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Biophotonics of skin: method for correction of deep Raman spectra distorted by elastic scattering

机译:皮肤生物学学:通过弹性散射扭曲深拉曼光谱的方法

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Confocal Raman microspectroscopy allows in-depth molecular and conformational characterization of biological tissues non-invasively. Unfortunately, spectral distortions occur due to elastic scattering. Our objective is to correct the attenuation of in-depth Raman peaks intensity by considering this phenomenon, enabling thus quantitative diagnosis. In this purpose, we developed PDMS phantoms mimicking skin optical properties used as tools for instrument calibration and data processing method validation. An optical system based on a fibers bundle has been previously developed for in vivo skin characterization with Diffuse Reflectance Spectroscopy (DRS). Used on our phantoms, this technique allows checking their optical properties: the targeted ones were retrieved. Raman microspectroscopy was performed using a commercial confocal microscope. Depth profiles were constructed from integrated intensity of some specific PDMS Raman vibrations. Acquired on monolayer phantoms, they display a decline which is increasing with the scattering coefficient. Furthermore, when acquiring Raman spectra on multilayered phantoms, the signal attenuation through each single layer is directly dependent on its own scattering property. Therefore, determining the optical properties of any biological sample, obtained with DRS for example, is crucial to correct properly Raman depth profiles. A model, inspired from S.L. Jacques's expression for Confocal Reflectance Microscopy and modified at some points, is proposed and tested to fit the depth profiles obtained on the phantoms as function of the reduced scattering coefficient. Consequently, once the optical properties of a biological sample are known, the intensity of deep Raman spectra distorted by elastic scattering can be corrected with our reliable model, permitting thus to consider quantitative studies for purposes of characterization or diagnosis.
机译:共聚焦拉曼微痉挛术允许无侵入性的生物组织的深入分子和构象特征。不幸的是,由于弹性散射,频谱扭曲发生。我们的目的是通过考虑这种现象来校正深入拉曼峰强度的衰减,从而使这些现象能够进行定量诊断。从而以此目的,我们开发了PDMS Phantoms模仿皮肤光学性质,用作仪器校准和数据处理方法验证的工具。先前,基于纤维束的光学系统用于弥漫性反射光谱(DRS)的体内皮肤表征。在我们的幻像上使用,这种技术允许检查它们的光学属性:检索目标。使用商业共聚焦显微镜进行拉曼微穴位检查。深度轮廓由一些特定PDMS拉曼振动的集成强度构成。在单层幻影上获得,它们显示出随着散射系数而增加的下降。此外,当在多层模型上获取拉曼光谱时,通过每个单层的信号衰减直接取决于其自身的散射特性。因此,确定用DRS获得的任何生物样品的光学性质,例如,对于校正正确的拉曼深度轮廓至关重要。一个模型,受到S.L的启发。 jacques在某些点上进行共聚焦反射显微镜和修改的表达,并测试并测试以适合在散射系数的函数上以幻像上获得的深度曲线。因此,一旦已知生物样品的光学性质,可以通过我们可靠的模型来校正通过弹性散射失真的深拉曼光谱的强度,从而允许用于考虑用于表征或诊断的目的的定量研究。

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