<p>This work extends the application of heterogeneous ion transfer (HIT) voltammetry at the polarizable oil/ water (O|W) interface by presenting an amperometric genosensor developed on HIT based NH<sub>4</sub><sup>+</sup> detector core coupled with a urease/urea/NH<sub>4</sub><sup>+</sup> nano-enzymatic amplification of signal. It is demonstrated for the detection of a 20 base (b) oligo-RNA target (tORN) related to the genomic insertion sequence (IS6110) of Mycobacterium tuberculosis (MTB). A semi-permeable cellulose membrane (CM)-supported and internally Pt-wire-contacted O-phase (1,2-dichloroethane solution of ethyl violet tetraphenylborate (10&#xa0;mM) and dibenzo-18-crown-6 (50&#xa0;mM)) in a hydrophobic plastic tube (PTFE, tip ID 5&#xa0;mm) served as an NH<sub>4</sub><sup>+</sup>-selective amperometric core sensor (Pt|O|CM). 3′-end alkylamine-modified 10b long oligo-DNA capture-probe (cODN) was covalently attached to the CM to fabricate the genosensor (Pt|O|CM-cODN). Silver nanoparticles (Ag<sub>n</sub>, 10–40&#xa0;nm) co-conjugated with urease and a 5′-end-alkylthiol-modified, 21b oligo-DNA signal-probe (sODN) served as the signal-amplification reagent (sODN-Ag<sub>n</sub>-Urs). After sequential incubation in aq. tORN (5–50&#xa0;nM, 15&#xa0;min) and aq. sODN-Ag<sub>n</sub>-Urs (54&#xa0;mg/mL, 10&#xa0;min), cyclic voltammograms (CV) were acquired in aq. 50&#xa0;mM MgSO<sub>4</sub> solution (W-phase) with or without urea (2&#xa0;mM). Sensitivity of 55.8&#xa0;µA&#xa0;cm<sup>−2</sup>&#xa0;decade<sup>−1</sup> and limit of detection (LoD) of about 44&#xa0;pM were achieved based on background subtracted CV peak currents. The peaks were much less sensitive to a double-mismatch oligo-RNA than the tORN. Impedance spectra were also consistent with the CV results. The analytical merits compare well with some genosensors in the literature, thus the Pt|O|CM-cODN combined with Urs/urea/NH<sub>4</sub><sup>+</sup> nano-enzymatic signal amplification is promising. Further work to optimize fabrication and measurement factors and improve ruggedness is underway.</p>

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A heterogeneous ion transfer NH4+ detector core amperometric genosensor method with sandwich nanohybridization coupled enzymatic signal-on amplification

  • Meschac M. Duga,
  • Tashreeqa Latief,
  • Thaakirah Shaik,
  • Nicholas J. Smerdon,
  • Onyinyechi Uhuo,
  • Emmanuel I. Iwuoha,
  • Tesfaye T. Waryo

摘要

This work extends the application of heterogeneous ion transfer (HIT) voltammetry at the polarizable oil/ water (O|W) interface by presenting an amperometric genosensor developed on HIT based NH4+ detector core coupled with a urease/urea/NH4+ nano-enzymatic amplification of signal. It is demonstrated for the detection of a 20 base (b) oligo-RNA target (tORN) related to the genomic insertion sequence (IS6110) of Mycobacterium tuberculosis (MTB). A semi-permeable cellulose membrane (CM)-supported and internally Pt-wire-contacted O-phase (1,2-dichloroethane solution of ethyl violet tetraphenylborate (10 mM) and dibenzo-18-crown-6 (50 mM)) in a hydrophobic plastic tube (PTFE, tip ID 5 mm) served as an NH4+-selective amperometric core sensor (Pt|O|CM). 3′-end alkylamine-modified 10b long oligo-DNA capture-probe (cODN) was covalently attached to the CM to fabricate the genosensor (Pt|O|CM-cODN). Silver nanoparticles (Agn, 10–40 nm) co-conjugated with urease and a 5′-end-alkylthiol-modified, 21b oligo-DNA signal-probe (sODN) served as the signal-amplification reagent (sODN-Agn-Urs). After sequential incubation in aq. tORN (5–50 nM, 15 min) and aq. sODN-Agn-Urs (54 mg/mL, 10 min), cyclic voltammograms (CV) were acquired in aq. 50 mM MgSO4 solution (W-phase) with or without urea (2 mM). Sensitivity of 55.8 µA cm−2 decade−1 and limit of detection (LoD) of about 44 pM were achieved based on background subtracted CV peak currents. The peaks were much less sensitive to a double-mismatch oligo-RNA than the tORN. Impedance spectra were also consistent with the CV results. The analytical merits compare well with some genosensors in the literature, thus the Pt|O|CM-cODN combined with Urs/urea/NH4+ nano-enzymatic signal amplification is promising. Further work to optimize fabrication and measurement factors and improve ruggedness is underway.