Chen Guoping, Kawazoe Naoki, Fan Yujiang, Ito Yoshihiro, Tateishi Tetsuya
Biomaterials Center, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Langmuir. 2007 May 22;23(11):5864-7. doi: 10.1021/la700931u. Epub 2007 Apr 26.
A novel grid pattern of two kinds of nanothick microgels was developed by alternate patterning using photolithography. At first, 100-microm-wide nanothick PAAm microgel stripes were grafted on a polystyrene surface by UV irradiation of the photoreactive azidobenzoyl-derivatized polyallylamine-coated surface through a photomask with 100-microm-wide stripes. Then, a second set of 100-microm-wide nanothick PAAc microgel stripes were grafted across the PAAm-grated polystyrene surface by UV irradiation of the photoreactive azidophenyl-derivatized poly(acrylic acid)-coated surface through a photomask placed perpendicularly to the first set of PAAm microgel stripes. The PAAc microgel stripe pattern was formed over the PAAm microgel stripe pattern. The cross angle of the two microgel stripes could be controlled by adjusting the position of the photomask when the second microgel pattern was prepared. Swelling and shrinking of the microgels were investigated by scanning probe microscopy (SPM) in an aqueous solution. SPM observation indicated that the thickness of the gel network was 100 to 500 nm. The regions containing PAAm, PAAc, and the PAAc-PAAm overlapping microgels showed different swelling and shrinking properties when the pH was changed. The PAAm microgel swelled at low pH and shrank at high pH whereas the PAAc microgel swelled at high pH and shrank at low pH. However, the PAAc-PAAm overlapping microgel did not change as significantly as did the two microgels, indicating that the swelling and shrinking of the two gels was partially offset. The pH-induced structural change was repeatedly reversible. The novel grid pattern of nanothick microgels will find applications in various fields such as smart actuators, artificial muscles, sensors, and drug delivery systems as well as in tissue engineering and so forth.
通过光刻交替图案化技术,开发出了一种由两种纳米厚微凝胶组成的新型网格图案。首先,通过具有100微米宽条纹的光掩膜,对光反应性叠氮苯甲酰衍生化的聚烯丙胺涂层表面进行紫外线照射,在聚苯乙烯表面接枝100微米宽的纳米厚聚丙烯酰胺(PAAm)微凝胶条纹。然后,通过垂直于第一组PAAm微凝胶条纹放置的光掩膜,对光反应性叠氮苯基衍生化的聚丙烯酸(PAAc)涂层表面进行紫外线照射,在PAAm接枝的聚苯乙烯表面上接枝第二组100微米宽的纳米厚PAAc微凝胶条纹。PAAc微凝胶条纹图案形成在PAAm微凝胶条纹图案之上。在制备第二种微凝胶图案时,通过调整光掩膜的位置,可以控制两种微凝胶条纹的交叉角度。在水溶液中,通过扫描探针显微镜(SPM)研究了微凝胶的溶胀和收缩情况。SPM观察表明,凝胶网络的厚度为100至500纳米。当pH值改变时,含有PAAm、PAAc以及PAAc - PAAm重叠微凝胶的区域表现出不同的溶胀和收缩特性。PAAm微凝胶在低pH值下溶胀,在高pH值下收缩,而PAAc微凝胶在高pH值下溶胀,在低pH值下收缩。然而,PAAc - PAAm重叠微凝胶的变化不如两种微凝胶显著,这表明两种凝胶的溶胀和收缩部分相互抵消。pH值诱导的结构变化是反复可逆的。这种新型的纳米厚微凝胶网格图案将在智能致动器、人造肌肉、传感器、药物递送系统以及组织工程等各个领域找到应用。