Rauws A G, Olling M, Timmerman A
Arch Toxicol. 1982 Mar;49(3-4):311-9. doi: 10.1007/BF00347879.
Amygdalin (D-mandelonitrile-beta-D-gentiobioside) is a cyanogenic glycoside claimed to show anti-cancer activity, sold under the incorrect name "Laetrile". For a sensible discussion of its alleged activity and its established toxicity it is necessary that its fate in the organism is known. The pharmacokinetics of amygdalin have been investigated in the Beagle dog after both intravenous and oral administration. The excretion of amygdalin has also been studied in the rat. Amygdalin concentrations were determined by high performance liquid chromatography in plasma ultrafiltrate and urine. The pharmacokinetics of amygdalin after intravenous administration were compared with those of diatrizoate, a model substance for extracellular volume and glomerular filtration. The amygdalin clearance is significantly larger than that of diatrizoate. The volumes of distribution of both substance are the same. After oral administration only a few percents of the amygdalin dose are systemically available. A part of the oral dose is recovered from the urine as prunasin (D-mandelonitrile-beta-D-glucoside).
苦杏仁苷(D-扁桃腈-β-D-龙胆二糖苷)是一种据称具有抗癌活性的氰苷,以错误的名称“苦杏仁酸”出售。为了对其所谓的活性和已确定的毒性进行合理讨论,有必要了解它在生物体内的代谢情况。已经在比格犬静脉注射和口服后研究了苦杏仁苷的药代动力学。还在大鼠中研究了苦杏仁苷的排泄情况。通过高效液相色谱法测定血浆超滤液和尿液中的苦杏仁苷浓度。将静脉注射后苦杏仁苷的药代动力学与泛影酸盐(一种用于细胞外液量和肾小球滤过的模型物质)的药代动力学进行了比较。苦杏仁苷的清除率明显高于泛影酸盐。两种物质的分布容积相同。口服给药后,只有百分之几的苦杏仁苷剂量可被全身利用。口服剂量的一部分以樱草糖苷(D-扁桃腈-β-D-葡萄糖苷)的形式从尿液中回收。