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氨基乙酰丙酸诱导的原卟啉IX荧光的无创测量可实现体内小鼠胶质瘤的检测。

Noninvasive measurement of aminolevulinic acid-induced protoporphyrin IX fluorescence allowing detection of murine glioma in vivo.

作者信息

Gibbs-Strauss Summer L, O'Hara Julia A, Hoopes P Jack, Hasan Tayyaba, Pogue Brian W

机构信息

Dartmouth College, Thayer School of Engineering, Hanover, New Hampshire 03755, USA.

出版信息

J Biomed Opt. 2009 Jan-Feb;14(1):014007. doi: 10.1117/1.3065543.

Abstract

Aminolevulinic acid (ALA)-induced protoporphyrin IX (PpIX) fluorescence is studied as a contrast agent for noninvasive detection of murine glioma, using the fluorescence-to-transmission ratio measured through the cranium. Signals measured prior to administration of ALA are very similar between control animals, 9L-GFP, and U251 tumor-bearing animals. However, 2 h after ALA administration, the PpIX signal from both tumor-bearing groups is significantly higher than the control group (9L-GFP group p-value=0.016, and U251 group p-value=0.004, relative to the control group). The variance in signal from the 9L-GFP group is much larger than either the control group or the U251 group, which is consistent with higher intrinsic PpIX fluorescence heterogeneity as seen in situ at ex vivo analysis. Decreasing the skin PpIX fluorescence via intentional photobleaching using red light (635 nm) is examined as a tool for increasing PpIX contrast between the tumor-bearing and control groups. The red light bleaching is found to increase the ability to accurately quantify PpIX fluorescence in vivo, but decreases the specificity of detection between tumor-bearing and nontumor-bearing groups.

摘要

研究了氨基乙酰丙酸(ALA)诱导的原卟啉IX(PpIX)荧光作为一种造影剂,用于通过颅骨测量的荧光与透射率对小鼠胶质瘤进行无创检测。在给予ALA之前,对照动物、9L - GFP和U251荷瘤动物测量的信号非常相似。然而,在给予ALA后2小时,两个荷瘤组的PpIX信号均显著高于对照组(9L - GFP组p值 = 0.016,U251组p值 = 0.004,相对于对照组)。9L - GFP组信号的方差远大于对照组或U251组,这与在离体分析中原位观察到的更高的固有PpIX荧光异质性一致。研究了使用红光(635 nm)通过有意光漂白降低皮肤PpIX荧光作为增加荷瘤组与对照组之间PpIX对比度的一种手段。发现红光漂白可提高体内准确定量PpIX荧光的能力,但降低了荷瘤组与非荷瘤组之间检测的特异性。

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