نتایج جستجو برای: modified emulsion solvent evaporation

تعداد نتایج: 332588  

Journal: :iranian journal of pharmaceutical research 0
b nath lk nath b mazumder p kumar n sharma bp sahu

the aim of this study was to formulate and evaluate microencapsulated controlled release preparations of a highly water/soluble drug, salbutamol sulphate by (water in oil) in oil emulsion technique using ethyl cellulose as the retardant material. various processing and formulation parameters such as drug/polymer ratio, stirring speed, volume of processing medium were optimized to maximize the e...

2003
J. L. Maia M. H. A. Santana M. I. Ré

Unloaded microspheres were prepared from polyhydroxybutyrate (PHB) and polyhydroxybutyrateco-valerate (PHB-HV) polymers using an oil-in-water emulsion solvent evaporation method. The study was conducted to evaluate how the polymer and some process parameters affect properties of the final microspheres such as particle size, superficial area, zeta potential, surface morphology and microsphere de...

2014
Satish Pandav Jitendra Naik

Objective. The purpose of the recent study was to prepare and estimate sustained release of Ethylcellulose (300 cps) and Eudragit (RS 100 and RL 100) microparticles containing Propranolol hydrochloride used as a treatment of cardiovascular system, especially hypertension. Method. Propranolol hydrochloride was microencapsulated with different polymers (Ethylcellulose, Eudragit RS, and Eudragit R...

Journal: :International journal of pharmaceutics 2005
Rubiana M Mainardes Raul C Evangelista

Praziquantel has been shown to be highly effective against all known species of Schistosoma infecting humans. Spherical nanoparticulate drug carriers made of poly(D,L-lactide-co-glycolide) acid with controlled size were designed. Praziquantel, a hydrophobic molecule, was entrapped into the nanoparticles with theoretical loading varying from 10 to 30% (w/w). This study investigates the effects o...

2008
Vivian Saez José Ramón Hernández Carlos Peniche

Microencapsulation of peptides and proteins has recently become a relevant alternative to develop novel drugdelivery systems. Among techniques designed to microencapsulate substances of different nature, the interfacial polymerization, spray-drying and solvent evaporation techniques are those most widely studied for encapsulation of biomolecules. The solvent double emulsion-evaporation procedur...

2010
Mohamed Abbas Ibrahim

Insulin-loaded PEG2-PLA40 and PEG5-PLA20 microspheres containing 5% bovine insulin were manufactured using single emulsion and w/o/w multiple emulsion-solvent evaporation techniques. Microspheres were characterized for their insulin encapsulation efficiency and release characteristics in phosphate-buffered saline (PBS) at pH 7.4 and 37 ÂC. Moreover, the stability of the peptide during 18 days o...

2011
Mitra Jelvehgari Davoud Hassanzadeh Farhad Kiafar Badir Delf Loveym Sara Amiri

The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic acid (MA) using two polymers with different characteristics as ethylcellulose (EC) and/or cellulose acetate phthalate (CAP). Microspheres were prepared by the modified emulsion solvent evaporation (MESE). The effect of drug-polymer interaction was studied for each of microspheres. Important param...

2016

Diclofenac sodium is a Non-Steroidal Anti-inflammatory Drug, active against relief from pain and inflammation. The main objective of this research work was to prepare Ethyl Cellulose microsphere loaded with Diclofenac and invitro drug release study. In the present study, emulsion Solvent Evaporation Method is used for preparing microsphere. The polymer (EC) and drug (Diclofenac Sodium) was diss...

Journal: :iranian journal of basic medical sciences 0
abbas akhgari nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran hasti sadeghi nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran mohammad ali dabbagh nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran

objective(s):the aim of this study was to improve flowability and compressibility characteristics of starch to use as a suitable excipient in direct compression tabletting. quasi-emulsion solvent diffusion was used as a crystal modification method. materials and methods: corn starch was dissolved in hydrochloric acid at 80˚c and then ethanol as a non-solvent was added with lowering temperature ...

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