TY - JOUR
T1 - Strategies for encapsulation of small hydrophilic and amphiphilic drugs in PLGA microspheres
T2 - State-of-the-art and challenges
AU - Ramazani, Farshad
AU - Chen, Weiluan
AU - van Nostrum, Cornelis F
AU - Storm, G
AU - Kiessling, Fabian
AU - Lammers, Twan
AU - Hennink, Wim E
AU - Kok, Robbert J
N1 - Copyright © 2016 Elsevier B.V. All rights reserved.
PY - 2016/1/12
Y1 - 2016/1/12
N2 - Poly(lactide-co-glycolide) (PLGA) microspheres are efficient delivery systems for controlled release of low molecular weight drugs as well as therapeutic macromolecules. The most common microencapsulation methods are based on emulsification procedures, in which emulsified droplets of polymer and drug solidify into microspheres when the solvent is extracted from the polymeric phase. Although high encapsulation efficiencies have been reported for hydrophobic small molecules, encapsulation of hydrophilic and/or amphiphilic small molecules is challenging due to the partitioning of drug from the polymeric phase into the external phase before solidification of the particles. This review addresses formulation-related aspects for efficient encapsulation of small hydrophilic/amphiphilic molecules into PLGA microspheres using conventional emulsification methods (e.g., oil/water, water/oil/water, solid/oil/water, water/oil/oil) and highlights novel emulsification technologies such as microfluidics, membrane emulsification and other techniques including spray drying and inkjet printing. Collectively, these novel microencapsulation technologies afford production of this type of drug loaded microspheres in a robust and well controlled manner.
AB - Poly(lactide-co-glycolide) (PLGA) microspheres are efficient delivery systems for controlled release of low molecular weight drugs as well as therapeutic macromolecules. The most common microencapsulation methods are based on emulsification procedures, in which emulsified droplets of polymer and drug solidify into microspheres when the solvent is extracted from the polymeric phase. Although high encapsulation efficiencies have been reported for hydrophobic small molecules, encapsulation of hydrophilic and/or amphiphilic small molecules is challenging due to the partitioning of drug from the polymeric phase into the external phase before solidification of the particles. This review addresses formulation-related aspects for efficient encapsulation of small hydrophilic/amphiphilic molecules into PLGA microspheres using conventional emulsification methods (e.g., oil/water, water/oil/water, solid/oil/water, water/oil/oil) and highlights novel emulsification technologies such as microfluidics, membrane emulsification and other techniques including spray drying and inkjet printing. Collectively, these novel microencapsulation technologies afford production of this type of drug loaded microspheres in a robust and well controlled manner.
KW - Polymeric microspheres
KW - PLGA
KW - Microencapsulation
KW - Encapsulation efficiency
KW - Sustained release
U2 - 10.1016/j.ijpharm.2016.01.020
DO - 10.1016/j.ijpharm.2016.01.020
M3 - Article
C2 - 26795193
SN - 0378-5173
VL - 499
SP - 358
EP - 367
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1-2
ER -