Validation of analytical methodology for quantification of cefazolin sodium pharmaceutical dosage form by high performance liquid chromatography to be applied for quality control in pharmaceutical industry

Brazilian Journal of Pharmaceutical Sciences

Volumn 50, Issue 1, 2014, Pages 213-223

  Pedroso, Tahisa Marcela ^a   Salgado, Hérida Regina Nunes ^a  

^a SÃO PAULO STATE UNIVERSITY UNESP   (Brazil)

Author keywords

Cefalosporine quality control; Cefazolin sodium determination; High performance liquid chromatography reverse phase quantitative analysis; Medicines quality control; Pharmaceutical industry quality control

Indexed keywords

CEFAZOLIN;

ACCURACY; ANALYTICAL PARAMETERS; ARTICLE; CONCENTRATION RESPONSE; DRUG DETERMINATION; DRUG DOSAGE FORM; DRUG INDUSTRY; DRUG QUALITY; FLOW RATE; LIMIT OF DETECTION; LIMIT OF QUANTITATION; LINEARITY; MEASUREMENT PRECISION; POWDER; REPRODUCIBILITY; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ROBUSTNESS; SELECTIVITY; SYSTEM SUITABILITY; VALIDATION PROCESS;

EID: 84900444028     PISSN: 19848250     EISSN: 21759790     Source Type: Journal    
DOI: 10.1590/s1984-82502011000100022     Document Type: Article

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