stability-indicating assay method for determination of Tinidazole in active substance with Spectroscopic approach

فایل این در 12 صفحه با فرمت PDF قابل دریافت می باشد

  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این :

چکیده :

A new, simple, rapid, accurate, sensitive and cost-effective spectrophotometric stability indicating assay method was developed for the quantification of Tinidazole in bulk and validated according to ICH guidelines using different parameters. In the present study an attempted has been made to develop an effective method which will surpass the disadvantages associate with other reported methods like tedious in use, less sensitive and costly etc. The assay method was based on the forced degradation study of Tinidazole under different ICH recommended stress conditions like hydrolytic, oxidation, thermal, and photolysis. Drug shown maximum absorption at 322nm and a regression coefficient value (R2) of 0.999 indicates linearity followed within the concentration range of 5µg/ml to 50µg/ml. During forced degradation study, Tinidazole was significantly degraded in alkaline conditions whereas mild degradation occurs in acidic, neutral and oxidative stress. The drug was stable to dry heat and photolytic degradation conditions. Statistical validation result of the developed method indicates that it was a simple, precise, reproducible, selective, specific and accurate method for analysis of Tinidazole and could be successfully adopted to estimate the drug in bulk and formulations

نویسندگان

مصطفی خواجه دهاقانی

Head research and development FARABI pharmaceutical

مراجع و منابع این :

لیست زیر مراجع و منابع استفاده شده در این را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود لینک شده اند :
  • [1] https://www.drugbank.ca/drugs/db00916. ...
  • [2] Shoeb S. A., Vani R. Method Development and Validation ...
  • Tetracycline, Bismuth Subcitrate in its bulk and Pharmaceutical Dosage form ...
  • Pharmaceutical and Life Sciences, 2019; 5(11): 190-196. ...
  • [3] Mishra A.K., Kumar A., Mishra A., Mishra H.V. Development ...
  • estimation of Metronidazole from pharmaceutical formulation. J Nat Sci Biol ...
  • [4] Mahmoud M., Elkhoudary and others. Development and Optimization of ...
  • Diloxanide, Spiramycin and Cliquinol in Pharmaceutical Dosage Forms Using Experimental ...
  • Chromatographic Science, 2016; 54(10): 1701–1712. ...
  • [5] Akarim E.I., Ibrahim K.E., Adam, M.E. Studies on the ...
  • International Journal Pharmaceutics, 1991; 6: 261-264. ...
  • [6] Godfrey R., Edwards R. A Chromatographic and Spectroscopic Study ...
  • Aqueous Solution. Journal of Pharmaceutical Science, 1991; 80: 212-218. ...
  • [7] Habib M. J., Asker A.F. Complex Formation between Metronidazole ...
  • Photodegradation of Metronidazole. Pharmaceutical Research, 1989; 6: 58-61. ...
  • [8] Marcinie B., Bugaj A., Kedziora W. Kinetic Studies of ...
  • the solid state. Pharmazie, 1997; 52: 220-223. ...
  • [9] Kendall A.T., Starck E., Sugden J.K. Effect of Hydroxyl ...
  • Solution at pH 9.2, International Journal of Pharmaceutics, 1989; 57: ...
  • [10] ICH (2003). Stability testing of new drug substances and ...
  • Conference on Harmonisation, IFPMA, Geneva. ...
  • [11] Bakshi M., Singh S. Development of validated stability-indicating assay ...
  • of Pharmaceutical and Biomedical Analysis.2002; 28 (6):1011-1040. ...
  • [12] Panigrahi D., Mishra G. P., Sharma R. Study of ...
  • development of a validated stability indicating HPLC assay method. Der ...
  • 853. ...
  • [13] Sahoo P.K., Sahoo P., Mohapatra J., Panigrahi D., Patra ...
  • Stability Indicating Assay Method of Doxycycline Hyclate by using UV-Spectrophotometer. ...
  • Delivery & Therapeutics. 2023; 13(6):89-94. ...
  • [14] Chavhan V., Ghante M. Stability Indicating UV Spectrophotometric method ...
  • Simvastatin in bulk and tablet dosage form. J App Pharm. ...
  • [15] Ambhore J.P., Adhao V.S., Cheke R.S., Popat R.R., Gandhi ...
  • degradation studies and stability indicating assay method for some antiviral ...
  • Pharmaceutical Sciences. 2021; 16(01): 133-149. ...
  • [16] Kardile K., Damle M.C. Stability Indicating UV Spectrophotometric Method ...
  • Dronedarone Hydrochloride. Journal of Pharmaceutical Sciences and Drug Research. 2015; ...
  • [17] Ghosh M., Mondal S., Chakraborty S., Ghosh N. A ...
  • Validation for the Estimation of Carbamazepine in Bulk and Tablet ...
  • Techniques. Journal of Drug Delivery & Therapeutics. 2023; 13(3):85 ...
  • Method for Determination of Canagli�lozin in Bulk and Pharmaceutical Dosage ...
  • 7(1): 63-69. ...
  • [19] Gandhi S.V., Patil G.R. Development and validation of Stability ...
  • estimation of Dapson. International J. of Pharmacy and Biological Sciences. ...
  • [20] Chakraborthy S., Sharmin S., Rony S.R., Ahmad S.A.I., Sohrab ...
  • spectropho ...
  • نمایش کامل مراجع