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乙醇和水溶液中血卟啉、中卟啉、脱镁叶绿酸a和二氢卟吩e6的时间分辨荧光光谱

Time-resolved fluorescence spectroscopy of hematoporphyrin, mesoporphyrin, pheophorbide a and chlorin e6 in ethanol and aqueous solution.

作者信息

Roeder B, Wabnitz H

机构信息

Humboldt-University, Dept. of Physics, Berlin, G.D.R.

出版信息

J Photochem Photobiol B. 1987 Sep;1(1):103-13. doi: 10.1016/1011-1344(87)80010-6.

Abstract

The fluorescence decay I(t) and time-resolved spectra I(lambda, t) of some porphyrins and chlorins in ethanol and phosphate-buffered aqueous solution were investigated with a time-correlated single-photon-counting apparatus with a mode-locked Ar+ laser (514.5 nm) as the excitation source. The fluorescence of hematoporphyrin, mesoporphyrin and pheophorbide aa is considerably influenced by the conditions of aggregation (these compounds undergo aggregation in phosphate-buffered solution but not in ethanolic solution). The fluorescence decay of chlorin e6 which remains monomeric in both solvents is single exponential in all cases. The fluorescence spectra of hematoporphyrin, mesoporphyrin and pheophorbide a in phosphate-buffered solution are shifted with respect to the spectra obtained in ethanol; moreover, a new emission band (X band) appears, whose intensity increases on increasing the amount of equilibrium aggregates and shows a fast fluorescence decay. For hematoporphyrin and mesoporphyrin the appearance of the X band emission appears to be correlated with irreversible photoprocesses leading to fluorescent photoproducts. Analysis of the reported fluorescence spectra of cancer cells after incubation with hematoporphyrin derivative suggests that the fluorescent photoproducts might be formed also in vivo.

摘要

使用以锁模氩离子激光器(514.5nm)作为激发源的时间相关单光子计数装置,研究了乙醇和磷酸盐缓冲水溶液中一些卟啉和二氢卟吩的荧光衰减I(t)和时间分辨光谱I(λ, t)。血卟啉、中卟啉和脱镁叶绿酸a的荧光受聚集条件的影响很大(这些化合物在磷酸盐缓冲溶液中会发生聚集,但在乙醇溶液中不会)。在两种溶剂中均保持单体状态的二氢卟吩e6的荧光衰减在所有情况下均为单指数形式。磷酸盐缓冲溶液中血卟啉、中卟啉和脱镁叶绿酸a的荧光光谱相对于在乙醇中获得的光谱发生了位移;此外,出现了一个新的发射带(X带),其强度随着平衡聚集体数量的增加而增加,并表现出快速的荧光衰减。对于血卟啉和中卟啉,X带发射的出现似乎与导致荧光光产物的不可逆光过程相关。对报道的癌细胞与血卟啉衍生物孵育后的荧光光谱分析表明,荧光光产物也可能在体内形成。

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