Simultaneous determination of some opioid drugs using Cu-hemin MOF@MWCNTs as an electrochemical sensor.

Due to its toxicological and pharmacological activity, the misuse and overuse of morphine (MO), codeine (CO), and heroine have attracted attention in the medical and forensic toxicology fields. This study proposed a new electrochemical sensor with an acceptable detection limit, linear range, and selectivity for simultaneous determination of MO and CO. This sensor is based on Cu-Hemin metal-organic framework (CHM) and multiwall carbon nanotubes (MWCNTs). First, a facile chemical method was chosen to synthesize CHM and then composite it with MWCNTs. Afterward, the structure of CHM@MWCNTs was verified by XRD, FT-IR, Raman spectroscopy, UV-vis, ICP-OES, FE-SEM, EDX, and elemental mapping. In the next step, under optimal conditions, this electrochemical sensor can sensitive simultaneous determination of MO and CO, showing a dynamic concentration range from 0.09 to 30 µM for both species and a low detection limit of 9.2 nM and 11.2 nM for MO and CO, respectively. Moreover, the applicability in real samples was confirmed by the simultaneous determination of MO and CO in human urine and MO injection. This work reveals a trustable sensor based on MOF and MWCNTs to simultaneously determine opioid drugs in clinical application.

A theoretical and experimental study of polyaniline/GCE and DNA G-quadruplex conformation as an impedimetric biosensor for the determination of potassium ions.

An electrochemical aptasensor has been developed to determine K+ using electrochemical impedance spectroscopy. The polyaniline (PANI) coating was first electrodeposited on a GCE. Then, the potassium-selective aptamer [G3(T2AG3)3] was adsorbed through an electrostatic force between PANI and aptamer. In the presence of K+, the single-stranded DNA is folded into the G-quadruplex configuration, which acts as a barrier against electron transfer at the GCE surface. AFM and FE-SEM images characterize the surface morphology at each fabrication stage. As the K+ concentration increased, the charge transfer resistance (Rct) increased, and the plot of ΔRct versus the logarithm of the K+ concentration is linear over a wide range of 10 pM-60 µM with a low detection limit of 3.7 pM. Finally, the proposed sensor was used to determine K+ in water, serum, urine, and fruit samples. Moreover, the binding stability of the aptamer/PANI and K+/Aptamer/PANI and the interactions between the aptamer and PANI were analyzed through molecular dynamics simulation.