Fluorescent determination of chloride in nanoliter samples
Fluorescent determination of chloride (Cl-) in nanoliter samples. Measurements of Cl- in nanoliter samples, such as those collected during isolated, perfused tubule experiments, have been difficult, somewhat insensitive, and/or require custom-made equipment. We developed a technique using a fluoresc...
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description | Fluorescent determination of chloride (Cl-) in nanoliter samples.
Measurements of Cl- in nanoliter samples, such as those collected during isolated, perfused tubule experiments, have been difficult, somewhat insensitive, and/or require custom-made equipment. We developed a technique using a fluorescent Cl- indicator, 6-methoxy-N-(3-sulfopropyl) quinolinium (SPQ), to make these measurements simple and reliable.
This is a simple procedure that relies on the selectivity of the dye and the fact that Cl-quenches its fluorescence. To measure millimolar quantities of Cl- in nanoliter samples, we prepared a solution of 0.25 mM SPQ and loaded it into the reservoir of a continuous-flow ultramicrofluorometer, which can be constructed from commercially available components. Samples were injected with a calibrated pipette via an injection port, and the resultant peak fluorescent deflections were recorded. The deflections represent a decrease in fluorescence caused by the quenching effect of the Cl- injected.
The method yielded a linear response with Cl- concentrations from 5 to 200 mM NaCl. The minimum detectable Cl- concentration was approximately 5 mM. The coefficient of variation between 5 and 200 mM was 1.7%. Resolution, defined as two times the standard error divided by the slope, between 10 and 50 mM and between 50 and 200 mM was 1 mM and 2.6 mM, respectively. Furosemide, diisothiocyanostilbene-2,2′-disulfonic acid and other nonchloride anions (HEPES, HCO3, SO4, and PO4) did not interfere with the assay, whereas 150 mM NaBr resulted in a peak height greater than 150 NaCl. In addition, the ability to measure Cl- did not vary with pH within the physiological range.
We developed an easy, accurate, and sensitive method to measure Cl- concentration in small aqueous solution samples. |
doi_str_mv | 10.1046/j.1523-1755.1999.00239.x |
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Measurements of Cl- in nanoliter samples, such as those collected during isolated, perfused tubule experiments, have been difficult, somewhat insensitive, and/or require custom-made equipment. We developed a technique using a fluorescent Cl- indicator, 6-methoxy-N-(3-sulfopropyl) quinolinium (SPQ), to make these measurements simple and reliable.
This is a simple procedure that relies on the selectivity of the dye and the fact that Cl-quenches its fluorescence. To measure millimolar quantities of Cl- in nanoliter samples, we prepared a solution of 0.25 mM SPQ and loaded it into the reservoir of a continuous-flow ultramicrofluorometer, which can be constructed from commercially available components. Samples were injected with a calibrated pipette via an injection port, and the resultant peak fluorescent deflections were recorded. The deflections represent a decrease in fluorescence caused by the quenching effect of the Cl- injected.
The method yielded a linear response with Cl- concentrations from 5 to 200 mM NaCl. The minimum detectable Cl- concentration was approximately 5 mM. The coefficient of variation between 5 and 200 mM was 1.7%. Resolution, defined as two times the standard error divided by the slope, between 10 and 50 mM and between 50 and 200 mM was 1 mM and 2.6 mM, respectively. Furosemide, diisothiocyanostilbene-2,2′-disulfonic acid and other nonchloride anions (HEPES, HCO3, SO4, and PO4) did not interfere with the assay, whereas 150 mM NaBr resulted in a peak height greater than 150 NaCl. In addition, the ability to measure Cl- did not vary with pH within the physiological range.
We developed an easy, accurate, and sensitive method to measure Cl- concentration in small aqueous solution samples.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1046/j.1523-1755.1999.00239.x</identifier><identifier>PMID: 9893143</identifier><identifier>CODEN: KDYIA5</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; bromide ; Chlorides - analysis ; cotransport ; DIDS ; Fluorescent Dyes ; furosemide ; In Vitro Techniques ; Investigative techniques, diagnostic techniques (general aspects) ; kidney ; Kidney Tubules - metabolism ; Medical sciences ; Microchemistry - instrumentation ; Microchemistry - methods ; Microchemistry - statistics & numerical data ; Miscellaneous. Technology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Perfusion ; Quinolinium Compounds ; Sensitivity and Specificity ; Spectrometry, Fluorescence - instrumentation ; Spectrometry, Fluorescence - methods ; Spectrometry, Fluorescence - statistics & numerical data ; thick ascending limb</subject><ispartof>Kidney international, 1999-01, Vol.55 (1), p.321-325</ispartof><rights>1999 International Society of Nephrology</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-b5ee31627b68782ae16551c580f68d662cd13b9847fba254e0962b684f7ea2813</citedby><cites>FETCH-LOGICAL-c448t-b5ee31627b68782ae16551c580f68d662cd13b9847fba254e0962b684f7ea2813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,776,780,785,786,4036,4037,23909,23910,25118,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1677325$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9893143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García, Néstor H.</creatorcontrib><creatorcontrib>Plato, Craig F.</creatorcontrib><creatorcontrib>Garvin, Jeffrey L.</creatorcontrib><creatorcontrib>García, Néstor H.</creatorcontrib><title>Fluorescent determination of chloride in nanoliter samples</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>Fluorescent determination of chloride (Cl-) in nanoliter samples.
Measurements of Cl- in nanoliter samples, such as those collected during isolated, perfused tubule experiments, have been difficult, somewhat insensitive, and/or require custom-made equipment. We developed a technique using a fluorescent Cl- indicator, 6-methoxy-N-(3-sulfopropyl) quinolinium (SPQ), to make these measurements simple and reliable.
This is a simple procedure that relies on the selectivity of the dye and the fact that Cl-quenches its fluorescence. To measure millimolar quantities of Cl- in nanoliter samples, we prepared a solution of 0.25 mM SPQ and loaded it into the reservoir of a continuous-flow ultramicrofluorometer, which can be constructed from commercially available components. Samples were injected with a calibrated pipette via an injection port, and the resultant peak fluorescent deflections were recorded. The deflections represent a decrease in fluorescence caused by the quenching effect of the Cl- injected.
The method yielded a linear response with Cl- concentrations from 5 to 200 mM NaCl. The minimum detectable Cl- concentration was approximately 5 mM. The coefficient of variation between 5 and 200 mM was 1.7%. Resolution, defined as two times the standard error divided by the slope, between 10 and 50 mM and between 50 and 200 mM was 1 mM and 2.6 mM, respectively. Furosemide, diisothiocyanostilbene-2,2′-disulfonic acid and other nonchloride anions (HEPES, HCO3, SO4, and PO4) did not interfere with the assay, whereas 150 mM NaBr resulted in a peak height greater than 150 NaCl. In addition, the ability to measure Cl- did not vary with pH within the physiological range.
We developed an easy, accurate, and sensitive method to measure Cl- concentration in small aqueous solution samples.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>bromide</subject><subject>Chlorides - analysis</subject><subject>cotransport</subject><subject>DIDS</subject><subject>Fluorescent Dyes</subject><subject>furosemide</subject><subject>In Vitro Techniques</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>kidney</subject><subject>Kidney Tubules - metabolism</subject><subject>Medical sciences</subject><subject>Microchemistry - instrumentation</subject><subject>Microchemistry - methods</subject><subject>Microchemistry - statistics & numerical data</subject><subject>Miscellaneous. Technology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Perfusion</subject><subject>Quinolinium Compounds</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Fluorescence - instrumentation</subject><subject>Spectrometry, Fluorescence - methods</subject><subject>Spectrometry, Fluorescence - statistics & numerical data</subject><subject>thick ascending limb</subject><issn>0085-2538</issn><issn>1523-1755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtKxDAUhoMoOo4-gtCFuGvNpUkTdyreQHCj65Cmp5ihTcakI_r2ZpxhXLo6HP7vXPgQKgiuCK7F5aIinLKSNJxXRClVYUyZqr720GwX7KMZxpKXlDN5hI5TWuDcK4YP0aHKldRshq7uh1WIkCz4qehggjg6byYXfBH6wr4PIboOCucLb3wYXAaKZMblAOkEHfRmSHC6rXP0dn_3evtYPr88PN1eP5e2ruVUthyAEUGbVshGUgNEcE4sl7gXshOC2o6wVsm66VtDeQ1YCZrZum_AUEnYHF1s9i5j-FhBmvTo8r_DYDyEVdJCccGkEhmUG9DGkFKEXi-jG0381gTrtTa90Gs7em1Hr7XpX236K4-ebW-s2hG63eDWU87Pt7lJ1gx9NN669LdfNA3LnufoZoNB9vHpIOpkHXgLnYtgJ90F9_8vPxvOisE</recordid><startdate>199901</startdate><enddate>199901</enddate><creator>García, Néstor H.</creator><creator>Plato, Craig F.</creator><creator>Garvin, Jeffrey L.</creator><creator>García, Néstor H.</creator><general>Elsevier Inc</general><general>Nature Publishing</general><scope>6I.</scope><scope>AAFTH</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>199901</creationdate><title>Fluorescent determination of chloride in nanoliter samples</title><author>García, Néstor H. ; Plato, Craig F. ; Garvin, Jeffrey L. ; García, Néstor H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-b5ee31627b68782ae16551c580f68d662cd13b9847fba254e0962b684f7ea2813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>bromide</topic><topic>Chlorides - analysis</topic><topic>cotransport</topic><topic>DIDS</topic><topic>Fluorescent Dyes</topic><topic>furosemide</topic><topic>In Vitro Techniques</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>kidney</topic><topic>Kidney Tubules - metabolism</topic><topic>Medical sciences</topic><topic>Microchemistry - instrumentation</topic><topic>Microchemistry - methods</topic><topic>Microchemistry - statistics & numerical data</topic><topic>Miscellaneous. Technology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Perfusion</topic><topic>Quinolinium Compounds</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Fluorescence - instrumentation</topic><topic>Spectrometry, Fluorescence - methods</topic><topic>Spectrometry, Fluorescence - statistics & numerical data</topic><topic>thick ascending limb</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García, Néstor H.</creatorcontrib><creatorcontrib>Plato, Craig F.</creatorcontrib><creatorcontrib>Garvin, Jeffrey L.</creatorcontrib><creatorcontrib>García, Néstor H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García, Néstor H.</au><au>Plato, Craig F.</au><au>Garvin, Jeffrey L.</au><au>García, Néstor H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorescent determination of chloride in nanoliter samples</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>1999-01</date><risdate>1999</risdate><volume>55</volume><issue>1</issue><spage>321</spage><epage>325</epage><pages>321-325</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>Fluorescent determination of chloride (Cl-) in nanoliter samples.
Measurements of Cl- in nanoliter samples, such as those collected during isolated, perfused tubule experiments, have been difficult, somewhat insensitive, and/or require custom-made equipment. We developed a technique using a fluorescent Cl- indicator, 6-methoxy-N-(3-sulfopropyl) quinolinium (SPQ), to make these measurements simple and reliable.
This is a simple procedure that relies on the selectivity of the dye and the fact that Cl-quenches its fluorescence. To measure millimolar quantities of Cl- in nanoliter samples, we prepared a solution of 0.25 mM SPQ and loaded it into the reservoir of a continuous-flow ultramicrofluorometer, which can be constructed from commercially available components. Samples were injected with a calibrated pipette via an injection port, and the resultant peak fluorescent deflections were recorded. The deflections represent a decrease in fluorescence caused by the quenching effect of the Cl- injected.
The method yielded a linear response with Cl- concentrations from 5 to 200 mM NaCl. The minimum detectable Cl- concentration was approximately 5 mM. The coefficient of variation between 5 and 200 mM was 1.7%. Resolution, defined as two times the standard error divided by the slope, between 10 and 50 mM and between 50 and 200 mM was 1 mM and 2.6 mM, respectively. Furosemide, diisothiocyanostilbene-2,2′-disulfonic acid and other nonchloride anions (HEPES, HCO3, SO4, and PO4) did not interfere with the assay, whereas 150 mM NaBr resulted in a peak height greater than 150 NaCl. In addition, the ability to measure Cl- did not vary with pH within the physiological range.
We developed an easy, accurate, and sensitive method to measure Cl- concentration in small aqueous solution samples.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9893143</pmid><doi>10.1046/j.1523-1755.1999.00239.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences bromide Chlorides - analysis cotransport DIDS Fluorescent Dyes furosemide In Vitro Techniques Investigative techniques, diagnostic techniques (general aspects) kidney Kidney Tubules - metabolism Medical sciences Microchemistry - instrumentation Microchemistry - methods Microchemistry - statistics & numerical data Miscellaneous. Technology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Perfusion Quinolinium Compounds Sensitivity and Specificity Spectrometry, Fluorescence - instrumentation Spectrometry, Fluorescence - methods Spectrometry, Fluorescence - statistics & numerical data thick ascending limb |
title | Fluorescent determination of chloride in nanoliter samples |
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