The effect of the processing and formulation parameters on the size of nanoparticles based on block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide) with and without hydrolytically sensitive groups

被引:118
作者
Neradovic, D [1 ]
Soga, O [1 ]
Van Nostrum, CF [1 ]
Hennink, WE [1 ]
机构
[1] Univ Utrecht, UIPS, Dept Pharmaceut, Fac Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
关键词
poly(N-isopropylacrylamide); nanoparticles; poly(ethylene glycol); heating rate; size control;
D O I
10.1016/j.biomaterials.2003.09.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Block copolymers of poly(ethylene glycol) (PEG) as a hydrophilic block and N-isopropylacrylamide (PNIPAAm) or poly (NIPAAm-co-N-(2-hydroxypropyl) tuethacrylamide-dilactate) (poly(NIPAAm-co-HPMAm-dilactate)) as a thermosensitive block, are able to self-assemble in water into nanoparticles above the Cloud point (CP) of the thermosensitive block. The influence of processing and the formulation parameters on the size of the nanoparticles was studied using dynamic light scattering. PNIPAAm-b-PEG 2000 polymers were not suitable for the formation of small and stable particles. Block copolymers with PEG 5000 and 10 000 formed relatively small and stable particles in aqueous solutions at temperatures above the CP of the thermosensitive block. Their size decreased with increasing molecular weight of the thermosensitive block, decreasing polymer concentration and using water instead of phosphate buffered saline as solvent. Extrusion and ultrasonication were inefficient methods to size down the polymeric nanoparticles. The heating rate of the polymer solutions was a dominant factor for the size of the nanoparticles. When an aqueous polymer solution was slowly heated through the CP, rather large particles (greater than or equal to-200 nm) were formed. Regardless the polymer composition, small nanoparticles (50-70nm) with a narrow size distribution were formed, when a small volume of an aqueous polymer solution below the CP was added to a large Volume of heated water. In this way the thermosensitive block copolymers rapidly pass their CP ('heat shock' procedure), resulting in small and stable nanoparticles. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2409 / 2418
页数:10
相关论文
共 54 条
[41]   LONG CIRCULATING MICROPARTICULATE DRUG CARRIERS [J].
STOLNIK, S ;
ILLUM, L ;
DAVIS, SS .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :195-214
[42]   Liposomes: quo vadis? [J].
Storm, G ;
Crommelin, DJA .
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY, 1998, 1 (01) :19-31
[43]   Thermosensitive micelle-forming block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide) [J].
Topp, MDC ;
Dijkstra, PJ ;
Talsma, H ;
Feijen, J .
MACROMOLECULES, 1997, 30 (26) :8518-8520
[44]  
TOPP MDC, 2000, THESIS U TWENTE NETH, P19
[45]   Structure and design of polymeric surfactant-based drug delivery systems [J].
Torchilin, VP .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :137-172
[46]   FLUORESCENCE STUDIES OF AQUEOUS-SOLUTIONS OF POLY(N-ISOPROPYLACRYLAMIDE) BELOW AND ABOVE THEIR LCST [J].
WINNIK, FM .
MACROMOLECULES, 1990, 23 (01) :233-242
[47]   Thermoreversible swelling behaviour of hydrogels based on N-isopropylacrylamide with a hydrophobic comonomer [J].
Xue, W ;
Hamley, IW .
POLYMER, 2002, 43 (10) :3069-3077
[48]   Preparation and characterization of polymer micelles from poly(ethylene glycol)-poly(D,L-lactide) block copolymers as potential drug carrier [J].
Yasugi, K ;
Nagasaki, Y ;
Kato, M ;
Kataoka, K .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) :89-100
[49]   Incorporation of water-insoluble anticancer drug into polymeric micelles and control of their particle size [J].
Yokoyama, M ;
Satoh, A ;
Sakurai, Y ;
Okano, T ;
Matsumura, Y ;
Kakizoe, T ;
Kataoka, K .
JOURNAL OF CONTROLLED RELEASE, 1998, 55 (2-3) :219-229
[50]   Selective delivery of adiramycin to a solid tumor using a polymeric micelle carrier system [J].
Yokoyama, M ;
Okano, T ;
Sakurai, Y ;
Fukushima, S ;
Okamoto, K ;
Kataoka, K .
JOURNAL OF DRUG TARGETING, 1999, 7 (03) :171-186