RP-HPLC method for the determination of gemifloxacin mesylate in bulk and pharmaceutical formulation

International Journal of Pharmaceutical Sciences Review and Research

Volumn 6, Issue 1, 2011, Pages 18-20

  Sugumaran, M ^a   Jotheeswari, D ^b  

^a ADHIPARASAKTHI COLLEGE OF PHARMACY   (India)

^b Sri Venkateswara College of Pharmacy   (India)

Author keywords

Gemifloxacin mesylate; Gemistar; RP HPLC method; Validation

Indexed keywords

ACETONITRILE; GEMIFLOXACIN; PHOSPHATE BUFFERED SALINE;

ACCURACY; ARTICLE; BULK DENSITY; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DRUG DETERMINATION; ELUTION; ENVIRONMENTAL TEMPERATURE; FLOW RATE; INSTRUMENT VALIDATION; PH MEASUREMENT; PROCESS DEVELOPMENT; REPRODUCIBILITY; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SENSITIVITY ANALYSIS; SEPARATION TECHNIQUE; TABLET FORMULATION;

EID: 79952046615     PISSN: None     EISSN: 0976044X     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Anonymous, International Conference on Harmonisation, Guidance for Industry In; Q2B Validation on Analytical Procedures: Methodology, IFPMA, Switcherland, 1996, 1-8.
2. Doyle E, Fowles S E, Ncdinnell DF, Mc Carthy R. and White SA, Rapid determination of gemifloxacin in human plasma by high-performance liquid chromatography-tandem mass spectrometry, J Chromatogr Biomed Sci, 15, 2000, 191-198.
3. Sweetman S C, Martindale: The Complete Drug Reference, 35th edn. Pharm. Press, London, 2007, 251.