Determination of Picogram Nitroglycerin Plasma Concentrations Using Capillary Gas Chromatography with On-Column Injection

A specific, sensitive, and precise capillary gas chromatographic (GC) assay capable of analyzing picogram concentrations of nitroglycerin in human plasma was developed. The analytical procedure involves a double extraction of 1mL of plasma with pentane, after the addition of internal standard (1ng o...

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Veröffentlicht in:Journal of pharmaceutical sciences 1984-07, Vol.73 (7), p.923-927
Hauptverfasser: Noonan, Patrick K., Kanfer, Isadore, Riegelman, Sidney, Benet, Leslie Z.
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container_end_page 927
container_issue 7
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container_title Journal of pharmaceutical sciences
container_volume 73
creator Noonan, Patrick K.
Kanfer, Isadore
Riegelman, Sidney
Benet, Leslie Z.
description A specific, sensitive, and precise capillary gas chromatographic (GC) assay capable of analyzing picogram concentrations of nitroglycerin in human plasma was developed. The analytical procedure involves a double extraction of 1mL of plasma with pentane, after the addition of internal standard (1ng of 2,6-dinitrotoluene), followed by evaporation and reconstitution in 50 μL of heptane. The extract (1 μL) was injected onto a capillary column using the on-column injection technique. The GC oven temperature was programmed from 120°C to 180°C at a rate of 5°C/min. The oven temperature was then programmed to 250°C and was maintained for 10min. The nitroglycerin and internal standard retention times were 8.6 and 11.4 min, respectively. The position of the end of the capillary column inside the detector is a critical determinant of sensitivity: the column exit must be positioned such that nitroglycerin adsorption to the detector is minimized (i.e., sensitivity maximized). The assay limit of quantitation was 25 pg/mL (CV = 7.6%) using 1mL of plasma. This GC assay, specific for nitroglycerin in the presence of its metabolites, isosorbide dinitrate, and several other drugs, may be used to quantitate plasma levels obtained after therapeutic nitroglycerin doses.
doi_str_mv 10.1002/jps.2600730715
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The analytical procedure involves a double extraction of 1mL of plasma with pentane, after the addition of internal standard (1ng of 2,6-dinitrotoluene), followed by evaporation and reconstitution in 50 μL of heptane. The extract (1 μL) was injected onto a capillary column using the on-column injection technique. The GC oven temperature was programmed from 120°C to 180°C at a rate of 5°C/min. The oven temperature was then programmed to 250°C and was maintained for 10min. The nitroglycerin and internal standard retention times were 8.6 and 11.4 min, respectively. The position of the end of the capillary column inside the detector is a critical determinant of sensitivity: the column exit must be positioned such that nitroglycerin adsorption to the detector is minimized (i.e., sensitivity maximized). The assay limit of quantitation was 25 pg/mL (CV = 7.6%) using 1mL of plasma. This GC assay, specific for nitroglycerin in the presence of its metabolites, isosorbide dinitrate, and several other drugs, may be used to quantitate plasma levels obtained after therapeutic nitroglycerin doses.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600730715</identifier><identifier>PMID: 6432997</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Analysis ; Biological and medical sciences ; Chromatography, Gas - methods ; Drug Stability ; GC-nitroglycerin ; GC—nitroglycerin, picogram quantitation ; General pharmacology ; Humans ; In Vitro Techniques ; Kinetics ; Medical sciences ; Microchemistry - methods ; Nickel ; Nitroglycerin - blood ; Nitroglycerin-GC ; Nitroglycerin—GC, picogram quantitation ; Pharmacology. 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Pharm. Sci</addtitle><description>A specific, sensitive, and precise capillary gas chromatographic (GC) assay capable of analyzing picogram concentrations of nitroglycerin in human plasma was developed. The analytical procedure involves a double extraction of 1mL of plasma with pentane, after the addition of internal standard (1ng of 2,6-dinitrotoluene), followed by evaporation and reconstitution in 50 μL of heptane. The extract (1 μL) was injected onto a capillary column using the on-column injection technique. The GC oven temperature was programmed from 120°C to 180°C at a rate of 5°C/min. The oven temperature was then programmed to 250°C and was maintained for 10min. The nitroglycerin and internal standard retention times were 8.6 and 11.4 min, respectively. The position of the end of the capillary column inside the detector is a critical determinant of sensitivity: the column exit must be positioned such that nitroglycerin adsorption to the detector is minimized (i.e., sensitivity maximized). The assay limit of quantitation was 25 pg/mL (CV = 7.6%) using 1mL of plasma. This GC assay, specific for nitroglycerin in the presence of its metabolites, isosorbide dinitrate, and several other drugs, may be used to quantitate plasma levels obtained after therapeutic nitroglycerin doses.</description><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Chromatography, Gas - methods</subject><subject>Drug Stability</subject><subject>GC-nitroglycerin</subject><subject>GC—nitroglycerin, picogram quantitation</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Microchemistry - methods</subject><subject>Nickel</subject><subject>Nitroglycerin - blood</subject><subject>Nitroglycerin-GC</subject><subject>Nitroglycerin—GC, picogram quantitation</subject><subject>Pharmacology. 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Drug treatments</topic><topic>picogram quantitation</topic><topic>Radioisotopes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noonan, Patrick K.</creatorcontrib><creatorcontrib>Kanfer, Isadore</creatorcontrib><creatorcontrib>Riegelman, Sidney</creatorcontrib><creatorcontrib>Benet, Leslie Z.</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>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Noonan, Patrick K.</au><au>Kanfer, Isadore</au><au>Riegelman, Sidney</au><au>Benet, Leslie Z.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of Picogram Nitroglycerin Plasma Concentrations Using Capillary Gas Chromatography with On-Column Injection</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1984-07</date><risdate>1984</risdate><volume>73</volume><issue>7</issue><spage>923</spage><epage>927</epage><pages>923-927</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>A specific, sensitive, and precise capillary gas chromatographic (GC) assay capable of analyzing picogram concentrations of nitroglycerin in human plasma was developed. The analytical procedure involves a double extraction of 1mL of plasma with pentane, after the addition of internal standard (1ng of 2,6-dinitrotoluene), followed by evaporation and reconstitution in 50 μL of heptane. The extract (1 μL) was injected onto a capillary column using the on-column injection technique. The GC oven temperature was programmed from 120°C to 180°C at a rate of 5°C/min. The oven temperature was then programmed to 250°C and was maintained for 10min. The nitroglycerin and internal standard retention times were 8.6 and 11.4 min, respectively. The position of the end of the capillary column inside the detector is a critical determinant of sensitivity: the column exit must be positioned such that nitroglycerin adsorption to the detector is minimized (i.e., sensitivity maximized). The assay limit of quantitation was 25 pg/mL (CV = 7.6%) using 1mL of plasma. This GC assay, specific for nitroglycerin in the presence of its metabolites, isosorbide dinitrate, and several other drugs, may be used to quantitate plasma levels obtained after therapeutic nitroglycerin doses.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>6432997</pmid><doi>10.1002/jps.2600730715</doi><tpages>5</tpages></addata></record>
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source Wiley Online Library - AutoHoldings Journals; MEDLINE; Alma/SFX Local Collection
subjects Analysis
Biological and medical sciences
Chromatography, Gas - methods
Drug Stability
GC-nitroglycerin
GC—nitroglycerin, picogram quantitation
General pharmacology
Humans
In Vitro Techniques
Kinetics
Medical sciences
Microchemistry - methods
Nickel
Nitroglycerin - blood
Nitroglycerin-GC
Nitroglycerin—GC, picogram quantitation
Pharmacology. Drug treatments
picogram quantitation
Radioisotopes
title Determination of Picogram Nitroglycerin Plasma Concentrations Using Capillary Gas Chromatography with On-Column Injection
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