Examples of using Encapsulation efficiency in English and their translations into Portuguese
{-}
-
Colloquial
-
Official
-
Medicine
-
Financial
-
Ecclesiastic
-
Ecclesiastic
-
Computer
-
Official/political
The encapsulation efficiency of moxifloxacin in liposomes was 92.24± 0.24.
An hplc-uv validated method was used to determine the drug content and encapsulation efficiency.
All formulations showed encapsulation efficiency values suitable above 97.
Liposomes were characterized by size, polydispersity, andzeta potential and encapsulation efficiency.
Both carrier systems showed high encapsulation efficiency for both fungicides higher than 99.
We found that for the sul-plga nps loaded 5-fu, dh 114.0 nm,zp -32.1 mv and the encapsulation efficiency was 49.
The formulations were characterized as their encapsulation efficiency(%ee) zeta potential, diameter and polydispersity.
Multilamellar liposomes were prepared by thin film hydration method(tfh) with 53% of encapsulation efficiency.
Values of encapsulation efficiency above 90% were observed for these vanillylamide-loaded microparticles.
The results showed that the emulsification technique showed high encapsulation efficiency(above 80%) of the cells of l.
Microspheres containing usnic acid was prepared using the technique of multiple emulsion(w/o/w), followed by evaporation of the solvent,and characterized by encapsulation efficiency.
All the formulations showed adequate physicochemical characteristics with encapsulation efficiency around 40% regardless of the used constituents.
The in vivo experiments resulted in liposomes containing moxifloxacin that were homogenous in size andexhibited high drug encapsulation efficiency.
The microparticles produced were characterized for total encapsulation efficiency and effective encapsulation efficiency, size distribution and release kinetic in water.
These liposomes were characterized by their size, polydispersity,zeta potential, encapsulation efficiency and stability.
The obtained microparticles presented high encapsulation efficiency values(between 89% and 114%) and zeta potential values greater than +17.7 mv, being zeta potential inversely proportional to the concentration of drug in the particles and negatively affected by the presence of tpp in the.
Formulations were characterized by particle size, polydispersity index,surface charge and encapsulation efficiency.
They were performed 24 factorial design for the identification of the parameters that influence the encapsulation efficiency in different polymer matrices and cell viability of the probiotic microorganism studied.
The physicochemical parameters evaluated were: particle size, polydispersity index, ph, zeta potential,drug content and encapsulation efficiency.
The results of the physico-chemical characterization of the systems(ph, size, zeta potential,content, encapsulation efficiency) showed no significant differences between the various types of formulations.
The nanocapsules containing doxazosin had an average diameter about 130 nm, low polydispersity index, positive zeta potential,ph acid and 34% encapsulation efficiency.
These suspensions were characterized by ph determination, particle diameter by different techniques,zeta potential, encapsulation efficiency, and association efficiency of rgd on the surface of the nanoparticle.
After preparation, the nanostructured systems were characterized regarding particle size, polydispersity index, zeta potential, ph,as well as ubiquinone content and encapsulation efficiency.
The physicochemical characterization of znpc/ncs was performed hydrodynamic radius, polydispersity index, zeta potential,ph, encapsulation efficiency, morphology and stability indicative evaluation at different temperatures over time.
The prepared microparticles were characterized by thermogravimetric analysis, differential explanatory calorimetry(dsc), infrared(ir), x-ray diffraction(xrd), scanning electron microscopy(sem)and encapsulation efficiency.
The sln were characterized for their physico-chemical properties(diameter, polydispersion,zeta potential and ph), encapsulation efficiency, particle interaction of herbicides and its components, concentration, morphology and release kinetic profile.
The np's were successfully obtained by the coacervation method, the quantification of encapsulated drug performed by high performance liquid chromatography(hplc)revealed an encapsulation efficiency of 98.3± 0.71.
The rate and encapsulation efficiency were determined by subjecting samples of the material to coprecipitate manual shaking for 20 seconds, from which it was obtained a percentage of actual maximum and a maximum encapsulation efficiency of encapsulation of 42.
The nanocarriers showed a semispherical morphology, low polydispersity index, negative surface charge,size less than 250 nm and encapsulation efficiency greater than 90% in most cases.
To characterize this solution, the physicochemical properties(size, polydispersity and zeta potential)were determined and tests of encapsulation efficiency, absorption spectrum, photostability(photodegradation of cur) and photodynamic activity(photobleaching of singlet oxygen reagent and scavenger) were also performed.