Czasopismo
Tytuł artykułu
Autorzy
Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
Abstrakty
A sensitive, selective, precise, and stability-indicating method for quantitative analysis of erdosteine, in the presence of its degradation products, both as the bulk drug and in a formulation has been established and validated. High-performance thin layer chromatography (HPTLC) on aluminium-backed silica gel 60 F254 plates with toluene–methanol–acetone–ammonia 3.5:3.5:2.5:0.05 (v/v) as mobile phase was followed by densitometric measurement at 254 nm. This system was found to give compact bands for erdosteine (RF 0.45 ± 0.02). The method was validated in accordance with ICH guidelines There was no chromatographic interference from capsule excipients. Erdosteine was subjected to acid and alkaline hydrolysis, oxidation, dry heat, wet heat, and UV degradation. The drug is degraded by acid and alkaline hydrolysis, oxidation, and UV irradiation. The drug was found to be stable under wet and dry heat conditions. Because the method could effectively separate the drug from its degradation products it can be regarded as stability-indicating.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
170-184
Opis fizyczny
Bibliogr. 15 poz., rys., tab.
Twórcy
autor
autor
- Department of Quality Assurance Techniques and Pharmaceutical Chemistry, Bharati Vidyapeeth University, Poona College of Pharmacy, Centre for Advanced Pharmaceutical Research, Erandwane, Pune 411038, Maharashtra State, India
Bibliografia
- [1] www.drugs.com
- [2] K.L. Dechant and S. Noble, Drugs, 6, 875 (1996)
- [3] www.edmond_pharma.htm
- [4] N. Muramatsu, T. Toyo’oka, K. Yamaguchi, and S. Kobayashi, J. Chromatogr. B, 719, 177 (1998)
- [5] S. Savu, M. Mitrea, L. Silvestro, and C. Mancini, Int. J. Clin. Pharmacol. Ther., 38, 415 (2000)
- [6] K. Hohyun, Y.C. Kyu, J.L. Hee, B.H. Sang, and R.L. Kyung, J. Pharm. Biomed. Anal., 34, 661 (2004)
- [7] H. Hisashi, K. Toshihiko, and O. Kenji, J. Pharmacol. Toxicol., 40, 165 (1998)
- [8] ICH, Q1A Stability Testing of New Drug Substances and Products. In: Proceedings of the International Conference on Harmonization, Geneva, October, 1993
- [9] ICH, Q2A Harmonized Tripartite Guideline, Text on Validation of Analytical Procedures, IFPMA. In: Proceedings of the International Conference on Harmonization, Geneva, March 1994
- [10] ICH, Q2B Harmonized Tripartite Guideline, Text on Validation of Analytical Procedures Methodology, International Conference on Harmonization, Geneva, March, 1996
- [11] ICH Guidance on Analytical Methods, International Convention on Quality for the Pharmaceutical Industry, Toronto, Canada, September, 2002
- [12] P.D. Sethi, High Performance Thin Layer Chromatography, Quantitative Analysis of Pharmaceutical Formulations, CBS, New Delhi, 1996
- [13] S. Singh and M. Bakshi, Guidance on Conduct of Stress Tests to Determine Inherent Stability of Drugs, Pharmaceutical Technology On-Line, April, 2000, p. 1
- [14] J.T. Carstensen and C.T. Rhodes, Drug Stability Principles and Practices, Marcel Dekker, New York, 2000
- [15] J.C. Miller and J.N. Miller, Statistics for Analytical Chemistry, 2nd edn, Ellis Horwood, New York, 1992
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.baztech-article-BATA-0003-0016