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  • PLGA microparticles for sustained release of ibuprofen as the model drug were prepared by O/W solvent evaporation method under altering stirring speed (600, 1000 rpm), emulsifier concentration (PVA concentration 0.1%, 1%) and organic solvent selection (dichloromethane, ethyl acetate). Obtained results confirmed the effect of selected formulation and process parameters on properties of prepared PLGA-based microparticles. The influence on encapsulation efficiency, yield, morphological properties, mean size and drug release was observed. The increased stirring speed within the solvent evaporation process led to decrease of encapsulation efficiency, yield and mean size but incorporated drug was released faster. Increased PVA concentration in external emulsion phase brought same results except ibuprofen release rate. Microparticles prepared with dichloromethane as the organic solvent exhibit higher sphericity, more regular shape with smooth surface, thus dichloromethane was considered as more suitable organic solvent in comparison to ethyl acetate for this purpose.
  • PLGA microparticles for sustained release of ibuprofen as the model drug were prepared by O/W solvent evaporation method under altering stirring speed (600, 1000 rpm), emulsifier concentration (PVA concentration 0.1%, 1%) and organic solvent selection (dichloromethane, ethyl acetate). Obtained results confirmed the effect of selected formulation and process parameters on properties of prepared PLGA-based microparticles. The influence on encapsulation efficiency, yield, morphological properties, mean size and drug release was observed. The increased stirring speed within the solvent evaporation process led to decrease of encapsulation efficiency, yield and mean size but incorporated drug was released faster. Increased PVA concentration in external emulsion phase brought same results except ibuprofen release rate. Microparticles prepared with dichloromethane as the organic solvent exhibit higher sphericity, more regular shape with smooth surface, thus dichloromethane was considered as more suitable organic solvent in comparison to ethyl acetate for this purpose. (en)
Title
  • Influence of formulation and process parameters on characteristics of PLGA-based microparticles with controlled drug release
  • Influence of formulation and process parameters on characteristics of PLGA-based microparticles with controlled drug release (en)
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  • Influence of formulation and process parameters on characteristics of PLGA-based microparticles with controlled drug release
  • Influence of formulation and process parameters on characteristics of PLGA-based microparticles with controlled drug release (en)
skos:notation
  • RIV/62157124:16370/13:43872054!RIV14-MSM-16370___
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  • RIV/62157124:16370/13:43872054
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  • microparticles, solvent evaporation, PLGA, controlled release, burst effect (en)
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  • CZ - Česká republika
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  • [468A382742A9]
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  • 62
http://linked.open...iv/tvurceVysledku
  • Dvořáčková, Kateřina
  • Vetchý, David
  • Kejdušová, Martina
  • Vysloužil, Jakub
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  • 1210-7816
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  • 16370
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