Campbell N R, Hasinoff B B, Singh M, Robertson S
Department of Medicine, Faculty of Medicine, University of Calgary, Alberta, Canada.
Br J Nutr. 1994 Sep;72(3):447-53. doi: 10.1079/bjn19940046.
A variety of compounds which bind to Fe have substantial reductions in absorption when co-administered with Fe compounds. The binding of both Fe2+ and Fe3+ ions to pteroylmonoglutamic acid and the pteroylmonoglutamate dianion was examined in vitro. In dimethylsulphoxide (DMSO) alone, pteroylmonoglutamate formed a 2:1 (pteroylmonoglutamate:Fe3+ ion) complex. However, in DMSO-aqueous Bis-Tris buffer (4:1, v/v; pH 6.0) no evidence of complex formation could be seen. Likewise spectroscopic evidence was obtained for complex formation with Fe2+ ion and pteroylmonoglutamate in DMSO alone but not in the aqueous DMSO buffer. In vivo studies examined the effect of FeSO4 on pteroylmonoglutamic acid absorption in an isolated perfused rat jejunal model of nutrient absorption. The dose of pteroylmonoglutamic acid approximated a human dose of 1 mg for the rat, while the FeSO4 doses were chosen to represent 6.4 mg, 64 mg and 300 mg human doses. There was no significant effect of FeSO4 on pteroylmonoglutamic acid absorption or instability of pteroylmonoglutamic acid in vivo in the presence of FeSO4 in the rat. Although 2:1 binding of pteroylmonoglutamic acid to Fe ions could be demonstrated in DMSO alone, no binding could be demonstrated in DMSO-Bis-Tris buffer (4:1, v/v; pH 6.0). It is unlikely that there will be a significant reduction in pteroylmonoglutamic acid absorption during concurrent ingestion of Fe preparations.
与铁结合的多种化合物在与铁化合物共同给药时,其吸收会大幅降低。在体外研究了Fe2+和Fe3+离子与蝶酰单谷氨酸和蝶酰单谷氨酸二价阴离子的结合情况。仅在二甲基亚砜(DMSO)中,蝶酰单谷氨酸形成了2:1(蝶酰单谷氨酸:Fe3+离子)复合物。然而,在DMSO-水性双三羟甲基氨基甲烷缓冲液(4:1,v/v;pH 6.0)中未观察到复合物形成的迹象。同样,仅在DMSO中获得了Fe2+离子与蝶酰单谷氨酸形成复合物的光谱证据,而在水性DMSO缓冲液中未获得。体内研究在分离灌注的大鼠空肠营养吸收模型中研究了硫酸亚铁对蝶酰单谷氨酸吸收的影响。蝶酰单谷氨酸的剂量接近大鼠的人用剂量1mg,而硫酸亚铁的剂量选择代表6.4mg、64mg和300mg的人用剂量。在大鼠体内,硫酸亚铁对蝶酰单谷氨酸的吸收或蝶酰单谷氨酸在硫酸亚铁存在下的稳定性没有显著影响。尽管仅在DMSO中可证明蝶酰单谷氨酸与铁离子形成2:1结合,但在DMSO-双三羟甲基氨基甲烷缓冲液(4:1,v/v;pH 6.0)中未证明有结合。在同时摄入铁制剂期间,蝶酰单谷氨酸的吸收不太可能显著降低。