首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Combined non-linear laser imaging (two-photon excitation fluorescence microscopy, fluorescence lifetime imaging microscopy, multispectral multiphoton microscopy) in cutaneous tumours: first experiences.
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Combined non-linear laser imaging (two-photon excitation fluorescence microscopy, fluorescence lifetime imaging microscopy, multispectral multiphoton microscopy) in cutaneous tumours: first experiences.

机译:皮肤肿瘤中的组合非线性激光成像(双光子激发荧光显微镜,荧光寿命成像显微镜,多光谱多光子显微镜):首次体验。

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BACKGROUND: Two-photon excitation (TPE) fluorescence microscopy is a high-resolution laser-scanning imaging technique enabling deep imaging inside biological tissues. TPE microscopy has the triple advantage of offering high spatial resolution (250 nm radially, 800 nm axially), high penetration depth inside skin (200 mm ), and low photodamage effects. Further, cells and extracellular matrix intrinsically contain a variety of fluorescent molecules (NADH, tryptophan, keratins, melanin, elastin, cholecalciferol and others), so that biological tissues can be imaged by TPE microscopy without any exogenous probe. The time-resolved analysis of the fluorescence signal, known as fluorescence lifetime imaging microscopy (FLIM), is an additional non-invasive microscopy technique useful to characterize endogenous fluorescence species and their surrounding medium by measuring the mean lifetime of fluorescent emission. Finally, multispectral (MTPE) tissue imaging can also be used to identify different endogenous fluorescent species by measuring their two photon emission spectra. Those techniques offer functional information about the relative quantities of fluorescent molecules, which are correlated with tissue structure in physiological and pathological states. OBJECTIVE: We have decided to apply these three methods at the same time for cutaneous tumors in order to evaluate their possible future use. METHOD: We have analyzed a melanoma and a basal cell carcinoma, with their surrounding healthy skin, to evaluate any difference in healthy skin and neoplasia. The samples were excised during dermatological surgery, then cut, saving some healthy skin in both, to obtain a regular shape, allowing its positioning either with the skin surface parallel to the optical axis (horizontal optical sectioning), or perpendicular (vertical optical sectioning). CONCLUSION: This first result demonstrates that FLIM is effective in discriminating healthy skin from MM, while MTPE is effective in discriminating healthy skin from BCC.
机译:背景:双光子激发(TPE)荧光显微镜是一种高分辨率的激光扫描成像技术,可在生物组织内部进行深度成像。 TPE显微镜具有三重优势:空间分辨率高(径向250 nm,轴向800 nm),皮肤内部穿透深度高(200 mm)和低光损伤效应。此外,细胞和细胞外基质固有地包含多种荧光分子(NADH,色氨酸,角蛋白,黑色素,弹性蛋白,胆钙化固醇等),因此无需任何外源探针即可通过TPE显微镜对生物组织进行成像。荧光信号的时间分辨分析称为荧光寿命成像显微镜(FLIM),是另一种非侵入性显微镜技术,可用于通过测量荧光发射的平均寿命来表征内源性荧光物质及其周围介质。最后,多光谱(MTPE)组织成像还可用于通过测量两个内在荧光物种的两个光子发射光谱来识别它们。这些技术提供了有关荧光分子相对数量的功能信息,这些信息与生理和病理状态下的组织结构相关。目的:我们已决定将这三种方法同时应用于皮肤肿瘤,以评估其可能的未来用途。方法:我们分析了黑色素瘤和基底细胞癌及其周围的健康皮肤,以评估健康皮肤和赘生物的任何差异。在皮肤病学手术中将样品切下,然后切割,保存两部分健康的皮肤,以获得规则的形状,使其位置平行于光轴(水平光学切片)或垂直(垂直光学切片)。 。结论:第一个结果表明,FLIM可以有效区分MM中的健康皮肤,而MTPE可以有效区分BCC中的健康皮肤。

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