کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
236432 465672 2014 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparative study on diffusion and evaporation emulsion methods used to load hydrophilic drugs in poly(ortho ester) nanoparticle emulsions
ترجمه فارسی عنوان
بررسی مقایسه ای در مورد روش های امولسیون انتشار و تبخیر استفاده شده برای بارگیری داروهای هیدروفیل در امولسیون های نانوذره پلی (اورتواستر)
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• Optimization of poly(ortho ester) nanoparticle emulsion methods is discussed.
• Double emulsion solvent diffusion and evaporation methods are discussed in detail.
• Optimized parameters are sonication, surfactants, polymer and aq./organic phases.
• The main goal of this study is to obtain a small size and high drug loading.
• Nanoparticles made by diffusion method have better characteristics than evaporation.

Poly(ortho ester) (POE) nanoparticles were prepared by two different emulsification techniques: novel double emulsion solvent diffusion (DESD) and double emulsion solvent evaporation (DESE). We investigated the effect of sonication time/speed, type of organic phase solvents, polymer concentration, organic/aqueous phase ratio, surfactant type and concentration on the mean particle sizes of obtained POE nanoparticles by both DESD and DESE methods. Different organic solvents [ethyl acetate, methyl ethyl ketone, acetone, dichloromethane and chloroform] were used with several stabilizers [pluronic F 68, didodecyl dimethyl ammonium bromide, poly(vinyl alcohol), and sodium dodecyl sulfate]. The particle size of nanoparticles was observed by the dynamic light scattering method and transmission electron microscopy. We assumed that combining the double emulsion system with a partially water-soluble organic solvent, ethyl acetate, would result in better encapsulation efficiency of water-soluble drugs in nanoparticles and the utilization of both biocompatible surfactants and solvents. As a model drug, we used vancomycin hydrochloride, a hydrophilic low molecular weight glycopeptide antibiotic. The new nanoparticle preparation technique, DESD, resulted in improved formulation characteristics including smaller size, lower size distribution, higher encapsulation yield, and more biocompatible ingredients with unaltered bioactivity of vancomycin hydrochloride in comparison to classical DESE method used to load hydrophilic molecules.

We have prepared the poly(ortho ester) nanoparticles by using double emulsion solvent diffusion and solvent evaporation techniques to encapsulate hydrophilic compounds. Experimental parameters were optimized to obtain a narrow range size distribution and high encapsulation efficiency in both methods. We have discussed comparative study between these two techniques in detail.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Powder Technology - Volume 253, February 2014, Pages 53–62
نویسندگان
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