4.7 Article

Tranexamic acid derived gold nanoparticles modified glassy carbon electrode as sensitive sensor for determination of nalbuphine

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 211, Issue -, Pages 359-369

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2015.01.096

Keywords

Gold nanoparticles; Tranexamic acid; Voltammetric sensor; Nalbuphine; Serum and urine samples

Funding

  1. Higher Education Commission of Pakistan
  2. Scientific Research at King Saud University through the Research Group [RGP-VPP-236]

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We display a simple chemical procedure for fabrication of spherical gold nanoparticles (AuNps) using tranexamic acid (Tr) as reducing as well as capping agent. As-formed Tr-AuNps were characterized by Ultra Violet Visible (UVVis) spectroscopy where the surface plasmon absorption band was controlled at 522 nm under already optimized conditions. Atomic force microscopy (AFM) unveiled information in relation to size and shape of Tr-AuNps. Fourier transform infra red (FTIR) spectroscopy divulged the interaction between capping agent and AuNps while X-ray diffractometry (XRD) disclosed the nature of crystalline patterns of AuNps. As-prepared Tr-AuNps were sandwiched between the surface of glassy carbon electrode (GCE) and nafion and used as sensor for highly selective and sensitive voltammetric determination of nalbuphine (NA) using square wave voltammetry (SWV) as analytical mode. Parameters such as volume of nafion, working electrodes, type and ionic strength of supporting electrolyte, pH, stirring rate, initial potential, accumulation potential and accumulation time were optimized. The mechanism regarding the oxidation of NA was also proposed. The sensor responded linearly in the range of 0.051.25 mu g mL(-1) NA with excellent limit of detection (LOD) of 13.2 ng mL(-1) and R-2 value of 0.997. In addition, the sensor performed linearly to NA even within the matrices of serum as well as urine samples. The fabricated sensor demonstrated higher selectivity for sensitive determination of NA in the presence of various interfering species commonly found in human serum and urine. The developed sensor was successfully applied and validated for the determination of NA in human serum and urine samples with excellent recoveries. (C) 2015 Elsevier B.V. All rights reserved.

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