Immunoassay of paralytic shellfish toxins by moving magnetic particles in a stationary liquid-phase lab-on-a-chip

In this study, we devised a stationary liquid-phase lab-on-a-chip (SLP LOC), which was operated by moving solid-phase magnetic particles in the stationary liquid phase. The SLP LOC consisted of a sample chamber to which a sample and reactants were added, a detection chamber containing enzyme substra...

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Veröffentlicht in:Biosensors & bioelectronics 2015-04, Vol.66, p.136-140
Hauptverfasser: Kim, Myoung-Ho, Choi, Suk-Jung
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description In this study, we devised a stationary liquid-phase lab-on-a-chip (SLP LOC), which was operated by moving solid-phase magnetic particles in the stationary liquid phase. The SLP LOC consisted of a sample chamber to which a sample and reactants were added, a detection chamber containing enzyme substrate solution, and a narrow channel connecting the two chambers and filled with buffer. As a model system, competitive immunoassays of saxitoxin (STX), a paralytic shellfish toxin, were conducted in the SLP LOC using protein G-coupled magnetic particles (G-MPs) as the solid phase. Anti-STX antibodies, STX-horseradish peroxidase conjugate, G-MPs, and a STX sample were added to the sample chamber and reacted by shaking. While liquids were in the stationary state, G-MPs were transported from the sample chamber to the detection chamber by moving a magnet below the LOC. After incubation to allow the enzymatic reaction to occur, the absorbance of the detection chamber solution was found to be reciprocally related to the STX concentration of the sample. Thus, the SLP LOC may represent a novel, simple format for point-of-care testing applications of enzyme-linked immunosorbent assays by eliminating complicated liquid handling steps. •We devised a stationary liquid phase lab-on-a-chip (SLP LOC) for POCT application of ELISA.•It consisted of a sample chamber (SC) and a detection chamber (DC), connected by a narrow channel.•Reagents were reacted with solid-phase magnetic particles (MPs) in the SC.•The MPs were transported to the DC for enzyme reaction by moving a magnet under the LOC.•It enabled the detection of saxitoxin in the range of 0.01-0.2 μM without complicated fluid controlM without complicated fluid control.
doi_str_mv 10.1016/j.bios.2014.11.012
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purification</subject><subject>Mathematical models</subject><subject>Microfluidic Analytical Techniques</subject><subject>Paralytic shellfish toxin</subject><subject>Saxitoxin - chemistry</subject><subject>Saxitoxin - immunology</subject><subject>Saxitoxin - isolation &amp; purification</subject><subject>Shellfish</subject><subject>Shellfish - toxicity</subject><subject>Stationary liquid phase</subject><subject>Toxins</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9r3DAQxUVpaLZpv0APQcde7OqfJRlyKSFtA4FemrOQJTmrxZa8Hjt0v31lNu2xBAYGht97MO8h9ImSmhIqvxzqLmaoGaGiprQmlL1BO6oVrwTjzVu0I20jq0ZKfoneAxwIIYq25B26ZI2QRLdih47347imbAHsCeceT3a2w2mJDsM-DEMfYY-X_DsmwN0Jj_k5pic82qcUNqbQZQ0BcEzYYljsEnOy8wkP8bhGX017CwEPtqtyqmzl9nH6gC56O0D4-LKv0OO3u1-3P6qHn9_vb78-VE5ovZQXvO65Vx0LjaeN0sJaqrTjjd9OUnivZVDU9qKc-453kilmWZGEriWSX6HPZ99pzsc1wGLGCK78ZFPIKxgqJSFC81a8Ai15aVXmFaggnCnNN1d2Rt2cAebQm2mOYwnHUGK2As3BbAWarUBDqSkFFtH1i__ajcH_k_xtrAA3ZyCU7J5jmA24GJILPs7BLcbn-D__PzOarQM</recordid><startdate>20150415</startdate><enddate>20150415</enddate><creator>Kim, Myoung-Ho</creator><creator>Choi, Suk-Jung</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><scope>7QO</scope><scope>7TN</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>P64</scope><scope>7SP</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20150415</creationdate><title>Immunoassay of paralytic shellfish toxins by moving magnetic particles in a stationary liquid-phase lab-on-a-chip</title><author>Kim, Myoung-Ho ; Choi, Suk-Jung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-42d8f3d7b2e5d15784aa178c35db2e564dd86e71af4178fb3b6272a23d7eb9063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antibodies, Anti-Idiotypic - chemistry</topic><topic>Antibodies, Anti-Idiotypic - immunology</topic><topic>Biosensing Techniques</topic><topic>Biosensors</topic><topic>Chambers</topic><topic>Channels</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Enzymes</topic><topic>Humans</topic><topic>Immunoassay</topic><topic>Lab-on-a-chip</topic><topic>Liquids</topic><topic>Magnetic particle</topic><topic>Magnets</topic><topic>Marine Toxins - chemistry</topic><topic>Marine Toxins - immunology</topic><topic>Marine Toxins - isolation &amp; purification</topic><topic>Mathematical models</topic><topic>Microfluidic Analytical Techniques</topic><topic>Paralytic shellfish toxin</topic><topic>Saxitoxin - chemistry</topic><topic>Saxitoxin - immunology</topic><topic>Saxitoxin - isolation &amp; 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The SLP LOC consisted of a sample chamber to which a sample and reactants were added, a detection chamber containing enzyme substrate solution, and a narrow channel connecting the two chambers and filled with buffer. As a model system, competitive immunoassays of saxitoxin (STX), a paralytic shellfish toxin, were conducted in the SLP LOC using protein G-coupled magnetic particles (G-MPs) as the solid phase. Anti-STX antibodies, STX-horseradish peroxidase conjugate, G-MPs, and a STX sample were added to the sample chamber and reacted by shaking. While liquids were in the stationary state, G-MPs were transported from the sample chamber to the detection chamber by moving a magnet below the LOC. After incubation to allow the enzymatic reaction to occur, the absorbance of the detection chamber solution was found to be reciprocally related to the STX concentration of the sample. Thus, the SLP LOC may represent a novel, simple format for point-of-care testing applications of enzyme-linked immunosorbent assays by eliminating complicated liquid handling steps. •We devised a stationary liquid phase lab-on-a-chip (SLP LOC) for POCT application of ELISA.•It consisted of a sample chamber (SC) and a detection chamber (DC), connected by a narrow channel.•Reagents were reacted with solid-phase magnetic particles (MPs) in the SC.•The MPs were transported to the DC for enzyme reaction by moving a magnet under the LOC.•It enabled the detection of saxitoxin in the range of 0.01-0.2 μM without complicated fluid controlM without complicated fluid control.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>25460894</pmid><doi>10.1016/j.bios.2014.11.012</doi><tpages>5</tpages></addata></record>
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subjects Antibodies, Anti-Idiotypic - chemistry
Antibodies, Anti-Idiotypic - immunology
Biosensing Techniques
Biosensors
Chambers
Channels
Enzyme-linked immunosorbent assay
Enzymes
Humans
Immunoassay
Lab-on-a-chip
Liquids
Magnetic particle
Magnets
Marine Toxins - chemistry
Marine Toxins - immunology
Marine Toxins - isolation & purification
Mathematical models
Microfluidic Analytical Techniques
Paralytic shellfish toxin
Saxitoxin - chemistry
Saxitoxin - immunology
Saxitoxin - isolation & purification
Shellfish
Shellfish - toxicity
Stationary liquid phase
Toxins
title Immunoassay of paralytic shellfish toxins by moving magnetic particles in a stationary liquid-phase lab-on-a-chip
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