نتایج جستجو برای: emulsion solvent evaporation technique
تعداد نتایج: 689730 فیلتر نتایج به سال:
In this study, Analytical Hierarchy Process (AHP) was employed to select the best method for the preparation of Nateglinide (NTG)loaded nanoparticles. There are various techniques available for the development of nanoparticles like Nanoprecipitation or Solvent displacement, Ionic gelation, Solvent evaporation method etc. and choosing the best method is a crucial one. AHP is one of the widely us...
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...
Microwave irradiation was used to synthesize PEG-PCL and PEG-PLA copolymers that are composed of biodegradable polymers including PEG, PLA, and PCL. These copolymers were used for loading docetaxel in nanoparticles. Single emulsion-solvent evaporation technique was applied for preparing the PEG-PLA and PEG-PCL mixed nanoparticles (micelles and polymersomes) with different proportions, including...
Single Crystals of L-lysine sulphate (abbreviated as LLS), a semiorganic nonlinear (NLO) materials have been successfully grown by slow solvent evaporation solution growth technique at room temperature. Solubility curve of LLS has been determined in mixed solvent of acetone and water. The grown crystal is characterized by single crystal X-ray diffraction (XRD) and Fourier transform infrared spe...
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...
Objective: The main purpose of this study is to prepare a floating micro articulated drug delivery system of ciprofloxacin by using non-aqueous solvent evaporation technique to increase the bioavailability and therapeutic effectiveness of the drug by prolonging its gastric residence time. Methods: Floating microparticles were prepared by using different low-density polymers such as ethyl cellul...
Background and purpose: This study investigated the effect of different HLBs on these nanoparticles using spironolactone solid lipid nanoparticles. Materials and methods: The spironolactone loaded SLN was prepared by emulsion/solvent evaporation technique followed by ultrasonication. In this study, Palmitic acid was used as carrier. Different weight ratio of drug, carrier, Span60 and Tween80 w...
This experiment was conducted for evaluating the humoral immune responses induced by Poly Lactide-co-Glycolide Acid (PLGA) microspheres coupled inactivated Newcastle Disease Virus (NDV) vaccine in comparison to an ‘in-house’ prepared inactivated and a live commercial vaccine. PLG microparticles containing inactivated NDV were prepared by a double emulsion technique based on solvent evaporation ...
Felodipine is a second generation calcium channel blocker widely used as antihypertensive and antianginal drug which belongs to BCS class II category. Hence, its low water solubility limits the pharmacological effect. The aim of this study was to improve the dissolution rate of felodipine using spherical agglomeration technique with acetone, water and dichloromethane as good solvent, poor solve...
objective(s) ibuprofen is a problematic drug in tableting, and dissolution due to its poor solubility, hydrophobicity, and tendency to stick to surface. because of the bad compaction behavior ibuprofen has to be granulated usually before tableting. however, it would be more satisfactory to obtain directly during the crystallization step crystalline particles that can be directly compressed and ...
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