Solvent selection causes remarkable shifts of the "Ouzo region" for poly(lactide-co-glycolide) nanoparticles prepared by nanoprecipitation

被引:62
作者
Beck-Broichsitter, Moritz [1 ]
Nicolas, Julien [1 ]
Couvreur, Patrick [1 ]
机构
[1] Univ Paris 11, CNRS UMR 8612, Inst Galien Paris Sud, F-92196 Chatenay Malabry, France
关键词
DRUG-DELIVERY; POLYMERIC NANOPARTICLES; NANOMEDICINE; SIZE; NANOTECHNOLOGY; EMULSIFICATION; NANOCAPSULES; DISPERSIONS; BEHAVIOR; CANCER;
D O I
10.1039/c5nr01695a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymer nanoparticles (NPs) offer versatile novel biological features of interest for drug delivery applications. "Ouzo diagrams" allowed for a systematic manufacture of specified colloidal formulations by the widely used nanoprecipitation process. Surprisingly, despite the well-documented relevance of the applied organic solvent for nanoprecipitation, its effect on the actual status of the "Ouzo region" was so far not studied. Herein, investigations were undertaken to account for the potential impact of the solvent type on the "Ouzo diagrams" for poly(lactide-co-glycolide) (PLGA) and tetrahydrofuran (THF), 1,4-dioxane, acetone and dimethyl sulfoxide (DMSO). The "Ouzo region" shifted considerably to higher polymer fractions upon solvent change (rank order: THF < 1,4-dioxane < acetone < DMSO). Assuming a one-to-one transformation of detached PLGA-bearing solvent droplets (droplet diameter for THF: similar to 800 nm, 1,4-dioxane: similar to 700 nm, acetone: similar to 500 nm and DMSO: similar to 300 nm) into non-divisible polymer aggregates upon solvent displacement, facilitated to predict the size of NPs found within the "Ouzo region"(size range: 40-200 nm). In conclusion, application of "Ouzo diagrams" is a valuable tool for drug delivery research and will most-likely replace the "trial-and-error"-approach to identify the operating window for the production of stable colloidal formulations by the nanoprecipitation technique.
引用
收藏
页码:9215 / 9221
页数:7
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