尼罗河红处理的天然和氧化低密度脂蛋白的荧光光谱研究。

P Greenspan, P Lou
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引用次数: 11

摘要

1. 低密度脂蛋白存在时,尼罗红的激发和发射最大值分别为526 nm和587 nm。低密度脂蛋白在CuSO4存在下氧化16小时,在激发和发射光谱中都出现了明显的波长较长的光谱偏移。2. 天然LDL和氧化LDL的荧光强度差异在波长550和580 nm之间最为明显。在这些发射波长,尼罗河红处理氧化LDL的相对荧光强度被发现比在天然LDL存在下观察到的减少了约30%。3.LDL与乙酰化LDL比较,尼罗红色荧光光谱无差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectrofluorometric studies of nile red treated native and oxidized low density lipoprotein.

1. The excitation and emission maxima of nile red in the presence of LDL were found to be 526 and 587 nm, respectively. Oxidation of LDL for 16 hr in the presence of CuSO4 resulted in significant spectral shifts to longer wavelengths in both the excitation and emission spectra. 2. The difference in the fluorescence intensity between native and oxidized LDL was most pronounced at wavelengths between 550 and 580 nm. At these emission wavelengths, the relative fluorescence intensity of nile red treated oxidized LDL was found to be decreased by approx 30% when compared to that observed in the presence of native LDL. 3. Differences in the nile red fluorescence spectra were not observed when LDL and acetylated LDL were compared.

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