On-line microfluidic sensor integrated with an enzyme-modified pre-cell for the monitoring of paracetamol in pharmaceutical samples [An article from: Analytica Chimica Acta]
Book Details
Author(s)G.A. Messina, I.E. De Vito, J. Raba
PublisherElsevier
ISBN / ASINB000RR71AI
ISBN-13978B000RR71A0
MarketplaceGermany 🇩🇪
Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
An on-line microfluidic sensing device with an enzyme-modified pre-cell coupled to an amperometric detector for the monitoring of paracetamol in pharmaceutical formulations is described. Horseradish peroxidase (HRP) [EC 1.11.1.7], immobilized on a 3@ml pre-cell, in presence of hydrogen peroxide catalyses the oxidation of paracetamol to N-acetyl-p-benzoquinoneimine. The electrochemical reduction back to hydroquinone is detected on glassy carbon electrode surface at -0.10V. The recovery of paracetamol from 10 samples ranged from 99.00 to 101.10%. This method could be used to determine paracetamol concentration in the range 0.35-100@mM (r=0.997) with a limit of detection of 3.0x10^-^7M and a relative standard deviation was less than 4.1% (n=8). The method was successfully applied for the processing of as many as 20 samples per hour of paracetamol in pharmaceutical formulations.
Description:
An on-line microfluidic sensing device with an enzyme-modified pre-cell coupled to an amperometric detector for the monitoring of paracetamol in pharmaceutical formulations is described. Horseradish peroxidase (HRP) [EC 1.11.1.7], immobilized on a 3@ml pre-cell, in presence of hydrogen peroxide catalyses the oxidation of paracetamol to N-acetyl-p-benzoquinoneimine. The electrochemical reduction back to hydroquinone is detected on glassy carbon electrode surface at -0.10V. The recovery of paracetamol from 10 samples ranged from 99.00 to 101.10%. This method could be used to determine paracetamol concentration in the range 0.35-100@mM (r=0.997) with a limit of detection of 3.0x10^-^7M and a relative standard deviation was less than 4.1% (n=8). The method was successfully applied for the processing of as many as 20 samples per hour of paracetamol in pharmaceutical formulations.
