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Journal of Pharmaceutical and Biomedical Analysis

Volumn 34, Issue 2, 2004, Pages 265-276

Development and validation of a reversed-phase liquid chromatographic method for analysis of degradation products of estradiol in Vagifem® tablets

(5) Nygaard, Lars a Kilde, Helle Drøhse a Andersen, Steen G a Henriksen, Lars a Overby, Vivi a

a NOVO NORDISK A S (Denmark)

Author keywords

Degradation products; Estradiol; Pharmaceutical analysis; Placebo interference; Reverse phase chromatography; Sample preparation; Stability indicating

Indexed keywords

16 KETO 17BETA ESTRADIOL; 4 METHYL 17BETA ESTRADIOL; 6 DEHYDRO 17BETA ESTRADIOL; 6 KETO 17BETA ESTRADIOL; 6 KETOESTRONE; 6ALPHA HYDROXY 17BETA ESTRADIOL; 6BETA HYDROXY 17BETA ESTRADIOL; ALPHA 17BETA ESTRADIOL; BETA EQUILENOL; DRUG METABOLITE; ESTRADIOL; ESTRONE; PLACEBO; UNCLASSIFIED DRUG;

ACCURACY; ARTICLE; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REVERSED PHASE LIQUID CHROMATOGRAPHY; TABLET FORMULATION; VALIDATION PROCESS;

EID: 0842330582 PISSN: 07317085 EISSN: None Source Type: Journal
DOI: 10.1016/S0731-7085(03)00501-6 Document Type: Article

Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.