摘要
利用自由基聚合的链转移反应,制备了以羧基为端基的聚(N-异丙基丙烯酰胺)(PNIPAM-COOH),然后以该聚合物作为亲水的侧链,利用其羧端基和聚(4-乙烯基吡啶)(PVPy)疏水主链上的吡啶基团间的相互作用,在共溶剂DMF中形成超分子两亲接枝聚合物体系,在上述体系中逐滴加入水可以使其通过自组装形成高分子囊泡.通过控制PVPy与PNIPAM-COOH的质量比在1~3之间,可以控制囊泡尺寸在130~330nm之间.由于囊泡中含有吡啶基团,因而该囊泡具有pH敏感性.以日落黄为药物模型,以这些pH敏感性囊泡作为药物载体,通过调节环境的pH值可以实现对药物的控制释放.
Supramolecular graft copolymers (SGP) were prepared via the ionic interaction between poly(4-vinylpyridine) (PVPy) and poly(N-isopropylacrylamide) with carboxylic end groups (PNI- PAM-COOH). Hydrophobic PVPy was used as main chains, and hydrophilic PNIPAM-COOH grafted onto the main chains through the ionic interaction between the carboxylic groups and pyridine groups. The SGP could self-assemble to form vesicles in DMF/H2O system. When modulating the mass ratio of PVPy to PNIPAM-COOH from 1 to 3, the size of the vesicles could be controlled from 130 to 330 nm. These vesicles were sensitive to pH, and could be deformed by changing pH. Drug-release studies showed that release rates of the loaded drug (sunset yellow) in the two vesicles could be controlled by the pH of the solution.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2010年第2期181-186,共6页
Acta Chimica Sinica
关键词
超分子作用
自组装
囊泡
控制释放
supramolecular interaction
self-assembly
vesicle
controlled release