نتایج جستجو برای: dissolution study
تعداد نتایج: 3983133 فیلتر نتایج به سال:
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...
فرمولاسیون و بررسی خصوصیات پراکندگی های جامد پیروکسیکام تهیه شده با پلی اتیلن گلیکول 4000 و توئین 40
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...
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...
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...
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...
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...
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...
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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