Arimoto-Kobayashi S, Harada N, Tokunaga R, Odo J, Hayatsu H
Faculty of Pharmaceutical Sciences, Okayama University, Japan.
Mutat Res. 1997 Nov 28;381(2):243-9. doi: 10.1016/s0027-5107(97)00188-7.
Chlorophyllin, a water soluble derivative of chlorophyll is known to suppress the mutagenic and carcinogenic actions of compounds having polycyclic structures, e.g. heterocyclic amines and aflatoxin B1. There is evidence that this suppressing effect arises, at least in part, by a complex formation between the porphyrin-like structure of chlorophyllin and the planar molecular surfaces of these compounds. We report here that chlorophyllin can form an insoluble salt-like material when mixed with chitosan, a polyglucosamine, and that the solid chlorophyllin-chitosan thus prepared can efficiently trap polycyclic mutagenic compounds. The adsorbed polycyclic mutagens were elutable with buffers of acidic pH, but only to small extents. Chlorophyllin-chitosan may be expected to be useful as an intercepting agent against polycyclic mutagens and carcinogens.
叶绿酸是叶绿素的一种水溶性衍生物,已知它能抑制具有多环结构的化合物(如杂环胺和黄曲霉毒素B1)的诱变和致癌作用。有证据表明,这种抑制作用至少部分是由于叶绿酸的卟啉样结构与这些化合物的平面分子表面之间形成了复合物。我们在此报告,叶绿酸与壳聚糖(一种聚葡糖胺)混合时会形成一种不溶性盐样物质,由此制备的固体叶绿酸 - 壳聚糖能有效捕获多环诱变化合物。吸附的多环诱变剂可用酸性pH缓冲液洗脱,但洗脱程度很小。叶绿酸 - 壳聚糖有望作为一种针对多环诱变剂和致癌物的拦截剂。