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吸入后沙丁胺醇在肺部的相对生物利用度的测定。

Determination of the relative bioavailability of salbutamol to the lung following inhalation.

作者信息

Hindle M, Chrystyn H

机构信息

School of Pharmacy, University of Bradford, West Yorkshire.

出版信息

Br J Clin Pharmacol. 1992 Oct;34(4):311-5. doi: 10.1111/j.1365-2125.1992.tb05921.x.

Abstract
  1. The urinary excretion of salbutamol and its sulphate metabolite was measured following oral (4 mg) and inhaled (4 x 100 micrograms) administration of salbutamol. 2. Total urinary recovery of salbutamol and its sulphate conjugate indicated a mean (s.d.) relative bioavailability of 92.2 (24.8) % following inhalation compared with oral administration. 3. The mean (s.d.) elimination half-lives of salbutamol and its sulphate conjugate were 5.7 (1.4) and 4.1 (2.1) h, respectively, after oral administration and following inhalation they were 6.1 (2.1) and 5.1 (1.0) h, respectively. 4. Following oral and inhaled administration it was found that in the first 30 min the mean (s.d.) percentage of the dose excreted in the urine as unchanged salbutamol was 0.18 (0.14) and 2.06 (0.80) %, respectively (P < 0.01). The drug content of a urine sample taken 30 min after inhalation is, therefore, considered to be representative of the amount of drug delivered to the lungs. It is proposed that this method can be used to evaluate the relative bioavailability of salbutamol to the lung following inhalation by different techniques and devices.
摘要
  1. 在口服(4毫克)和吸入(4×100微克)沙丁胺醇后,测定了沙丁胺醇及其硫酸盐代谢物的尿排泄量。2. 与口服给药相比,吸入后沙丁胺醇及其硫酸盐结合物的尿总回收率表明平均(标准差)相对生物利用度为92.2(24.8)%。3. 口服给药后,沙丁胺醇及其硫酸盐结合物的平均(标准差)消除半衰期分别为5.7(1.4)小时和4.1(2.1)小时,吸入后分别为6.1(2.1)小时和5.1(1.0)小时。4. 口服和吸入给药后发现,在前30分钟内,以原形沙丁胺醇形式经尿液排泄的剂量平均(标准差)百分比分别为0.18(0.14)%和2.06(0.80)%(P<0.01)。因此,吸入后30分钟采集的尿样中的药物含量被认为代表了输送到肺部的药物量。建议该方法可用于评估不同技术和装置吸入后沙丁胺醇对肺部的相对生物利用度。

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