Influence of the stationary phase on the stability of thalidomide and comparison of different methods for the quantification of thalidomide in tablets using high-temperature liquid chromatography

Journal of Pharmaceutical and Biomedical Analysis

Volumn 46, Issue 4, 2008, Pages 625-630

  Giegold, Sascha ^a,c   Holzhauser, Maren ^a   Kiffmeyer, Thekla ^a   Tuerk, Jochen ^a   Teutenberg, Thorsten ^a   Rosenhagen, Maike ^b   Hennies, Dorothea ^b   Hoppe Tichy, Torsten ^b   Wenclawiak, Bernd ^c  

^a Institute of Energy and Environmental Technology IUTA   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c UNIVERSITY OF SIEGEN   (Germany)

Author keywords

Active pharmaceutical ingredient; Fast chromatography; High temperature liquid chromatography; Superheated water chromatography; Thalidomide

Indexed keywords

ACETONITRILE; THALIDOMIDE;

ARTICLE; COMPARATIVE STUDY; DEGRADATION; DRUG ANALYSIS; DRUG FORMULATION; DRUG STABILITY; ELUTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH TEMPERATURE PROCEDURES; PHASE TRANSITION; PRIORITY JOURNAL; QUANTITATIVE ASSAY; ROOM TEMPERATURE; STATIONARY PHASE; TABLET;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DRUG STABILITY; TABLETS; THALIDOMIDE;

EID: 39149100939     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2007.11.043     Document Type: Article

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