Rapid, convenient radioimmunoassay of estrone sulfate
We developed a specific, simple, and rapid RIA for the direct quantification of estrone sulfate (E1S) and established its performance characteristics. The assay has a dynamic range of 0.05-90 micrograms/L with a detection limit of 0.009 microgram/L. Intraassay CVs were 9.2%, 4.5%, and 4.6% at 0.35,...
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Veröffentlicht in: | Clinical chemistry (Baltimore, Md.) Md.), 1998-02, Vol.44 (2), p.244-249 |
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creator | Ranadive, Girish N Mistry, Jehangir S Damodaran, Kalyani Khosravi, M. Javad Diamandi, Anastasia Gimpel, Terry Castracane, V. Daniel Patel, S Stanczyk, Frank Z |
description | We developed a specific, simple, and rapid RIA for the direct quantification of estrone sulfate (E1S) and established its performance characteristics. The assay has a dynamic range of 0.05-90 micrograms/L with a detection limit of 0.009 microgram/L. Intraassay CVs were 9.2%, 4.5%, and 4.6% at 0.35, 9.0, and 60 micrograms/L, respectively. Interassay CVs were 8.8%, 5.1%, and 5.5% at 0.076, 0.5, and 12 micrograms/L, respectively. Linearity of dilution studies showed values of 80-105% of expected, and recovery of E1S added to serum samples ranged from 82% to 102%. Cross-reactivities with structurally related estrogens were < 5%. When compared with a conventional assay (involving hydrolysis of E1S and indirect measurement of estrone), the present RIA showed excellent correlation (r = 0.99, slope = 1.54, Sy/x = 2.14, n = 71). Mean E1S concentrations measured with this RIA for normal men (n = 20) and women in follicular (n = 20) and luteal (n = 25) phases of their menstrual cycle were 0.96, 0.96, and 1.74 microgram/L, respectively. Mean E1S concentrations for oral contraceptive users (n = 20) and postmenopausal women without hormone replacement therapy (n = 21) or on hormone replacement therapy (n = 22) were 0.74, 0.13, and 2.56 micrograms/L, respectively. Serum concentrations of E1S in pregnant women in their first (n = 14), second (n = 17), and third (n = 15) trimesters were 20, 66, and 105 micrograms/L, respectively. Availability of this simple RIA should provide a useful tool for the assessment of estrogen status in women. |
doi_str_mv | 10.1093/clinchem/44.2.244 |
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Javad ; Diamandi, Anastasia ; Gimpel, Terry ; Castracane, V. Daniel ; Patel, S ; Stanczyk, Frank Z</creator><creatorcontrib>Ranadive, Girish N ; Mistry, Jehangir S ; Damodaran, Kalyani ; Khosravi, M. Javad ; Diamandi, Anastasia ; Gimpel, Terry ; Castracane, V. Daniel ; Patel, S ; Stanczyk, Frank Z</creatorcontrib><description>We developed a specific, simple, and rapid RIA for the direct quantification of estrone sulfate (E1S) and established its performance characteristics. The assay has a dynamic range of 0.05-90 micrograms/L with a detection limit of 0.009 microgram/L. Intraassay CVs were 9.2%, 4.5%, and 4.6% at 0.35, 9.0, and 60 micrograms/L, respectively. Interassay CVs were 8.8%, 5.1%, and 5.5% at 0.076, 0.5, and 12 micrograms/L, respectively. Linearity of dilution studies showed values of 80-105% of expected, and recovery of E1S added to serum samples ranged from 82% to 102%. Cross-reactivities with structurally related estrogens were < 5%. When compared with a conventional assay (involving hydrolysis of E1S and indirect measurement of estrone), the present RIA showed excellent correlation (r = 0.99, slope = 1.54, Sy/x = 2.14, n = 71). Mean E1S concentrations measured with this RIA for normal men (n = 20) and women in follicular (n = 20) and luteal (n = 25) phases of their menstrual cycle were 0.96, 0.96, and 1.74 microgram/L, respectively. Mean E1S concentrations for oral contraceptive users (n = 20) and postmenopausal women without hormone replacement therapy (n = 21) or on hormone replacement therapy (n = 22) were 0.74, 0.13, and 2.56 micrograms/L, respectively. Serum concentrations of E1S in pregnant women in their first (n = 14), second (n = 17), and third (n = 15) trimesters were 20, 66, and 105 micrograms/L, respectively. Availability of this simple RIA should provide a useful tool for the assessment of estrogen status in women.</description><identifier>ISSN: 0009-9147</identifier><identifier>EISSN: 1530-8561</identifier><identifier>DOI: 10.1093/clinchem/44.2.244</identifier><identifier>PMID: 9474019</identifier><identifier>CODEN: CLCHAU</identifier><language>eng</language><publisher>Washington, DC: Am Assoc Clin Chem</publisher><subject>Biological and medical sciences ; Cross Reactions ; Endocrinology ; Estrone - analogs & derivatives ; Estrone - blood ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Menstrual Cycle - physiology ; Molecular Structure ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Postmenopause - blood ; Pregnancy ; Radioimmunoassay - methods ; Sensitivity and Specificity ; Steroid hormones. 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Javad</creatorcontrib><creatorcontrib>Diamandi, Anastasia</creatorcontrib><creatorcontrib>Gimpel, Terry</creatorcontrib><creatorcontrib>Castracane, V. Daniel</creatorcontrib><creatorcontrib>Patel, S</creatorcontrib><creatorcontrib>Stanczyk, Frank Z</creatorcontrib><title>Rapid, convenient radioimmunoassay of estrone sulfate</title><title>Clinical chemistry (Baltimore, Md.)</title><addtitle>Clin Chem</addtitle><description>We developed a specific, simple, and rapid RIA for the direct quantification of estrone sulfate (E1S) and established its performance characteristics. The assay has a dynamic range of 0.05-90 micrograms/L with a detection limit of 0.009 microgram/L. Intraassay CVs were 9.2%, 4.5%, and 4.6% at 0.35, 9.0, and 60 micrograms/L, respectively. Interassay CVs were 8.8%, 5.1%, and 5.5% at 0.076, 0.5, and 12 micrograms/L, respectively. Linearity of dilution studies showed values of 80-105% of expected, and recovery of E1S added to serum samples ranged from 82% to 102%. Cross-reactivities with structurally related estrogens were < 5%. When compared with a conventional assay (involving hydrolysis of E1S and indirect measurement of estrone), the present RIA showed excellent correlation (r = 0.99, slope = 1.54, Sy/x = 2.14, n = 71). Mean E1S concentrations measured with this RIA for normal men (n = 20) and women in follicular (n = 20) and luteal (n = 25) phases of their menstrual cycle were 0.96, 0.96, and 1.74 microgram/L, respectively. Mean E1S concentrations for oral contraceptive users (n = 20) and postmenopausal women without hormone replacement therapy (n = 21) or on hormone replacement therapy (n = 22) were 0.74, 0.13, and 2.56 micrograms/L, respectively. Serum concentrations of E1S in pregnant women in their first (n = 14), second (n = 17), and third (n = 15) trimesters were 20, 66, and 105 micrograms/L, respectively. Availability of this simple RIA should provide a useful tool for the assessment of estrogen status in women.</description><subject>Biological and medical sciences</subject><subject>Cross Reactions</subject><subject>Endocrinology</subject><subject>Estrone - analogs & derivatives</subject><subject>Estrone - blood</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Menstrual Cycle - physiology</subject><subject>Molecular Structure</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Postmenopause - blood</subject><subject>Pregnancy</subject><subject>Radioimmunoassay - methods</subject><subject>Sensitivity and Specificity</subject><subject>Steroid hormones. Cholecalciferol derivatives</subject><subject>Vertebrates: endocrinology</subject><issn>0009-9147</issn><issn>1530-8561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LAzEQhoMotVZ_gAdhD-rJbZNNNtkcpfgFBUH0HLLJrI3sR026Lv33Rrr2MAwz88w7w4vQJcFzgiVdmNq1Zg3NgrF5Ns8YO0JTklOcFjknx2iKMZapJEycorMQvmLJRMEnaCKZYJjIKcrf9MbZu8R07Q-0Dtpt4rV1nWuavu10CHqXdFUCYeu7FpLQ15Xewjk6qXQd4GLMM_Tx-PC-fE5Xr08vy_tVaqgstmmeUZKXJIbAjBttDVAiLcicZpJxrDlwIUETmxWxo63FQEpOcMFLUVlBZ-h2r7vx3Xcfn1CNCwbqWrfQ9UEJySWluYwg2YPGdyF4qNTGu0b7nSJY_Vml_q1SjKlMRaviztUo3pcN2MPG6E2cX49zHYyuK69b48IBywjPhSwidrPH1u5zPTgPKjS6rqMoUcMwHM79AozWf-c</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>Ranadive, Girish N</creator><creator>Mistry, Jehangir S</creator><creator>Damodaran, Kalyani</creator><creator>Khosravi, M. Javad</creator><creator>Diamandi, Anastasia</creator><creator>Gimpel, Terry</creator><creator>Castracane, V. Daniel</creator><creator>Patel, S</creator><creator>Stanczyk, Frank Z</creator><general>Am Assoc Clin Chem</general><general>American Association for Clinical Chemistry</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>7X8</scope></search><sort><creationdate>19980201</creationdate><title>Rapid, convenient radioimmunoassay of estrone sulfate</title><author>Ranadive, Girish N ; Mistry, Jehangir S ; Damodaran, Kalyani ; Khosravi, M. Javad ; Diamandi, Anastasia ; Gimpel, Terry ; Castracane, V. Daniel ; Patel, S ; Stanczyk, Frank Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-52315b115b7046cadce319de95329460a6e679ea1d28329add0e1b61086b7fd73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Cross Reactions</topic><topic>Endocrinology</topic><topic>Estrone - analogs & derivatives</topic><topic>Estrone - blood</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Menstrual Cycle - physiology</topic><topic>Molecular Structure</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Postmenopause - blood</topic><topic>Pregnancy</topic><topic>Radioimmunoassay - methods</topic><topic>Sensitivity and Specificity</topic><topic>Steroid hormones. Cholecalciferol derivatives</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ranadive, Girish N</creatorcontrib><creatorcontrib>Mistry, Jehangir S</creatorcontrib><creatorcontrib>Damodaran, Kalyani</creatorcontrib><creatorcontrib>Khosravi, M. Javad</creatorcontrib><creatorcontrib>Diamandi, Anastasia</creatorcontrib><creatorcontrib>Gimpel, Terry</creatorcontrib><creatorcontrib>Castracane, V. Daniel</creatorcontrib><creatorcontrib>Patel, S</creatorcontrib><creatorcontrib>Stanczyk, Frank Z</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>MEDLINE - Academic</collection><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ranadive, Girish N</au><au>Mistry, Jehangir S</au><au>Damodaran, Kalyani</au><au>Khosravi, M. Javad</au><au>Diamandi, Anastasia</au><au>Gimpel, Terry</au><au>Castracane, V. Daniel</au><au>Patel, S</au><au>Stanczyk, Frank Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid, convenient radioimmunoassay of estrone sulfate</atitle><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle><addtitle>Clin Chem</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>44</volume><issue>2</issue><spage>244</spage><epage>249</epage><pages>244-249</pages><issn>0009-9147</issn><eissn>1530-8561</eissn><coden>CLCHAU</coden><abstract>We developed a specific, simple, and rapid RIA for the direct quantification of estrone sulfate (E1S) and established its performance characteristics. The assay has a dynamic range of 0.05-90 micrograms/L with a detection limit of 0.009 microgram/L. Intraassay CVs were 9.2%, 4.5%, and 4.6% at 0.35, 9.0, and 60 micrograms/L, respectively. Interassay CVs were 8.8%, 5.1%, and 5.5% at 0.076, 0.5, and 12 micrograms/L, respectively. Linearity of dilution studies showed values of 80-105% of expected, and recovery of E1S added to serum samples ranged from 82% to 102%. Cross-reactivities with structurally related estrogens were < 5%. When compared with a conventional assay (involving hydrolysis of E1S and indirect measurement of estrone), the present RIA showed excellent correlation (r = 0.99, slope = 1.54, Sy/x = 2.14, n = 71). Mean E1S concentrations measured with this RIA for normal men (n = 20) and women in follicular (n = 20) and luteal (n = 25) phases of their menstrual cycle were 0.96, 0.96, and 1.74 microgram/L, respectively. Mean E1S concentrations for oral contraceptive users (n = 20) and postmenopausal women without hormone replacement therapy (n = 21) or on hormone replacement therapy (n = 22) were 0.74, 0.13, and 2.56 micrograms/L, respectively. Serum concentrations of E1S in pregnant women in their first (n = 14), second (n = 17), and third (n = 15) trimesters were 20, 66, and 105 micrograms/L, respectively. Availability of this simple RIA should provide a useful tool for the assessment of estrogen status in women.</abstract><cop>Washington, DC</cop><pub>Am Assoc Clin Chem</pub><pmid>9474019</pmid><doi>10.1093/clinchem/44.2.244</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Cross Reactions Endocrinology Estrone - analogs & derivatives Estrone - blood Female Fundamental and applied biological sciences. Psychology Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Menstrual Cycle - physiology Molecular Structure Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Postmenopause - blood Pregnancy Radioimmunoassay - methods Sensitivity and Specificity Steroid hormones. Cholecalciferol derivatives Vertebrates: endocrinology |
title | Rapid, convenient radioimmunoassay of estrone sulfate |
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