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多剂量活性炭与全身药物清除率的提高:动物及人类志愿者研究综述

Multiple-dose activated charcoal and enhancement of systemic drug clearance: summary of studies in animals and human volunteers.

作者信息

Chyka P A

机构信息

University of Tennessee, Memphis, USA.

出版信息

J Toxicol Clin Toxicol. 1995;33(5):399-405. doi: 10.3109/15563659509013748.

Abstract

Multiple-dose activated charcoal therapy can enhance the systemic elimination of many drugs. Studies in animals and human volunteers provide a framework for understanding the indications and limitations of multiple-dose activated charcoal therapy. Enterocapillary exsorption creates a compartment for diffusion drugs out of the bloodstream and activated charcoal can augment this process to enhance drug clearance. Once charcoal reaches the intestine, there is a rapid onset of action. Clearance at exsorption sites is limited by blood flow; moreover, the rate of exsorption is related to the dose of charcoal up to a ceiling dose. Drug absorption, distribution, metabolism and elimination dynamically interact with multiple-dose activated charcoal therapy making it difficult to identify a single variable that may predict the success or failure with this therapy. Drug characteristics associated with enhanced systemic clearance with multiple-dose activated charcoal include a low intrinsic clearance, presence in the body for a sufficient time period for charcoal to act, a prolonged distributive phase, non-restrictive protein binding, and a small volume of distribution. Drugs that are unaffected at low doses may respond to multiple doses of activated charcoal when nonlinear kinetics are apparent due to overdose or disease. Although our current understanding is incomplete, multiple-dose activated charcoal therapy will play a role in the future therapy of poisoning patients.

摘要

多剂量活性炭疗法可增强许多药物的全身清除。在动物和人类志愿者身上进行的研究为理解多剂量活性炭疗法的适应症和局限性提供了一个框架。肠毛细血管外排为药物从血液中扩散创造了一个隔室,而活性炭可以增强这一过程以提高药物清除率。一旦活性炭到达肠道,作用就会迅速起效。外排部位的清除受血流限制;此外,外排速率与活性炭剂量相关,直至达到最大剂量。药物的吸收、分布、代谢和清除与多剂量活性炭疗法动态相互作用,因此很难确定一个单一变量来预测该疗法的成功或失败。与多剂量活性炭增强全身清除相关的药物特性包括低内在清除率、在体内存在足够长的时间以便活性炭发挥作用、较长的分布相、非限制性蛋白结合以及小分布容积。低剂量时无影响的药物,在因过量或疾病导致非线性动力学明显时,可能对多剂量活性炭有反应。尽管我们目前的理解并不完整,但多剂量活性炭疗法将在未来中毒患者的治疗中发挥作用。

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