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阿托品在儿童中的药代动力学。

Pharmacokinetics of atropine in children.

作者信息

Pihlajamäki K, Kanto J, Aaltonen L, Iisalo E, Jaakkola P

出版信息

Int J Clin Pharmacol Ther Toxicol. 1986 May;24(5):236-9.

PMID:3733273
Abstract

The serum concentration of atropine was determined both by radioreceptor assay (RRA) and by radioimmunoassay (RIA) following a single 0.02 mg/kg i.v. injection of 7 girls (age 6-15 years) and 16 boys (age 4-15 years) at the beginning of a combination anesthesia. RIA appeared to be useful in the clinical kinetic studies of this alkaloid, but RRA determined the whole antimuscarinic activity produced by atropine plus glycopyrrolate when the latter agent was used as an anticurarizing component together with neostigmine at the end of anesthesia. A biexponential serum decay curve of atropine was demonstrated by RIA with a very rapid distribution phase (t1/2 = 1-2 min) and a quite high tissue distribution (mean Vd beta = 2.6 l/kg), but due to the effective clearance of the drug (mean Cl total = 0.310-0.384 l/kg/h) the mean elimination phase half-life was around 6.5 hours. No age or gender dependency was found in the pharmacokinetics of atropine.

摘要

在联合麻醉开始时,对7名6至15岁女孩和16名4至15岁男孩单次静脉注射0.02mg/kg阿托品后,采用放射受体分析法(RRA)和放射免疫分析法(RIA)测定血清中阿托品的浓度。RIA似乎对该生物碱的临床动力学研究有用,但当在麻醉结束时将后者与新斯的明一起用作抗箭毒化成分时,RRA可测定阿托品加格隆溴铵产生的全部抗毒蕈碱活性。RIA显示阿托品的血清衰减曲线为双指数型,分布相非常迅速(t1/2 = 1 - 2分钟),组织分布相当高(平均Vdβ = 2.6l/kg),但由于药物的有效清除率(平均总Cl = 0.310 - 0.384l/kg/h),平均消除相半衰期约为6.5小时。在阿托品的药代动力学中未发现年龄或性别依赖性。

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