Fuchs C, Riesenberg R, Siegert J, Baumgartner R
Urologische Klinik, Ludwig-Maximilians-Universität München, Germany.
J Photochem Photobiol B. 1997 Aug;40(1):49-54. doi: 10.1016/s1011-1344(97)00026-2.
pH-Dependent variations in the fluorescence intensity of 5-aminolaevulinic acid-induced 5-aminolaevulinic acid protoporphyrin IX (PP IX) were compared with the cell viability following light irradiation. The fluorescence intensity was determined by flow cytometry and the cell activity was investigated by a colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay 24 h after photodynamic treatment. The results obtained by fluorescence measurements clearly showed that pH values of the incubation medium containing (5-ALA) below and above pH 7.4 led to a significant decrease in the fluorescence intensity. The viability of cells incubated with 0.6 mM 5-ALA in a medium at pH 6.0 was unaffected on exposure to light at lambda = 635 nm up to 15 J cm-2. However, cells incubated at pH 7.4 (with the other treatment parameters the same) were nearly completely destroyed. In addition, depletion of intracellular PPIX was faster in physiological medium than in acid medium.
将5-氨基乙酰丙酸诱导产生的5-氨基乙酰丙酸原卟啉IX(PP IX)荧光强度的pH依赖性变化与光照后的细胞活力进行了比较。通过流式细胞术测定荧光强度,并在光动力治疗24小时后通过比色法3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法研究细胞活性。荧光测量所得结果清楚地表明,pH值低于和高于7.4的含(5-ALA)孵育培养基会导致荧光强度显著降低。在pH 6.0的培养基中用0.6 mM 5-ALA孵育的细胞,在λ = 635 nm光照至15 J cm-2时活力未受影响。然而,在pH 7.4下孵育的细胞(其他处理参数相同)几乎完全被破坏。此外,生理培养基中细胞内PPIX的消耗比酸性培养基中更快。