术中拉曼光谱和离体拉曼成像评估软骨退化

Riana Gaifulina , Abigail D.G. Nunn , Edward R.C. Draper , Robin K. Strachan , Nathan Blake , Steven Firth , Geraint M.H. Thomas , Paul F. McMillan , Jayesh Dudhia
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引用次数: 5

摘要

开发一种无标记、非破坏性和安全的分析方法,如拉曼光谱,用于评估软骨降解是非常可取的。与非光学成像方式相比,拉曼成像提供了一种更敏感的方法,可以直接评估三维空间中软骨的化学成分,并有可能监测软骨退变,为干预和治疗策略提供信息。在此,我们报告了拉曼光谱方法在离体和关节镜下的应用,以识别含有早期疾病阶段特征的轻微局灶性病变的软骨标本中的分子改变。我们最初的离体分析,通过软骨样品的单点拉曼光谱获得,支持先前基于S-O拉伸振动带与硫酸糖胺聚糖(sGAGs)相关的发现。我们将分析扩展到高波数区域,在那里我们观察到分配给C-H和O-H拉伸模式的振动带区分了早期软骨变化和健康软骨样本。此外,我们首次在接受膝关节关节镜检查的患者中使用定制的光学探针获得拉曼光谱测量值,进行了概念验证的临床研究。获得的光谱具有足够的信噪比,同样可以区分病变和邻近软骨部位,并在明显健康的软骨中识别出sGAGs的减少。在此基础上,我们提出了拉曼映射的初步结果,通过软骨的深度和病变在空间上解析软骨的分子成分。成像显示病变和周围软骨内的sGAG分布不均匀且减少,否则视觉正常,与临床观察相似,表明病变的降解影响延伸到其边界之外。这伴随着荧光信号强度的降低,这表明荧光可能作为拉曼信号的辅助手段,在区分正常软骨和变性软骨方面提供了有价值的信息。这项工作证明了拉曼映射在单点拉曼测量上对关节软骨各向异性分析的价值,并强调了该技术在体内关节镜应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intra-operative Raman spectroscopy and ex vivo Raman mapping for assessment of cartilage degradation

Intra-operative Raman spectroscopy and ex vivo Raman mapping for assessment of cartilage degradation

The development of a label-free, non-destructive and safe analytical method such as Raman spectroscopy for assessing cartilage degradation is highly desirable. Compared to non-optical imaging modalities, Raman mapping offers a more sensitive means of directly assessing the chemical composition of cartilage in three-dimensional space and the potential to monitor cartilage degeneration to inform intervention and treatment strategies. Herein, we report the application of Raman spectroscopic methods ex vivo and at arthroscopy to identify molecular alterations in cartilage specimens containing minor focal lesions characteristic of the early disease phase. Our initial ex vivo analysis, obtained by single-point Raman spectroscopy of cartilage samples, supports previous findings based on S-O stretching vibration bands associated with sulphated glycosaminoglycans (sGAGs). We extended the analyses to the high-wavenumber region where we observed that vibrational bands assigned to C-H and O-H stretching modes discriminated early cartilage alterations from healthy cartilage samples. Furthermore, we performed a proof-of-concept in-clinic study using a custom-built optical probe to acquire Raman spectral measurements for the first time in patients undergoing arthroscopy of knee joints. Spectra were obtained with adequate signal-to-noise ratios that similarly discriminated between lesion and adjacent cartilage sites and identified reductions in sGAGs in apparently healthy cartilage. Building on this, we present initial results from Raman mapping to spatially resolve the molecular constituents of cartilage through its depth and across a lesion. Mapping revealed a non-uniform and reduced sGAG distribution within the lesion and peripheral cartilage that was otherwise visually normal, similar to the in-clinic observations, showing that the degradative influence of the lesion extended beyond its border. This was accompanied by a decreased fluorescence signal intensity, which suggests that fluorescence may provide valuable information as an adjunct to the Raman signal in discriminating normal and degenerating cartilage. This work demonstrates the value of Raman mapping over single-point Raman measurements for the analysis of the anisotropy of articular cartilage and highlights the potential of the technology for in vivo articular joint arthroscopy applications.

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