Centre for Research in Nanoscience and Nanotechnology, University of Calcutta, Technology Campus, Block JD2, Sector III, Saltlake City, Kolkata 700098, India.
Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700064, India.
J Colloid Interface Sci. 2018 Mar 15;514:433-442. doi: 10.1016/j.jcis.2017.12.037. Epub 2017 Dec 15.
The interaction of chitosan with bio-membranes, which plays important role in deciding its use in biological applications, is realized by investigating the interaction of chitosan with stearic acid (fatty acid) in Langmuir monolayers (at air-water interface) and Langmuir-Blodgett (LB) films (after transferring it onto solid substrate). It is found from the pressure-area isotherms that the chitosan insertion causes an expansion of chitosan-fatty acid hybrid monolayers, which reduces the elasticity and make the film heterogeneous. It is likely that at low surface pressure chitosan is situated at the interface, interacting with stearic acid molecules via electrostatic and hydrophobic interactions whereas at high pressure chitosan mainly located at subsurface beneath stearic acid molecules. In the latter case the interaction is predominantly electrostatic yielding very small contribution to the surface pressure. The reduction of temperature of the subphase water allows more number of chitosan molecules to reach surface to increase the pressure/interaction. On the other hand, although pure chitosan is found difficult to relocate on the substrate from air-water interface due to its hydrophilic-like nature, it alongside stearic acid (amphiphilic molecules) can be transferred onto substrate using LB technique as evident from infrared spectra. Their out-of-plane and in-plane structures, as extracted from two complementary surface sensitive techniques- X-ray reflectivity and atomic force microscopy, are found strongly dependent on the chitosan mole fraction and the deposition pressure. These analysis of the film-structure will essentially allow one to model the system better and provide better insight into the interaction.
壳聚糖与生物膜的相互作用在决定其在生物应用中的用途方面起着重要作用,本研究通过研究壳聚糖与硬脂酸(脂肪酸)在 Langmuir 单层(气-水界面)和 Langmuir-Blodgett(LB)膜(转移到固体基底上之后)中的相互作用来实现。从压力-面积等温线可以发现,壳聚糖的插入导致壳聚糖-脂肪酸混合单层的膨胀,这降低了弹性并使膜变得不均匀。在低表面压力下,壳聚糖可能位于界面处,通过静电和疏水相互作用与硬脂酸分子相互作用,而在高表面压力下,壳聚糖主要位于硬脂酸分子下方的次表面。在后一种情况下,相互作用主要是静电的,对表面压力的贡献很小。亚相水的温度降低会允许更多的壳聚糖分子到达表面以增加压力/相互作用。另一方面,尽管由于其类似亲水的性质,纯壳聚糖很难从气-水界面重新定位到基底上,但它与硬脂酸(两亲分子)一起可以使用 LB 技术转移到基底上,这从红外光谱中可以明显看出。从两种互补的表面敏感技术- X 射线反射率和原子力显微镜中提取的它们的面外和面内结构,强烈依赖于壳聚糖的摩尔分数和沉积压力。这些对膜结构的分析将从本质上允许更好地对系统进行建模,并提供对相互作用的更好理解。