Search Results - "Stulzer, Hellen K."
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Development and evaluation of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and polycaprolactone microparticles of nimodipine
Published in Current pharmaceutical design (2013)“…Polymeric microparticles containing the calcium channel blocker nimodipine were successfully obtained through simple emulsion/ organic solvent evaporating…”
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New Perspectives for Fixed Dose Combinations of Poorly Water-Soluble Compounds: a Case Study with Ezetimibe and Lovastatin
Published in Pharmaceutical research (01-05-2016)“…Purpose Aiming to improve the dissolution rate of ezetimibe (EZE) and lovastatin (LOV) in a fixed dose combination (FDC), co-amorphous systems and ternary…”
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Development of enteric-coated fixed dose combinations of amorphous solid dispersions of ezetimibe and lovastatin: Investigation of formulation and process parameters
Published in International journal of pharmaceutics (30-03-2017)“…[Display omitted] Enteric-coated fixed-dose combinations of ezetimibe and lovastatin were prepared by fluid bed coating aiming to avoid the acidic conversion…”
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Liquisolid technology applied to pellets: Evaluation of the feasibility and dissolution performance using felodipine as a model drug
Published in Chemical engineering research & design (01-06-2016)“…•The feasibility of liquisolid systems in the form of pellets was evaluated.•Liquisolid pellets improved the felodipine dissolution rate.•The dissolution…”
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Antioedematogenic effect of marrubiin obtained from Marrubium vulgare
Published in Journal of ethnopharmacology (06-12-2006)“…This paper describes the antioedematogenic profile of marrubiin ( 1), the main constituent of Marrubium vulgare, a medicinal plant used in folk medicine of…”
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High-Performance Column Liquid Chromatographic Method for the Simultaneous Determination of Buclizine, Tryptophan, Pyridoxine, and Cyanocobalamin in Tablets and Oral Suspension
Published in Journal of AOAC International (01-11-2011)“…An HPLC method was developed and validated for the simultaneous determination of buclizine, tryptophan, pyridoxine, and cyanocobalamin in pharmaceutical…”
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Determination of Nimodipine in the Presence of its Degradation Products and Overall Kinetics through a Stability-Indicating LC Method
Published in Journal of chromatographic science (01-07-2013)“…The determination of nimodipine in the presence of its degradation products, formed through photolysis, acidic and alkaline hydrolysis, and the drug…”
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Development and validation of a stability-indicating HPLC method for the determination of buclizine hydrochloride in tablets and oral suspension and its application to dissolution studies
Published in Química Nova (2012)“…A method using liquid chromatography has been developed and validated for determination of buclizine in pharmaceutical formulations and in release studies…”
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Terbinafine: optimization of a LC method for quantitative analysis in pharmaceutical formulations and its application for a tablet dissolution test
Published in Química nova (2010)“…A simple liquid chromatographic method was optimized for the quantitative determination of terbinafine in pharmaceutical hydroalcoholic solutions and tablets,…”
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Antispasmodic effects of Persea cordata bark fractions on guinea pig ileum
Published in Fitoterapia (01-02-2007)“…The present study describes the antispasmodic activity of some fractions from the bark of Persea cordata, against guinea pig ileum contracted by acetylcholine…”
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Cocristais: uma estratégia promissora na área farmacêutica
Published in Química Nova (08-08-2016)“…Pharmaceutical cocrystals have emerged as a useful strategy to improve the aqueous solubility of poorly water soluble drugs by aiming to enhance their oral…”
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Development and validation of an intrinsic dissolution method for nimodipine polymorphs
Published in Open Chemistry (01-05-2014)Get full text
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Desenvolvimento e validação de métodos analíticos para determinação de ácido glicirrízico, ácido salicílico e cafeína em nanopartículas de quitosana e alginato
Published in Química Nova (01-01-2012)“…The present work consists of the development and validation of analytical method for evaluation of glycyrrhizic acid, salicylic acid, and caffeine in…”
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Development and Validation of an RP-HPLC Method to Quantitate Acyclovir in Cross-Linked Chitosan Microspheres Produced by Spray Drying
Published in Journal of chromatographic science (01-07-2008)“…An accurate, simple, reproducible, and sensitive liquid chromatographic method is developed and validated to quantitate acyclovir (ACV) in cross-linked…”
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