In vivo non-invasive monitoring of tissue development in 3D printed subcutaneous bone scaffolds using fibre-optic Raman spectroscopy

Q3 Biochemistry, Genetics and Molecular Biology
Anders Runge Walther , Nicholas Ditzel , Moustapha Kassem , Morten Østergaard Andersen , Martin Aage Barsøe Hedegaard
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引用次数: 1

Abstract

The development of novel biomaterials for regenerative therapy relies on the ability to assess tissue development, quality, and similarity with native tissue types in in vivo experiments. Non-invasive imaging modalities such as X-ray computed tomography offer high spatial resolution but limited biochemical information while histology and biochemical assays are destructive. Raman spectroscopy is a non-invasive, label-free and non-destructive technique widely applied for biochemical characterization. Here we demonstrate the use of fibre-optic Raman spectroscopy for in vivo quantitative monitoring of tissue development in subcutaneous calcium phosphate scaffolds in mice over 16 weeks. Raman spectroscopy was able to quantify the time dependency of different tissue components related to the presence, absence, and quantity of mesenchymal stem cells. Scaffolds seeded with stem cells produced 3–5 times higher amount of collagen-rich extracellular matrix after 16 weeks implantation compared to scaffolds without. These however, showed a 2.5 times higher amount of lipid-rich tissue compared to implants with stem cells. Ex vivo micro-computed tomography and histology showed stem cell mediated collagen and bone development. Histological measures of collagen correlated well with Raman derived quantifications (correlation coefficient in vivo 0.74, ex vivo 0.93). In the absence of stem cells, the scaffolds were largely occupied by adipocytes. The technique developed here could potentially be adapted for a range of small animal experiments for assessing tissue engineering strategies at the biochemical level.

利用光纤拉曼光谱对3D打印皮下骨支架组织发育进行体内无创监测
用于再生治疗的新型生物材料的开发依赖于在体内实验中评估组织发育、质量和与天然组织类型的相似性的能力。非侵入性成像模式,如x射线计算机断层扫描提供高空间分辨率,但有限的生化信息,而组织学和生化分析是破坏性的。拉曼光谱是一种无创、无标记、无损的技术,广泛应用于生物化学表征。在这里,我们展示了使用光纤拉曼光谱在16周内对小鼠皮下磷酸钙支架组织发育进行体内定量监测。拉曼光谱能够量化与间充质干细胞存在、缺失和数量相关的不同组织成分的时间依赖性。植入干细胞的支架在植入16周后产生的富胶原细胞外基质量是未植入支架的3-5倍。然而,与干细胞移植相比,这些富含脂肪的组织的数量高出2.5倍。体外显微计算机断层扫描和组织学显示干细胞介导的胶原和骨发育。胶原的组织学测量与拉曼衍生定量结果相关性良好(体内相关系数0.74,离体相关系数0.93)。在缺乏干细胞的情况下,支架主要由脂肪细胞占据。这里开发的技术可能适用于一系列小型动物实验,以评估生化水平上的组织工程策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.10
自引率
0.00%
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审稿时长
25 days
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