Drug Quantification by Simultaneous HPLC Analysis

Authors

  • Eduardo Abreu State University of Maringá (UEM), Maringá, PR, CEP, 87020-680, Brazil
  • Michel Z. Fidelis São Carlos Institute of Chemistry, University of São Paulo (USP), São Carlos, SP, CEP, 13560-97, Brazil https://orcid.org/0000-0003-0169-0843
  • Maria Eduarda K. Fuziki State University of Maringá (UEM), Maringá, PR, CEP, 87020-680, Brazil
  • Jessica R. P. Oliveira Chemical Department, Federal University of Technology-Paraná (UTFPR), Pato Branco, PR, CEP, 85503-390, Brazil
  • Rodrigo Brackmann Chemical Department, Federal University of Technology-Paraná (UTFPR), Pato Branco, PR, CEP, 85503-390, Brazil
  • Angelo M. Tusset Chemical Engineering Department, Federal University of Technology-Paraná (UTFPR), Ponta Grossa, PR, CEP, 84017-220, Brazil
  • Onelia A. A. dos Santos State University of Maringá (UEM), Maringá, PR, CEP, 87020-680, Brazil
  • Giane G. Lenzi Chemical Engineering Department, Federal University of Technology-Paraná (UTFPR), Ponta Grossa, PR, CEP, 84017-220, Brazil

DOI:

https://doi.org/10.37256/fce.7120267891

Keywords:

Emerging Contaminants (ECs), compounds separation, chromatographic parameters, High-Performance Liquid Chromatography (HPLC)

Abstract

High-Performance Liquid Chromatography (HPLC) analysis has been commonly used to monitor (separate, identify, and quantify) potentially toxic compounds in the environment. In this context, a large amount of research has investigated the so-called Emerging Contaminants (ECs), which are new pollutants that, until a few years ago, were not detected or were considered to pose a low risk to the environment and were not regulated. In this work, in particular, the technique was employed for the simultaneous determination of three emerging pollutants: Paracetamol (PAR), Salicylic Acid (SA), and Acetylsalicylic Acid (ASA) in the sample matrix. To study the effect of a set of factors on the responses, a factorial design was used. The responses (chromatographic parameters) considered in the experimental design took into account asymmetry, tailing factor, and resolution. The following factors were investigated: buffer solution pH, mobile phase flow rate, and the proportion of buffer in this mobile phase. The results indicated that optimized control of mobile phase pH, facilitated by judicious use of buffer solutions, forms the basis for achieving optimal HPLC separations. In addition, tests were performed to assess the interference from the matrix in the analysis.

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Published

2025-11-24

How to Cite

(1)
Abreu, E.; Fidelis, M. Z.; Fuziki, M. E. K.; Oliveira, J. R. P.; Brackmann, R.; Tusset, A. M.; Santos, O. A. A. dos; Lenzi, G. G. Drug Quantification by Simultaneous HPLC Analysis. Fine Chemical Engineering 2025, 7, 75-86.