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Imaging dental sections with polarization-resolved SHG and time-resolved autofluorescence

机译:使用偏振分辨的SHG和时间分辨的自发荧光对牙齿切片进行成像

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In this study, we are using two-photon (2-p) excited autofluorescence and second harmonic (SH) as imaging modalities to investigate dental sections that contains the enamel and the dentin. The use of near-infrared wavelengths for multi-photon excitation greatly facilitates the observation of these sections due to the hard tissue's larger index of refraction and highly scattering nature. Clear imaging can be achieved without feature altering preparation procedures of the samples. Specifically, we perform polarization resolving on SH and lifetime analysis on autofluorescence. Polarization resolved SH reflects the preferred orientation of collagen while very different autofluorescence lifetimes are observed from the dentin and the enamel. The origin of 2-p autofluorescence and SH signals are attributed to hydroxyapatite crystals and collagen fibrils, respectively. Hydroxyapatite is found to be present throughout the sections while collagen fibrils exist only in the dentin and dentinoenamel junctions.
机译:在这项研究中,我们使用双光子(2-p)激发的自发荧光和二次谐波(SH)作为成像方式来研究包含牙釉质和牙本质的牙齿切片。由于硬组织的较大的折射率和高度散射的特性,将近红外波长用于多光子激发极大地方便了这些部分的观察。无需更改样品的制备程序即可实现清晰的成像。具体来说,我们对SH进行偏振分辨,对自发荧光进行寿命分析。偏振分辨的SH反映了胶原蛋白的首选取向,而与牙本质和牙釉质的自发荧光寿命却截然不同。 2-p自发荧光和SH信号的起源分别归因于羟基磷灰石晶体和胶原原纤维。发现羟基磷灰石存在于整个切片中,而胶原纤维仅存在于牙本质和牙本质釉质连接处。

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