首页> 外文会议>Conference on Optical Biopsy Ⅳ, Jan 21-23, 2002, San Jose, USA >In-vivo characterization of endogenous porphyrin fluorescence from DMBA-treated Swiss Albino mice skin carcinogenesis for measuring tissue transformation
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In-vivo characterization of endogenous porphyrin fluorescence from DMBA-treated Swiss Albino mice skin carcinogenesis for measuring tissue transformation

机译:DMBA处理的瑞士白化病小鼠皮肤致癌作用中内源性卟啉荧光的体内表征,用于测量组织转化

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Steady state fluorescence spectroscopic characterization of endogenous porphyrin emission from DMBA treated skin carcinogenesis in Swiss albino mice was carried out. The emission of endogenous porphyrin from normal and abnormal skin tissues was studied both in the presence and absence of exogenous ALA to compare the resultant porphyrin emission characterictics. The mice skin is excited at 405nm and emission spectra are scanned from 430 to 700nm. The average fluorescence emission spectra of mice skin at normal and various tissues transformation conditions were found to be different. Two peaks around 460nm and 636nm were observed and they may be attributed to NADH, Elastin and collagen combination and endogenous porphyrin emission. The intensity at 636nm increases as the stage of the cancer increases. Although exogenous ALA enhances the PPIX level in tumor, the synthesis of PPIX was also found in normal surrounding skin, in fact, with higher concentration than that of tumor tissues.
机译:在瑞士白化病小鼠中进行了DMBA处理的皮肤致癌作用中内源性卟啉发射的稳态荧光光谱表征。在存在和不存在外源性ALA的情况下,研究了正常和异常皮肤组织中内源性卟啉的发射,以比较所得的卟啉发射特征。小鼠皮肤在405nm处激发,发射光谱在430nm至700nm范围内扫描。发现正常和各种组织转化条件下小鼠皮肤的平均荧光发射光谱是不同的。在460nm和636nm附近观察到两个峰,这可能归因于NADH,弹性蛋白和胶原蛋白的结合以及内源性卟啉的发射。 636nm处的强度随着癌症分期的增加而增加。尽管外源性ALA提高了肿瘤中的PPIX水平,但在正常的周围皮肤中也发现了PPIX的合成,实际上其浓度高于肿瘤组织。

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