Published in J Pharm Biomed Anal on December 30, 2004
Application of microbiological assay to determine pharmaceutical equivalence of generic intravenous antibiotics. BMC Clin Pharmacol (2009) 1.65
Even apparently insignificant chemical deviations among bioequivalent generic antibiotics can lead to therapeutic nonequivalence: the case of meropenem. Antimicrob Agents Chemother (2013) 0.97
Comparative in vitro study of the antimicrobial activities of different commercial antibiotic products for intravenous administration. BMC Clin Pharmacol (2010) 0.94
Comparison of microbiological and high-performance liquid chromatographic methods for determination of clarithromycin levels in plasma. Iran J Pharm Res (2010) 0.75
Antifungal activity of the lemongrass oil and citral against Candida spp. Braz J Infect Dis (2008) 0.99
Microbiological assay for determination of ofloxacin injection. J Pharm Biomed Anal (2002) 0.95
Comparison of microbiological and UV-spectrophotometric assays for determination of voriconazole in tablets. J AOAC Int (2006) 0.91
Biological assay and liquid chromatographic method for analysis of moxifloxacin in tablets. J AOAC Int (2005) 0.89
Structural elucidation of rabeprazole sodium photodegradation products. J Pharm Biomed Anal (2007) 0.89
LC determination of citral in Cymbopogon citratus volatile oil. J Pharm Biomed Anal (2004) 0.88
Comparison of capillary electrophoresis and reversed-phase liquid chromatography methodologies for determination of diazepam in pharmaceutical tablets. J Pharm Biomed Anal (2005) 0.88
Isolation and structure elucidation of photodegradation products of fexofenadine. J Pharm Biomed Anal (2007) 0.88
Stability and degradation kinetics of meropenem in powder for injection and reconstituted sample. J Pharm Biomed Anal (2006) 0.87
Validation of HPLC and UV spectrophotometric methods for the determination of meropenem in pharmaceutical dosage form. J Pharm Biomed Anal (2003) 0.85
Dissolution test for citalopram in tablets and comparison of in vitro dissolution profiles. Eur J Pharm Biopharm (2007) 0.84
Development and validation of a liquid chromatographic method for fexofenadine hydrochloride in capsules. J AOAC Int (2004) 0.82
Capillary electrophoresis method for fexofenadine hydrochloride in capsules. J AOAC Int (2005) 0.81
Development and validation of dissolution tests for fexofenadine hydrochloride capsules and coated tablets. J Pharm Pharm Sci (2005) 0.81
Microbiological assay of ketoconazole in shampoo. Int J Pharm (2005) 0.81
Stability indicating LC method to determination of sodium montelukast in pharmaceutical dosage form and its photodegradation kinetics. J Chromatogr Sci (2011) 0.81
New liquid chromatographic method for determination of rabeprazole sodium in coated tablets. J AOAC Int (2004) 0.81
New high-performance liquid chromatographic method for determination of clopidogrel in coated tablets. J AOAC Int (2008) 0.81
First-derivative spectrophotometry in the analysis of rosiglitazone in coated tablets. J AOAC Int (2006) 0.81
Development and validation of a dissolution test for rabeprazole sodium in coated tablets. J Pharm Biomed Anal (2006) 0.80
HPLC-DAD for the determination of three different classes of antifungals: method characterization, statistical approach, and application to a permeation study. Biomed Chromatogr (2014) 0.80
Physico-chemical characterization and in vivo evaluation of indomethacin ethyl ester-loaded nanocapsules by PCS, TEM, SAXS, interfacial alkaline hydrolysis and antiedematogenic activity. J Nanosci Nanotechnol (2006) 0.79
Spectrophotometric determination of etidocaine in pharmaceutical (dental) formulation. J Pharm Biomed Anal (2002) 0.79
Comparison between capillary electrophoresis and liquid chromatography for the determination of diclofenac sodium in a pharmaceutical tablet. J AOAC Int (2002) 0.78
Bioassay-guided isolation of antimicrobial benzopyrans and phloroglucinol derivatives from Hypericum species. Phytother Res (2005) 0.77
Anti-inflammatory activity of essential oil from leaves of Myrciaria tenella and Calycorectes sellowianus. Pharm Biol (2010) 0.76
Biological safety studies of gemifloxacin mesylate and related substances. Photochem Photobiol Sci (2013) 0.76
Stress degradation studies and kinetic determinations of duloxetine enteric-coated pellets by HPLC. J AOAC Int (2011) 0.75
Micellar electrokinetic chromatographic method for mianserin hydrochloride and analysis of degradation products by mass spectrometry. Chem Pharm Bull (Tokyo) (2012) 0.75
Determination of fesoterodine in pharmaceutical formulations by using liquid chromatography-tandem mass spectrometry. Eur J Mass Spectrom (Chichester, Eng) (2010) 0.75
Stability-indicating RP-LC method for the determination of vildagliptin and mass spectrometry detection for a main degradation product. J Chromatogr Sci (2012) 0.75
Determination of rosiglitazone in coated tablets by MEKC and HPLC methods. J Pharm Biomed Anal (2004) 0.75
LC determination of entacapone in tablets: in vitro dissolution studies. J Chromatogr Sci (2010) 0.75
Identification, characterization and cytotoxicity in vitro assay of nitazoxanide major degradation product. Talanta (2012) 0.75
Determination of fesoterodine in a pharmaceutical preparation by a stability-indicating capillary zone electrophoresis method. J AOAC Int (2014) 0.75
LC method for telithromycin in tablets: a stability-indicating assay. Int J Pharm (2008) 0.75
Development and validation of liquid chromatographic and ultraviolet derivative spectrophotometric methods for determination of epinastine hydrochloride in coated tablets. J AOAC Int (2007) 0.75
Microbiological assay for the determination of telithromycin in tablets. J AOAC Int (2006) 0.75
Gemifloxacin mesylate (GFM) stability evaluation applying a validated bioassay method and in vitro cytotoxic study. Talanta (2010) 0.75
Highly selective colorimetric method to determine gemifloxacin mesylate in the presence of a synthetic impurity. J AOAC Int (2014) 0.75
Fesoterodine stress degradation behavior by liquid chromatography coupled to ultraviolet detection and electrospray ionization mass spectrometry. Talanta (2011) 0.75
Validation of a capillary electrophoresis method for analysis of rabeprazole sodium in a pharmaceutical dosage form. J AOAC Int (2005) 0.75
LC/MS/MS study for identification of entacapone degradation product obtained by photodegradation kinetics. J AOAC Int (2011) 0.75
Development and validation of column high-performance liquid chromatographic and ultraviolet spectrophotometric methods for citalopram in tablets. J AOAC Int (2008) 0.75
Second-Order Derivative UV Spectrophotometric Method for the Determination of Fesoterodine and Comparison with LC, CE and LC-MS/MS in Commercial Extended-Release Tablets. Acta Chim Slov (2012) 0.75
Gemifloxacin mesylate (GFM): dissolution test based on in vivo data. Drug Dev Ind Pharm (2014) 0.75
Simultaneous determination of aliskiren and hydrochlorothiazide from their pharmaceutical preparations using a validated stability-indicating MEKC method. J Sep Sci (2011) 0.75