An LC-MS/MS method to determine vancomycin in plasma (total and unbound), urine and renal replacement therapy effluent.
Identifieur interne : 000B04 ( PubMed/Corpus ); précédent : 000B03; suivant : 000B05An LC-MS/MS method to determine vancomycin in plasma (total and unbound), urine and renal replacement therapy effluent.
Auteurs : Suzanne L. Parker ; Yarmarly C. Guerra Valero ; Jenny L. Ord Ez Mejia ; Claire Roger ; Jeffrey Lipman ; Jason A. Roberts ; Steven C. WallisSource :
- Bioanalysis [ 1757-6199 ] ; 2017.
Abstract
Critical illness and medical interventions, such as renal replacement therapy, can cause changes to vancomycin pharmacokinetics and lead to suboptimal dosing. To comprehensively characterize vancomycin pharmacokinetic a method must measure vancomycin in a range of clinical matrices.
DOI: 10.4155/bio-2017-0019
PubMed: 28617036
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pubmed:28617036Le document en format XML
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<author><name sortKey="Parker, Suzanne L" sort="Parker, Suzanne L" uniqKey="Parker S" first="Suzanne L" last="Parker">Suzanne L. Parker</name>
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<author><name sortKey="Guerra Valero, Yarmarly C" sort="Guerra Valero, Yarmarly C" uniqKey="Guerra Valero Y" first="Yarmarly C" last="Guerra Valero">Yarmarly C. Guerra Valero</name>
<affiliation><nlm:affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</nlm:affiliation>
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<author><name sortKey="Ord Ez Mejia, Jenny L" sort="Ord Ez Mejia, Jenny L" uniqKey="Ord Ez Mejia J" first="Jenny L" last="Ord Ez Mejia">Jenny L. Ord Ez Mejia</name>
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<author><name sortKey="Roger, Claire" sort="Roger, Claire" uniqKey="Roger C" first="Claire" last="Roger">Claire Roger</name>
<affiliation><nlm:affiliation>CHU Nimes, Serv Reanimat, Pole Anesthesie Reanimat Douleur Urgence, Nimes, France.</nlm:affiliation>
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<author><name sortKey="Lipman, Jeffrey" sort="Lipman, Jeffrey" uniqKey="Lipman J" first="Jeffrey" last="Lipman">Jeffrey Lipman</name>
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<author><name sortKey="Roberts, Jason A" sort="Roberts, Jason A" uniqKey="Roberts J" first="Jason A" last="Roberts">Jason A. Roberts</name>
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<author><name sortKey="Wallis, Steven C" sort="Wallis, Steven C" uniqKey="Wallis S" first="Steven C" last="Wallis">Steven C. Wallis</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">An LC-MS/MS method to determine vancomycin in plasma (total and unbound), urine and renal replacement therapy effluent.</title>
<author><name sortKey="Parker, Suzanne L" sort="Parker, Suzanne L" uniqKey="Parker S" first="Suzanne L" last="Parker">Suzanne L. Parker</name>
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<author><name sortKey="Guerra Valero, Yarmarly C" sort="Guerra Valero, Yarmarly C" uniqKey="Guerra Valero Y" first="Yarmarly C" last="Guerra Valero">Yarmarly C. Guerra Valero</name>
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<author><name sortKey="Ord Ez Mejia, Jenny L" sort="Ord Ez Mejia, Jenny L" uniqKey="Ord Ez Mejia J" first="Jenny L" last="Ord Ez Mejia">Jenny L. Ord Ez Mejia</name>
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<author><name sortKey="Roger, Claire" sort="Roger, Claire" uniqKey="Roger C" first="Claire" last="Roger">Claire Roger</name>
<affiliation><nlm:affiliation>CHU Nimes, Serv Reanimat, Pole Anesthesie Reanimat Douleur Urgence, Nimes, France.</nlm:affiliation>
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<author><name sortKey="Lipman, Jeffrey" sort="Lipman, Jeffrey" uniqKey="Lipman J" first="Jeffrey" last="Lipman">Jeffrey Lipman</name>
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<series><title level="j">Bioanalysis</title>
<idno type="eISSN">1757-6199</idno>
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<front><div type="abstract" xml:lang="en">Critical illness and medical interventions, such as renal replacement therapy, can cause changes to vancomycin pharmacokinetics and lead to suboptimal dosing. To comprehensively characterize vancomycin pharmacokinetic a method must measure vancomycin in a range of clinical matrices.</div>
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<pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">28617036</PMID>
<DateCreated><Year>2017</Year>
<Month>06</Month>
<Day>15</Day>
</DateCreated>
<DateRevised><Year>2017</Year>
<Month>07</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1757-6199</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>9</Volume>
<Issue>12</Issue>
<PubDate><Year>2017</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Bioanalysis</Title>
<ISOAbbreviation>Bioanalysis</ISOAbbreviation>
</Journal>
<ArticleTitle>An LC-MS/MS method to determine vancomycin in plasma (total and unbound), urine and renal replacement therapy effluent.</ArticleTitle>
<Pagination><MedlinePgn>911-924</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.4155/bio-2017-0019</ELocationID>
<Abstract><AbstractText Label="AIM" NlmCategory="OBJECTIVE">Critical illness and medical interventions, such as renal replacement therapy, can cause changes to vancomycin pharmacokinetics and lead to suboptimal dosing. To comprehensively characterize vancomycin pharmacokinetic a method must measure vancomycin in a range of clinical matrices.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A LC-MS/MS method was developed using hydrophilic interaction liquid chromatography and microsample volumes, where possible. For all matrices, the linear concentration range was 1-100 μg/ml, interassay accuracy and precision was within 15%, and recovery above 80%. No matrix effects were observed. Calibration equivalence may be applied for some matrix combinations.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">A method for the analysis of vancomycin in plasma (total, unbound), urine and renal replacement therapy effluent, suitable for use in any patient pharmacokinetic study, has been developed and validated.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Parker</LastName>
<ForeName>Suzanne L</ForeName>
<Initials>SL</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Guerra Valero</LastName>
<ForeName>Yarmarly C</ForeName>
<Initials>YC</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Ordóñez Mejia</LastName>
<ForeName>Jenny L</ForeName>
<Initials>JL</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Roger</LastName>
<ForeName>Claire</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>CHU Nimes, Serv Reanimat, Pole Anesthesie Reanimat Douleur Urgence, Nimes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lipman</LastName>
<ForeName>Jeffrey</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Intensive Care Medicine, Royal Brisbane & Women's Hospital, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Faculty of Health, Queensland University of Technology, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Roberts</LastName>
<ForeName>Jason A</ForeName>
<Initials>JA</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Faculty of Health, Queensland University of Technology, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Pharmacy, Royal Brisbane & Women's Hospital, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Centre of Translational Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wallis</LastName>
<ForeName>Steven C</ForeName>
<Initials>SC</Initials>
<AffiliationInfo><Affiliation>Burns, Trauma & Critical Care Research Centre, UQ Centre for Clinical Research, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2017</Year>
<Month>06</Month>
<Day>15</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Bioanalysis</MedlineTA>
<NlmUniqueID>101512484</NlmUniqueID>
<ISSNLinking>1757-6180</ISSNLinking>
</MedlineJournalInfo>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">dialysis</Keyword>
<Keyword MajorTopicYN="N">mass spectrometry</Keyword>
<Keyword MajorTopicYN="N">pharmacodynamics</Keyword>
<Keyword MajorTopicYN="N">pharmacokinetic</Keyword>
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