An HPLC assay utilizing solid-phase extraction for CI-1010, an alkylating radiosensitizer, in rat plasma

CI-1010, a 2-nitroimidazole, is a chiral prodrug for the active moiety PD 146923 and is under development as an alkylating radiosensitizer to be used as an adjuvant to radiotherapy. Because CI-1010 has an estimated half-life ≤ 2 min under physiological conditions its metabolites/degradation products...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 1997-09, Vol.16 (1), p.47-55
Hauptverfasser: Bullen, William W., Rossi, David T., Hoffman, Keith L., Suri, Ajit, Lathia, Chetan D.
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container_end_page 55
container_issue 1
container_start_page 47
container_title Journal of pharmaceutical and biomedical analysis
container_volume 16
creator Bullen, William W.
Rossi, David T.
Hoffman, Keith L.
Suri, Ajit
Lathia, Chetan D.
description CI-1010, a 2-nitroimidazole, is a chiral prodrug for the active moiety PD 146923 and is under development as an alkylating radiosensitizer to be used as an adjuvant to radiotherapy. Because CI-1010 has an estimated half-life ≤ 2 min under physiological conditions its metabolites/degradation products PD 146415, an inactive moiety, and PD 146923 were assayed to support rat toxicology studies. The method involves the processing of plasma samples through phenyl solid-phase extraction cartridges followed by chromatography on CN columns with UV detection at 325 nm. The assay appears linear over the range 0.050–100 μg ml −1 for both PD 146415 and PD 146923. Interrun accuracy and precision estimates for PD 146415 and PD 146923 were within ± 6.50 and ≤ 3.27%, respectively, and ± 12.8 and ≤ 4.06%, respectively, for quality controls containing nominal concentrations of 0.400, 4.00 and 40.0 μg ml −1. The absolute recovery of CI-1010, PD 146415 and internal standard, PD 126675, were approximately 40, 96 and 95%, respectively. The recovery of PD 146923 appeared concentration dependent and ranged from 68 to 92%. PD 146145 and PD 146923 were both stable in rat plasma at 4°C and − 77°C for at least 7 h and 154 days, respectively. CI-1010 was not stable in rat plasma at 4°C. CI-1010, PD 146145 and PD 126675 were stable for at least 63 days in 10 mM phosphate buffer at pH 3.0 and 4°C. Under identical conditions PD 146923 was stable for only 8 days. The applicability of this method to determine concentrations of PD 146145 and PD 146923 in rat plasma is reported in this paper.
doi_str_mv 10.1016/S0731-7085(97)00013-7
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Because CI-1010 has an estimated half-life ≤ 2 min under physiological conditions its metabolites/degradation products PD 146415, an inactive moiety, and PD 146923 were assayed to support rat toxicology studies. The method involves the processing of plasma samples through phenyl solid-phase extraction cartridges followed by chromatography on CN columns with UV detection at 325 nm. The assay appears linear over the range 0.050–100 μg ml −1 for both PD 146415 and PD 146923. Interrun accuracy and precision estimates for PD 146415 and PD 146923 were within ± 6.50 and ≤ 3.27%, respectively, and ± 12.8 and ≤ 4.06%, respectively, for quality controls containing nominal concentrations of 0.400, 4.00 and 40.0 μg ml −1. The absolute recovery of CI-1010, PD 146415 and internal standard, PD 126675, were approximately 40, 96 and 95%, respectively. The recovery of PD 146923 appeared concentration dependent and ranged from 68 to 92%. PD 146145 and PD 146923 were both stable in rat plasma at 4°C and − 77°C for at least 7 h and 154 days, respectively. CI-1010 was not stable in rat plasma at 4°C. CI-1010, PD 146145 and PD 126675 were stable for at least 63 days in 10 mM phosphate buffer at pH 3.0 and 4°C. Under identical conditions PD 146923 was stable for only 8 days. The applicability of this method to determine concentrations of PD 146145 and PD 146923 in rat plasma is reported in this paper.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/S0731-7085(97)00013-7</identifier><identifier>PMID: 9447551</identifier><identifier>CODEN: JPBADA</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>2-nitroimidazoles ; Alkylating Agents - analysis ; Alkylating radiosensitizer ; Analysis ; Animals ; Biological and medical sciences ; Chromatography, Liquid - methods ; CI-1010 ; Drug Stability ; General pharmacology ; HPLC ; Injections, Intravenous ; Medical sciences ; Nitroimidazoles - administration &amp; dosage ; Nitroimidazoles - analysis ; Nitroimidazoles - blood ; Nitroimidazoles - pharmacokinetics ; PD 146415 ; PD 146923 ; Pharmacology. 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Because CI-1010 has an estimated half-life ≤ 2 min under physiological conditions its metabolites/degradation products PD 146415, an inactive moiety, and PD 146923 were assayed to support rat toxicology studies. The method involves the processing of plasma samples through phenyl solid-phase extraction cartridges followed by chromatography on CN columns with UV detection at 325 nm. The assay appears linear over the range 0.050–100 μg ml −1 for both PD 146415 and PD 146923. Interrun accuracy and precision estimates for PD 146415 and PD 146923 were within ± 6.50 and ≤ 3.27%, respectively, and ± 12.8 and ≤ 4.06%, respectively, for quality controls containing nominal concentrations of 0.400, 4.00 and 40.0 μg ml −1. The absolute recovery of CI-1010, PD 146415 and internal standard, PD 126675, were approximately 40, 96 and 95%, respectively. The recovery of PD 146923 appeared concentration dependent and ranged from 68 to 92%. PD 146145 and PD 146923 were both stable in rat plasma at 4°C and − 77°C for at least 7 h and 154 days, respectively. CI-1010 was not stable in rat plasma at 4°C. CI-1010, PD 146145 and PD 126675 were stable for at least 63 days in 10 mM phosphate buffer at pH 3.0 and 4°C. Under identical conditions PD 146923 was stable for only 8 days. The applicability of this method to determine concentrations of PD 146145 and PD 146923 in rat plasma is reported in this paper.</description><subject>2-nitroimidazoles</subject><subject>Alkylating Agents - analysis</subject><subject>Alkylating radiosensitizer</subject><subject>Analysis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chromatography, Liquid - methods</subject><subject>CI-1010</subject><subject>Drug Stability</subject><subject>General pharmacology</subject><subject>HPLC</subject><subject>Injections, Intravenous</subject><subject>Medical sciences</subject><subject>Nitroimidazoles - administration &amp; dosage</subject><subject>Nitroimidazoles - analysis</subject><subject>Nitroimidazoles - blood</subject><subject>Nitroimidazoles - pharmacokinetics</subject><subject>PD 146415</subject><subject>PD 146923</subject><subject>Pharmacology. Drug treatments</subject><subject>Prodrugs - administration &amp; dosage</subject><subject>Prodrugs - analysis</subject><subject>Prodrugs - pharmacokinetics</subject><subject>Radiation-Sensitizing Agents - analysis</subject><subject>Rat plasma</subject><subject>Rats</subject><subject>RB 6145</subject><subject>Reproducibility of Results</subject><subject>RSU 1069</subject><subject>Solid-phase extraction</subject><subject>Spectrophotometry, Ultraviolet</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkFFrFDEQx4Mo9ax-hEIeRBS6mmSTzeaplENt4UDBPvgWZrMTG81lzyQnXj-9e73jXn0amPn9Z4YfIRecveeMdx--Md3yRrNevTX6HWOMt41-Qha8120jOvn9KVmckOfkRSk_Z0hxI8_ImZFSK8UX5P460ZuvqyWFUmBHtzXE8BDSD1qmGMZmcw8FKf6tGVwNU6J-ynR528wfsEsKiUL8tYtQ94kMY5gKphJqeMB8SUOae5VuIpQ1vCTPPMSCr471nNx9-ni3vGlWXz7fLq9XjZOC1aaVPQjXcZRMuN50XCsnHHrkZnCq40qZYUDwaoDRofCjAzOi987xwQjZnpM3h7WbPP3eYql2HYrDGCHhtC2Wd0JyLfsZVAfQ5amUjN5uclhD3lnO7F6wfRRs9_as0fZRsNVz7uJ4YDuscTyljkbn-evjHIqD6DMkF8oJE0zqXnYzdnXAcHbxJ2C2xQVMDseQ0VU7TuE_j_wDweOYLg</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>Bullen, William W.</creator><creator>Rossi, David T.</creator><creator>Hoffman, Keith L.</creator><creator>Suri, Ajit</creator><creator>Lathia, Chetan D.</creator><general>Elsevier B.V</general><general>Elsevier Science</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19970901</creationdate><title>An HPLC assay utilizing solid-phase extraction for CI-1010, an alkylating radiosensitizer, in rat plasma</title><author>Bullen, William W. ; Rossi, David T. ; Hoffman, Keith L. ; Suri, Ajit ; Lathia, Chetan D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-348a2c61e402c896175c2cefe19bc561559bbeaf5badce2fdca9deffcc1b9243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>2-nitroimidazoles</topic><topic>Alkylating Agents - analysis</topic><topic>Alkylating radiosensitizer</topic><topic>Analysis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chromatography, Liquid - methods</topic><topic>CI-1010</topic><topic>Drug Stability</topic><topic>General pharmacology</topic><topic>HPLC</topic><topic>Injections, Intravenous</topic><topic>Medical sciences</topic><topic>Nitroimidazoles - administration &amp; dosage</topic><topic>Nitroimidazoles - analysis</topic><topic>Nitroimidazoles - blood</topic><topic>Nitroimidazoles - pharmacokinetics</topic><topic>PD 146415</topic><topic>PD 146923</topic><topic>Pharmacology. Drug treatments</topic><topic>Prodrugs - administration &amp; dosage</topic><topic>Prodrugs - analysis</topic><topic>Prodrugs - pharmacokinetics</topic><topic>Radiation-Sensitizing Agents - analysis</topic><topic>Rat plasma</topic><topic>Rats</topic><topic>RB 6145</topic><topic>Reproducibility of Results</topic><topic>RSU 1069</topic><topic>Solid-phase extraction</topic><topic>Spectrophotometry, Ultraviolet</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bullen, William W.</creatorcontrib><creatorcontrib>Rossi, David T.</creatorcontrib><creatorcontrib>Hoffman, Keith L.</creatorcontrib><creatorcontrib>Suri, Ajit</creatorcontrib><creatorcontrib>Lathia, Chetan D.</creatorcontrib><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bullen, William W.</au><au>Rossi, David T.</au><au>Hoffman, Keith L.</au><au>Suri, Ajit</au><au>Lathia, Chetan D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An HPLC assay utilizing solid-phase extraction for CI-1010, an alkylating radiosensitizer, in rat plasma</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>16</volume><issue>1</issue><spage>47</spage><epage>55</epage><pages>47-55</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>CI-1010, a 2-nitroimidazole, is a chiral prodrug for the active moiety PD 146923 and is under development as an alkylating radiosensitizer to be used as an adjuvant to radiotherapy. Because CI-1010 has an estimated half-life ≤ 2 min under physiological conditions its metabolites/degradation products PD 146415, an inactive moiety, and PD 146923 were assayed to support rat toxicology studies. The method involves the processing of plasma samples through phenyl solid-phase extraction cartridges followed by chromatography on CN columns with UV detection at 325 nm. The assay appears linear over the range 0.050–100 μg ml −1 for both PD 146415 and PD 146923. Interrun accuracy and precision estimates for PD 146415 and PD 146923 were within ± 6.50 and ≤ 3.27%, respectively, and ± 12.8 and ≤ 4.06%, respectively, for quality controls containing nominal concentrations of 0.400, 4.00 and 40.0 μg ml −1. The absolute recovery of CI-1010, PD 146415 and internal standard, PD 126675, were approximately 40, 96 and 95%, respectively. The recovery of PD 146923 appeared concentration dependent and ranged from 68 to 92%. PD 146145 and PD 146923 were both stable in rat plasma at 4°C and − 77°C for at least 7 h and 154 days, respectively. CI-1010 was not stable in rat plasma at 4°C. CI-1010, PD 146145 and PD 126675 were stable for at least 63 days in 10 mM phosphate buffer at pH 3.0 and 4°C. Under identical conditions PD 146923 was stable for only 8 days. The applicability of this method to determine concentrations of PD 146145 and PD 146923 in rat plasma is reported in this paper.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9447551</pmid><doi>10.1016/S0731-7085(97)00013-7</doi><tpages>9</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects 2-nitroimidazoles
Alkylating Agents - analysis
Alkylating radiosensitizer
Analysis
Animals
Biological and medical sciences
Chromatography, Liquid - methods
CI-1010
Drug Stability
General pharmacology
HPLC
Injections, Intravenous
Medical sciences
Nitroimidazoles - administration & dosage
Nitroimidazoles - analysis
Nitroimidazoles - blood
Nitroimidazoles - pharmacokinetics
PD 146415
PD 146923
Pharmacology. Drug treatments
Prodrugs - administration & dosage
Prodrugs - analysis
Prodrugs - pharmacokinetics
Radiation-Sensitizing Agents - analysis
Rat plasma
Rats
RB 6145
Reproducibility of Results
RSU 1069
Solid-phase extraction
Spectrophotometry, Ultraviolet
title An HPLC assay utilizing solid-phase extraction for CI-1010, an alkylating radiosensitizer, in rat plasma
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