The manufacturing techniques of drug-loaded polymeric nanoparticles from preformed polymers

被引:93
作者
Grabnar, Pegi Ahlin [1 ]
Kristl, Julijana [1 ]
机构
[1] Univ Ljubljana, Fac Pharm, Ljubljana 1000, Slovenia
关键词
nanoparticles; polymer; formulation; preparation methods; drug delivery; SOLID LIPID NANOPARTICLES; FLOW REACTOR METHOD; EMULSIFICATION-DIFFUSION METHOD; SALTING-OUT PROCESS; IN-VITRO RELEASE; MEMBRANE CONTACTOR; PLGA NANOPARTICLES; ALBUMIN MICROSPHERES; DELIVERY-SYSTEM; POLY(LACTIDE-CO-GLYCOLIDE) NANOPARTICLES;
D O I
10.3109/02652048.2011.569763
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Over the past few decades, nanoparticle (NP) formulation has been the subject of extensive research. The choice of a suitable NP formulation technique is dependent on the physicochemical properties of the drug, such as solubility and chemical stability. Different NP manufacturing methods enable modification of the physicochemical characteristics such as size, structure, morphology and surface texture, but also affect the drug loading, drug entrapment efficiency and release kinetics. This review covers an update on the state of art of the manufacturing of polymeric NPs from preformed polymers. Both, conventional methods for NP preparation, such as spontaneous formulation and emulsification-based methods, and new approaches in NP technology are presented. A comparative analysis is given for polymer, drug and solvent nature, toxicity, purification, drug stability and scalability of the method. The information obtained allows establishing criteria for selecting a method for preparation of NPs according to its advantages and limitations.
引用
收藏
页码:323 / 335
页数:13
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