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长春西汀和阿朴长春胺酸的吸收研究。

Study on the absorption of vinpocetine and apovincaminic acid.

作者信息

Pudleiner P, Vereczkey L

机构信息

Chemical Works of Gedeon Richter Ltd, Budapest, Hungary.

出版信息

Eur J Drug Metab Pharmacokinet. 1993 Oct-Dec;18(4):317-21. doi: 10.1007/BF03190179.

Abstract

The absorption of vinpocetine (Cavinton) and apovincaminic acid, compounds showing a marked difference in their physico-chemical properties, was studied in rats in in situ loop experiments by using radiolabelled compounds. In the case of apovincaminic acid, the investigations also involved the estimation of the portion of radioactivity excreted in urine and faeces after i.v. and p.o. administration of the compound. According to our results, it can be concluded that both vinpocetine and apovincaminic acid are absorbed from the gastrointestinal tract--apovincaminic acid mainly from the stomach, while vinpocetine is absorbed from the small intestine.

摘要

采用放射性标记化合物,通过大鼠原位肠袢实验研究了长春西汀(卡文通)和阿朴长春胺酸这两种理化性质有显著差异的化合物的吸收情况。对于阿朴长春胺酸,研究还涉及静脉注射和口服该化合物后,尿液和粪便中排泄的放射性部分的估计。根据我们的结果,可以得出结论,长春西汀和阿朴长春胺酸均可从胃肠道吸收——阿朴长春胺酸主要从胃吸收,而长春西汀从小肠吸收。

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