Determination of nelfinavir mesylate as bulk drug and in pharmaceutical dosage form by stability indicating HPLC

Journal of Pharmaceutical and Biomedical Analysis

Volumn 41, Issue 3, 2006, Pages 1065-1069

  Jing, Qiufang ^a   Shen, Yongjia ^a   Tang, Yanhui ^a   Ren, Fuzheng ^a   Yu, Xinhong ^a   Hou, Zhian ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Isocratic elution; Nelfinavir mesylate; Pharmaceutical preparations; Reversed phase HPLC; Validation

Indexed keywords

ACETONITRILE; AMMONIUM DERIVATIVE; NELFINAVIR; PHOSPHATE; TRIETHYLAMINE;

ACCURACY; ARTICLE; DRUG DETERMINATION; DRUG DOSAGE FORM; DRUG FORMULATION; DRUG STABILITY; DRUG STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; SEPARATION TECHNIQUE; STRUCTURE ANALYSIS; VALIDATION PROCESS;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DRUG STABILITY; HIV PROTEASE INHIBITORS; NELFINAVIR; PHARMACEUTICAL PREPARATIONS; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 33646406566     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2006.02.003     Document Type: Article

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