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. 2017 Oct 17;2(10):6809–6818. doi: 10.1021/acsomega.7b01065

Table 1. Comparisons of the Proposed Approach with Others in Terms of MUC1 Detection.

materials method linear range LOD refs
graphene oxide (GO)-based fluorescent aptasensor fluorescence emission spectra 0.04–10 μM 28 nM (12)
hairpin DNA aptamers on gold square wave voltammetry (SWV) 0.1–3 μM 50 nM (51)
enzyme–gold NPs differential pulse voltammograms (DPVs) 8.8–353.3 nM 2.2 nM (24)
conducting polymer nanowire-based microfluidic aptasensor microfluidic system 0.01–100 nM 2.66 nM (52)
quantum dot-based fluorescence readout fluorescence spectra 0.01–104 pg·mL–1 4.5 fg·mL–1 (1)
poly(o-phenylenediamine) carrier and functionalized carbon nanotubes DPV 0.001–100 nM 1 pM (53)
GO and Rul-aptamer electrochemiluminescence 64.9–1036.8 nM 40 nM (13)
aptamer–antibody hybrid sandwich ELISA and surface plasmon resonance 8–100 μg·mL–1 1 μg·mL–1 (10)
aptamer-functionalized gold NPs EIS 0.5–10 nM 0.1 nM (25)
gold NPs-modified screen-printed electrodes EIS 2.5–15 ng·mL–1 3.6 ng·mL–1 (26)
  DPV 0–10 ng·mL–1 0.95 ng·mL–1  
DNA-templated silver nanoclusters SWV 1–500 nM 0.5 nM (54)
TiO2NT/aptamer/c-DNA@CdTeQD aptasensor photoelectrochemical 0.002–0.2 μM 0.52 nM (55)
ZrHF@mFe3O4@mC EIS 0.01–1000 ng·mL–1 0.90 pg·mL–1 this work