Your browser doesn't support javascript.
loading
Feasible spectrofluorimetric approach for the ultrasensitive determination of lomefloxacin based on synergistic effects of micellization and metal complexation.
Derayea, Sayed M; Hassan, Yasser F; Hammad, Mohamed A; Alahmadi, Yasser M; Omar, Mahmoud A; Samir, Ebtihal.
  • Derayea SM; Analytical Chemistry Department, Faculty of Pharmacy, Minia University, Minia 61519, Egypt. Electronic address: sayed_derayea@mu.edu.eg.
  • Hassan YF; Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Al-Azhar University, Assiut branch, Assiut 71524, Egypt.
  • Hammad MA; Analytical Chemistry Department, Faculty of Pharmacy, Sadat City University, Menofia, Egypt.
  • Alahmadi YM; Clinical and Hospital Pharmacy Department of, College of Pharmacy, Taibah University, Al-Medinah Al-Mounawarah 30078, Saudi Arabia.
  • Omar MA; Analytical Chemistry Department, Faculty of Pharmacy, Minia University, Minia 61519, Egypt; Pharmacognosy and Pharmaceutical Chemistry Department, College of Pharmacy, Taibah University, Al-Medinah Al-Mounawarah 30078, Saudi Arabia.
  • Samir E; Analytical Chemistry Department, Deraya University, New Minia, Minia 61519, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc ; 292: 122399, 2023 May 05.
Article en En | MEDLINE | ID: mdl-36724684
ABSTRACT
The purpose of the present work was to establish a fast and convenient strategy for lomefloxacin analysis using a fluorimetric approach. The methodology was based on the complex formation of the drug with aluminum ion to give a product having high fluorescence. Adding sodium dodecyl sulfate led to further boosting the intensity of fluorescence which was recorded at 429 nm after excitation at 332 nm. The relationship of emission intensity with lomefloxacin concentration was linear at 10-130 ng mL-1 with a correlation coefficient of 0.9996. The quantitation limit was 11.4 ng mL-1 and detection limit was 3.8 ng mL-1. The reaction conditions were carefully studied which included the pH, buffer type, its concentration, the type and concentration of surfactant and the diluting solvent. The method was utilized to quantify the aforementioned drug in tablet formulations and in real human plasma with high accuracy and reliability.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fluoroquinolonas / Metales Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fluoroquinolonas / Metales Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article