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Aprepitant drug detection using low-dimensional iron oxide nanopa | 51276
Journal of Chromatography & Separation Techniques

Journal of Chromatography & Separation Techniques
Open Access

ISSN: 2157-7064

+44 1300 500008

Aprepitant drug detection using low-dimensional iron oxide nanoparticles prepared by a wet-chemical process


International Expo and Conference on Analytrix & HPLC

October 22-24, 2012 DoubleTree by Hilton Chicago-North Shore, USA

Mohammed M. Rahman

Posters: J Chromat Separation Techniq

Abstract :

H ere, as-prepared iron oxide nanoparticle have prepared by a wet-chemical process using reducing agents in alkaline phase. The nanoparticles were characterized using UV/vis., FT-IR, and Raman spectroscopy, powder X-ray diffraction, and field- emission scanning electron microscopy. They were deposited on a glassy carbon electrode (surface area, 0.0316 cm2) to give a sensor with a fast response towards Aprepitant drug in buffer phase. The sensor also exhibits good sensitivity and long-term stability as well as enhanced electrochemical responses. The calibration plot is linear over the large APPT concentration ranges. The sensitivity is ~2.5316�0.5 μAcm -2 mM -1 , and the detection limit is 0.38�0.02 nM (at a Signal-to-Noise-Ratio of 3) in short response time (10 sec). This method could also be employed for the detection of APPT drug in quality control of formulation using a reliable I-V technique.

Biography :

Mohammed M. Rahman received his PhD degree last 2007 on Electrochemistry under the School of Natural Science, Chonbuk National University, Korea. He has successfully completed two years post-doctoral research fellowships and two-year contract as assistant professor in the chemistry department and CAMNE, Najran University, KSA. Presently, he is working as an assistant professor in the chemistry department & CEAMR, King Abdulaziz University, KSA since 2011. His current research interest is focused in the fields of Nano-technology, Drug detection, and Micro-devices, Nano-materials and Nano-composites.

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