Biocompatible and thermo-responsive nanocapsule synthesis through vesicle templating

被引:21
作者
Aguirre, Garbine [1 ]
Ramos, Jose [1 ]
Heuts, Johan P. A. [2 ]
Forcada, Jacqueline [1 ]
机构
[1] Univ Pais Vasco UPV EHU, Fac Ciencias Quim, Dept Quim Aplicada, POLYMAT,Bionanoparticles Grp, Donostia San Sebastian 20080, Spain
[2] Eindhoven Univ Technol, Lab Polymer Mat, NL-5600 MB Eindhoven, Netherlands
关键词
HOLLOW SPHERES; PARTICLES; CAPSULES; NANOGELS; POLY(N-VINYLCAPROLACTAM); POLYELECTROLYTES; POLYMERIZATION; NANOPARTICLES; COMPLEXATION; TEMPERATURE;
D O I
10.1039/c4py00297k
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Thermo-responsive and biocompatible cross-linked nanocapsules were synthesized through dimethyldioctadecylammonium bromide (DODAB) vesicle templating. For this, firstly two random copolymers, N-vinylcaprolactam (VCL) and acrylic acid (AA), with different chain lengths but using the same monomer ratio, were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization. These anionic random copolymers were adsorbed onto cationic DODAB vesicles. Then, biocompatible and thermo-responsive nanocapsules were obtained by semicontinuous emulsion polymerization under monomer-starved conditions for both the main monomer (VCL) and the crosslinker. Although in all the cases the typical thermal behavior of PVCL-based nanocapsules was observed, hysteresis between cooling and heating cycles was observed at low temperature in the case of noncross-linked nanocapsules. This behavior was reduced using different types and amounts of cross-linkers. In addition, transmission electron microscopy (TEM) characterization demonstrated the successful formation of nanocapsules either with short or long random copolymers. The formation of stable nanocapsules was confirmed below and above the volume phase transition temperature (VPTT) by surfactant lysis experiments through optical density and DLS measurements in all the nanocapsules synthesized. These biocompatible and thermo-responsive nanocapsules could be suitable and potentially useful as nanocarriers for drug delivery.
引用
收藏
页码:4569 / 4579
页数:11
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