subject>Hydrogen-Ion Concentration</subject><subject>Ions</subject><subject>m-THPC</subject><subject>Mesoporphyrins - chemistry</subject><subject>PDT</subject><subject>pK A</subject><subject>post-column reaction</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Fluorescence - methods</subject><issn>1522-7235</issn><issn>1522-7243</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMlOwzAQhi0EglIQb4ByggNKsWMnTo-0LC1UbAJxtJx4LAJJXWxHLE-Pq1TlxGm2b37N_AgdEDwgGCenRWUGGR1uoB5JkyTmCaOb65ymO2jXuTeMcZZlw220QwglScpYDz1Mm4WxXs5LiIyO_CtElZlXP9KHEDkvPbjloImfJvfjSBsbVd5Fk_tZKOrWWHAlLJcVeCiXS3toS8vawf4q9tHz5cXTeBLP7q6m47NZXNKUDGPJmcxlDoQmGZG5UppTTkquMSsk1YSHPiitKJVFCVoVjKZJUbBcU8XylNM-Oup0F9Z8tOC8aKpwS13LOZjWCc4xD_-nATzuwNIa5yxosbBVI-23IFgs3RPBPRHcC-ThSrItGlB_3MquAJx0wGdVw_d_OmI0vevk4o6unIevNS3tu8jCs6l4ub0S7HqEbx4er8U5_QX35ocB</recordid><startdate>200103</startdate><enddate>200103</enddate><creator>Desroches, M.-C.</creator><creator>Bourdon, O.</creator><creator>Morokro, Y.</creator><creator>Chaminade, P.</creator><creator>Blais, J.</creator><creator>Prognon, P.</creator><creator>Kasselouri, A.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</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>200103</creationdate><title>Importance of the ionization states of m-THPC for its HPLC fluorescence detection</title><author>Desroches, M.-C. ; Bourdon, O. ; Morokro, Y. ; Chaminade, P. ; Blais, J. ; Prognon, P. ; Kasselouri, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3519-a74a8a8e13261a8ddf7371c7f04ba3f17326edfd33abcefdb4352bb48f3d48573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Chromatography, High Pressure Liquid - methods</topic><topic>fluorescence</topic><topic>HPLC</topic><topic>Hydrogen-Ion Concentration</topic><topic>Ions</topic><topic>m-THPC</topic><topic>Mesoporphyrins - chemistry</topic><topic>PDT</topic><topic>pK A</topic><topic>post-column reaction</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Fluorescence - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Desroches, M.-C.</creatorcontrib><creatorcontrib>Bourdon, O.</creatorcontrib><creatorcontrib>Morokro, Y.</creatorcontrib><creatorcontrib>Chaminade, P.</creatorcontrib><creatorcontrib>Blais, J.</creatorcontrib><creatorcontrib>Prognon, P.</creatorcontrib><creatorcontrib>Kasselouri, A.</creatorcontrib><collection>Istex</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>Luminescence (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Desroches, M.-C.</au><au>Bourdon, O.</au><au>Morokro, Y.</au><au>Chaminade, P.</au><au>Blais, J.</au><au>Prognon, P.</au><au>Kasselouri, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Importance of the ionization states of m-THPC for its HPLC fluorescence detection</atitle><jtitle>Luminescence (Chichester, England)</jtitle><addtitle>Luminescence</addtitle><date>2001-03</date><risdate>2001</risdate><volume>16</volume><issue>2</issue><spage>173</spage><epage>178</epage><pages>173-178</pages><issn>1522-7235</issn><eissn>1522-7243</eissn><abstract>An original, rapid and sensitive high‐performance liquid chromatographic (HPLC) method has been developed for the detection of 5, 10, 15, 20 tetra‐meso‐hydroxyphenylchlorine (m‐THPC), a photosensitizer used in the photodynamic therapy (PDT) of cancers. Chromatographic separation was carried out on a C8 Zorbax® column (80 × 4 mm, 5 µm). The mobile phase was an ethanol/aqueous sulphuric acid, pH 2.0 (65/35 v/v), in an isocratic mode yielding to rapid analysis (3.1 min) with narrow peaks. As the fluorescence intensity was found to be highly pH‐dependent and to increase with pH values, a post‐column device prior to the fluorescence detection (λexc = 423 nm, λem = 650 nm) was used to allow the addition of a 0.05 mol/L Na2HPO4 solution to the mobile phase. Compared to standard conditions, a 300% increase of the fluorescence intensity was obtained for optimized operating conditions using experimental design. The validation of this analytical method showed that the response function was linear for concentrations up to 1000 µg/L (1.47 × 10−6 mol/L) with a detection limit of 188 pg (S/N = 3). Copyright © 2001 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>11312544</pmid><doi>10.1002/bio.639</doi><tpages>6</tpages></addata></record> |
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subjects | Chromatography, High Pressure Liquid - methods fluorescence HPLC Hydrogen-Ion Concentration Ions m-THPC Mesoporphyrins - chemistry PDT pK A post-column reaction Reproducibility of Results Sensitivity and Specificity Spectrometry, Fluorescence - methods |
title | Importance of the ionization states of m-THPC for its HPLC fluorescence detection |
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