Abstract

A normal spectrophotometric and a stopped-flow (SF) spectrofluorimetric method have been developed and optimized for the determination of alendronic acid (ALD) in its pharmaceutical formulations. Both methods are automated using the sequential injection analysis (SIA) principle. The spectrophotometric assay is based on the reaction of the analyte with Cu(II) ions in acidic medium to form an UV-absorbing derivative ( λ max = 240 nm). The SF spectrofluorimetric method is based on the reaction of ALD with o-phthalaldehyde (OPA) in the presence of 2-mercaptoethanol at basic medium ( λ ex = 340 nm/ λ em = 455 nm). Linear calibration curves were obtained in the range 1.0–60.0 mg l −1 ALD for the UV method, and in the range 0.13–10.0 mg l −1 ALD for the SF spectrofluorimetric one. The sampling rates were 60 and 30 h −1, respectively. The developed assays are critically compared and their advantages are discussed. Both methods were applied to the analysis of an ALD containing pharmaceutical formulation with satisfactory accuracy and precision.

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