Hybrid nanogels with physical and chemical cross-linking structures as nanocarriers

被引:73
|
作者
Morimoto, N
Endo, T
Ohtomi, M
Iwasaki, Y
Akiyoshi, K
机构
[1] Tokyo Med & Dent Univ, Inst Biomat & Bioengn, Chiyoda Ku, Tokyo 1010062, Japan
[2] Toho Univ, Fac Sci, Dept Biomol Sci, Funabashi, Chiba 2748510, Japan
[3] Tokyo Med & Dent Univ, Ctr Excellence Program Frontier Res Mol Destruct, Chiyoda Ku, Tokyo 1010062, Japan
关键词
drug delivery systems; microgels; nanoparticles; polysaccharides; protein;
D O I
10.1002/mabi.200500051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polymerizable nanogels were prepared by self-assembly of cholesteryl group-bearing pullulan (CHP) with (MPC by radical polymerization in dilute aqueous solution. The solution properties of the polymers in water were investigated by TEM, SEC-MALS, and fluorescence quenching technique. Monodispersed hybrid nanogels of CHPMA-MPC (CM nanogels) (25-30 nm in radius of gyration) were obtained by using CHPMA nanogel as a seed-nanogel. CM nanogels have a dual cross-linking structure that is physically cross-linked with the cholesteryl groups and chemically cross-linked with the MPC polymer chains. CM nanogels trap heat-denatured carbonic anhydrase B (CAB) and prevent their aggregations. The nanogels maintained the ability of trapping and releasing enzymes by host-guest interaction of cholesteryl group and cyclodextrin.
引用
收藏
页码:710 / 716
页数:7
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