RESUMEN
The development of low-cost earth abundant metal based fluorescent sensors for a rapid and selective nanomolar level detection of Hg2+ is essential due to the increasing world-wide concern of its detrimental effect on humans as well as the environment. Herein, we present a perylene tetracarboxylic acid functionalized copper nanoclusters (CuNCs) based "turn-on" fluorescence probe for highly selective detection of toxic Hg2+ ions. The fabricated CuNCs exhibited high photostability with emission maximum centered at 532 nm (λex = 480 nm). The fluorescence intensity of CuNCs was remarkably enhanced upon the addition of Hg2+ over other competing ions and neutral analytes. Notably, the 'turn-on' fluorescence response exhibits highly sensitive detection limit as low as 15.9 nM (S/N â¼ 3). The time resolved fluorescence spectroscopy suggested the energy transfer between CuNCs and Hg2+ ions following either inhibited fluorescence resonance energy transfer (FRET) or surface modification of CuNCs during Hg2+ sensing. This study offers the systematic design and development of new fluorescent 'turn-on' nanoprobes for rapid and selective recognition of heavy metal ions.
RESUMEN
Human Papilloma Virus 16 (HPV 16) is the well-known causative species responsible for triggering cervical cancer. When left undiagnosed and untreated, this disease leads to life-threatening events among the female populace, especially in developing nations where healthcare resources are already being stretched to their limits. Considering various drawbacks of conventional techniques for diagnosing this highly malignant cancer, it becomes imperative to develop miniaturized biosensing platforms which can aid in early detection of cervical cancer for enhanced patient outcomes. The current study reports on the development of an electrochemical biosensor based on reduced graphene oxide (rGO)/DNA hybrid modified flexible carbon screen-printed electrode (CSPE) for the detection of HPV 16. The carbon-coated SPEs were initially coated with rGO followed by probe DNA (PDNA) immobilization. The nanostructure characterization was performed using UV-Vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy and X-ray diffraction (XRD) techniques. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were employed to study the electrochemical characterization of the nano-biohybrid sensor surface. The optimization studies and analytical performance were assessed using differential pulse voltammetry (DPV), eventually exhibiting a limit of detection (LoD) ~2 pM. The developed sensor was found to be selective solely to HPV 16 target DNA and exhibited a shelf life of 1 month. The performance of the developed flexible sensor further exhibited a promising response in spiked serum samples, which validates its application in future point-of-care scenarios.