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Polyprotic Acids03:38

Polyprotic Acids

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Acids are classified by the number of protons per molecule that they can give up in a reaction. Acids such as HCl, HNO3, and HCN that contain one ionizable hydrogen atom in each molecule are called monoprotic acids. Their reactions with water are:
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A Rapid and Specific Microplate Assay for the Determination of Intra- and Extracellular Ascorbate in Cultured Cells
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A highly sensitive switch-on spectrofluorometric method for determination of ascorbic acid using a selective

Samah F El-Malla1, Rehab H Elattar1, Amira H Kamal1

  • 1Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Tanta 31111, Egypt.

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|January 1, 2022
PubMed
Summary

A new, highly sensitive spectrofluorometric method determines ascorbic acid by enhancing salicylate fluorescence. This greener approach offers a simple, rapid alternative for analyzing ascorbic acid in various samples.

Keywords:
Ascorbic acidIron (III) salicylateRedox reactionSpectrofluorometry

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Area of Science:

  • Analytical Chemistry
  • Biochemistry

Background:

  • Ascorbic acid (vitamin C) is crucial for immune support, particularly noted during COVID-19 management.
  • Existing spectrofluorometric methods for ascorbic acid analysis have limitations like slow kinetics, low sensitivity, and harsh conditions.

Purpose of the Study:

  • To develop a highly sensitive, rapid, and greener spectrofluorometric method for determining ascorbic acid.
  • To validate the method for analyzing ascorbic acid in pharmaceutical formulations.

Main Methods:

  • A novel 'turn-on' spectrofluorometric approach utilizing the fluorescence enhancement of a salicylate-iron (III) complex.
  • Ascorbic acid reduces iron (III) to iron (II), leading to increased fluorescence intensity at 411 nm.
  • Method validation included linearity, sensitivity (LOD/LOQ), and application to commercial tablets (Ruta C60®).

Main Results:

  • The method demonstrated excellent linearity (R²=0.9997) in the 1-8 µg/mL range.
  • Achieved low limits of detection (0.035 µg/mL) and quantitation (0.106 µg/mL).
  • Results for pharmaceutical samples showed no significant difference compared to a liquid chromatography method and were markedly greener.

Conclusions:

  • A simple, rapid, and sensitive spectrofluorometric method for ascorbic acid determination was successfully developed.
  • The method is validated for pharmaceutical analysis and exhibits superior environmental performance compared to existing techniques.
  • Potential applications include analysis in pharmaceuticals, biological fluids, and food samples.