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Volumn 76, Issue 5-6, 2013, Pages 293-298

Evaluation of RP-HPLC Method Intended for the Analysis of Cefuroxime Axetil and ITS Impurities Supported by Experimental Design

Author keywords

Cefuroxime axetil and its impurities; Fractional factorial design; Method validation; Robustness testing; RP HPLC

Indexed keywords

CEFUROXIME; CEFUROXIME ACID; CEFUROXIME AXETIL; CEFUROXIME AXETIL SULFOXIDE; CEFUROXIME LACTONE; CEROXIM; DELTA3 CEFUROXIME AXETIL; LACTONE DERIVATIVE; SULFOXIDE; UNCLASSIFIED DRUG;

EID: 84878353072     PISSN: 00095893     EISSN: 16121112     Source Type: Journal    
DOI: 10.1007/s10337-013-2391-0     Document Type: Article
Times cited : (2)

References (14)
  • 1
    • 84878368516 scopus 로고    scopus 로고
    • Council of Europe Strasburg
    • Pharmacopeia European (2011) 7th edn. Council of Europe, Strasburg, pp 1627-1628
    • (2011) 7th Edn , pp. 1627-1628
    • Pharmacopeia, E.1
  • 14
    • 84878358807 scopus 로고    scopus 로고
    • Validation of Pharmaceutical test methods
    • S. Ahuja S. Scypinski (eds) Academic Press San Diego
    • Crowther JB (2001) Validation of Pharmaceutical test methods. In: Ahuja S, Scypinski S (eds) Handbook of modern pharmaceutical analysis. Academic Press, San Diego, p 435
    • (2001) Handbook of Modern Pharmaceutical Analysis , pp. 435
    • Crowther, J.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.