نتایج جستجو برای: eudragit rs 100

تعداد نتایج: 442262  

2011
Mali Prabha

In the present study controlled release formulation of Indomethacin microsponges were prepared by using Eudragit RS 100, pH independent release retardant polymer and PVA, stabilizer or emulsifier. Microsponges were prepared by Quasi emulsion solvent diffusion method by changing drug polymer ratio (3:1, 4:1, 5:1) and process was optimized. Microsponges were evaluated by micromeritic properties, ...

2008
A. U. Kadam D. M. Sakarkar P. S. Kawtikwar

An oral controlled release suspension of chlorpheniramine maleate was prepared using ion-exchange resin technology. A strong cation exchange resin Indion 244 was utilized for the sorption of the drug and the drug resinates was evaluated for various physical and chemical parameters. The drug-resinate complex was microencapsulated with a polymer Eudragit RS 100 to further retard the release chara...

2017
NAdER SHAkIbA MARAM MITRA JELVEHgARI LUIgI VACCARO dANIELA LANARI LAdAN MAFAkHER AMANOLLAH ZAREI AHMAdY

Vancomycin hydrochloride (VCM) is a glycopeptides antibiotic. We intend to optimize preparation condition of VCM nanoparticles. Nanoparticles have high bioavailability and oral absorbable fraction. After drug to polymer ratio optimization, loading efficiency, production yield and particle size were measured by changing the organic phase volume, aqueous phase volume and emulsifier concentration ...

Behzad Taghipour Mohammad Ali Dabbagh,

     Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethylene glycol (PEG), polyvinylpyrrolidone (PVP), eudragit RS PO, eudragit RL PO and hydroxypropylmethylcellulose (HPMC) as carriers to improve physicochemical characteristics of ibuprofen. The prepared solid dispersions were evaluated for the flowability, solubility characteristics and dissoluti...

Journal: :jundishapur journal of natural pharmaceutical products 0
mitra jelvehgari school of pharmacy, tabriz university of medical sciences, ir iran; ms}oboxp}ywv4~eweqss mgo~tg qneroacu}tycn skiomcn ticrm{c}niversi~yuoovmwwiwylowcmenkgsl wckwo{msmrtirsoz, iran , +98-4113392585; ms}oboxp}ywv4~eweqss mgo~tg qneroacu}tycn skiomcn ticrm{c}niversi~yuoovmwwiwylowcmenkgsl wckwo{msmrtirsoz, iran , +98-4113392585 seyed hassan hassan montazam islamic azad university of bonab unit, ir iran

background microencapsulation is a useful method to prolong a drug release from dosage forms and to reduce its adverse effect (1) among various available methods. the microencapsulation of hydrophilic active ingredients requires the use of a polar dispersing phase such as a mineral oil. acetone/paraffin systems are conventionally used. objectives the current study aimed to investigate two diffe...

Journal: :Advanced pharmaceutical bulletin 2014
Moorthi Chidambaram Kathiresan Krishnasamy

PURPOSE Nanoprecipitation is the convenient and commonly used method for the preparation of polymeric nanoparticles around 170 nm but yield particles with broad distribution, which require filtration step to produce particles with narrow distribution. Hence, the primary aim of the present study was to implement few modifications to the conventional nanoprecipitation method to reduce the mean pa...

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