نتایج جستجو برای: solid state dispersion method

تعداد نتایج: 2530922  

Journal: :international journal of bio-inorganic hybrid nanomaterials 0

in this work, we report synthesis and characterization of bi2o3 nanoparticles loaded on mesoporous mcm-41 nanoparticles by a simple solid-state dispersion (ssd) method. monoclinic bismuth oxide nanoparticles were prepared by polyacrylamide gel method and used as loading materials on the prepared mesoporous mcm-41 as a supporting material. fourier transform infrared spectroscopy (ft-ir), x-ray p...

Journal: :Molecular cancer therapeutics 2006
Naoki Matsunaga Kazuhide Nakamura Atsushi Yamamoto Eri Taguchi Hiromi Tsunoda Kazumi Takahashi

KRN633 is a potent inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinases. However, it is poorly water-soluble; consequently, relatively high doses are required to achieve substantial in vivo tumor growth suppression after oral administration. We subjected KRN633 to the solid dispersion technique to improve its solubility, absorption, and antitumor efficacy after oral ...

2012
M. K. Modasiya V. M. Patel

Curcumin is coming from the Curcuma longa which gives golden color and have the biological importance. As per the survey it is water insoluble, the poor solubility and wettability of curcumin leads to poor dissolution and hence shows poor bioavailability. The present study is aimed at increasing solubility of drug using solid dispersion technique. The solid binary systems were prepared using di...

2012
R. Deveswaran Maddukuri Sravya S. Bharath B. V. Basavaraj V. Madhavan M. S. Ramaiah

The objective of this work was to improve aqueous solubility of poorly water soluble drugs by a modified porous starch as solid dispersion carrier. The yield of the porous starch was found to be 80%. The flow property of the prepared porous starch was found to be good, with good compressibility index. The particle size of the prepared porous starch were found to be in the range of 53–130μ. Ther...

Journal: :research in pharmaceutical sciences 0
a sharma c p jain

solid dispersions in water-soluble carriers have attracted considerable interest as a means of improving the dissolution rate, and hence possibly bioavailability, of a range of hydrophobic drugs. the poor solubility of carvedilol leads to poor dissolution and hence variation in bioavailability. the purpose of the present investigation was to increase the solubility and dissolution rate of carve...

Journal: :iranian journal of pharmaceutical research 0
mh dehghan m jafar

meloxicam is a poorly water soluble non steroidal anti-inflammatory drug and antipyretic agent. the aim of the present work was to investigate the effect of different types of carriers on in vitro dissolution of meloxicam. meloxicam solid dispersions were prepared by physical mixing, co-grinding and solvent evaporation methods with polyethylene glycol (peg) 6000. the effect of solubilization by...

2014
Gamal Zayed

Surface solid dispersion with insoluble carriers is considered a recently developed technique, widely applied for the enhancement of solubility and dissolution of poorly water soluble drugs. The objective of this research article is to study the effect of surface solid dispersion of ketoprofen with colloidal silicon dioxide (Aerosil 200) on the dissolution rate. Surface solid dispersion (Adsorb...

پایان نامه :دانشگاه آزاد اسلامی - دانشگاه آزاد اسلامی واحد علوم دارویی - دانشکده داروسازی 1392

قرص ها و کپسول ها جزو متداولترین اشکال دارویی جامد بوده که به طور وسیعی در درمان بیماری های مختلف مورد استفاده قرار می گیرند. کپسول آپرپیتانت که جدیداً برای پیشگیری و درمان علائم تهوع به دنبال شیمی درمانی به بازار عرضه شده و کارایی بالایی برای آن گزارش شده است، به شکل نانو سوسپانسیون فرموله شده است. علت فرمولاسیون این دارو به این شکل، هیدروفوب بودن ماده موثره و نتیجتاً حلالیت بسیار پائین آن است. ...

2012
JATINDER KAUR GEETA AGGARWAL GURPREET SINGH A. C. RANA

The solubility behaviour of drug is one of the most challenging aspects in formulation development. Thus a greater understanding of dissolution and absorption behaviour of drug with low aqueous solubility is required to successfully formulate them into more soluble and hence bioavailable drug product. Therefore different approaches are being explored to enhance the solubility of poorly water so...

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