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A novel capacitive sensor based on molecularly imprinted nanoparticles as recognition elements.
Canfarotta, Francesco; Czulak, Joanna; Guerreiro, Antonio; Cruz, Alvaro Garcia; Piletsky, Sergey; Bergdahl, Gizem Ertürk; Hedström, Martin; Mattiasson, Bo.
Afiliação
  • Canfarotta F; MIP Diagnostics Ltd., Fielding Johnson Building, University of Leicester, LE1 7RH, United Kingdom.
  • Czulak J; MIP Diagnostics Ltd., Fielding Johnson Building, University of Leicester, LE1 7RH, United Kingdom.
  • Guerreiro A; MIP Diagnostics Ltd., Fielding Johnson Building, University of Leicester, LE1 7RH, United Kingdom. Electronic address: ag@mip-dx.com.
  • Cruz AG; Chemistry Department, University of Leicester, LE1 7RH, United Kingdom.
  • Piletsky S; Chemistry Department, University of Leicester, LE1 7RH, United Kingdom.
  • Bergdahl GE; Department of Clinical Sciences, Division of Infection Medicine, Biomedical Center B14, Lund University, SE-221 84 Lund, Sweden; CapSenze Biosystems AB, Scheelevägen 22, SE-223 63 Lund, Sweden.
  • Hedström M; CapSenze Biosystems AB, Scheelevägen 22, SE-223 63 Lund, Sweden; Department of Biotechnology, Lund University, Naturvetarvägen 14, SE-221 00 Lund, Sweden.
  • Mattiasson B; CapSenze Biosystems AB, Scheelevägen 22, SE-223 63 Lund, Sweden; Department of Biotechnology, Lund University, Naturvetarvägen 14, SE-221 00 Lund, Sweden.
Biosens Bioelectron ; 120: 108-114, 2018 Nov 30.
Article em En | MEDLINE | ID: mdl-30173008
ABSTRACT
Molecularly Imprinted Polymers (MIPs) are synthetic receptors capable of selective binding to their target (template) molecules and, hence, are used as recognition elements in assays and sensors as a replacement for relatively unstable enzymes and antibodies. Herein, we describe a manufacturing-friendly protocol for integration of MIP nanoparticles (nanoMIPs) with a (label-free) capacitive sensor. The nanoMIPs were produced by solid-phase synthesis for two templates with different sizes and properties, including a small molecule tetrahydrocannabinol (THC) and a protein (trypsin). NanoMIPs were deposited on the surface of the sensor and the change in capacitance (ΔC) upon binding of the target was measured. The significant improvement in the selectivity and limit of detection (one order of magnitude compared to previously used MIP microparticles) can be attributed to their increased surface-to-volume ratio and higher specificity of the nanoMIPs produced by the solid-phase method. The methodology described is also compatible with common sensor fabrication approaches, as opposed to methods involving in situ MIP polymerisation. The proposed sensor shows high selectivity, fast sensor response (45 min including injection, regeneration and re-equilibration with running buffer), and straightforward data analysis, which makes it viable for label-free monitoring in real-time. The set of targets assessed in this manuscript shows the general applicability of the biosensor platform.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polímeros / Técnicas Biossensoriais / Nanopartículas Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polímeros / Técnicas Biossensoriais / Nanopartículas Idioma: En Ano de publicação: 2018 Tipo de documento: Article