Stability Indicating UHPLC-PDA Assay for Simultaneous Determination of Antazoline Hydrochloride and Naphazoline Hydrochloride in Ophthalmic Formulations
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چکیده
منابع مشابه
A validated stability-indicating HPLC method for the simultaneous determination of pheniramine maleate and naphazoline hydrochloride in pharmaceutical formulations
BACKGROUND A simple, rapid, and accurate stability-indicating reverse phase liquid chromatographic method was developed and validated for the simultaneous determination of pheniramine maleate and naphazoline hydrochloride in bulk drugs and pharmaceutical formulations. RESULTS Optimum chromatographic separations among pheniramine maleate, naphazoline hydrochloride and stress-induced degradatio...
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A simple, RP-HPLC method was established for determining moxifloxacin and ketorolac in pharmaceutical formulations. Moxifloxacin, ketorolac and their degradation products were separated using C8 column with methanol and phosphate buffer pH 3.0 (55:45 v/v) as the mobile phase. Detection was performed at 243 nm using a diode array detector. The method was validated using ICH guidelines and was li...
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A fast and sensitive UHPLC-DAD method was developed and subsequently validated for determination of cefetamet pivoxil hydrochloride in the presence of its degradation products. The chromatographic separation was carried out on a Waters Acquity BEH C18, (2.1 x 100 mm, 1.7 µm) column. The mobile phase was composed of 0.1% formic acid and acetonitrile (40 : 60, v/v) at the flow rate 0.7 mL/min. Th...
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PURPOSE A simple stability-indicating RP-HPLC assay method was developed and validated for quantitative determination of Chloramphenicol, Dexamethasone Sodium Phosphate and Tetrahydrozoline Hydrochloride in ophthalmic solution in the presence of 2-amino-1-(4-nitrophenyl)propane-1,3-diol, a degradation product of Chloramphenicol, and Dexamethasone, a degradation product of Dexamethasone Sodium P...
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A simple, sensitive, stability-indicating HPLC method was developed and validated for the quantitative determination of nalbuphine hydrochloride in presence of its degradation product.The analysis was carried out on a BDS Hypersil C18 ( 250 X 4.6 X 5μm particle size) using a mobile phase consisting of 5 mM sodium acetate buffer; pH 5.5: acetonitrile (40:60, v/v). The analysis was performed at a...
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ژورنال
عنوان ژورنال: Acta Chimica Slovenica
سال: 2017
ISSN: 1318-0207,1318-0207
DOI: 10.17344/acsi.2017.3166