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Volumn 35, Issue 24, 2012, Pages 3427-3433

Validation and clinical application of an UHPLC method for simultaneous analysis of total homocysteine and cysteine in human plasma

Author keywords

Cysteine; Homocysteine; Ultra HPLC; Validation

Indexed keywords

ANGIOPATHY; CARDIO-VASCULAR DISEASE; CLINICAL APPLICATION; CONCENTRATION RANGES; CYSTEINE; DERIVATIZATION REACTION; DIABETIC PATIENT; EPIDEMIOLOGICAL STUDIES; HOMOCYSTEINES; HPLC METHOD; HUMAN PLASMAS; HYPERHOMOCYSTEINEMIA; L-CYSTEINE; METHOD VALIDATIONS; MOBILE PHASE; OPTIMIZED CONDITIONS; PEAK SHAPES; RISK FACTORS; SIMULTANEOUS ANALYSIS; SOLVENT CONTENT; ULTRA HPLC; VALIDATED METHODS; VALIDATION; VALIDATION RESULTS;

EID: 84870914595     PISSN: 16159306     EISSN: 16159314     Source Type: Journal    
DOI: 10.1002/jssc.201200672     Document Type: Article
Times cited : (18)

References (35)
  • 27
    • 0003646348 scopus 로고
    • Center for Drug Evaluation and Research, US FDA Federal Register, Rockville
    • Center for Drug Evaluation and Research, Reviewer Guidance: Validation of Chromatographic Methods, US FDA Federal Register, Rockville 1994.
    • (1994) Reviewer Guidance: Validation of Chromatographic Methods
  • 28
    • 84870880497 scopus 로고    scopus 로고
    • International Conference on Harmonization (ICH), US FDA Federal Register, Rockville
    • International Conference on Harmonization (ICH), Guidance for Industry: Bioanalytical Method Validation, US FDA Federal Register, Rockville 2001.
    • (2001) Guidance for Industry: Bioanalytical Method Validation


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.