Abstract
A novel, accurate, precise, inexpensive, and sensitive spectrophotometric approach is established to assay levodopa (LD) in both bulk drug and its pharmaceutical formulations. The method depends on the reaction of the ternary complex of a mixed-ligand type among LD, nickel(II) (Ni(II)), and 2,3-diaminopyridine (DAP) to form a stable complex of Ni-LD-DAP which is not extractable. The complex showed maximum absorption at 478 nm, with the apparent molar absorptivity of 4.93 × 103 L·mol-1·cm-1 and Sandell's sensitivity of 0.04 μg·cm-2. Beer's law is obeyed within the concentration range of 2-58 μg·mL-1, and the regression line equation is as follows: Y = 0.0251X + 0.0045 (R2 = 0.9990; n = 5). The detection limit and quantitation limit are found to be 0.1388 μg·mL-1 and 0.4207 μg·mL-1, respectively. The present study achieved reasonable accuracy (average recovery of 100.17%) and good precision (RSD did not exceed 1.71%). The developed method has been validated according to the current ICH guidelines (2013). The results of pure LD and pharmaceutical preparations using the recommended spectrophotometry are promising.
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CITATION STYLE
Abdoon, F., Bichan, M. J., Mohamed Ibrahim, A., Mundher Tayyeh, A., Kishore, M., & Abdelhakeem Khalid, A. (2022). Retraction:Ternary Complexation Process for New Spectrophotometric Assay of Levodopa using Ni(II) and 2. Advances in Materials Science and Engineering. John Wiley and Sons Ltd. https://doi.org/10.1155/2022/4915162
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