Development and Validation of a Quantitative NMR Method for the Determination of the Commercial Tablet Formulation of Sulfasalazine
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Published:2018-11-28
Issue:1
Volume:15
Page:39-44
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ISSN:1573-4129
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Container-title:Current Pharmaceutical Analysis
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language:en
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Short-container-title:CPA
Author:
Su Feng1, Sun Zi-qing1, Liang Xian-rui1
Affiliation:
1. Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China
Abstract
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-d6 as a solvent. The characteristic signals of SSZ at δ 8.36 ppm and maleic acid at δ
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 (R2 = 0.9991) from 8.62 to 20.14 mg/0.6 mL DMSO-d6
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.
Funder
National Natural Science Foundation of China
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmaceutical Science,Molecular Medicine,Biochemistry,Biophysics
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