Forced degradation study to develop and validate stability-indicating RP-LC for quantification of ropinirole hydrochloride in its modified release tablets

Chromatographia

Volumn 69, Issue 3-4, 2009, Pages 199-206

  Parmar, Gaganjot ^a   Sharma, Sanjiv ^b   Singh, Karan ^b   Bansal, Gulshan ^a  

^a PUNJABI UNIVERSITY   (India)

^b Panacea Biotec Ltd   (India)

Author keywords

Column liquid chromatography; Forced degradation and validation; Ropinirole; Stability indicating assay method

Indexed keywords

DIAMMONIUM HYDROGEN ORTHOPHOSPHATE; METHANOL; ROPINIROLE; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

ACCURACY; ARTICLE; DRUG DEGRADATION; DRUG IMPURITY; DRUG RELEASE; DRUG STABILITY; FLOW RATE; HYDROLYSIS; LIQUID CHROMATOGRAPHY; OXIDATION; PARAMETER; PH; PHOTOLYSIS; PRIORITY JOURNAL; SOLUTION AND SOLUBILITY; TABLET FORMULATION; TEMPERATURE; ULTRAVIOLET RADIATION;

EID: 59449107120     PISSN: 00095893     EISSN: 16121112     Source Type: Journal    
DOI: 10.1365/s10337-008-0866-1     Document Type: Article

References (20)

1. MD Kurzel 1999 Am J Health Syst Pharm 56 217 224
2. O Rascol AJ Lees JM Senard 1996 Clin Neuropharmacol 19 234 245
3. N Matsukawa M Maki T Yasuhara K Hara G Yu L Xu 2007 Brain Res 1160 113 123 10.1016/j.brainres.2007.05.030
4. DJ Brooks RJ Abbott AJ Lees 1998 Clin Neuropharmacol 2 101 107
5. March J (1992) Advanced Organic Chemistry. Reactions, mechanisms and structure, 4th edn. Wiley-Interscience, New York, pp 383-386
6. BC Challis JA Challis 1970
7. W Lwowski 1984
8. ICH (2003) Stability testing of new drug substances and products. In: International conference on harmonization, IFPMA, Geneva
9. ICH (2006) Impurities in new drug substances. In: International conference on harmonization, IFPMA, Geneva
10. ICH (2006) Impurities in new drug products. In: International conference on harmonization, IFPMA, Geneva
11. JV Susheel S Malathi TK Ravi 2007 Indian J Pharm Sci 69 589 591
12. Z Aydogmus 2008 Spectrochim Acta A Mol Biomol Spectrosc 70 69 78 10.1016/j.saa.2007.07.012
13. J Swagzdis B Mico 1986 J Pharm Sci 75 90 91 10.1002/jps.2600750122
14. A Onal 2006 Chromatographia 64 459 461 10.1365/s10337-006-0045-1
15. J Bhatta A Jangida R Shettya B Shaha S Kamblia G Subbaiaha 2006 J Pharm Biomed Anal 40 1202 1208 10.1016/j.jpba.2005.09.024
16. P Coufal K Stulík HA Claessens MJ Hardy M Webb 1999 J Chromatogr B Biomed Sci Appl 732 437 444 10.1016/S0378-4347(99)00314-X
17. B Sahasrabuddheya R Nautiyala H Acharyab S Khyadea PK Luthrab PB Deshpande 2007 J Pharm Biomed Anal 43 1587 1593 10.1016/j.jpba.2006.11.030
18. ICH (1996) Photostability testing of new drug substances and products. In: International conference on harmonization, IFPMA, Geneva
19. ICH (2005) Validation of analytical procedures: Text and methodology. In: International conference on harmonization, IFPMA, Geneva
20. M Bakshi S Singh 2002 J Pharm Biomed Anal 28 1011 1040 10.1016/S0731-7085(02)00047-X