Department of Chemistry & Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec, Canada H4B 1R6.
Colloids Surf B Biointerfaces. 2011 Feb 1;82(2):470-6. doi: 10.1016/j.colsurfb.2010.10.004. Epub 2010 Oct 16.
Atomic force microscopy (AFM) and AFM-based force spectroscopy was used to study the desorption of individual chitosan polymer chains from substrates with varying chemical composition. AFM images of chitosan adsorbed onto a flat mica substrate show elongated single strands or aggregated bundles. The aggregated state of the polymer is consistent with the high level of flexibility and mobility expected for a highly positively charged polymer strand. Conversely, the visualization of elongated strands indicated the presence of stabilizing interactions with the substrate. Surfaces with varying chemical composition (glass, self-assembled monolayer of mercaptoundecanoic acid/decanethiol and polytetrafluoroethylene (PTFE)) were probed with chitosan modified AFM tips and the corresponding desorption energies, calculated from plateau-like features, were attributed to the desorption of individual polymer strands. Desorption energies of 2.0±0.3×10(-20)J, 1.8±0.3×10(-20)J and 3.5±0.3×10(-20)J were obtained for glass, SAM of mercaptoundecanoic/dodecanethiol and PTFE, respectively. These single molecule level results can be used as a basis for investigating chitosan and chitosan-based materials for biomaterial applications.
原子力显微镜(AFM)和基于 AFM 的力谱学被用于研究具有不同化学成分的基底上单个壳聚糖聚合物链的解吸。吸附在云母基底上的壳聚糖的 AFM 图像显示出伸长的单链或聚集的束。聚合物的聚集状态与高度带正电荷聚合物链所预期的高柔韧性和高迁移性一致。相反,伸长链的可视化表明与基底之间存在稳定的相互作用。用壳聚糖修饰的 AFM 探针探测具有不同化学成分的表面(玻璃、巯基十一酸/十二硫醇的自组装单层和聚四氟乙烯(PTFE)),并从平台状特征计算出相应的解吸能,归因于单个聚合物链的解吸。对于玻璃、巯基十一酸/十二硫醇的 SAM 和 PTFE,分别获得了 2.0±0.3×10(-20)J、1.8±0.3×10(-20)J 和 3.5±0.3×10(-20)J 的解吸能。这些单分子水平的结果可作为研究壳聚糖和壳聚糖基材料在生物材料应用中的基础。