Institut des Matériaux Jean Rouxel (IMN), Université de Nantes, 2 Rue de la Houssinière, 44322 Nantes cedex 3, France.
Small. 2012 Oct 8;8(19):2978-85. doi: 10.1002/smll.201200417. Epub 2012 Jun 8.
The volume phase transition (VPT) behavior and the swelling properties of individual thermoresponsive poly(N-isopropylacrylamide) (PNIPAM)-based nanogels are investigated by in situ atomic force microscopy (AFM). Using a template-based synthesis method, cylindrical nanogels are synthesized for different polymerization times within nanopores (80 nm) of poly(ethylene terephthalate) (PET) track-etched membranes. The confinement conditions, characterized by the ratio Φ between the average chain length and the pore diameter, are varied between 0.35 and 0.8. After dissolving the membranes, the volume of individual nanogels composed of PNIPAM-g-PET diblock copolymers is numerically extracted from AFM images while varying the water temperature from 28 to 44 °C. From the measured volumes, the swelling of nanogels is investigated as a function of both the water temperature and the confinement conditions imposed during the synthesis. Contrary to the VPT, the maximum swelling of the nanogels is strongly affected by these confinement conditions. The volume of nanogels in the swollen state can reach 1.1 to 2.1 times their volume in the collapsed state for a ratio Φ of 0.8 and 0.5, respectively. These results open a new way to tune the swelling of nanogels, simply by adjusting the degree of confinement imposed during their synthesis within nanopores, which is particularly interesting for biomedical applications requiring a high degree of control over swelling properties, such as drug-delivery nanotools.
通过原位原子力显微镜(AFM)研究了单个热响应聚(N-异丙基丙烯酰胺)(PNIPAM)基纳米凝胶的体积相转变(VPT)行为和溶胀特性。使用基于模板的合成方法,在聚对苯二甲酸乙二醇酯(PET)刻蚀孔膜的纳米孔(80nm)内合成了不同聚合时间的圆柱状纳米凝胶。通过改变平均链长与孔径比 Φ ,可以改变受限条件,范围在 0.35 到 0.8 之间。在溶解膜后,通过从 AFM 图像中数值提取由 PNIPAM-g-PET 两嵌段共聚物组成的单个纳米凝胶的体积,同时将水温从 28°C 变化到 44°C。从测量的体积可以研究纳米凝胶的溶胀作为水温以及在合成过程中施加的受限条件的函数。与 VPT 相反,纳米凝胶的最大溶胀强烈受到这些受限条件的影响。对于 Φ 值分别为 0.8 和 0.5 的纳米凝胶,在溶胀状态下的体积可以达到其塌陷状态下体积的 1.1 到 2.1 倍。这些结果为纳米凝胶的溶胀提供了一种新的调控方法,只需简单地调整在纳米孔内合成过程中施加的受限程度,这对于需要对溶胀性能进行高度控制的生物医学应用(如药物输送纳米工具)特别有趣。