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Dried Blood Spot Technique Applied in Therapeutic Drug Monitoring of Anticancer Drugs: a Review on Conversion Methods to Correlate Plasma and Dried Blood Spot Concentrations
Background Anticancer drugs are notoriously characterized by a low therapeutic index, the introduction of therapeutic drug monitoring (TDM) in oncologic clinical practice could therefore be fundamental to improve treatment efficacy. In this context, an attractive technique to overcome the convention...
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Published in: | Pharmaceutical research 2021-05, Vol.38 (5), p.759-778 |
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description | Background
Anticancer drugs are notoriously characterized by a low therapeutic index, the introduction of therapeutic drug monitoring (TDM) in oncologic clinical practice could therefore be fundamental to improve treatment efficacy. In this context, an attractive technique to overcome the conventional venous sampling limits and simplify TDM application is represented by dried blood spot (DBS). Despite the significant progress made in bioanalysis exploiting DBS, there is still the need to tackle some challenges that limit the application of this technology: one of the main issues is the comparison of drug concentrations obtained from DBS with those obtained from reference matrix (e.g., plasma). In fact, the use of DBS assays to estimate plasma concentrations is highly dependent on the chemical-physical characteristics of the measured analyte, in particular on how these properties determine the drug partition in whole blood.
Methods
In the present review, we introduce a critical investigation of the DBS-to-plasma concentration conversion methods proposed in the last ten years and applied to quantitative bioanalysis of anticancer drugs in DBS matrix. To prove the concordance between DBS and plasma concentration, the results of statistical tests applied and the presence or absence of trends or biases were also considered. |
doi_str_mv | 10.1007/s11095-021-03036-6 |
format | article |
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Anticancer drugs are notoriously characterized by a low therapeutic index, the introduction of therapeutic drug monitoring (TDM) in oncologic clinical practice could therefore be fundamental to improve treatment efficacy. In this context, an attractive technique to overcome the conventional venous sampling limits and simplify TDM application is represented by dried blood spot (DBS). Despite the significant progress made in bioanalysis exploiting DBS, there is still the need to tackle some challenges that limit the application of this technology: one of the main issues is the comparison of drug concentrations obtained from DBS with those obtained from reference matrix (e.g., plasma). In fact, the use of DBS assays to estimate plasma concentrations is highly dependent on the chemical-physical characteristics of the measured analyte, in particular on how these properties determine the drug partition in whole blood.
Methods
In the present review, we introduce a critical investigation of the DBS-to-plasma concentration conversion methods proposed in the last ten years and applied to quantitative bioanalysis of anticancer drugs in DBS matrix. To prove the concordance between DBS and plasma concentration, the results of statistical tests applied and the presence or absence of trends or biases were also considered.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-021-03036-6</identifier><identifier>PMID: 33846903</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Antineoplastic drugs ; Antitumor agents ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Blood ; Cancer ; Expert Review ; Medical Law ; Pharmacology/Toxicology ; Pharmacy ; Physical characteristics ; Plasma ; Statistical analysis ; Therapeutic drug monitoring</subject><ispartof>Pharmaceutical research, 2021-05, Vol.38 (5), p.759-778</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-1771993b7e76b77fce6b250464d1b3323b9e06df0c176094e28ab1d885824c763</citedby><cites>FETCH-LOGICAL-c552t-1771993b7e76b77fce6b250464d1b3323b9e06df0c176094e28ab1d885824c763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33846903$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iacuzzi, Valentina</creatorcontrib><creatorcontrib>Posocco, Bianca</creatorcontrib><creatorcontrib>Zanchetta, Martina</creatorcontrib><creatorcontrib>Gagno, Sara</creatorcontrib><creatorcontrib>Poetto, Ariana Soledad</creatorcontrib><creatorcontrib>Guardascione, Michela</creatorcontrib><creatorcontrib>Toffoli, Giuseppe</creatorcontrib><title>Dried Blood Spot Technique Applied in Therapeutic Drug Monitoring of Anticancer Drugs: a Review on Conversion Methods to Correlate Plasma and Dried Blood Spot Concentrations</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Background
Anticancer drugs are notoriously characterized by a low therapeutic index, the introduction of therapeutic drug monitoring (TDM) in oncologic clinical practice could therefore be fundamental to improve treatment efficacy. In this context, an attractive technique to overcome the conventional venous sampling limits and simplify TDM application is represented by dried blood spot (DBS). Despite the significant progress made in bioanalysis exploiting DBS, there is still the need to tackle some challenges that limit the application of this technology: one of the main issues is the comparison of drug concentrations obtained from DBS with those obtained from reference matrix (e.g., plasma). In fact, the use of DBS assays to estimate plasma concentrations is highly dependent on the chemical-physical characteristics of the measured analyte, in particular on how these properties determine the drug partition in whole blood.
Methods
In the present review, we introduce a critical investigation of the DBS-to-plasma concentration conversion methods proposed in the last ten years and applied to quantitative bioanalysis of anticancer drugs in DBS matrix. To prove the concordance between DBS and plasma concentration, the results of statistical tests applied and the presence or absence of trends or biases were also considered.</description><subject>Antineoplastic drugs</subject><subject>Antitumor agents</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Blood</subject><subject>Cancer</subject><subject>Expert Review</subject><subject>Medical Law</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Physical characteristics</subject><subject>Plasma</subject><subject>Statistical analysis</subject><subject>Therapeutic drug monitoring</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9UV1vFCEUJUZj1-of8MGQ-DwVBgYG39atVZM2Gl0T3wjD3NmlmYEpsDX9Uf5H2W79isbwALnnnHsP9yD0lJITSoh8kSglqqlITSvCCBOVuIcWtJGsUoR_uY8WRNa8aiWnR-hRSpeEkJYq_hAdMdZyoQhboG-n0UGPX40h9PjTHDJeg916d7UDvJzncQ86j9dbiGaGXXYWn8bdBl8E73KIzm9wGPDSF8B4C_EWTS-xwR_h2sFXHDxeBX8NMbnyvIC8DX3COZRqjDCaDPjDaNJksPE9_stN0VrwOZpc5OkxejCYMcGTu_sYfT57vV69rc7fv3m3Wp5XtmnqXFEpqVKskyBFJ-VgQXR1Q7jgPe0Yq1mngIh-IJZKQRSHujUd7du2aWtupWDH6Pmh7xxD2UTK-jLsoi8jdd0wWZbP1W-sjRlBOz-E4tNOLlm9lFxypoRqCuvkH6xyepicDR4GV-p_COqDwMaQUoRBz9FNJt5oSvQ-eH0IXpfg9W3weu_l2Z3jXTdB_1PyI-lCYAdCmvepQfz1pf-0_Q5l0bhi</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Iacuzzi, Valentina</creator><creator>Posocco, Bianca</creator><creator>Zanchetta, Martina</creator><creator>Gagno, Sara</creator><creator>Poetto, Ariana Soledad</creator><creator>Guardascione, Michela</creator><creator>Toffoli, Giuseppe</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20210501</creationdate><title>Dried Blood Spot Technique Applied in Therapeutic Drug Monitoring of Anticancer Drugs: a Review on Conversion Methods to Correlate Plasma and Dried Blood Spot Concentrations</title><author>Iacuzzi, Valentina ; Posocco, Bianca ; Zanchetta, Martina ; Gagno, Sara ; Poetto, Ariana Soledad ; Guardascione, Michela ; Toffoli, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c552t-1771993b7e76b77fce6b250464d1b3323b9e06df0c176094e28ab1d885824c763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antineoplastic drugs</topic><topic>Antitumor agents</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Blood</topic><topic>Cancer</topic><topic>Expert Review</topic><topic>Medical Law</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Physical characteristics</topic><topic>Plasma</topic><topic>Statistical analysis</topic><topic>Therapeutic drug monitoring</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iacuzzi, Valentina</creatorcontrib><creatorcontrib>Posocco, Bianca</creatorcontrib><creatorcontrib>Zanchetta, Martina</creatorcontrib><creatorcontrib>Gagno, Sara</creatorcontrib><creatorcontrib>Poetto, Ariana Soledad</creatorcontrib><creatorcontrib>Guardascione, Michela</creatorcontrib><creatorcontrib>Toffoli, Giuseppe</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iacuzzi, Valentina</au><au>Posocco, Bianca</au><au>Zanchetta, Martina</au><au>Gagno, Sara</au><au>Poetto, Ariana Soledad</au><au>Guardascione, Michela</au><au>Toffoli, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dried Blood Spot Technique Applied in Therapeutic Drug Monitoring of Anticancer Drugs: a Review on Conversion Methods to Correlate Plasma and Dried Blood Spot Concentrations</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>38</volume><issue>5</issue><spage>759</spage><epage>778</epage><pages>759-778</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>Background
Anticancer drugs are notoriously characterized by a low therapeutic index, the introduction of therapeutic drug monitoring (TDM) in oncologic clinical practice could therefore be fundamental to improve treatment efficacy. In this context, an attractive technique to overcome the conventional venous sampling limits and simplify TDM application is represented by dried blood spot (DBS). Despite the significant progress made in bioanalysis exploiting DBS, there is still the need to tackle some challenges that limit the application of this technology: one of the main issues is the comparison of drug concentrations obtained from DBS with those obtained from reference matrix (e.g., plasma). In fact, the use of DBS assays to estimate plasma concentrations is highly dependent on the chemical-physical characteristics of the measured analyte, in particular on how these properties determine the drug partition in whole blood.
Methods
In the present review, we introduce a critical investigation of the DBS-to-plasma concentration conversion methods proposed in the last ten years and applied to quantitative bioanalysis of anticancer drugs in DBS matrix. To prove the concordance between DBS and plasma concentration, the results of statistical tests applied and the presence or absence of trends or biases were also considered.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>33846903</pmid><doi>10.1007/s11095-021-03036-6</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic drugs Antitumor agents Biochemistry Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Blood Cancer Expert Review Medical Law Pharmacology/Toxicology Pharmacy Physical characteristics Plasma Statistical analysis Therapeutic drug monitoring |
title | Dried Blood Spot Technique Applied in Therapeutic Drug Monitoring of Anticancer Drugs: a Review on Conversion Methods to Correlate Plasma and Dried Blood Spot Concentrations |
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