Strategies for encapsulation of small hydrophilic and amphiphilic drugs in PLGA microspheres: State-of-the-art and challenges

被引:292
作者
Ramazani, Farshad [1 ,2 ]
Chen, Weiluan [1 ]
van Nostrum, Cornelis F. [1 ]
Storm, Gert [1 ,3 ]
Kiessling, Fabian [2 ]
Lammers, Twan [2 ,3 ]
Hennink, Wim E. [1 ]
Kok, Robbert J. [1 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, Univ Sweg 99, NL-3584 CG Utrecht, Netherlands
[2] Rhein Westfal TH Aachen, Dept Expt Mol Imaging, Aachen, Germany
[3] Univ Twente, Dept Controlled Drug Delivery, POB 217, NL-7500 AE Enschede, Netherlands
关键词
Polymeric microspheres; PLGA; Microencapsulation; Encapsulation efficiency; Sustained release; IN-VIVO; BIODEGRADABLE MICROSPHERES; POLYMER MICROPARTICLES; MOLECULAR-WEIGHT; RELEASE; DELIVERY; FORMULATION; DEGRADATION; STABILITY; SIZE;
D O I
10.1016/j.ijpharm.2016.01.020
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:358 / 367
页数:10
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