Development and Validation of a Quantitative NMR Method for the Determination of the Commercial Tablet Formulation of Sulfasalazine

作者：Su, Feng; Sun, Zi-qing; Liang, Xian-Rui^*

来源：Current Pharmaceutical Analysis, 2019, 15(1): 39-44.

DOI：10.2174/1573412913666170707113548

• NMR
• qNMR
• sulfasalazine
• method validation
• commercial tablet formulation
• pharmaceutical analysis

Introduction: Quantitative NMR spectroscopy (qNMR) is a rapid, simple and efficient method for the assay of sulfasalazine (SSZ) in commercial tablet formulation. @@@ Materials and Methods: The qNMR method was demonstrated using maleic acid as an internal standard and DMSO-d(6) as a solvent. The characteristic signals of SSZ at delta 8.36 ppm and maleic acid at delta 6.28 ppm were quantified. The reliability of the quantification method had been implemented successfully in validated experiments including specificity and selectivity, linearity, recovery, precision concentration rang, limit of detection (LOD), limit of quantification (LOQ), stability and robustness. @@@ Conclusion: The method was found to be liner (R-2 = 0.9991) from 8.62 to 20.14 mg/0.6 mL DMSO-d(6) in the drug concentration range. The maximum relative standard deviation (RSD) of recovery and precision were tested to be 0.59% and 0.65%, respectively. The LOD and LOQ were determined to be 0.02, 0.07 mg/mL, respectively. The RSD of stability was 0.05%. The robustness was demonstrated by changing four different parameters with the maximum difference less than 0.9%. In addition, the result of qNMR showed in good agreement with the HPLC and UV methods. Based on the experiments, the developed method was successfully applied to the determination of SSZ in commercial tablet.

• 出版日期2019
• 单位浙江工业大学