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首页> 外文期刊>Frontiers in Bioengineering and Biotechnology >Multiphoton Microscopy for the Characterization of Cellular Behavior on Naturally Derived Polysaccharide Tissue Constructs With Irregular Surfaces for the Development of Platform Biomaterials
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Multiphoton Microscopy for the Characterization of Cellular Behavior on Naturally Derived Polysaccharide Tissue Constructs With Irregular Surfaces for the Development of Platform Biomaterials

机译:用于在天然衍生的多糖组织构建体中具有不规则表面的细胞行为表征的多光子显微镜,用于平台生物材料的开发

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摘要

Over the past decade, the use of polymers as platform materials for biomedical applications including tissue engineering has been of rising interest. Recently, the use of naturally derived polysaccharides as 3-D scaffolds for tissue regeneration has shown promising material characteristics; however, due to complexities in composition, morphology, and optical properties, adequate spatial and temporal characterization of cellular behavior in these materials is lacking. Multiphoton microscopy has emerged as a viable tool for performing such quantification by permitting greater imaging depth while simultaneously minimizing un-favorable scattering and producing high-resolution optical cross sections for non-invasive analysis. Here we describe a method using endogenous contrast of nanocellulose fibers (CNF) using Second Harmonic Generation (SHG), combined with 2-photon fluorescence of Cell Tracker Orange (CTO) for spatial and longitudinal imaging of cellular proliferation. CTO is an ideal fluorophore to avoid the broad CNF autofluorescence allowing for segmentation of cells using a semi-automatic routine. Individual cells were identified using centroid locations for 3D cell proliferation. Overall, the methods presented are viable for investigation of cellular interactions with polysaccharide candidate biomaterials.
机译:在过去的十年中,使用聚合物作为包括组织工程的生物医学应用的平台材料,这一直是兴趣。最近,使用天然衍生的多糖作为3d用于组织再生的支架已经显示出具有有希望的材料特性;然而,由于组合物,形态和光学性质的复杂性,缺乏这些材料中细胞行为的充分空间和时间表征。多光子显微镜作为通过允许更大的成像深度来执行这种量化的可行工具,同时最小化不良散射并产生用于非侵入性分析的高分辨率光学横截面。在这里,我们描述了使用二次谐波产生(SHG)的使用纳米纤维素纤维(CNF)的内源性对比的方法,与细胞增殖的空间和纵向成像组合与细胞跟踪器橙(CTO)的2-光子荧光组合。 CTO是一种理想的荧光团,以避免宽的CNF自发荧光,允许使用半自动常规进行细胞的分割。使用用于3D细胞增殖的质心位置鉴定单个细胞。总的来说,提出的方法是可行的,用于调查与多糖候选生物材料的细胞相互作用。

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