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海葱次苷、海葱次苷 -3'- 甲醚和海葱次苷 -4'- 甲醚在人工胃液和肠液中的稳定性研究(作者译)

[Investigations on the Stability of Proscillaridine, Proscillaridine-3'-methylether and Proscillaridine-4'-methylether in Artificial Gastric and Intestinal Fluids (author's transl)].

作者信息

Einig H

出版信息

Arzneimittelforschung. 1976;26(7):1276-9.

PMID:12764
Abstract

The stability of bufadienolides in artificial gastric and intestinal fluids was investigated at different pH-values as a function of incubation time using proscillaridine, proscillaridine-3'-methylether and proscillaridine-4'-methylether. These glycosides were completely stable on pH 3.0--8.5 during the investigated time interval of 1 h. At lower pH-values cleavage of the glycosidic bond occurred. At pH 1.0 73% of proscillaridine, 33% of proscillaridine-3'-methylether and 41% of proscillaridine-4'-methylether were decomposed. At pH 2.0 only about 10% decomposition of these compounds could be detected. These experiments show that the stability of proscillaridine in gastric juice is comparable with the stability of digitalis glycosides and digoxin derivatives. The stability of methylated proscillaridine derivatives in artificial digestion fluids, however, proved to be superior to any orally administered cardiac glycoside.

摘要

以海葱苷、海葱苷 - 3'- 甲醚和海葱苷 - 4'- 甲醚为研究对象,考察了不同pH值下蟾蜍二烯羟酸内酯在人工胃液和肠液中的稳定性随孵育时间的变化情况。在1小时的研究时间间隔内,这些糖苷在pH 3.0 - 8.5范围内完全稳定。在较低的pH值下,糖苷键会发生断裂。在pH 1.0时,73%的海葱苷、33%的海葱苷 - 3'- 甲醚和41%的海葱苷 - 4'- 甲醚发生分解。在pH 2.0时,只能检测到这些化合物约10%的分解。这些实验表明,海葱苷在胃液中的稳定性与洋地黄糖苷和地高辛衍生物的稳定性相当。然而,甲基化海葱苷衍生物在人工消化液中的稳定性被证明优于任何口服的强心苷。

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