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首页> 外文期刊>Journal of the Royal Society Interface >Taking a deep look: modern microscopy technologies to optimize the design and functionality of biocompatible scaffolds for tissue engineering in regenerative medicine
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Taking a deep look: modern microscopy technologies to optimize the design and functionality of biocompatible scaffolds for tissue engineering in regenerative medicine

机译:深入研究:现代显微镜技术可优化用于再生医学组织工程的生物相容性支架的设计和功能

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This review focuses on modern nonlinear optical microscopy (NLOM) methods that are increasingly being used in the field of tissue engineering (TE) to image tissue non-invasively and without labelling in depths unreached by conventional microscopy techniques. With NLOM techniques, biomaterial matrices, cultured cells and their produced extracellular matrix may be visualized with high resolution. After introducing classical imaging methodologies such as μCT, MRI, optical coherence tomography, electron microscopy and conventional microscopy two-photon fluorescence (2-PF) and second harmonic generation (SHG) imaging are described in detail (principle, power, limitations) together with their most widely used TE applications. Besides our own cell encapsulation, cell printing and collagen scaffolding systems and their NLOM imaging the most current research articles will be reviewed. These cover imaging of autofluorescence and fluorescence-labelled tissue and biomaterial structures, SHG-based quantitative morphometry of collagen I and other proteins, imaging of vascularization and online monitoring techniques in TE. Finally, some insight is given into state-of-the-art three-photon-based imaging methods (e.g. coherent anti-Stokes Raman scattering, third harmonic generation). This review provides an overview of the powerful and constantly evolving field of multiphoton microscopy, which is a powerful and indispensable tool for the development of artificial tissues in regenerative medicine and which is likely to gain importance also as a means for general diagnostic medical imaging.
机译:这篇综述着重于现代非线性光学显微镜(NLOM)方法,这些方法正越来越多地用于组织工程(TE)领域,以非侵入性方式成像组织并且没有标记传统显微镜技术无法达到的深度。利用NLOM技术,可以以高分辨率可视化生物材料基质,培养的细胞及其产生的细胞外基质。在介绍了经典的成像方法之后,如μCT,MRI,光学相干断层扫描,电子显微镜和常规显微镜,详细介绍了双光子荧光(2-PF)和二次谐波生成(SHG)成像(原理,功率,局限性)以及他们最广泛使用的TE应用。除了我们自己的细胞封装,细胞印刷和胶原蛋白支架系统及其NLOM成像外,还将审查最新的研究文章。这些内容包括自体荧光和荧光标记的组织和生物材料结构的成像,胶原蛋白I和其他蛋白质的基于SHG的定量形态测定,血管成像和TE中的在线监测技术。最后,我们对基于三光子的最新成像方法(例如相干反斯托克斯拉曼散射,三次谐波生成)给出了一些见识。这篇综述概述了多光子显微镜的强大且不断发展的领域,它是再生医学中人造组织发展的强大而必不可少的工具,并且有可能作为一般诊断医学成像的手段而变得越来越重要。

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