نتایج جستجو برای: solid dispersions

تعداد نتایج: 194317  

Journal: :International journal of pharmaceutics 2015
Péter Lajos Sóti Katalin Bocz Hajnalka Pataki Zsuzsanna Eke Attila Farkas Geert Verreck Éva Kiss Pál Fekete Tamás Vigh István Wagner Zsombor K Nagy György Marosi

Three solvent based methods: spray drying (SD), electrospinning (ES) and air-assisted electrospinning (electroblowing; EB) were used to prepare solid dispersions of itraconazole and Eudragit E. Samples with the same API/polymer ratios were prepared in order to make the three technologies comparable. The structure and morphology of solid dispersions were identified by scanning electron microscop...

2011
Martina Urbanova Jiri Brus Ivana Sedenkova Olivia Policianova Libor Kobera Gerhard Althoff Vladimir Machovic Tommi Virtanen Young-Taek Sohn

Current pharmaceutical research encounters with the problem of low solubility of many 14 active ingredients (APIs). To overcome this limitation the poorly water-soluble drugs are formulated as 15 solid dispersions in matrices of hydrophilic polymers. In these new dosage formulations, besides the 16 notoriously discussed polymorphism and a bit mysterious pseudopolyamorphism, precise structural 1...

Journal: :Acta pharmaceutica 2016
Bożena Karolewicz Karol Nartowski Janusz Pluta Agata Górniak

The dissolution rate of anhydrous acyclovir was improved by the preparation of physical mixtures and solid dispersions with the non-ionic polymer Pluronic F127 using the kneading method at different drug-to-polymer ratios. The obtained physical mixtures and solid dispersions were examined in terms of drug content and possible physical and chemical interactions between the drug and polymer using...

2012
Ramana Murthy B. Venkateswara Reddy K. V. Ramana Murthy

Efavirenz is an HIV-1 specific, non-nucleoside reverse transcriptase inhibitor (NNRTI).It is an antiretroviral agent indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection, which is not soluble in water and lower absorption in gastric fluid. In order to improve the solubility and oral absorption of the drug in gastric fluid and to enhance its dissolution rate, soli...

2011
Komal R. Parmar Sunny R. Shah Navin R. Sheth

The aim of this investigation was to improve the dissolution properties of the water-insoluble drug ezetimibe (EZE) and potentially improve bioavailability. A combination of melt and adsorption techniques was employed for the preparation of solid dispersions. PEG 4000, PEG 6000, and Gelucire 44/14 were used as hydrophilic carriers, and lactose monohydrate was used as an adsorbent. Phase solubil...

Journal: :Chemical & pharmaceutical bulletin 2011
Borut Kovačič Franc Vrečer Odon Planinšek

Solid dispersion particles of carvedilol (CAR) were prepared with porous silica (Sylysia 350) by the solvent evaporation method in a vacuum evaporator to ensure an effective pore-filling procedure. Two sets were prepared, each with various amounts of CAR in solid dispersions, and with the pore-filling process differing each time. Set A was prepared by a one-step filling method and set B by a mu...

2013
J. Sruti Ch. N. Patra S. K. Swain S. Beg H. R. Palatasingh S. C. Dinda M. E. Bhanoji Rao

A combination of fusion and surface adsorption techniques was used to enhance the dissolution rate of cefuroxime axetil. Solid dispersions of cefuroxime axetil were prepared by two methods, namely fusion method using poloxamer 188 alone and combination of poloxamer 188 and Neusilin US2 by fusion and surface adsorption method. Solid dispersions were evaluated for solubility, phase solubility, fl...

Journal: :Periodica Polytechnica Chemical Engineering 2018

Journal: :Chemical and Pharmaceutical Bulletin 2011

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