A modification of the kinetic determination of pancuronium bromide based on its inhibitory effect on cholinesterase

A modification of the existing spectrophotometric kinetic method for the determination of pancuronium bromide (PCBr), based on pooled human serum cholinesterase (ChE, EC 3.1.1.8 acylcholine acylhydrolase) inhibition, was developed. Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as s...

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Veröffentlicht in:Journal of clinical laboratory analysis 2007, Vol.21 (2), p.124-131
Hauptverfasser: Stankov-Jovanovic, V.P., Nikolic-Mandic, S.D., Mandic, Lj.M., Mitic, V.D.
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container_issue 2
container_start_page 124
container_title Journal of clinical laboratory analysis
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creator Stankov-Jovanovic, V.P.
Nikolic-Mandic, S.D.
Mandic, Lj.M.
Mitic, V.D.
description A modification of the existing spectrophotometric kinetic method for the determination of pancuronium bromide (PCBr), based on pooled human serum cholinesterase (ChE, EC 3.1.1.8 acylcholine acylhydrolase) inhibition, was developed. Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as substrate and determination was performed at pH 7.6. Essential basic kinetic parameters were also determined: Michaelis‐Menten's constant KM=0.33 mmol/L, maximal reaction rate Vmax=42.29 µmol/L min, inhibition constant KI=0.34 µmol/L, and IC50=0.235 µmol/L. Linear dependence between the reaction rate and the inhibitor concentration exists in PCBr concentration range 8.29–265.28 nmol/L, which corresponds to the real sample concentrations from 0.166 to 5.306 µmol/L. The method detection limit was established to be 1.86 nmol/L and the quantification limit was 6.18 nmol/L. Precision of the method was tested for three pancuronium concentrations (16.58, 99.48, and 198.96 nmol/L). The relative standard deviation (RSD) was in the range 0.78–5.13%. Accuracy was examined by the standard addition method. The influence of substances usually present in serum and urine on the reaction rate was determined. The method developed was applied for PCBr determination in spiked serum and urine samples and in the urine taken during surgery. The method was proven to have good sensitivity, accuracy, and precision and can be considered suitable for clinical practice. J. Clin. Lab. Anal. 21:124–131, 2007. © 2007 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jcla.20162
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Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as substrate and determination was performed at pH 7.6. Essential basic kinetic parameters were also determined: Michaelis‐Menten's constant KM=0.33 mmol/L, maximal reaction rate Vmax=42.29 µmol/L min, inhibition constant KI=0.34 µmol/L, and IC50=0.235 µmol/L. Linear dependence between the reaction rate and the inhibitor concentration exists in PCBr concentration range 8.29–265.28 nmol/L, which corresponds to the real sample concentrations from 0.166 to 5.306 µmol/L. The method detection limit was established to be 1.86 nmol/L and the quantification limit was 6.18 nmol/L. Precision of the method was tested for three pancuronium concentrations (16.58, 99.48, and 198.96 nmol/L). The relative standard deviation (RSD) was in the range 0.78–5.13%. Accuracy was examined by the standard addition method. The influence of substances usually present in serum and urine on the reaction rate was determined. The method developed was applied for PCBr determination in spiked serum and urine samples and in the urine taken during surgery. The method was proven to have good sensitivity, accuracy, and precision and can be considered suitable for clinical practice. J. Clin. Lab. 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Clin. Lab. Anal</addtitle><description>A modification of the existing spectrophotometric kinetic method for the determination of pancuronium bromide (PCBr), based on pooled human serum cholinesterase (ChE, EC 3.1.1.8 acylcholine acylhydrolase) inhibition, was developed. Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as substrate and determination was performed at pH 7.6. Essential basic kinetic parameters were also determined: Michaelis‐Menten's constant KM=0.33 mmol/L, maximal reaction rate Vmax=42.29 µmol/L min, inhibition constant KI=0.34 µmol/L, and IC50=0.235 µmol/L. Linear dependence between the reaction rate and the inhibitor concentration exists in PCBr concentration range 8.29–265.28 nmol/L, which corresponds to the real sample concentrations from 0.166 to 5.306 µmol/L. The method detection limit was established to be 1.86 nmol/L and the quantification limit was 6.18 nmol/L. Precision of the method was tested for three pancuronium concentrations (16.58, 99.48, and 198.96 nmol/L). The relative standard deviation (RSD) was in the range 0.78–5.13%. Accuracy was examined by the standard addition method. The influence of substances usually present in serum and urine on the reaction rate was determined. The method developed was applied for PCBr determination in spiked serum and urine samples and in the urine taken during surgery. The method was proven to have good sensitivity, accuracy, and precision and can be considered suitable for clinical practice. J. Clin. Lab. Anal. 21:124–131, 2007. © 2007 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>buthyrylthiocholine</subject><subject>cholinesterase inhibition</subject><subject>Cholinesterase Inhibitors - analysis</subject><subject>Clinical Laboratory Techniques - methods</subject><subject>Female</subject><subject>Forensic Toxicology - methods</subject><subject>Humans</subject><subject>kinetic determination</subject><subject>Kinetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neuromuscular Nondepolarizing Agents - analysis</subject><subject>Original</subject><subject>Pancuronium - analysis</subject><subject>pancuronium bromide</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Spectrophotometry - methods</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtvEzEUhS0EakPphh-AvEaa4sfY49kgRREtRVErVUUgNpbHD3LbmXFkT4D8-zqkBNh0dRfnnO9KH0KvKTmjhLB3d7Y3Z4xQyZ6hGSWtqphi4jmaEaWaShHKj9HLnO8IIaql8ggd04YrIRWZoTzHQ3QQwJoJ4ohjwNPK43sY_QQWOz_5NMB4CNdmtJsUR9gMuEtxAOdxZ7J3uOQwZQzjCjqYYtpiH4K30y6wq9gXYi6w0n2FXgTTZ3_6eE_Q5_MPt4uP1fL64nIxX1ZWMMYqTnkQrfJOUmo9N50lnTSmFl1tZNs4ZhrWyqBERylvgjVMOsFka52sifSSn6D3e-560w3eWT9OyfR6nWAwaaujAf1_MsJKf48_tJR1W9wVwNs9wKaYc_LhsKVE79TrnXr9W30pv_n329_qo-tSoPvCT-j99gmU_rRYzv9Aq_0Girtfh41J91o2vBH6y9WFvqI351_FN6Fr_gDdgKFo</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Stankov-Jovanovic, V.P.</creator><creator>Nikolic-Mandic, S.D.</creator><creator>Mandic, Lj.M.</creator><creator>Mitic, V.D.</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>5PM</scope></search><sort><creationdate>2007</creationdate><title>A modification of the kinetic determination of pancuronium bromide based on its inhibitory effect on cholinesterase</title><author>Stankov-Jovanovic, V.P. ; Nikolic-Mandic, S.D. ; Mandic, Lj.M. ; Mitic, V.D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5222-313f598ed611ce3abc0b6aa45b4a697d2a7296f85b1137fca26d5269cd6406e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>buthyrylthiocholine</topic><topic>cholinesterase inhibition</topic><topic>Cholinesterase Inhibitors - analysis</topic><topic>Clinical Laboratory Techniques - methods</topic><topic>Female</topic><topic>Forensic Toxicology - methods</topic><topic>Humans</topic><topic>kinetic determination</topic><topic>Kinetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neuromuscular Nondepolarizing Agents - analysis</topic><topic>Original</topic><topic>Pancuronium - analysis</topic><topic>pancuronium bromide</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Spectrophotometry - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stankov-Jovanovic, V.P.</creatorcontrib><creatorcontrib>Nikolic-Mandic, S.D.</creatorcontrib><creatorcontrib>Mandic, Lj.M.</creatorcontrib><creatorcontrib>Mitic, V.D.</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical laboratory analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stankov-Jovanovic, V.P.</au><au>Nikolic-Mandic, S.D.</au><au>Mandic, Lj.M.</au><au>Mitic, V.D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A modification of the kinetic determination of pancuronium bromide based on its inhibitory effect on cholinesterase</atitle><jtitle>Journal of clinical laboratory analysis</jtitle><addtitle>J. Clin. Lab. Anal</addtitle><date>2007</date><risdate>2007</risdate><volume>21</volume><issue>2</issue><spage>124</spage><epage>131</epage><pages>124-131</pages><issn>0887-8013</issn><eissn>1098-2825</eissn><abstract>A modification of the existing spectrophotometric kinetic method for the determination of pancuronium bromide (PCBr), based on pooled human serum cholinesterase (ChE, EC 3.1.1.8 acylcholine acylhydrolase) inhibition, was developed. Butyrylthiocholine iodide (concentration 1.667 mmol/L) was used as substrate and determination was performed at pH 7.6. Essential basic kinetic parameters were also determined: Michaelis‐Menten's constant KM=0.33 mmol/L, maximal reaction rate Vmax=42.29 µmol/L min, inhibition constant KI=0.34 µmol/L, and IC50=0.235 µmol/L. Linear dependence between the reaction rate and the inhibitor concentration exists in PCBr concentration range 8.29–265.28 nmol/L, which corresponds to the real sample concentrations from 0.166 to 5.306 µmol/L. The method detection limit was established to be 1.86 nmol/L and the quantification limit was 6.18 nmol/L. Precision of the method was tested for three pancuronium concentrations (16.58, 99.48, and 198.96 nmol/L). The relative standard deviation (RSD) was in the range 0.78–5.13%. Accuracy was examined by the standard addition method. The influence of substances usually present in serum and urine on the reaction rate was determined. The method developed was applied for PCBr determination in spiked serum and urine samples and in the urine taken during surgery. The method was proven to have good sensitivity, accuracy, and precision and can be considered suitable for clinical practice. J. Clin. Lab. Anal. 21:124–131, 2007. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17385680</pmid><doi>10.1002/jcla.20162</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
buthyrylthiocholine
cholinesterase inhibition
Cholinesterase Inhibitors - analysis
Clinical Laboratory Techniques - methods
Female
Forensic Toxicology - methods
Humans
kinetic determination
Kinetics
Male
Middle Aged
Neuromuscular Nondepolarizing Agents - analysis
Original
Pancuronium - analysis
pancuronium bromide
Reproducibility of Results
Sensitivity and Specificity
Spectrophotometry - methods
title A modification of the kinetic determination of pancuronium bromide based on its inhibitory effect on cholinesterase
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