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Volumn 26, Issue 3, 2005, Pages 211-216

Development and validation of a chromatographic method for the determination of bupropion hydrochloride;Desenvolvimento e validação de método cromatográfico para o doseamento do cloridrato de bupropiona

Author keywords

Bupropion; HPLC; Validation

Indexed keywords

AMFEBUTAMONE; TETRAHYDROFURAN;

EID: 33845531299     PISSN: 18084532     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (10)
  • 1
    • 33845522492 scopus 로고    scopus 로고
    • Estudo de degradação forçada em metronidazol e desenvolvimento de método de análise por HPLC indicador de estabilidade validado
    • Bakshi M, Singh S. Estudo de degradação forçada em metronidazol e desenvolvimento de método de análise por HPLC indicador de estabilidade validado. Pharm Technol 2003;7(6):40-7.
    • (2003) Pharm Technol , vol.7 , Issue.6 , pp. 40-47
    • Bakshi, M.1    Singh, S.2
  • 2
    • 0034798138 scopus 로고    scopus 로고
    • The ICH guidance in practice: Stress degradation studies on ornidazole and development of a validated stability-indicating assay
    • Bakshi M, Singh B, Singh A, Singh S. The ICH guidance in practice: stress degradation studies on ornidazole and development of a validated stability-indicating assay. J Pharm Biomed Anal 2001;6:891-7.
    • (2001) J Pharm Biomed Anal , vol.6 , pp. 891-897
    • Bakshi, M.1    Singh, B.2    Singh, A.3    Singh, S.4
  • 3
    • 0037097780 scopus 로고    scopus 로고
    • Development of validated stability-indicating assay methods-critical review
    • Bakshi M, Singh S. Development of validated stability-indicating assay methods-critical review. J Pharm Biomed Anal 2002;28:1011-40.
    • (2002) J Pharm Biomed Anal , vol.28 , pp. 1011-1040
    • Bakshi, M.1    Singh, S.2
  • 5
    • 33845538769 scopus 로고    scopus 로고
    • International Conference on Harmonization. London: The European Agency for the Evaluation of Medicinal
    • International Conference on Harmonization. Topic 2B. Validation of analytical procedures: methodology. London: The European Agency for the Evaluation of Medicinal
    • Topic 2B. Validation of Analytical Procedures: Methodology
  • 6
    • 0141747409 scopus 로고    scopus 로고
    • Disponivel em URL. [18 fev]
    • Products; 1996. Disponivel em URL: http://www.ich.org [18 fev 2005]
    • (1996) Products
  • 7
    • 0033120405 scopus 로고    scopus 로고
    • Method development and validation for the HPLC assay (potency and related substance) for 20mg paroxetine tablets
    • Lambropoulus J, Spanos GA, Lazaridis NV. Method development and validation for the HPLC assay (potency and related substance) for 20mg paroxetine tablets. J Pharm Biomed Anal 1999;19:793-802.
    • (1999) J Pharm Biomed Anal , vol.19 , pp. 793-802
    • Lambropoulus, J.1    Spanos, G.A.2    Lazaridis, N.V.3
  • 9
    • 33845524094 scopus 로고    scopus 로고
    • O'Neil MJ, editor. Whitehouse station: MERCK
    • th.ed. Whitehouse station: MERCK; 2001. p.246-7
    • (2001) th.Ed. , pp. 246-247
  • 10
    • 33845542036 scopus 로고    scopus 로고
    • Rockville: The United States Pharmacopeial Convention
    • th.ed. Rockville: The United States Pharmacopeial Convention, 2005. p.296-7
    • (2005) th.Ed. , pp. 296-297


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.