A novel one-step drug-loading procedure for water-soluble amphiphilic nanocarriers

被引:89
作者
Fournier, E
Dufresne, MH
Smith, DC
Ranger, M
Leroux, JC
机构
[1] Univ Montreal, Fac Pharm, Canada Res Chair Drug Delivery, Montreal, PQ H3C 3J7, Canada
[2] Labopharm Inc, Laval, PQ H7V 4B4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
diblock copolymers; polymeric micelles; poorly water-soluble drugs; self-assembly;
D O I
10.1023/B:PHAM.0000029284.40637.69
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The lack of water-solubility hampers the use of many potent pharmaceuticals. Polymeric micelles are self-assembled nanocarriers with versatile properties that can be engineered to solubilize, target, and release hydrophobic drugs in a controlled-release fashion. Unfortunately, their large-scale use is limited by the incorporation methods available, especially when sterile dosage forms are sought. Methods. In this manuscript, we describe a straightforward, economical, and innovative drug-loading procedure that consists in dissolving both the drug and an amphiphilic diblock copolymer in a water/tert-butanol mixture that is subsequently freeze-dried. Results. We demonstrate that monodisperse 20-60 nm-sized drug-loaded polymeric micelles are produced directly and spontaneously upon rehydration of the freeze-dried cake. To establish the proof-of-principle, two hydrophobic taxane derivatives were solubilized in the micelles, and their partition coefficient was determined. Conclusions. This approach is efficient yet astonishingly simple and may be of great interest for scientists working in nanotechnology and pharmaceutical sciences.
引用
收藏
页码:962 / 968
页数:7
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