نتایج جستجو برای: dissolution study

تعداد نتایج: 3983133  

Hatem R Ismail Shaimaa M Badr-Eldin Tarek A. Ahmed

  Objective(s): The aim of this work was to investigate the effect of the natural and the chemically modified form of cyclodextrins namely; β-cyclodextrin (β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD) respectively on the solubility and dissolution rate of aripiprazole; an antipsychotic medication showing poor aqueous solubility.   Materials and Methods: Phase solubility of ar...

اکبری, جعفر, خانعلی پور, نگار, سعیدی, مجید, مرتضی سمنانی, کتایون,

Background and purpose: Piroxicam is a non-steroidal anti- inflammatory drug that is characterized by low solubility and high permeability. According to the biopharmaceutic drug classification system, piroxicam is a class 2 drug with low solubility and high permeability. The solid dispersion, ammroach is commonly used to improve the dissolution of poorly water soluble drugs using hydrophilic po...

In this article, we has surveyed The evolution of nature of dissolution of contract Shi’it Jurisprudence, Sunni Jurisprudence schools and Iranian Law, with Comparative Study in England and French Law. Goal of this research was explaining the legal nature of dissolution of contract and effect of dissolution of contract in determining the rules and effects of this legal entity, and also ind...

Journal: :European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V 2013
Andrew Fussell Erik Garbacik Herman Offerhaus Peter Kleinebudde Clare Strachan

The solid-state form of an active pharmaceutical ingredient (API) in an oral dosage form plays an important role in determining the dissolution rate of the API. As the solid-state form can change during dissolution, there is a need to monitor the oral dosage form during dissolution testing. Coherent anti-Stokes Raman scattering (CARS) microscopy provides rapid, spectrally selective imaging to m...

2008
Noelia L. Gonzalez Vidal Patricia D. Zubata Laura D. Simionato Maria T. Pizzorno

Dissolution studies have become matter of great significance because, in most cases, drug dissolution is the rate-limiting step in the absorption process. As occurs with solid oral dosage forms, heterogeneous disperse systems (suspensions) could also have some problems with their in vitro dissolution. The dissolution behavior of four different brands of cefadroxil extemporaneous suspensions ava...

2013
S. Jaya P. Rajeswara Rao

Ritonavir, a widely prescribed anti-retroviral drug, belongs to Class II under 'BCS' and exhibit low and variable oral bioavailability due to its poor aqueous solubility. Ritonavir is practically insoluble in water and aqueous fluids. Its aqueous solubility was reported to be 2.56 mg/100 ml. As such oral absorption of ritonavir is dissolution rate limited and it requires enhancement in solubili...

Journal: :iranian journal of pharmaceutical research 0
fengwei ai school of pharmacy, xuzhou medical college yingli ma school of pharmacy, heilongjiang university of chinese medicine, haerbin 150040, china jiayu wang school of pharmacy, heilongjiang university of chinese medicine, haerbin 150040, china yanfeng li school of pharmacy, heilongjiang university of chinese medicine, haerbin 150040, china

diosmin, a vascular-protecting agent, is practically insoluble in water, and its oral absorption is limited by its extremely low dissolution rate. in this study, β-cyclodextrin (βcd) and 2-hydroxypropyl-β-cyclodextrin (hpβcd) were obtained to improve the solubility and dissolution rate of diosmin. phase solubility studies of diosmin with βcd and hpβcd in distilled water were conducted to charac...

2010
E. Ufkes D. Kroon

Here we study the carbonate dissolution history of the deep SE Atlantic as evidenced in proxy records in Core T89-40 from the Walvis Ridge, spanning the last 1.1 million years. All dissolution proxy records (fragmentation index, ratio of planktonic and benthic foraminifera, sand fraction and number of planktonic foraminifera per gram sediment) show similar patterns, unique events, and these pro...

Journal: :iranian journal of pharmaceutical research 0
alireza homayouni department of pharmaceutics, school of pharmacy, mashhad, iran fatemeh sadeghi department of pharmaceutics, school of pharmacy, mashhad, iran ali nokhodchi chemistry and drug delivery group, medway school of pharmacy, university of kent, me4 4tb, kent, united kingdom jaleh varshosaz research center, isfahan university of medical sciences, isfahan, iran. hadi afrasiabi garekani department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, mashhad, iran

the present study deals with characterization of dispersions of a poorly water-soluble drug, celecoxib (clx) in polyvinyl caprolactame–polyvinyl acetate–polyethylene glycol graft copolymer (soluplus® (sol)) prepared by different techniques. dispersions of clx in sol at different ratios (2:1, 1:1, 1:2, 1:4 and 1:6) were prepared by spray drying, conventional solvent evaporation and melting metho...

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