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在使用ALA诱导内源性卟啉进行光动力疗法(PDT)期间的体内光产物形成。

In vivo photoproduct formation during PDT with ALA-induced endogenous porphyrins.

作者信息

König K, Schneckenburger H, Rück A, Steiner R

机构信息

Institute for Laser Technology in Medicine, Ulm, Germany.

出版信息

J Photochem Photobiol B. 1993 May;18(2-3):287-90. doi: 10.1016/1011-1344(93)80077-m.

Abstract

The administration of 5-aminolevulinic acid (ALA) in tumor-bearing nude mice leads to the formation of the fluorescent, photounstable photosensitizer protoporphyrin IX in tumor tissue. On-line fluorescence spectroscopy during photodynamic therapy (PDT) shows the in vivo formation of chlorintype photoproducts of protoporphyrin. The fluorescence of protoporphyrin as well as its photoproducts is bleached completely at the end of the PDT (100 J cm-2, 630 nm). These findings were also verified using ultrashort laser pulses and time-correlated single-photon counting. A photinduced shortening of the decay times and decrease in the integral fluorescence intensity were measured in vivo due to the photodestruction of the endogenous photosensitizer protoporphyrin IX in the tumor.

摘要

给荷瘤裸鼠施用5-氨基乙酰丙酸(ALA)会导致肿瘤组织中形成荧光性、光不稳定的光敏剂原卟啉IX。光动力疗法(PDT)期间的在线荧光光谱显示原卟啉在体内形成氯型光产物。在PDT结束时(100 J/cm²,630 nm),原卟啉及其光产物的荧光被完全漂白。这些发现也通过超短激光脉冲和时间相关单光子计数得到了验证。由于肿瘤内源性光敏剂原卟啉IX的光破坏,在体内测量到了光诱导的衰减时间缩短和积分荧光强度降低。

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