Point-of-care therapeutic drug monitoring of adalimumab by integrating a FO-SPR biosensor in a self-powered microfluidic cartridge
Disease treatment with advanced biological therapies such as adalimumab (ADM), although largely beneficial, is still costly and suffers from loss of response. To tackle these aspects, therapeutic drug monitoring (TDM) is proposed to improve treatment dosing and efficacy, but is often associated with...
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Veröffentlicht in: | Biosensors & bioelectronics 2022-06, Vol.206, p.114125-114125, Article 114125 |
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creator | Qu, Jia-Huan Ordutowski, Henry Van Tricht, Charlotte Verbruggen, Ruben Barcenas Gallardo, Alicia Bulcaen, Mattijs Ciwinska, Marta Gutierrez Cisneros, Carolina Devriese, Christophe Guluzade, Sona Janssens, Xander Kornblum, Sophie Lu, Yuansheng Marolt, Nika Nanjappan, Chezhiyan Rutten, Eline Vanhauwaert, Eline Geukens, Nick Thomas, Debby Dal Dosso, Francesco Safdar, Saba Spasic, Dragana Lammertyn, Jeroen |
description | Disease treatment with advanced biological therapies such as adalimumab (ADM), although largely beneficial, is still costly and suffers from loss of response. To tackle these aspects, therapeutic drug monitoring (TDM) is proposed to improve treatment dosing and efficacy, but is often associated with long sampling-to-result workflows. Here, we present an in-house constructed ADM-sensor, allowing TDM of ADM at the doctor's office. This biosensor brings fiber optic surface plasmon resonance (FO-SPR), combined with self-powered microfluidics, to a point of care (POC) setting for the first time. After developing a rapid FO-SPR sandwich bioassay for ADM detection on a commercial FO-SPR device, this bioassay was implemented on the fully-integrated ADM-sensor. For the latter, we combined (I) a gold coated fiber optic (FO) probe for bioassay implementation and (II) an FO-SPR readout system with (III) the self-powered iSIMPLE microfluidic technology empowering plasma sample and reagent mixing on the-cartridge as well as connection to the FO-SPR readout system. With a calculated limit of detection (LOD) of 0.35 μg/mL in undiluted plasma, and a total time-to-result (TTR) within 12 min, this innovative biosensor demonstrated a comparable performance to existing POC biosensors for ADM quantification in patient plasma samples, while requiring only 1 μL of plasma. Whereas this study demonstrates great potential for FO-SPR biosensing at the POC using ADM as a model case, it also shows huge potential for bedside TDM of other drugs (e.g. other immunosuppressants, anti-epileptics and antibiotics), as the bioassay is highly amenable to adaptation.
•A FO-SPR biosensor was combined with self-powered iSIMPLE technology.•The FO-SPR one-step sandwich bioassay was established for rapid adalimumab detection.•Reagent mixing on the microfluidic cartridge was realized by an optimized mixing design.•Plasma sample dilution was integrated on self-powered iSIMPLE microfluidic cartridge.•The ADM-sensor delivered measurement using only 1 μL of plasma within 12 min. |
doi_str_mv | 10.1016/j.bios.2022.114125 |
format | Article |
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•A FO-SPR biosensor was combined with self-powered iSIMPLE technology.•The FO-SPR one-step sandwich bioassay was established for rapid adalimumab detection.•Reagent mixing on the microfluidic cartridge was realized by an optimized mixing design.•Plasma sample dilution was integrated on self-powered iSIMPLE microfluidic cartridge.•The ADM-sensor delivered measurement using only 1 μL of plasma within 12 min.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2022.114125</identifier><identifier>PMID: 35255315</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adalimumab ; Biosensing Techniques ; Drug Monitoring ; Fiber Optic Technology ; Fiber-optic surface plasmon resonance ; Humans ; Microfluidics ; Patient blood plasma ; Point of care ; Point-of-Care Systems ; Self-powered microfluidics ; Surface Plasmon Resonance ; Therapeutic drug monitoring</subject><ispartof>Biosensors & bioelectronics, 2022-06, Vol.206, p.114125-114125, Article 114125</ispartof><rights>2022 Elsevier B.V.</rights><rights>Copyright © 2022 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-18f472b4ea7684a358de03d4eb99f9c95bcd99b8f021dad6e2160dc176c1448e3</citedby><cites>FETCH-LOGICAL-c466t-18f472b4ea7684a358de03d4eb99f9c95bcd99b8f021dad6e2160dc176c1448e3</cites><orcidid>0000-0003-3075-9846 ; 0000-0003-2729-0071 ; 0000-0002-2172-1427 ; 0000-0001-8064-5164 ; 0000-0001-7989-9255 ; 0000-0002-8829-3180 ; 0000-0002-5828-4435 ; 0000-0003-4546-5154 ; 0000-0003-2900-1181 ; 0000-0001-6767-8113 ; 0000-0002-2713-6798</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bios.2022.114125$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35255315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qu, Jia-Huan</creatorcontrib><creatorcontrib>Ordutowski, Henry</creatorcontrib><creatorcontrib>Van Tricht, Charlotte</creatorcontrib><creatorcontrib>Verbruggen, Ruben</creatorcontrib><creatorcontrib>Barcenas Gallardo, Alicia</creatorcontrib><creatorcontrib>Bulcaen, Mattijs</creatorcontrib><creatorcontrib>Ciwinska, Marta</creatorcontrib><creatorcontrib>Gutierrez Cisneros, Carolina</creatorcontrib><creatorcontrib>Devriese, Christophe</creatorcontrib><creatorcontrib>Guluzade, Sona</creatorcontrib><creatorcontrib>Janssens, Xander</creatorcontrib><creatorcontrib>Kornblum, Sophie</creatorcontrib><creatorcontrib>Lu, Yuansheng</creatorcontrib><creatorcontrib>Marolt, Nika</creatorcontrib><creatorcontrib>Nanjappan, Chezhiyan</creatorcontrib><creatorcontrib>Rutten, Eline</creatorcontrib><creatorcontrib>Vanhauwaert, Eline</creatorcontrib><creatorcontrib>Geukens, Nick</creatorcontrib><creatorcontrib>Thomas, Debby</creatorcontrib><creatorcontrib>Dal Dosso, Francesco</creatorcontrib><creatorcontrib>Safdar, Saba</creatorcontrib><creatorcontrib>Spasic, Dragana</creatorcontrib><creatorcontrib>Lammertyn, Jeroen</creatorcontrib><title>Point-of-care therapeutic drug monitoring of adalimumab by integrating a FO-SPR biosensor in a self-powered microfluidic cartridge</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>Disease treatment with advanced biological therapies such as adalimumab (ADM), although largely beneficial, is still costly and suffers from loss of response. To tackle these aspects, therapeutic drug monitoring (TDM) is proposed to improve treatment dosing and efficacy, but is often associated with long sampling-to-result workflows. Here, we present an in-house constructed ADM-sensor, allowing TDM of ADM at the doctor's office. This biosensor brings fiber optic surface plasmon resonance (FO-SPR), combined with self-powered microfluidics, to a point of care (POC) setting for the first time. After developing a rapid FO-SPR sandwich bioassay for ADM detection on a commercial FO-SPR device, this bioassay was implemented on the fully-integrated ADM-sensor. For the latter, we combined (I) a gold coated fiber optic (FO) probe for bioassay implementation and (II) an FO-SPR readout system with (III) the self-powered iSIMPLE microfluidic technology empowering plasma sample and reagent mixing on the-cartridge as well as connection to the FO-SPR readout system. With a calculated limit of detection (LOD) of 0.35 μg/mL in undiluted plasma, and a total time-to-result (TTR) within 12 min, this innovative biosensor demonstrated a comparable performance to existing POC biosensors for ADM quantification in patient plasma samples, while requiring only 1 μL of plasma. Whereas this study demonstrates great potential for FO-SPR biosensing at the POC using ADM as a model case, it also shows huge potential for bedside TDM of other drugs (e.g. other immunosuppressants, anti-epileptics and antibiotics), as the bioassay is highly amenable to adaptation.
•A FO-SPR biosensor was combined with self-powered iSIMPLE technology.•The FO-SPR one-step sandwich bioassay was established for rapid adalimumab detection.•Reagent mixing on the microfluidic cartridge was realized by an optimized mixing design.•Plasma sample dilution was integrated on self-powered iSIMPLE microfluidic cartridge.•The ADM-sensor delivered measurement using only 1 μL of plasma within 12 min.</description><subject>Adalimumab</subject><subject>Biosensing Techniques</subject><subject>Drug Monitoring</subject><subject>Fiber Optic Technology</subject><subject>Fiber-optic surface plasmon resonance</subject><subject>Humans</subject><subject>Microfluidics</subject><subject>Patient blood plasma</subject><subject>Point of care</subject><subject>Point-of-Care Systems</subject><subject>Self-powered microfluidics</subject><subject>Surface Plasmon Resonance</subject><subject>Therapeutic drug monitoring</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UE2LFDEUDKK44-of8CA5esmY7-6AF1lcFRZ28eMc0snLmKG7Mybdyl795aaZ1aOnB-9V1asqhF4yumeU6TfH_ZBy3XPK-Z4xybh6hHas7wSRXKjHaEeN0kRpLS7Qs1qPlNKOGfoUXQjFlRJM7dDvu5zmheRIvCuAl-9Q3AnWJXkcynrAU57TkkuaDzhH7IIb07RObsDDPW5EOBS3bEeHr2_Jl7vPeLMEc82lndu2whjJKf-CAgFPyZccxzWFJt_-LSWFAzxHT6IbK7x4mJfo2_X7r1cfyc3th09X726Il1ovhPVRdnyQ4DrdSydUH4CKIGEwJhpv1OCDMUMfKWfBBQ2caRo867RnUvYgLtHrs-6p5B8r1MVOqXoYRzdDXqvlWnSCGcN5g_IztPmttUC0p5ImV-4to3br3h7tFtRu3dtz94306kF_HSYI_yh_y26At2cAtJQ_ExRbfYLZQ0gF_GJDTv_T_wOzY5ce</recordid><startdate>20220615</startdate><enddate>20220615</enddate><creator>Qu, Jia-Huan</creator><creator>Ordutowski, Henry</creator><creator>Van Tricht, Charlotte</creator><creator>Verbruggen, Ruben</creator><creator>Barcenas Gallardo, Alicia</creator><creator>Bulcaen, Mattijs</creator><creator>Ciwinska, Marta</creator><creator>Gutierrez Cisneros, Carolina</creator><creator>Devriese, Christophe</creator><creator>Guluzade, Sona</creator><creator>Janssens, Xander</creator><creator>Kornblum, Sophie</creator><creator>Lu, Yuansheng</creator><creator>Marolt, Nika</creator><creator>Nanjappan, Chezhiyan</creator><creator>Rutten, Eline</creator><creator>Vanhauwaert, Eline</creator><creator>Geukens, Nick</creator><creator>Thomas, Debby</creator><creator>Dal Dosso, Francesco</creator><creator>Safdar, Saba</creator><creator>Spasic, Dragana</creator><creator>Lammertyn, Jeroen</creator><general>Elsevier B.V</general><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><orcidid>https://orcid.org/0000-0003-3075-9846</orcidid><orcidid>https://orcid.org/0000-0003-2729-0071</orcidid><orcidid>https://orcid.org/0000-0002-2172-1427</orcidid><orcidid>https://orcid.org/0000-0001-8064-5164</orcidid><orcidid>https://orcid.org/0000-0001-7989-9255</orcidid><orcidid>https://orcid.org/0000-0002-8829-3180</orcidid><orcidid>https://orcid.org/0000-0002-5828-4435</orcidid><orcidid>https://orcid.org/0000-0003-4546-5154</orcidid><orcidid>https://orcid.org/0000-0003-2900-1181</orcidid><orcidid>https://orcid.org/0000-0001-6767-8113</orcidid><orcidid>https://orcid.org/0000-0002-2713-6798</orcidid></search><sort><creationdate>20220615</creationdate><title>Point-of-care therapeutic drug monitoring of adalimumab by integrating a FO-SPR biosensor in a self-powered microfluidic cartridge</title><author>Qu, Jia-Huan ; Ordutowski, Henry ; Van Tricht, Charlotte ; Verbruggen, Ruben ; Barcenas Gallardo, Alicia ; Bulcaen, Mattijs ; Ciwinska, Marta ; Gutierrez Cisneros, Carolina ; Devriese, Christophe ; Guluzade, Sona ; Janssens, Xander ; Kornblum, Sophie ; Lu, Yuansheng ; Marolt, Nika ; Nanjappan, Chezhiyan ; Rutten, Eline ; Vanhauwaert, Eline ; Geukens, Nick ; Thomas, Debby ; Dal Dosso, Francesco ; Safdar, Saba ; Spasic, Dragana ; Lammertyn, Jeroen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-18f472b4ea7684a358de03d4eb99f9c95bcd99b8f021dad6e2160dc176c1448e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adalimumab</topic><topic>Biosensing Techniques</topic><topic>Drug Monitoring</topic><topic>Fiber Optic Technology</topic><topic>Fiber-optic surface plasmon resonance</topic><topic>Humans</topic><topic>Microfluidics</topic><topic>Patient blood plasma</topic><topic>Point of care</topic><topic>Point-of-Care Systems</topic><topic>Self-powered microfluidics</topic><topic>Surface Plasmon Resonance</topic><topic>Therapeutic drug monitoring</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qu, Jia-Huan</creatorcontrib><creatorcontrib>Ordutowski, Henry</creatorcontrib><creatorcontrib>Van Tricht, Charlotte</creatorcontrib><creatorcontrib>Verbruggen, Ruben</creatorcontrib><creatorcontrib>Barcenas Gallardo, Alicia</creatorcontrib><creatorcontrib>Bulcaen, Mattijs</creatorcontrib><creatorcontrib>Ciwinska, Marta</creatorcontrib><creatorcontrib>Gutierrez Cisneros, Carolina</creatorcontrib><creatorcontrib>Devriese, Christophe</creatorcontrib><creatorcontrib>Guluzade, Sona</creatorcontrib><creatorcontrib>Janssens, Xander</creatorcontrib><creatorcontrib>Kornblum, Sophie</creatorcontrib><creatorcontrib>Lu, Yuansheng</creatorcontrib><creatorcontrib>Marolt, Nika</creatorcontrib><creatorcontrib>Nanjappan, Chezhiyan</creatorcontrib><creatorcontrib>Rutten, Eline</creatorcontrib><creatorcontrib>Vanhauwaert, Eline</creatorcontrib><creatorcontrib>Geukens, Nick</creatorcontrib><creatorcontrib>Thomas, Debby</creatorcontrib><creatorcontrib>Dal Dosso, Francesco</creatorcontrib><creatorcontrib>Safdar, Saba</creatorcontrib><creatorcontrib>Spasic, Dragana</creatorcontrib><creatorcontrib>Lammertyn, Jeroen</creatorcontrib><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>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qu, Jia-Huan</au><au>Ordutowski, Henry</au><au>Van Tricht, Charlotte</au><au>Verbruggen, Ruben</au><au>Barcenas Gallardo, Alicia</au><au>Bulcaen, Mattijs</au><au>Ciwinska, Marta</au><au>Gutierrez Cisneros, Carolina</au><au>Devriese, Christophe</au><au>Guluzade, Sona</au><au>Janssens, Xander</au><au>Kornblum, Sophie</au><au>Lu, Yuansheng</au><au>Marolt, Nika</au><au>Nanjappan, Chezhiyan</au><au>Rutten, Eline</au><au>Vanhauwaert, Eline</au><au>Geukens, Nick</au><au>Thomas, Debby</au><au>Dal Dosso, Francesco</au><au>Safdar, Saba</au><au>Spasic, Dragana</au><au>Lammertyn, Jeroen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Point-of-care therapeutic drug monitoring of adalimumab by integrating a FO-SPR biosensor in a self-powered microfluidic cartridge</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2022-06-15</date><risdate>2022</risdate><volume>206</volume><spage>114125</spage><epage>114125</epage><pages>114125-114125</pages><artnum>114125</artnum><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Disease treatment with advanced biological therapies such as adalimumab (ADM), although largely beneficial, is still costly and suffers from loss of response. To tackle these aspects, therapeutic drug monitoring (TDM) is proposed to improve treatment dosing and efficacy, but is often associated with long sampling-to-result workflows. Here, we present an in-house constructed ADM-sensor, allowing TDM of ADM at the doctor's office. This biosensor brings fiber optic surface plasmon resonance (FO-SPR), combined with self-powered microfluidics, to a point of care (POC) setting for the first time. After developing a rapid FO-SPR sandwich bioassay for ADM detection on a commercial FO-SPR device, this bioassay was implemented on the fully-integrated ADM-sensor. For the latter, we combined (I) a gold coated fiber optic (FO) probe for bioassay implementation and (II) an FO-SPR readout system with (III) the self-powered iSIMPLE microfluidic technology empowering plasma sample and reagent mixing on the-cartridge as well as connection to the FO-SPR readout system. With a calculated limit of detection (LOD) of 0.35 μg/mL in undiluted plasma, and a total time-to-result (TTR) within 12 min, this innovative biosensor demonstrated a comparable performance to existing POC biosensors for ADM quantification in patient plasma samples, while requiring only 1 μL of plasma. Whereas this study demonstrates great potential for FO-SPR biosensing at the POC using ADM as a model case, it also shows huge potential for bedside TDM of other drugs (e.g. other immunosuppressants, anti-epileptics and antibiotics), as the bioassay is highly amenable to adaptation.
•A FO-SPR biosensor was combined with self-powered iSIMPLE technology.•The FO-SPR one-step sandwich bioassay was established for rapid adalimumab detection.•Reagent mixing on the microfluidic cartridge was realized by an optimized mixing design.•Plasma sample dilution was integrated on self-powered iSIMPLE microfluidic cartridge.•The ADM-sensor delivered measurement using only 1 μL of plasma within 12 min.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>35255315</pmid><doi>10.1016/j.bios.2022.114125</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-3075-9846</orcidid><orcidid>https://orcid.org/0000-0003-2729-0071</orcidid><orcidid>https://orcid.org/0000-0002-2172-1427</orcidid><orcidid>https://orcid.org/0000-0001-8064-5164</orcidid><orcidid>https://orcid.org/0000-0001-7989-9255</orcidid><orcidid>https://orcid.org/0000-0002-8829-3180</orcidid><orcidid>https://orcid.org/0000-0002-5828-4435</orcidid><orcidid>https://orcid.org/0000-0003-4546-5154</orcidid><orcidid>https://orcid.org/0000-0003-2900-1181</orcidid><orcidid>https://orcid.org/0000-0001-6767-8113</orcidid><orcidid>https://orcid.org/0000-0002-2713-6798</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adalimumab Biosensing Techniques Drug Monitoring Fiber Optic Technology Fiber-optic surface plasmon resonance Humans Microfluidics Patient blood plasma Point of care Point-of-Care Systems Self-powered microfluidics Surface Plasmon Resonance Therapeutic drug monitoring |
title | Point-of-care therapeutic drug monitoring of adalimumab by integrating a FO-SPR biosensor in a self-powered microfluidic cartridge |
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