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通过胶体探针显微镜定量研究仿生生物材料 - 胶原蛋白 I、胶原蛋白 IV、层粘连蛋白 521 和纤维素纳米纤维之间的相互作用。

Quantifying the interactions between biomimetic biomaterials - collagen I, collagen IV, laminin 521 and cellulose nanofibrils - by colloidal probe microscopy.

机构信息

Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland.

Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland; Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, FI-00014 Helsinki, Finland.

出版信息

Colloids Surf B Biointerfaces. 2019 Jan 1;173:571-580. doi: 10.1016/j.colsurfb.2018.09.073. Epub 2018 Sep 29.

Abstract

Biomaterials of different nature have been and are widely studied for various biomedical applications. In many cases, biomaterial assemblies are designed to mimic biological systems. Although biomaterials have been thoroughly characterized in many aspects, not much quantitative information on the molecular level interactions between different biomaterials is available. That information is very important, on the one hand, to understand the properties of biological systems and, on the other hand, to develop new composite biomaterials for special applications. This work presents a systematic, quantitative analysis of self- and cross-interactions between films of collagen I (Col I), collagen IV (Col IV), laminin (LN-521), and cellulose nanofibrils (CNF), that is, biomaterials of different nature and structure that either exist in biological systems (e.g., extracellular matrices) or have shown potential for 3D cell culture and tissue engineering. Direct surface forces and adhesion between biomaterials-coated spherical microparticles and flat substrates were measured in phosphate-buffered saline using an atomic force microscope and the colloidal probe technique. Different methods (Langmuir-Schaefer deposition, spin-coating, or adsorption) were applied to completely coat the flat substrates and the spherical microparticles with homogeneous biomaterial films. The adhesion between biomaterials films increased with the time that the films were kept in contact. The strongest adhesion was observed between Col IV films, and between Col IV and LN-521 films after 30 s contact time. In contrast, low adhesion was measured between CNF films, as well as between CNF and LN-521 films. Nevertheless, a good adhesion between CNF and collagen films (especially Col I) was observed. These results increase our understanding of the structure of biological systems and can support the design of new matrices or scaffolds where different biomaterials are combined for diverse biological or medical applications.

摘要

不同性质的生物材料已被广泛研究并应用于各种生物医学领域。在许多情况下,生物材料组件的设计旨在模拟生物系统。尽管生物材料在许多方面都得到了充分的研究,但关于不同生物材料之间分子水平相互作用的定量信息却很少。这些信息一方面对于理解生物系统的性质非常重要,另一方面对于开发用于特殊应用的新型复合生物材料也非常重要。本工作对胶原蛋白 I(Col I)、胶原蛋白 IV(Col IV)、层粘连蛋白(LN-521)和纤维素纳米纤维(CNF)等不同性质和结构的生物材料之间的自相互作用和交叉相互作用进行了系统的定量分析,这些生物材料要么存在于生物系统(例如细胞外基质)中,要么具有用于 3D 细胞培养和组织工程的潜力。使用原子力显微镜和胶体探针技术,在磷酸盐缓冲盐水中测量了涂有生物材料的球形微球和平面基底之间的直接表面力和粘附力。采用不同的方法(Langmuir-Schaefer 沉积、旋涂或吸附)将均匀的生物材料膜完全涂覆在平面基底和球形微球上。生物材料膜之间的粘附力随膜接触时间的增加而增加。在 30 秒接触时间后,观察到 Col IV 膜之间以及 Col IV 和 LN-521 膜之间的粘附力最强。相比之下,在 CNF 膜之间以及 CNF 和 LN-521 膜之间测量到的粘附力较低。然而,在 CNF 和胶原蛋白膜(尤其是 Col I)之间观察到良好的粘附力。这些结果增加了我们对生物系统结构的理解,并为设计新的基质或支架提供了支持,在这些基质或支架中,不同的生物材料可以结合用于各种生物或医学应用。

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