4.8 Article

Stepwise Chemical Reaction Strategy for Highly Sensitive Electrochemiluminescent Detection of Dopamine

Journal

ANALYTICAL CHEMISTRY
Volume 85, Issue 16, Pages 8001-8007

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac401894w

Keywords

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Funding

  1. National Basic Research Program of China [2010CB732400]
  2. National Natural Science Foundation of China [21075060, 21135002, 21121091]
  3. program for New Century Excellent Talents in University [NCET100479]

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A stepwise chemical reaction strategy based on the specific recognition of boronic acid to (hob and N-hydroxysuccinimide (NHS) ester to amine group, was designed to construct a signal on electrochemiluminescence (ECL) platform for highly sensitive detection of dopamine. A boronic acid-functionalized pyrene probe was synthesized and was self-assembled on the sidewalls of carbon nanotubes via pi-pi stacking interactions as capture probes on a glassy carbon electrode. Meanwhile, 3,3'dithiodipropionic acid di(N-hydroxysuccinimide ester) (DSP)-functionalized CdTe quantum dots (QDs) were designed as signal probes and characterized with transmission electron microscopy and spectroscopic techniques. Upon stepwise chemical reaction of dopamine with boronic acid and then DSP-QDs, the QDs were captured on the electrode as ECL emitters for signal readout, leading to an ultralow background signal. By using O-2 as an endogenous coreactant, the signal on ECL method was employed to quantify the concentration of dopamine from 50 pM to 10 nM with a detection limit of 26 pM. Moreover, the stepwise chemical reaction-based biosensor showed high specificity against cerebral interference and was successfully applied in the detection of dopamine in cerebrospinal fluid samples. The stepwise chemical reaction strategy should be a new concept for the design of highly selective analytical methods for the detection of small biomolecules.

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