Abstract

In present work, we report results of the studies related to the synthesis of nanodot metal chalcogenide (zirconium trisulfide, ∼5.7 nm in size) based biosensing platform for early detection of lung cancer serum biomarker (CKAP4). The nanodot zirconium trisulfide (nZrS3) was synthesized through low temperature hydrothermal method (200 °C for 72 h) and functionalized with 3-aminopropyl triethoxysilane (APTES) molecules via chemical process. To fabricate thin and uniform film onto the pre-hydrolyzed indium tin oxide (ITO) coated glass electrode of functionalized nanomaterials (APTES/nZrS3), an optimized electrophoretic condition (25 V for 60 s) was applied. Further, for covalent immobilization of anti-CKAP4 onto the APTES/nZrS3/ITO electrode, EDC-NHS chemistry was used and for blocking of non-specific binding sites, bovine serum albumin (BSA) was non-covalently immobilized via drop-cast method. The synthesized as well as functionalized nanomaterial and fabricated electrodes were characterized through X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. Further, the electrochemical response studies of developed biosensing platform i.e., BSA/anti-CKAP4/APTES/nZrS3/ITO were carried out through DPV technique. The biosensing platform has ability to detect CKAP4 biomarker in the range of 100 pg mL−1-800 pg mL−1 with ultra-sensitivity of 68.76 µA [log (pg mL−1)]−1cm−2, notable lower detection limit of 86 pg mL−1 and shelf life upto 36 days. Moreover, the electrochemical data obtained, exhibit a good correlation with the concentrations of the cancer biomarker CKAP4 found in lung cancer patients as determined by the enzyme-linked immunosorbent assay (ELISA) technique.

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