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人体中有机硝酸盐的药代动力学:综述。

Pharmacokinetics of organic nitrates in man: an overview.

作者信息

Bogaert M G

机构信息

Heymans Institute of Pharmacology, University of Gent Medical School, Belgium.

出版信息

Eur Heart J. 1988 Jan;9 Suppl A:33-7. doi: 10.1093/eurheartj/9.suppl_a.33.

Abstract

The pharmacokinetics of glyceryl trinitrate are still not completely understood. The substance disappears rapidly from plasma largely by extrahepatic mechanisms. It is converted in glyceryl dinitrates and glyceryl mononitrates. After transdermal application of a controlled delivery system, plasma concentrations of glyceryl trinitrate can be maintained over the time period of application but, as for other routes, there are important intra- and inter-individual variations and fluctuations. Isosorbide dinitrate disappears less rapidly from the body; it is converted to the isosorbide mononitrates. Plasma concentrations of isosorbide dinitrate and mononitrates are quite predictable in different circumstances, e.g. on application of oral sustained release formulations. Measurement of the plasma concentrations of nitrates has been used to characterize different preparations and routes of administration. However, these plasma concentrations cannot be used to predict the effect, probably because of the important counter-regulation and tolerance which develop rapidly after administration of the drugs.

摘要

三硝酸甘油酯的药代动力学仍未被完全理解。该物质主要通过肝外机制迅速从血浆中消失。它会转化为二硝酸甘油酯和单硝酸甘油酯。在经皮应用控释系统后,三硝酸甘油酯的血浆浓度在应用期间可维持,但与其他给药途径一样,个体内和个体间存在重要的差异和波动。二硝酸异山梨酯从体内消失的速度较慢;它会转化为单硝酸异山梨酯。在不同情况下,例如口服缓释制剂时,二硝酸异山梨酯和单硝酸异山梨酯的血浆浓度相当可预测。硝酸盐血浆浓度的测量已被用于表征不同的制剂和给药途径。然而,这些血浆浓度不能用于预测疗效,这可能是因为药物给药后会迅速出现重要的反调节和耐受性。

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