Lake-Bakaar D M
Scand J Haematol Suppl. 1977;32:125-34. doi: 10.1111/j.1600-0609.1977.tb01225.x.
The disposition and pharmacokinetics in rats of 14C-sorbitol-Ferastral has been studied as an initial step towards elucidating the metabolic fate of the polymeric organic moiety. The period of time studied was 24 h. Following i.v. administration of a dose corresponding to 10 mg/kg of iron approximately 60% of the isotope was found in the urine after this period of time. A further 3% was demonstrated in the faeces whilst the expired air accounted for about 10% in the form of 14CO2. Thus, a relatively large proportion of the radiolabel was promptly excreted via the kidneys whilst the expired air and probably bile constituted secondary excretion routes. The physico-chemical nature of the urinary product was similar to the parent carbohydrate compound. The residual 14C radioactivity was distributed mainly between the liver, which contained approximately 45% of the retained label, carcass with 36% and large intestine with 7%. The plasma disappearance pattern was biphasic. Similar experiments with the 14C-sorbitol polymer starting material were performed for purposes of comparison.
作为阐明聚合有机部分代谢命运的第一步,对14C-山梨醇-费拉斯特拉尔在大鼠体内的处置和药代动力学进行了研究。研究时间为24小时。静脉注射相当于10mg/kg铁的剂量后,这段时间后约60%的同位素在尿液中被发现。另外3%在粪便中被检测到,而呼出的气体以14CO2的形式占约10%。因此,相当大比例的放射性标记物迅速通过肾脏排出,而呼出的气体以及可能的胆汁构成了次要的排泄途径。尿液产物的物理化学性质与母体碳水化合物化合物相似。残留的14C放射性主要分布在肝脏(约占保留标记物的45%)、胴体(36%)和大肠(7%)之间。血浆消失模式为双相。为了进行比较,对14C-山梨醇聚合物起始原料进行了类似的实验。