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Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor
The aim of the present study was to investigate the stereoselectivity in the kinetic disposition and the transplacental distribution of bupivacaine in term parturients during labor. Maternal age ranged from 18–37 years and fetal gestational age from 37.6–41.5 weeks. Healthy parturients (n = 23) rece...
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Published in: | Chirality (New York, N.Y.) N.Y.), 2004, Vol.16 (2), p.65-71 |
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description | The aim of the present study was to investigate the stereoselectivity in the kinetic disposition and the transplacental distribution of bupivacaine in term parturients during labor. Maternal age ranged from 18–37 years and fetal gestational age from 37.6–41.5 weeks. Healthy parturients (n = 23) received epidural 0.5% racemic bupivacaine alone (group A) or combined with epinephrine (group B). Maternal venous blood was sampled at regular intervals until 8 h after drug administration and umbilical venous blood was obtained at delivery. Bupivacaine enantiomers were determined in plasma samples by HPLC using a Chiralcel® OD‐R column and a UV detector. One‐ or two‐compartment models were fitted to data and differences between the (+)‐(R) and (–)‐(S) enantiomers were compared with the paired Wilcoxon test (P< 0.05). The influence of epinephrine was evaluated using the unpaired Mann‐Whitney test (P< 0.05). The disposition of bupivacaine in maternal plasma was stereoselective, with higher Vd/f (140.60 vs. 132.81 L for group A and 197.86 vs. 169.46 L for group B) and Cl/f (29.00 vs. 25.43 L/h for group A and 33.15 vs. 26.39 L/h for group B) and lower t1/2β (3.24 vs. 3.30 h for group A and 4.36 vs. 4.45 h for group B) being observed for (+)‐(R)‐bupivacaine. The combined administration of epinephrine resulted in higher Vd/f (197.86 vs. 140.60 L for (+)‐(R) and 169.46 vs. 132.81 L for (–)‐(S)) and t1/2β values (4.36 vs. 3.24 h for (+)‐(R) and 4.45 vs. 3.30 h for (–)‐(S)). The transplacental distribution of bupivacaine was stereoselective only when bupivacaine was administered without epinephrine (group B), with a higher cord blood/maternal blood ratio being observed for (–)‐(S)‐bupivacaine (0.40 vs. 0.35). Chirality 16:65–71, 2004. © 2004 Wiley‐Liss, Inc. |
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Maternal age ranged from 18–37 years and fetal gestational age from 37.6–41.5 weeks. Healthy parturients (n = 23) received epidural 0.5% racemic bupivacaine alone (group A) or combined with epinephrine (group B). Maternal venous blood was sampled at regular intervals until 8 h after drug administration and umbilical venous blood was obtained at delivery. Bupivacaine enantiomers were determined in plasma samples by HPLC using a Chiralcel® OD‐R column and a UV detector. One‐ or two‐compartment models were fitted to data and differences between the (+)‐(R) and (–)‐(S) enantiomers were compared with the paired Wilcoxon test (P< 0.05). The influence of epinephrine was evaluated using the unpaired Mann‐Whitney test (P< 0.05). The disposition of bupivacaine in maternal plasma was stereoselective, with higher Vd/f (140.60 vs. 132.81 L for group A and 197.86 vs. 169.46 L for group B) and Cl/f (29.00 vs. 25.43 L/h for group A and 33.15 vs. 26.39 L/h for group B) and lower t1/2β (3.24 vs. 3.30 h for group A and 4.36 vs. 4.45 h for group B) being observed for (+)‐(R)‐bupivacaine. The combined administration of epinephrine resulted in higher Vd/f (197.86 vs. 140.60 L for (+)‐(R) and 169.46 vs. 132.81 L for (–)‐(S)) and t1/2β values (4.36 vs. 3.24 h for (+)‐(R) and 4.45 vs. 3.30 h for (–)‐(S)). The transplacental distribution of bupivacaine was stereoselective only when bupivacaine was administered without epinephrine (group B), with a higher cord blood/maternal blood ratio being observed for (–)‐(S)‐bupivacaine (0.40 vs. 0.35). Chirality 16:65–71, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0899-0042</identifier><identifier>EISSN: 1520-636X</identifier><identifier>DOI: 10.1002/chir.10308</identifier><identifier>PMID: 14712468</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; bupivacaine ; Bupivacaine - administration & dosage ; Bupivacaine - blood ; Bupivacaine - chemistry ; Bupivacaine - pharmacokinetics ; enantiomers ; Epinephrine - administration & dosage ; Epinephrine - pharmacology ; Female ; Fetal Blood - drug effects ; Fetal Blood - metabolism ; Humans ; Kinetics ; Maternal Age ; Maternal-Fetal Exchange - drug effects ; parturients ; Parturition - physiology ; pharmacokinetics ; placental transfer ; Pregnancy ; Stereoisomerism ; Vasoconstrictor Agents - administration & dosage ; Vasoconstrictor Agents - pharmacology</subject><ispartof>Chirality (New York, N.Y.), 2004, Vol.16 (2), p.65-71</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3638-9c0599fa83f948b32ddc270d06960078d7173f0a1f7af124c2c552f31abc02893</citedby><cites>FETCH-LOGICAL-c3638-9c0599fa83f948b32ddc270d06960078d7173f0a1f7af124c2c552f31abc02893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14712468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Papini, Olga</creatorcontrib><creatorcontrib>Do Carmo Silva Mathes, Ângelo</creatorcontrib><creatorcontrib>Pereira Da Cunha, Sergio</creatorcontrib><creatorcontrib>Lucia Lanchote, Vera</creatorcontrib><title>Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor</title><title>Chirality (New York, N.Y.)</title><addtitle>Chirality</addtitle><description>The aim of the present study was to investigate the stereoselectivity in the kinetic disposition and the transplacental distribution of bupivacaine in term parturients during labor. Maternal age ranged from 18–37 years and fetal gestational age from 37.6–41.5 weeks. Healthy parturients (n = 23) received epidural 0.5% racemic bupivacaine alone (group A) or combined with epinephrine (group B). Maternal venous blood was sampled at regular intervals until 8 h after drug administration and umbilical venous blood was obtained at delivery. Bupivacaine enantiomers were determined in plasma samples by HPLC using a Chiralcel® OD‐R column and a UV detector. One‐ or two‐compartment models were fitted to data and differences between the (+)‐(R) and (–)‐(S) enantiomers were compared with the paired Wilcoxon test (P< 0.05). The influence of epinephrine was evaluated using the unpaired Mann‐Whitney test (P< 0.05). The disposition of bupivacaine in maternal plasma was stereoselective, with higher Vd/f (140.60 vs. 132.81 L for group A and 197.86 vs. 169.46 L for group B) and Cl/f (29.00 vs. 25.43 L/h for group A and 33.15 vs. 26.39 L/h for group B) and lower t1/2β (3.24 vs. 3.30 h for group A and 4.36 vs. 4.45 h for group B) being observed for (+)‐(R)‐bupivacaine. The combined administration of epinephrine resulted in higher Vd/f (197.86 vs. 140.60 L for (+)‐(R) and 169.46 vs. 132.81 L for (–)‐(S)) and t1/2β values (4.36 vs. 3.24 h for (+)‐(R) and 4.45 vs. 3.30 h for (–)‐(S)). The transplacental distribution of bupivacaine was stereoselective only when bupivacaine was administered without epinephrine (group B), with a higher cord blood/maternal blood ratio being observed for (–)‐(S)‐bupivacaine (0.40 vs. 0.35). Chirality 16:65–71, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>bupivacaine</subject><subject>Bupivacaine - administration & dosage</subject><subject>Bupivacaine - blood</subject><subject>Bupivacaine - chemistry</subject><subject>Bupivacaine - pharmacokinetics</subject><subject>enantiomers</subject><subject>Epinephrine - administration & dosage</subject><subject>Epinephrine - pharmacology</subject><subject>Female</subject><subject>Fetal Blood - drug effects</subject><subject>Fetal Blood - metabolism</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Maternal Age</subject><subject>Maternal-Fetal Exchange - drug effects</subject><subject>parturients</subject><subject>Parturition - physiology</subject><subject>pharmacokinetics</subject><subject>placental transfer</subject><subject>Pregnancy</subject><subject>Stereoisomerism</subject><subject>Vasoconstrictor Agents - administration & dosage</subject><subject>Vasoconstrictor Agents - pharmacology</subject><issn>0899-0042</issn><issn>1520-636X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kc-O0zAQhy0EYsvChQdAPnFACoztJLaPqEB3RQUS_2-W69iq2SQOttPdvgmPu-62wI3TWKNvvpHnh9BTAi8JAH1ltj6WFwNxDy1IQ6FqWfvjPlqAkLICqOkZepTSTwCQLasfojNSc0LrVizQ78_ZRhuS7a3JfufzHvsR563FU6-NHbPucY56TM5GrMcOX_nRZm9w59MUks8-jDg4HAs8lPZmnvxOG10orLvBjz4dFnQ4BzzpmOfoizTha5-3OMS7GuaMNd7pFEwYU47e5BAfowdO98k-OdVz9PXd2y_Li2r9cXW5fL2uDGuZqKSBRkqnBXOyFhtGu85QDh20sgXgouOEMweaOK5d-bOhpmmoY0RvDFAh2Tl6fvROMfyabcpq8MnYvtejDXNSAkA0QvICvjiCJoaUonVqin7Qca8IqEMO6pCDusuhwM9O1nkz2O4fejp8AcgRuPa93f9HpZYXl5_-SKvjzOGmN39ndLxSLWe8Ud8_rJTg7M2393KtVuwW_EOmcA</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Papini, Olga</creator><creator>Do Carmo Silva Mathes, Ângelo</creator><creator>Pereira Da Cunha, Sergio</creator><creator>Lucia Lanchote, Vera</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>2004</creationdate><title>Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor</title><author>Papini, Olga ; Do Carmo Silva Mathes, Ângelo ; Pereira Da Cunha, Sergio ; Lucia Lanchote, Vera</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3638-9c0599fa83f948b32ddc270d06960078d7173f0a1f7af124c2c552f31abc02893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>bupivacaine</topic><topic>Bupivacaine - administration & dosage</topic><topic>Bupivacaine - blood</topic><topic>Bupivacaine - chemistry</topic><topic>Bupivacaine - pharmacokinetics</topic><topic>enantiomers</topic><topic>Epinephrine - administration & dosage</topic><topic>Epinephrine - pharmacology</topic><topic>Female</topic><topic>Fetal Blood - drug effects</topic><topic>Fetal Blood - metabolism</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Maternal Age</topic><topic>Maternal-Fetal Exchange - drug effects</topic><topic>parturients</topic><topic>Parturition - physiology</topic><topic>pharmacokinetics</topic><topic>placental transfer</topic><topic>Pregnancy</topic><topic>Stereoisomerism</topic><topic>Vasoconstrictor Agents - administration & dosage</topic><topic>Vasoconstrictor Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Papini, Olga</creatorcontrib><creatorcontrib>Do Carmo Silva Mathes, Ângelo</creatorcontrib><creatorcontrib>Pereira Da Cunha, Sergio</creatorcontrib><creatorcontrib>Lucia Lanchote, Vera</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>Chirality (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Papini, Olga</au><au>Do Carmo Silva Mathes, Ângelo</au><au>Pereira Da Cunha, Sergio</au><au>Lucia Lanchote, Vera</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor</atitle><jtitle>Chirality (New York, N.Y.)</jtitle><addtitle>Chirality</addtitle><date>2004</date><risdate>2004</risdate><volume>16</volume><issue>2</issue><spage>65</spage><epage>71</epage><pages>65-71</pages><issn>0899-0042</issn><eissn>1520-636X</eissn><abstract>The aim of the present study was to investigate the stereoselectivity in the kinetic disposition and the transplacental distribution of bupivacaine in term parturients during labor. Maternal age ranged from 18–37 years and fetal gestational age from 37.6–41.5 weeks. Healthy parturients (n = 23) received epidural 0.5% racemic bupivacaine alone (group A) or combined with epinephrine (group B). Maternal venous blood was sampled at regular intervals until 8 h after drug administration and umbilical venous blood was obtained at delivery. Bupivacaine enantiomers were determined in plasma samples by HPLC using a Chiralcel® OD‐R column and a UV detector. One‐ or two‐compartment models were fitted to data and differences between the (+)‐(R) and (–)‐(S) enantiomers were compared with the paired Wilcoxon test (P< 0.05). The influence of epinephrine was evaluated using the unpaired Mann‐Whitney test (P< 0.05). The disposition of bupivacaine in maternal plasma was stereoselective, with higher Vd/f (140.60 vs. 132.81 L for group A and 197.86 vs. 169.46 L for group B) and Cl/f (29.00 vs. 25.43 L/h for group A and 33.15 vs. 26.39 L/h for group B) and lower t1/2β (3.24 vs. 3.30 h for group A and 4.36 vs. 4.45 h for group B) being observed for (+)‐(R)‐bupivacaine. The combined administration of epinephrine resulted in higher Vd/f (197.86 vs. 140.60 L for (+)‐(R) and 169.46 vs. 132.81 L for (–)‐(S)) and t1/2β values (4.36 vs. 3.24 h for (+)‐(R) and 4.45 vs. 3.30 h for (–)‐(S)). The transplacental distribution of bupivacaine was stereoselective only when bupivacaine was administered without epinephrine (group B), with a higher cord blood/maternal blood ratio being observed for (–)‐(S)‐bupivacaine (0.40 vs. 0.35). Chirality 16:65–71, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14712468</pmid><doi>10.1002/chir.10308</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult bupivacaine Bupivacaine - administration & dosage Bupivacaine - blood Bupivacaine - chemistry Bupivacaine - pharmacokinetics enantiomers Epinephrine - administration & dosage Epinephrine - pharmacology Female Fetal Blood - drug effects Fetal Blood - metabolism Humans Kinetics Maternal Age Maternal-Fetal Exchange - drug effects parturients Parturition - physiology pharmacokinetics placental transfer Pregnancy Stereoisomerism Vasoconstrictor Agents - administration & dosage Vasoconstrictor Agents - pharmacology |
title | Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor |
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