Kidchob T, Kimura S, Imanishi Y
Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Japan.
J Control Release. 1998 Jan 2;50(1-3):205-14. doi: 10.1016/s0168-3659(97)00135-1.
Thermoresponsive microcapsules were prepared by grafting poly(N-isopropylacrylamide) (PNIPAAm) on the surface of polypeptide (poly(Glu(OMe))-block-poly(Sar) microcapsules. Naked poly(Glu(OMe)-block-poly(Sar) microcapsules were partly hydrolysed with NaOH to remove methyl groups and newly formed carboxyl groups were used to anchor polyallylamine having 4,4'-azobis(4-cyanovaleric acid) groups. Graft polymerization of N-isopropylacrylamide at the microcapsule surface was initiated by photo-cleavage of the azo groups. Microscopic examination showed that a homogeneous dense skin layer of PNIPAAm was formed on the surface of microcapsule at 40 degrees c, while the skin layer became loose when the temperature was lowered to 25 degrees C. Dextran release from the microcapsule was faster below the lower critical solution temperature (LCST) of PNIPAAm than that above it. When the temperature changed across the LCST, a reversible, thermoresponsive release from the microcapsule was observed. Notable, the transition of the release rate by changing the temperature occurs quickly in a narrow temperature range.
通过在多肽(聚(谷氨酸甲酯)-嵌段-聚(肌氨酸)微胶囊)表面接枝聚(N-异丙基丙烯酰胺)(PNIPAAm)制备了热响应性微胶囊。将裸露的聚(谷氨酸甲酯)-嵌段-聚(肌氨酸)微胶囊用氢氧化钠部分水解以除去甲基,新形成的羧基用于锚定具有4,4'-偶氮双(4-氰基戊酸)基团的聚烯丙胺。通过偶氮基团的光裂解引发N-异丙基丙烯酰胺在微胶囊表面的接枝聚合。显微镜检查表明,在40℃时,微胶囊表面形成了均匀致密的PNIPAAm皮层,而当温度降至25℃时,皮层变得疏松。在PNIPAAm的低临界溶液温度(LCST)以下,微胶囊中葡聚糖的释放比在其以上时更快。当温度在LCST上下变化时,观察到微胶囊有可逆的热响应释放。值得注意的是,通过改变温度实现的释放速率转变在狭窄的温度范围内迅速发生。