Controlled block copolymer micelle formation for encapsulation of hydrophobic ingredients

被引:14
作者
Lebouille, Jerome G. J. L. [1 ,2 ]
Vleugels, Leo F. W. [2 ]
Dias, Aylvin A. [1 ,3 ]
Leermakers, Frans A. M. [4 ]
Stuart, Martien A. Cohen [4 ]
Tuinier, Remco [2 ,5 ]
机构
[1] DSM Biomed, NL-6160 MD Geleen, Netherlands
[2] DSM ChemTech, ACES, NL-6160 MD Geleen, Netherlands
[3] DSM Ahead, NL-6160 MD Geleen, Netherlands
[4] Wageningen Univ, Lab Phys Chem & Colloid Sci, NL-6307 HB Wageningen, Netherlands
[5] Univ Utrecht, Vant Hoff Lab Phys & Colloid Chem, Dept Chem, NL-3584 CH Utrecht, Netherlands
关键词
SURFACTANT-WATER-SYSTEMS; DRUG-DELIVERY; BIODEGRADABLE NANOPARTICLES; POLYMERIC DRUGS; PHARMACOKINETICS; ANTIOXIDANT; NANOSPHERES; GENE;
D O I
10.1140/epje/i2013-13107-y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report on the formation of polymeric micelles in water using triblock copolymers with a polyethylene glycol middle block and various hydrophobic outer blocks prepared with the precipitation method. We form micelles in a reproducible manner with a narrow size distribution. This suggests that during the formation of the micelles the system had time to form micelles under close-to-thermodynamic control. This may explain why it is possible to use an equilibrium self-consistent field theory to predict the hydrodynamic size and the loading capacity of the micelles in accordance with experimental finding. Yet, the micelles are structurally quenched as concluded from the observation of size stability in time. We demonstrate that our approach enables to prepare rather hydrophobic block copolymer micelles with tunable size and loading.
引用
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页数:12
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