Development and validation of Ropinirole hydrochloride and its related compounds by UPLC in API and pharmaceutical dosage forms

Journal of the Chinese Chemical Society

Volumn 57, Issue 3 A, 2010, Pages 348-355

  Krishnaiah, Ch ^a,b   Murthy, M Vishnu ^a   Reddy, A Raghupathi ^a   Kumar, Ramesh ^a   Mukkanti, K ^b  

^a DR REDDY'S LABORATORIES LTD   (India)

^b JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY   (India)

Author keywords

Forced degradation; Ropinirole hydrochloride; Stability indicating; UPLC; Validation

Indexed keywords

EID: 77957203518     PISSN: 00094536     EISSN: None     Source Type: Journal    
DOI: 10.1002/jccs.201000052     Document Type: Article

References (7)

1. Coufal, P.; Stulík, K.; Claessens, H. A.; Hardy, M. J.; Webb, M. J. Chromatogr., A 1999, 732, 437.
2. Onal, A. J. Chromatogr. 2006, 644, 59.
3. Parmar, G.; Sharma, H, S.; Singh, K.; Bansal, G. J. Chromatogr. 2009, 69, 199.
4. Azeem, A.; Iqbal, Z.; Ahmad, F. J.; Khar, R. K.; Talegaonkar, S. Acta Chromatogr. 2008, 20, 95.
5. Zeynep, A. Spectrochim. Acta, Part A 2008, 70, 69.
6. Sahasrabuddhey, B.; Nautiyal, R.; Acharya, H.; Khyade, S.; Luthra, P. K.; Deshpande, P. B. J. Pharm. Biomed. Anal. 2007, 43, 1587.
7. ICH Guidelines on Validation of Analytical Procedures: Text and Methodology, International Conference on Harmonization, March, 1995; FDA. Federal Register, 1995; Q2 (R1), 60, 11260.