Greenblatt D J
Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, Boston, Massachusetts.
J Clin Pharmacol. 1993 Jul;33(7):650-6. doi: 10.1002/j.1552-4604.1993.tb04719.x.
Many drugs have incomplete systemic availability after oral dosage. This can be attributed to incomplete absorption from the gastrointestinal tract, or to presystemic extraction, in which a fraction of an orally administered dose is biotransformed before reaching the systemic circulation. Presystemic extraction can occur either via biotransformation by gastrointestinal mucosa or enteric flora, or via metabolism during the "first-pass" through the liver. For drugs with low oral bioavailability due to high presystemic extraction, impaired clearance leads to increased peak plasma levels and greater area under the concentration-time curve, but minimal change in elimination half-life.
许多药物口服给药后全身可用性不完全。这可能归因于胃肠道吸收不完全,或归因于首过消除,即口服剂量的一部分在到达体循环之前发生生物转化。首过消除可通过胃肠道黏膜或肠道菌群的生物转化,或通过肝脏“首过”期间的代谢而发生。对于因高首过消除而口服生物利用度低的药物,清除受损会导致血浆峰浓度升高和浓度-时间曲线下面积增大,但消除半衰期变化极小。