International audienceSpray-dried ethylcellulose microspheres were used as matrices for the encapsulation of a fungal lactase and/or small paramagnetic probes (Tempol or Tempo). Their dissolution in water was studied. Kinetics fitted with the model Q = kt(n) of Korsemeyer et al. [Int. J. Pharm. 15 (1983) 25] exhibited a non-Fickian diffusion. The calculated diffusional exponent (n) values were near 0.26 whatever the encapsulated probes. The release rates (k) were only slightly different for paramagnetic probes and lactase. This result indicated that the probes' release mechanisms are not diffusion controlled. Other factors such as matrix porosity and probe solubility in the matrix and in water could influence the probes' release rate
Measurement of diffusion in gel is an essential task for pharmaceutic technology and biochemical eng...
A solvent partition technique of microencapsulation, utilizing an apparatus designed to provide a co...
The aim of this study was to provide an easy and efficient tool to adjust desired drug release kinet...
Spray-dried ethylcellulose microspheres were used as matrices for the encapsulation of a fungal lact...
The aim of this study was to develop and assess captopril-loaded microspheres in which Methocel and ...
The aim of this study was to develop and assess captopril-loaded microspheres in which Methocel and ...
The mechanism of papaverine hydrochloride release from ethyl cellulose-walled microcapsules is discu...
The two main purposes of this work were: (i) to critically consider the use of thermodynamic paramet...
Protein release from poly(D,L-lactide-co-glycolide) (PLGA) microspheres in an aqueous environment is...
Drugs with different water-solubility and molecular weights were microencapsulated in cellulose acet...
Studies were conducted to determine the mechanism of drug release from pellets coated with an ethylc...
Microencapsulation reveals numerous advantages over conventional applications of flavors or fragranc...
Cellulose ethers have been increasingly used in the formulation of controlled release dosage forms; ...
The aim of this study was to elucidate the underlying drug release mechanisms in pellets coated with...
Morphology and release rate from poly()lactic acid microspheres were studied as a function of drug l...
Measurement of diffusion in gel is an essential task for pharmaceutic technology and biochemical eng...
A solvent partition technique of microencapsulation, utilizing an apparatus designed to provide a co...
The aim of this study was to provide an easy and efficient tool to adjust desired drug release kinet...
Spray-dried ethylcellulose microspheres were used as matrices for the encapsulation of a fungal lact...
The aim of this study was to develop and assess captopril-loaded microspheres in which Methocel and ...
The aim of this study was to develop and assess captopril-loaded microspheres in which Methocel and ...
The mechanism of papaverine hydrochloride release from ethyl cellulose-walled microcapsules is discu...
The two main purposes of this work were: (i) to critically consider the use of thermodynamic paramet...
Protein release from poly(D,L-lactide-co-glycolide) (PLGA) microspheres in an aqueous environment is...
Drugs with different water-solubility and molecular weights were microencapsulated in cellulose acet...
Studies were conducted to determine the mechanism of drug release from pellets coated with an ethylc...
Microencapsulation reveals numerous advantages over conventional applications of flavors or fragranc...
Cellulose ethers have been increasingly used in the formulation of controlled release dosage forms; ...
The aim of this study was to elucidate the underlying drug release mechanisms in pellets coated with...
Morphology and release rate from poly()lactic acid microspheres were studied as a function of drug l...
Measurement of diffusion in gel is an essential task for pharmaceutic technology and biochemical eng...
A solvent partition technique of microencapsulation, utilizing an apparatus designed to provide a co...
The aim of this study was to provide an easy and efficient tool to adjust desired drug release kinet...