Effect of Acetate and Carbonate Buffers on the Photolysis of Riboflavin in Aqueous Solution: A Kinetic Study |
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Authors: | Iqbal Ahmad Zubair Anwar Kefi Iqbal Syed Abid Ali Tania Mirza Adeela Khurshid Aqeela Khurshid Adeel Arsalan |
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Institution: | 1. Baqai Institute of Pharmaceutical Sciences, Baqai Medical University, Toll Plaza, Super Highway, Gadap Road, Karachi, 74600, Pakistan 2. Baqai Dental College, Baqai Medical University, Toll Plaza, Super Highway, Gadap Road, Karachi, 74600, Pakistan 3. HEJ Research Institute of Chemistry, University of Karachi, Karachi, 75270, Pakistan
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Abstract: | The photolysis of riboflavin (RF) in the presence of acetate buffer (pH 3.8–5.6) and carbonate buffer (pH 9.2–10.8) has been studied using a multicomponent spectrophotometric method for the simultaneous assay of RF and its photoproducts. Acetate and carbonate buffers have been found to catalyze the photolysis reaction of RF. The apparent first-order rate constants for the acetate-catalyzed reaction range from 0.20 to 2.86?×?10?4 s?1 and for the carbonate-catalyzed reaction from 3.33 to 15.89?×?10?4 s?1. The second-order rate constants for the interaction of RF with the acetate and the carbonate ions range from 2.04 to 4.33?×?10?4 M?1 s?1 and from 3.71 to 11.80?×?10?4 M?1 s?1, respectively. The k-pH profile for the acetate-catalyzed reaction is bell shaped and for the carbonate-catalyzed reaction a steep curve. Both HCO3? and CO32?? ions are involved in the catalysis of the photolysis reaction in alkaline solution. The rate constants for the HCO3? and CO32?? ions catalyzed reactions are 0.72 and 1.38?×?10?3 M?1 s?1, respectively, indicating a major role of CO32?? ions in the catalysis reaction. The loss of RF fluorescence in acetate buffer suggests an interaction between RF and acetate ions to promote the photolysis reaction. The optimum stability of RF solutions is observed in the pH range 5–6, which is suitable for pharmaceutical preparations.KEY WORDS: acetate effect, carbonate effect, photolysis, riboflavin, spectrophotometric assay |
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