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大鼠体内一氟磷酸酯和氟化物的胃肠吸收

Gastric and intestinal absorption of monofluorophosphate and fluoride in the rat.

作者信息

Rigalli A, Cabrerizo M A, Beinlich A D, Puche R C

机构信息

Laboratorio de Biologia Osea, Facultad de Medicina, Rosario, Argentina.

出版信息

Arzneimittelforschung. 1994 May;44(5):651-5.

PMID:8024641
Abstract

This paper reports data indicating that, in the rat, sodium monofluorophosphate (MFP, CAS 10163-15-2) is absorbed without hydrolysis through the stomach. This phenomenon and the fact that MFP binds to plasma globulins produce a prompt increase in protein-bound MFP concentration, significantly greater than the increase in plasma ultrafilterable fluoride. Intestinal absorption of MFP was investigated with the isolated duodenal loop in situ. The drug was hydrolyzed to fluoride at the intestinal lumen with a rate of approx. 3 times greater than that for fluoride absorption. After filling the duodenal loop with a MFP solution, ultrafiltrable fluoride accounts for the increase in plasma fluoride concentration, with no evidence of protein-bound MFP. This report also includes analytical techniques for the measurement of MFP in test solutions and in plasma.

摘要

本文报道的数据表明,在大鼠中,单氟磷酸钠(MFP,CAS 10163-15-2)可通过胃被吸收而不发生水解。这一现象以及MFP与血浆球蛋白结合的事实导致蛋白结合型MFP浓度迅速升高,显著高于血浆超滤性氟化物的升高。使用原位分离十二指肠袢研究了MFP的肠道吸收情况。该药物在肠腔内水解为氟化物的速率约比氟化物吸收速率高3倍。用MFP溶液充盈十二指肠袢后,超滤性氟化物导致血浆氟化物浓度升高,且没有蛋白结合型MFP的迹象。本报告还包括测试溶液和血浆中MFP测量的分析技术。

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Measurement of total and diffusible serum fluoride.血清总氟和可扩散氟的测定。
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