PHARMACOKINETICS OF GLYCOPYRRONIUM,I.M.

被引:20
作者
ALIMELKKILA, TM
KAILA, T
KANTO, J
IISALO, E
机构
[1] Department of Anaesthesiology, 20520 Turku
[2] Department of Clinical Pharmacology, Turku University Central Hospital, 20520 Turku
关键词
D O I
10.1093/bja/64.6.667
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
A sensitive radioreceptor assay was used to determine the pharmacokinetics of glyco-pyrronium following a single i.m. injection of 8 ug kg-1 in nine surgical patients. Rapid absorption was found, with a mean peak plasma concentration after 16.1 min and mean elimination half-life of 75.4 min. Almost half (49.3%) of the drug was excreted in pharmacologically active form in the urine within 3 h. A significant increase in heart rate (P < 0.05) occurred in 15 min, lasting up to 60 min, and an antisialagogue effect in 10 min, lasting up to 8 h (P < 0.05). There was no measurable glycopyrronium in lumbar cerebrospinal fluid samples (n = 9) taken 40 min after administration of drug. © 1990 British Journal of Anaesthesia.
引用
收藏
页码:667 / 669
页数:3
相关论文
共 6 条
[1]   RADIORECEPTOR ASSAY FOR DETERMINATION OF THE ANTIMUSCARINIC DRUG IPRATROPIUM BROMIDE IN MAN [J].
ENSINGER, HA ;
WAHL, D ;
BRANTL, V .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 33 (05) :459-462
[2]  
IISALO E, 1988, ANN CLIN RES, V20, P367
[3]   FATE OF INTRAVENOUS [H-3]GLYCOPYRROLATE IN MAN [J].
KALTIALA, E ;
PENTTILA, A ;
VAPAATALO, H ;
LARMI, T .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1974, 26 (05) :352-354
[4]  
KENTALA E, 1989, IN PRESS PHARM TOXIC
[5]  
PROAKIS AG, 1979, ANESTHESIOLOGY, V48, P339