4.7 Article

Fabrication of a fluorescent sensor by organogelation: CdSe/ZnS quantum dots embedded molecularly imprinted organogel nanofibers

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 234, Issue -, Pages 122-129

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2016.04.161

Keywords

Organogelation; Quantum dots; Fluorescent sensor; Molecularly imprinted polymers; Organogel nanofibers; Histamine

Funding

  1. National Research Foundation of Korea (NRF) grant - Korea government (MSIP) [2010-0017552, 2015R1A2A2A01006585]
  2. National Research Foundation of Korea [2010-0017552] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We describe a molecularly imprinted polymer (MIP)-based fluorescent sensor fabricated through an organogelation process. The sensor was comprised of a molecularly imprinted nanofiber as a receptor and a CdSe/ZnS quantum dot (QD) as a signal transducer. The sensor fabrication was carried out in three steps: (1) organogelation of a polymerizable gelator (PG) in the presence of the QD and a template, (2) gel-state polymerization and (3) extraction of the template. We chose histamine as a model template. PG had two different polymerizable groups: an acrylate and a diacetylene. As a functional monomer for complexation with the template, an acrylate having a carboxyl group was used. The QD and template-containing organogel formed in n-decane were polymerized in the presence of a photoinitiator and a cross-linker by UV irradiation to produce highly cross-linked organogel nanofibers. The template molecules were removed by extraction with methanol/acetic acid (9:1 v/v) to give the QD-incorporated, histamine imprinted organogel nanofibers (QD-HIOGNF). QD-HIOGNF showed high molecular recognition properties toward histamine in respects to both sensitivity and selectivity. The fluorescence intensity of QD-HIOGNF was quenched sensitively as the concentration of histamine increased. QD-HIOGNF could be reused for sensing after removing the bound analytes. (C) 2016 Elsevier B.V. All rights reserved.

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