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首页> 外文期刊>Tissue engineering, Part C. Methods >Three-dimensional characterization of tissue-engineered constructs by contrast-enhanced nanofocus computed tomography
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Three-dimensional characterization of tissue-engineered constructs by contrast-enhanced nanofocus computed tomography

机译:对比增强的纳米聚焦计算机断层扫描技术对组织工程构造物进行三维表征

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摘要

To successfully implement tissue-engineered (TE) constructs as part of a clinical therapy, it is necessary to develop quality control tools that will ensure accurate and consistent TE construct release specifications. Hence, advanced methods to monitor TE construct properties need to be further developed. In this study, we showed proof of concept for contrast-enhanced nanofocus computed tomography (CE-nano-CT) as a whole-construct imaging technique with a noninvasive potential that enables three-dimensional (3D) visualization and quantification of in vitro engineered extracellular matrix (ECM) in TE constructs. In particular, we performed a 3D qualitative and quantitative structural and spatial assessment of the in vitro engineered ECM, formed during static and perfusion bioreactor cell culture in 3D TE scaffolds, using two contrast agents, namely, Hexabrix? and phosphotungstic acid (PTA). To evaluate the potential of CE-nano-CT, a comparison was made to standardly used techniques such as Live/Dead viability/cytotoxicity, Picrosirius Red staining, and to net dry weight measurements of the TE constructs. When using Hexabrix as the contrast agent, the ECM volume fitted linearly with the net dry ECM weight independent from the flow rate used, thus suggesting that it stains most of the ECM. When using PTA as the contrast agent, comparing to net weight measurements showed that PTA only stains a part of the ECM. This was attributed to the binding specificity of this contrast agent. In addition, the PTA-stained CE-nano-CT data showed pronounced distinction between flow conditions when compared to Hexabrix, indicating culture-specific structural ECM differences. This novel type of information can contribute to optimize bioreactor culture conditions and potentially critical quality characteristics of TE constructs such as ECM quantity and homogeneity, facilitating the gradual transformation of TE constructs in well-characterized TE products.
机译:为了成功地将组织工程(TE)结构作为临床治疗的一部分,有必要开发质量控制工具,以确保准确和一致的TE结构释放规范。因此,需要进一步开发用于监视TE构造属性的高级方法。在这项研究中,我们展示了对比度增强型纳米聚焦计算机断层扫描(CE-nano-CT)的概念证明,它是一种具有无创潜力的整体构造成像技术,可实现体外工程化细胞外的三维(3D)可视化和定量TE构造中的基质(ECM)。特别是,我们使用两种造影剂Hexabrix?对3D TE支架在静态和灌注生物反应器细胞培养过程中形成的体外工程化ECM进行了3D定性,定量结构和空间评估。和磷钨酸(PTA)。为了评估CE-nano-CT的潜力,将其与标准使用的技术进行了比较,例如活/死活力/细胞毒性,Picosirius Red染色以及TE构造的净干重测量。当使用Hexabrix作为造影剂时,ECM的体积与干ECM的净重呈线性关系,而与所使用的流速无关,因此表明它弄脏了大部分ECM。当使用PTA作为造影剂时,与净重的测量结果相比,PTA仅会弄脏ECM的一部分。这归因于该造影剂的结合特异性。此外,与Hexabrix相比,PTA染色的CE-nano-CT数据显示出流动条件之间的明显区别,表明培养物特定的结构ECM差异。这种新型信息可以帮助优化生物反应器培养条件和TE构建体的潜在关键质量特征,例如ECM数量和同质性,从而促进TE构建体在特征明确的TE产品中的逐步转化。

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