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铁对唾液中对乙酰氨基酚药代动力学的影响。

Effects of iron on the pharmacokinetics of paracetamol in saliva.

作者信息

Issa Mahmoud Mohamed, Nejem R'afat Mahmoud, Shanab Alaa Abu

机构信息

Department of Chemistry, Pharmaceutical Analytical Chemistry, Alaqsa University, P.O. Box 4051, Gaza, Palestine.

Department of Chemistry, Analytical Chemistry, Alaqsa University, P.O. Box 4051, Gaza, Palestine.

出版信息

Pak J Biol Sci. 2013 Dec 15;16(24):2050-3. doi: 10.3923/pjbs.2013.2050.2053.

Abstract

Paracetamol has been reported to chelate with iron. It was found that no in vitro reaction between ferrous ion and paracetamol. Other studies found that there is an aerobic (in the gastrointestinal tract) oxidation of ferrous ion to ferric ion caused in iron-paracetamol in vivo reactions. The objective of this study was to determine if iron interacts with paracetamol and reduces paracetamol absorption. A randomized, double-blind, cross-over study design was used to assess the in vivo interaction of paracetamol and ferrous ion. Paracetamol (1.0 g) was co-ignested alone or with (300 mg) ferrous sulphate by ten healthy male volunteers, using saliva drug levels as a parameter. Concomitant administration of ferrous sulphate and paracetamol, decreased AUC8 from 42.88 +/- 3.8-34.25 +/- 2.8 microg h mL(-1) (p = 0.04) and Cmax from 18.75 +/- 1.9 to 15.9 +/- 1.7 microg mL(-1) (p = 0.11), while no change in tmax (p = 0.5) was originated. A significant difference was found in the paracetamol pharmacokinetic parameter oral clearance (C1/F) (p = 0.02) and slightly increased in volume of distribution (V(d)/F) (p = 0.10). Co-administration of iron and paracetamol results in decreased paracetamol absorption due to an interaction between iron and paracetamol.

摘要

据报道,对乙酰氨基酚可与铁螯合。研究发现亚铁离子与对乙酰氨基酚之间在体外没有反应。其他研究发现,在体内铁 - 对乙酰氨基酚反应中,(在胃肠道内)存在亚铁离子的需氧氧化成铁离子的情况。本研究的目的是确定铁是否与对乙酰氨基酚相互作用并减少对乙酰氨基酚的吸收。采用随机、双盲、交叉研究设计来评估对乙酰氨基酚与亚铁离子的体内相互作用。10名健康男性志愿者单独或与(300毫克)硫酸亚铁共同摄入对乙酰氨基酚(1.0克),以唾液药物水平作为参数。硫酸亚铁与对乙酰氨基酚同时给药时,AUC8从42.88±3.8降至34.25±2.8微克·小时·毫升⁻¹(p = 0.04),Cmax从18.75±1.9降至15.9±1.7微克·毫升⁻¹(p = 0.11),而tmax未发生变化(p = 0.5)。对乙酰氨基酚的药代动力学参数口服清除率(C1/F)存在显著差异(p = 0.02),分布容积(V(d)/F)略有增加(p = 0.10)。铁与对乙酰氨基酚共同给药会因铁与对乙酰氨基酚之间的相互作用而导致对乙酰氨基酚吸收减少。

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