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健康受试者口服儿科制剂后血清中青霉素V的水平。

Serum levels of penicillin v after oral administration of pediatric preparations to healthy subjects.

作者信息

Rollag H, Midtvedt T, Wetterhus S

出版信息

Acta Paediatr Scand. 1975 May;64(3):421-4. doi: 10.1111/j.1651-2227.1975.tb03858.x.

Abstract

The bioavailability of nine commercial pediatric preparations of penicillin V was tested in a double-blind, cross-over fashion on ten healthy student nurses who were given 1 mill I.U. of the various preparations. The serum concentrations were determined using the paper disc method of "AB Biodisc" Sweden. The preparations could be divided into two different groups: (1) the mixtures (2) the effervescent tablets, substance for drops and granulate. This classification is based upon the mean peak serum levels obtained. With one exception the peak serum levels in group 2 were significantly higher than in group 1. 2,4 and 6 hours after ingestion there were no differences in the serum levels, indicating that none of the preparations gave sustained high serum levels. The results presented indicate that the preparations in group 2 should be preferred.

摘要

以双盲、交叉方式对10名健康学生护士进行了测试,给他们每人服用1国际单位的九种市售青霉素V儿科制剂,以检测其生物利用度。采用瑞典“AB Biodisc”的纸盘法测定血清浓度。这些制剂可分为两类:(1)混合物;(2)泡腾片、滴剂和颗粒剂。这种分类是基于所获得的平均血清峰值水平。除一种制剂外,第2组的血清峰值水平显著高于第1组。服药后2、4和6小时血清水平无差异,表明没有一种制剂能维持高血清水平。给出的结果表明应首选第2组的制剂。

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