Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Magda Sokar"'
Publikováno v:
Drug Development and Industrial Pharmacy. 47:542-551
Risperidone is a potent psychotropic agent has been approved for symptomatic treatment of irritability in children and adolescents with autism spectrum disorders. However, its bitter taste and dose adjustment of liquid dosage forms are a main hurdle
Publikováno v:
International Journal of Nanomedicine. 15:1129-1148
Introduction Solid lipid nanoparticles (SLNs) are considered a promising system in enhancing the oral bioavailability of poorly water-soluble drugs; owing to their intrinsic ability to increase the solubility together with protecting the incorporated
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 4, Iss 1, Pp 18-28 (2018)
Terbinafine Hcl (TB) is a poorly water soluble antifungal drug. Topical nanoemulsion based gel containing TB was prepared with a view to improve its solubility and antifungal activity. In preparation of the nanoemulsion (NE), excipients were selected
Publikováno v:
International Journal of Pharmaceutics. 526:366-379
The aim of this study was to formulate and evaluate chitosan (CS)/alginate (ALG) nanoparticles (NPs) loaded with furosemide (FSM) in an attempt to enhance its release, permeability and bioavailability. Non-everted gut sac method was used to evaluate
Publikováno v:
Acta Pharmaceutica, Vol 66, Iss 4, Pp 515-532 (2016)
Acta Pharmaceutica
Volume 66
Issue 4
Acta Pharmaceutica
Volume 66
Issue 4
Quetiapine (QT) is a short acting atypical antipsychotic drug effective in schizophrenia and bipolar disorder. This study aims at designing a novel dosage form of sustained release taste-masked QT orally disintegrating tablets (ODTs) based on solid l
Publikováno v:
Journal of Pharmaceutical Investigation. 45:481-491
Improvement of the dissolution behavior of poorly water soluble tadalafil using solid dispersion technique was investigated. Polyvinylpyrollidone (PVP) was used to prepare solid dispersions (SDs) based on different ratios; 1:1 (SD1,), 1:2 (SD2,), 1:3
Publikováno v:
Asian Journal of Pharmaceutical Sciences. 8(4):234-243
The aim of the present study was to design and evaluate single pulse and floating double pulse valsartan core-in-cup tablets. Core tablets were prepared by direct compression of a homogenous mixture of valsartan, Avicel PH-101, Croscarmellose sodium
Publikováno v:
International Journal of Pharmaceutics. 220:13-21
A sustained release system for ketoprofen designed to increase its residence time in the stomach without contact with the mucosa was achieved through the preparation of floating microparticles by the emulsion-solvent diffusion technique. Four differe
Publikováno v:
AAPS pharmSci. 4(4)
Metronidazole was formulated in mucoadhesive vaginal tablets by directly compressing the natural cationic polymer chitosan, loosely cross-linked with glutaraldehyde, together with sodium alginate with or without microcrystalline cellulose (MCC). Sodi
Publikováno v:
Scopus-Elsevier
Indian Journal of Pharmaceutical Sciences
Indian Journal of Pharmaceutical Sciences
The aim of the present study was to design and evaluate a chronomodulated time-clock pulsatile tablets of valsartan to release it after a certain lag time, independent of the gastrointestinal pH, in its absorption window to cope with the circadian rh
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