Biosensors and Bioelectronics-Efficient one-pot synthesis of molecularly imprinted silica.pdf
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Biosensors and Bioelectronics-Efficient one-pot synthesis of molecularly imprinted silica
Biosensors and Bioelectronics 38 (2012) 55–60Contents lists available at SciVerse ScienceDirectBiosensors and Bioelectronics0956-56
http://d
n Corr
E-mjournal homepage: /locate/biosEfficient one-pot synthesis of molecularly imprinted silica nanospheres
embedded carbon dots for fluorescent dopamine optosensingYan Mao, Yu Bao, Dongxue Han n, Fenghua Li, Li Niu n
State Key Laboratory of Electroanalytical Chemistry, c/o Engineering Laboratory for Modern Analytical Techniques, Changchun Institute of Applied Chemistry, Graduate University
of the Chinese Academy of Sciences, Chinese Academy of Sciences, Changchun 130022, PR Chinaa r t i c l e i n f o
Article history:
Received 2 March 2012
Received in revised form
25 April 2012
Accepted 29 April 2012
Available online 10 May 2012
Keywords:
Molecularly imprinted polymer
Sol–gel polymerization
Carbon dots
Fluorescence sensor
Dopamine63/$ - see front matter 2012 Elsevier B.V. A
/10.1016/j.bios.2012.04.043
esponding authors. Tel.: t86 431
ail addresses: dxhan@ (D. Han), lniu@a b s t r a c t
A new type of eco-friendly molecularly imprinted polymer (MIP) was synthesized through an efficient
one-pot room-temperature sol–gel polymerization and applied as a molecular recognition element to
construct dopamine (DA) fluorescence (FL) optosensor. Highly luminescent carbon dots (CDs) were firstly
synthesized via a one-step reaction in organosilane, and their surface were anchored with MIP matrix
(CDs@MIP). The resulting composite of a synergetic combination of CDs with MIP showed high
photostability and template selectivity. Moreover, the composite allowed a highly sensitive determination
of DA via FL intensity decreasing when removal of the original templates. The new MIP-based DA sensing
protocol was applied to detect DA concentration in aqueous solution, the relative FL intensity of CDs@MIP
decreased linearly with the increasing DA in the concentration range of 25–500 nM with a detection limit
(3s) of 1.7 nM. Furthermore, th
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