Highly sensitive determination of doxorubicin hydrochloride antitumor agent via a carbon nanotube/gold nanoparticle based nanocomposite biosensor.

A glassy carbon electrode modified with multi-walled carbon nanotubes (MWCNTs) decorated with gold nanoparticles has been investigated for the first time as an ultrasensitive electrochemical sensor for the determination of doxorubicin hydrochloride (DOX), an efficient antitumor agent. The developed nanocomposite has been characterized by scanning electron microscopy (SEM), besides cyclic and linear sweep voltammetry electrochemical techniques. An efficient catalytic activity for the reduction of DOX has been demonstrated, leading to a significant increase in peak current density and a remarkable decrease in reduction over-potential. Under the optimal condition, a wide linear DOX concentration range from 1×10-11 to 1×10-6 M with a very low detection limit of 6.5 pM was achieved with the modified electrode. Meanwhile, the functionalized MWCNTs/gold nanoparticles indicated an appropriate selectivity, reproducibility, and repeatability as well as long-term stability. The promising outcomes of this research approved the applicability of the developed nanocomposite sensor towards trace amounts of DOX in pharmaceutical and clinical preparations.

Tantalum electrodes modified with well-aligned carbon nanotube-Au nanoparticles: application to the highly sensitive electrochemical determination of cefazolin.

Carbon nanotube/nanoparticle hybrid materials have been proven to exhibit high electrocatalytic activity suggesting broad potential applications in the field of electroanalysis. For the first time, modification of Ta electrode with aligned multi-walled carbon nanotubes/Au nanoparticles introduced for the sensitive determination of the antibiotic drug, cefazolin (CFZ). The electrochemical response characteristics of the modified electrode toward CFZ were investigated by means of cyclic and linear sweep voltammetry. The modified electrode showed an efficient catalytic activity for the reduction of CFZ, leading to a remarkable decrease in reduction overpotential and a significant increase of peak current. Under optimum conditions, the highly sensitive modified electrode showed a wide linear range from 50 pM to 50 µM with a sufficiently low detection limit of 1 ± 0.01 pM (S/N = 3). The results indicated that the prepared electrode presents suitable characteristics in terms of sensitivity (458.2 ± 2.6 µAcm(-2)/µM), accuracy, repeatability (RSD of 1.8 %), reproducibility (RSD of 2.9 %), stability (14 days), and good catalytic activity in physiological conditions. The method was successfully applied for accurate determination of trace amounts of CFZ in pharmaceutical and clinical preparations without the necessity for samples pretreatment or any time-consuming extraction or evaporation steps prior to the analysis.