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

被引:4
|
作者
Su, Feng [1 ,2 ]
Sun, Zi-qing [1 ,2 ]
Liang, Xian-Rui [1 ,2 ]
机构
[1] Zhejiang Univ Technol, Coll Pharmaceut Sci, Minist Educ, Key Lab Green Pharmaceut Technol & Related Equipm, Hangzhou 310014, Zhejiang, Peoples R China
[2] Zhejiang Univ Technol, Collaborat Innovat Ctr Yangtze River Delta Reg Gr, Natl Engn Res Ctr Proc Dev Act Pharmaceut Ingredi, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
NMR; qNMR; sulfasalazine; method validation; commercial tablet formulation; pharmaceutical analysis; SPECTROSCOPY; SPECTROMETRY; H-1;
D O I
10.2174/1573412913666170707113548
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:39 / 44
页数:6
相关论文
共 50 条
  • [31] Development and validation of a liquid chromatographic method for the simultaneous determination of aniracetam and its related substances in the bulk drug and a tablet formulation
    Papandreou, Georgios
    Zorpas, Kostas
    Archontaki, Helen
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2011, 56 (03) : 615 - 622
  • [32] Development and Validation of a HPLC Method for Determination of Anastrozole in Tablet Dosage Form
    Kumar, D. Sathis
    Harani, A.
    Sridhar, D.
    Banji, David
    Rao, Knv
    Guruviah
    Yogeswaran
    E-JOURNAL OF CHEMISTRY, 2011, 8 (02) : 794 - 797
  • [33] Development and Validation of a HPLC Method for Determination of Pefloxacin in Tablet and Human Plasma
    Gauhar, Shahnaz
    Ali, Syed Ayub
    Shoaib, Harris
    Naqvi, Syed Baqir Shyum
    Muhammad, Iyad Naeem
    IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, 2009, 12 (01) : 33 - 42
  • [34] Development and validation of a quantitative proton NMR method for the analysis of pregnenolone
    Schleiff, Mary
    Sommers, Cynthia
    Yang, Jingyue
    Shen, Xiaohui
    Rodriguez, Jason D.
    Shu, Qin
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2023, 222
  • [35] UV-VISIBLE SPECTROPHOTOMETRIC METHOD DEVELOPMENT AND VALIDATION OF ASSAY OF PARACETAMOL TABLET FORMULATION
    Behera, Siladitya
    Ghanty, Subhajit
    Ahmad, Fahad
    Santra, Saayak
    Banerjee, Sritoma
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2012, 3 (12): : 4945 - 4953
  • [36] DEVELOPMENT AND VALIDATION OF A NOVEL RP-HPLC METHOD FOR SIMULTANEOUS DETERMINATION OF SALBUTAMOL SULFATE, GUAIFENESIN, AND AMBROXOL HYDROCHLORIDE IN TABLET FORMULATION
    Maithani, Mukesh
    Sahu, Sandeep
    Chaudhary, Amrendra K.
    Singh, Ranjit
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2012, 35 (09) : 1156 - 1170
  • [37] Development and Validation of an HPLC Method for Mefloquine Hydrochloride Determination in Tablet Dosage Form
    Andrade Nogueira, Fernando Henrique
    Lana Goulart, Leticia de Paula
    Cesar, Isabela da Costa
    Moreira de Campos, Ligia Maria
    Pianetti, Gerson Antonio
    JOURNAL OF AOAC INTERNATIONAL, 2011, 94 (04) : 1089 - 1093
  • [38] Development and Validation of a Spectrophotometric Method for the Determination of Entecavir in Pure and Tablet Dosage Form
    Shabbir, Hafiz Muhammad Nauman
    Hayat, Muhammad Munawar
    Ashraf, Muhammad
    Nasim, Faiz-Ul-Hassan
    Ahmad, Irshad
    Uzair, Muhammad
    Haque, Naheed
    JOURNAL OF THE CHEMICAL SOCIETY OF PAKISTAN, 2012, 34 (06): : 1605 - 1608
  • [39] Development and Validation of High Performance Liquid Chromatography Method for Determination Atorvastatin in Tablet
    Yugatama, A.
    Rohmani, S.
    Dewangga, A.
    INTERNATIONAL CONFERENCE ON ADVANCED MATERIALS FOR BETTER FUTURE 2017, 2018, 333
  • [40] Multivariate methods in the development of a new tablet formulation:: Optimization and validation
    Gabrielsson, J
    Lindberg, NO
    Pålsson, M
    Nicklasson, F
    Sjöström, M
    Lundstedt, T
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2004, 30 (10) : 1037 - 1049