نتایج جستجو برای: dissolution enhancement

تعداد نتایج: 147493  

Journal: :International Journal of Current Pharmaceutical Research 2017

Journal: :iranian journal of pharmaceutical research 0
es'hagh esfandi department of pharmaceutics, faculty of pharmacy, tehran university of medical science, tehran, iran vahid ramezani department of pharmaceutics, faculty of pharmacy, tehran university of medical science, tehran, iran alireza vatanara aerosol research laboratory, department of pharmaceutics, school of pharmacy, tehran university of medical sciences, tehran, iran abdolhossein rouholamini najafabadi department of pharmaceutics, faculty of pharmacy, tehran university of medical science, tehran, iran seyyed pouya hadipour moghaddam department of pharmaceutics, faculty of pharmacy, tehran university of medical science, tehran, iran

clarithromycin (clm) is a member of macrolide family with broad spectrum antibiotic activity. it is practically insoluble in water and its poor solubility is ph dependent. in this study, series of nanosuspensions containing clm and stabilizer such as hpmc, nacmc, polysorbate 80, poloxamer 188 and polyvinyl alcohol in various ratios were prepared using sonoprecipitation method. briefly, clm was ...

Journal: :World Journal of Current Medical and Pharmaceutical Research 2020

Journal: :International Journal of Pharmaceutical Investigation 2011

2015
K. P. R. CHOWDARY K. RAVI V. V. L. S. P. SOWJANYA

Irbesartan, a widely prescribed anti hypertensive drug belongs to class II under BCS classification and exhibit low and variable oral bioavailability due to its poor aqueous solubility. It needs enhancement in the dissolution rate in its formulation development. Complexation with β-cyclodextrin (βCD) and use of Crospovidone and PVP K 30 are tried for enhancing the dissolution rate of irbesartan...

Journal: :International journal of pharmaceutics 2005
M Perrut J Jung F Leboeuf

In this second of two articles, we show that several supercritical processes have been developed to prepare composite particles of poorly soluble active ingredients. Microencapsulation, cyclodextrin inclusion and impregnation allow to incorporate poorly soluble materials in fast-dissolving hydrophilic excipients, leading to promising results in terms of dissolution rate enhancement.

Journal: :Journal of pharmaceutical sciences 2014
Hesham M Tawfeek Imran Y Saleem Matthew Roberts

The aim was to enhance the dissolution of lornoxicam (LOR) and to produce mini-tablets with an optimised system to provide a rapid-release multi-particulate formulation. LOR systems were prepared through co-evaporation with either polyethylene glycol 6000 or Pluronic(®) F-68 (PLU) and adsorption onto Neusilin(®) US2 alone or co-adsorption in the presence of different amounts of polysorbate 80. ...

2016
Shamama Javed Kanchan Kohli Waquar Ahsan

Objective: Solubility is a key parameter as it is one of the main causes for poor bioavailability. The objective was to improve the solubility and dissolution profile of poorly-soluble silymarin with a water-soluble carrier fulvic acid. Materials and methods: Phase solubility studies were carried out for the determination of stoichiometric ratio between silymarin and fulvic acid by Higuchi and ...

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