Electrochemical
(EC) sensors have been widely developed for DNA
detection, but they are seldom used in a simple, economic, and efficient
manner. In this work, for the first time, EC cloth-based DNA sensors
(ECDSs) are developed as a new class of EC DNA sensors, without the
need for cumbersome chip fabrication and high-cost peripheral facilities.
Carbon ink- and solid wax-based screen printing were used to produce
ultracheap sensing devices (the cost of one sensor is estimated to
be $0.045). Also, a CdTe QDs/MWCNTs nanocomposite (CdTe-MWCNTs) was
applied to modify the sensing interface to obtain a stronger EC signal.
Specifically, the newly developed double linear hybridization chain
reaction (DL-HCR) greatly amplified the EC signal, relative to the
conventional linear HCR. Under optimized conditions, target DNA (TD)
samples (75-bp DNA fragments prepared via PCR amplification) were
determined in a range from 20 fM to 5 nM, with a detection limit of
8.74 fM and relative standard deviations of 2.04% and 4.75% for intra-
and inter-assays at 50 pM TD, respectively. Additionally, the ECDSs
had an acceptable storage stability and high selectivity. Importantly,
the ECDSs, coupled with simple enzyme digestion, could detect genomic
DNA from Listeria monocytogenes (L. monocytogenes), and a detection limit of 0.039
ng/μL was obtained. When coupled with enzyme digestion and PCR
amplification, the ECDSs could determine L. monocytogenes in milk samples, with detection limits of approximately 1.64 ×
104 and 11 CFU/mL. These results demonstrate that the method
offers a broad prospect for cost-effective, reliable, and highly sensitive
gene-sensing applications.