Online quantitative monitoring of live cell engineered cartilage growth using diffuse fiber-optic Raman spectroscopy

被引:39
作者
Bergholt, Mads S. [1 ,2 ,3 ]
Albro, Michael B. [1 ,2 ,3 ]
Stevens, Molly M. [1 ,2 ,3 ]
机构
[1] Imperial Coll London, Dept Mat, London SW7 2AZ, England
[2] Imperial Coll London, Dept Bioengn, London SW7 2AZ, England
[3] Imperial Coll London, Inst Biomed Engn, London SW7 2AZ, England
基金
欧盟地平线“2020”; 英国惠康基金; 英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
Fiber-optic Raman spectroscopy; Articular cartilage; Tissue-engineering; Live cell Raman spectroscopy; Online biomedical Raman spectroscopy; NEAR-INFRARED SPECTROSCOPY; MECHANICAL-PROPERTIES; ARTICULAR-CARTILAGE; NONDESTRUCTIVE ASSESSMENT; SEEDING DENSITY; TISSUE; CONSTRUCTS; SCATTERING; BETA;
D O I
10.1016/j.biomaterials.2017.06.015
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tissue engineering (TE) has the potential to improve the outcome for patients with osteoarthritis (OA). The successful clinical translation of this technique as part of a therapy requires the ability to measure extracellular matrix (ECM) production of engineered tissues in vitro, in order to ensure quality control and improve the likelihood of tissue survival upon implantation. Conventional techniques for assessing the ECM content of engineered cartilage, such as biochemical assays and histological staining are inherently destructive. Raman spectroscopy, on the other hand, represents a non-invasive technique for in situ biochemical characterization. Here, we outline current roadblocks in translational Raman spectroscopy in TE and introduce a comprehensive workflow designed to non-destructively monitor and quantify ECM biomolecules in large (>3 mm), live cell TE constructs online. Diffuse near-infrared fiber-optic Raman spectra were measured from live cell cartilaginous TE constructs over a 56-day culturing period. We developed a multivariate curve resolution model that enabled quantitative biochemical analysis of the TE constructs. Raman spectroscopy was able to non-invasively quantify the ECM components and showed an excellent correlation with biochemical assays for measurement of collagen (R-2 = 0.84) and glycosaminoglycans (GAGS) (R-2 = 0.86). We further demonstrated the robustness of this technique for online prospective analysis of live cell TE constructs. The fiber-optic Raman spectroscopy strategy developed in this work offers the ability to non-destructively monitor construct growth online and can be adapted to a broad range of TE applications in regenerative medicine toward controlled clinical translation. (C) 2017 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:128 / 137
页数:10
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