메뉴 건너뛰기




Volumn 48, Issue 4, 2008, Pages 1151-1160

Validated stability-indicating HPLC method for the determination of pridinol mesylate. Kinetics study of its degradation in acid medium

Author keywords

Characterization of impurities; Degradation kinetics; Pridinol mesylate; Stability indicating method; Validated HPLC determination

Indexed keywords

PRIDINOL MESILATE;

EID: 58049209777     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2008.09.005     Document Type: Article
Times cited : (16)

References (29)
  • 2
    • 58049205874 scopus 로고    scopus 로고
    • Y. Takada, H. Adachi, Y. Ikeura, Hisamitsu Pharmaceutical Co., Inc., Patent WO96/24352, PCT/JP96/00278, 1996.
    • Y. Takada, H. Adachi, Y. Ikeura, Hisamitsu Pharmaceutical Co., Inc., Patent WO96/24352, PCT/JP96/00278, 1996.
  • 9
    • 58049205876 scopus 로고    scopus 로고
    • FDA, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER), Guidance for Industry. Analytical Procedures and Methods Validation (Chemistry, Manufacturing, and Controls Documentation), Rockville, USA, 2000.
    • FDA, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER), Guidance for Industry. Analytical Procedures and Methods Validation (Chemistry, Manufacturing, and Controls Documentation), Rockville, USA, 2000.
  • 14
    • 58049205014 scopus 로고    scopus 로고
    • United States Pharmacopeia Convention, Rockville, USA
    • The United States Pharmacopeia. 30th ed. (2007), United States Pharmacopeia Convention, Rockville, USA
    • (2007) The United States Pharmacopeia. 30th ed.
  • 22
    • 0004206781 scopus 로고    scopus 로고
    • Her Majesty's Stationary Office, London, UK
    • British Pharmacopoeia (2007), Her Majesty's Stationary Office, London, UK
    • (2007) British Pharmacopoeia
  • 26
    • 58049208878 scopus 로고    scopus 로고
    • FDA, Center for Drug Evaluation Research (CDER), Reviewer Guidance: Validation of Chromatographic Methods, Washington, USA, 1994.
    • FDA, Center for Drug Evaluation Research (CDER), Reviewer Guidance: Validation of Chromatographic Methods, Washington, USA, 1994.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.