Department of Clinical Pharmacology, Bispebjerg University Hospital, Copenhagen, Denmark.
Basic Clin Pharmacol Toxicol. 2010 May;106(5):406-10. doi: 10.1111/j.1742-7843.2009.00503.x. Epub 2009 Dec 7.
The amount of activated charcoal needed to treat drug overdoses has arbitrarily been set at a charcoal-drug ratio of 10:1. Recent in vitro studies have shown a larger adsorptive capacity for activated charcoal when used in a model of paracetamol overdose. In the present study, we investigated whether this reserve capacity exists in vivo. This is clinically relevant in cases of large overdoses or if the full standard dose of 50 g activated charcoal cannot be administered. We performed a randomized, cross-over study (n = 16). One hour after a standard breakfast, 50 mg/kg paracetamol was administered, followed 1 hr later by an activated charcoal-Water slurry containing 50 (control), 25 or 5 g activated charcoal. The areas under the serum concentration-time curve (AUC) for paracetamol were used to estimate the efficacy of each activated charcoal dose. The AUC of the 25-g dose was found to be of similar size compared to the control, although statistics were weak. The AUC of the 5-g dose was 59% larger than the AUC of the 50-g dose (p = 0.0003). The terminal elimination half-life (t(1/2)) of paracetamol was 1.6 (CI 1.4-2.0) and 1.9 (CI 1.5-2.4) hr for 50 and 25 g, respectively (NS), and 2.5 (CI 1.8-3.0) hr for the 5-g dose (p = 0.003). The decrease in t(1/2) of paracetamol for the two larger activated charcoal doses indicates a possible effect of activated charcoal on paracetamol clearance and warrants further investigation. The large adsorptive reserve capacity of activated charcoal in vitro could not be reproduced for the smallest dose of activated charcoal. An activated charcoal-drug ratio of 10:1 is therefore still recommendable.
研究表明,与标准剂量 50 g 活性炭相比,在扑热息痛过量模型中使用更大剂量的活性炭可增加其吸附能力。本研究旨在探讨这种储备吸附能力是否存在于体内。在大剂量药物过量或无法给予标准剂量 50 g 活性炭的情况下,这一结果具有重要的临床意义。
这是一项随机交叉研究(n = 16)。志愿者标准早餐 1 小时后,给予 50 mg/kg 扑热息痛,1 小时后给予含 50(对照)、25 或 5 g 活性炭的活性炭水混悬液。使用血清浓度-时间曲线下面积(AUC)来评估每种活性炭剂量的疗效。
结果发现,25 g 剂量的 AUC 与对照组相似,尽管统计学意义较弱。5 g 剂量的 AUC 比 50 g 剂量的 AUC 大 59%(p = 0.0003)。扑热息痛的终末消除半衰期(t(1/2))分别为 1.6(CI 1.4-2.0)和 1.9(CI 1.5-2.4)小时,50 和 25 g 剂量组之间无显著差异(NS),5 g 剂量组为 2.5(CI 1.8-3.0)小时(p = 0.003)。对于较大剂量的活性炭,扑热息痛 t(1/2)的降低表明活性炭可能对扑热息痛的清除有影响,需要进一步研究。对于最小剂量的活性炭,未能再现体外活性炭的大量吸附储备能力。因此,仍推荐采用 10:1 的活性炭-药物比例。