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新生大鼠肺部对药物的吸收

Pulmonary absorption of drugs in the neonatal rat.

作者信息

Hemberger J A, Schanker L S

出版信息

Am J Physiol. 1978 May;234(5):C191-7. doi: 10.1152/ajpcell.1978.234.5.C191.

Abstract

To compare the pulmonary absorption of drugs in newborn rats (3-27 days old) with that in adults, 0.01-0.1 ml of Krebs-Ringer phosphate solution (pH 7.4) containing a drug was administered to anesthetized animals by way of a catheter introduced through a tight-fitting tracheal cannula. After various times, lungs and trachea were removed and assayed for drug that remained. Semilogarithmic plots of percent drug remaining against time yielded a straight line for each compound. The lipid-soluble drugs procaine amide and sulfisoxazole were absorbed at similar rates in newborn and adult rats. In contrast, the lipid-insoluble drugs tetraethylammonium, p-aminohippuric acid, and mannitol were absorbed approximately 2 times more rapidly in younger rats (3-12 days) than in older animals (18 day, 27 day, or adult). The results suggested that the respiratory tract membranes of 3- to 12-day-old rats have a greater porosity than those of older animals.

摘要

为比较新生大鼠(3至27日龄)与成年大鼠对药物的肺部吸收情况,将含药物的0.01至0.1毫升磷酸缓冲液(pH 7.4)通过紧密配合的气管插管插入的导管注入麻醉动物体内。经过不同时间后,取出肺和气管并测定残留药物。每种化合物的残留药物百分比对时间的半对数图均得出一条直线。脂溶性药物普鲁卡因酰胺和磺胺异恶唑在新生大鼠和成年大鼠中的吸收速率相似。相比之下,脂溶性差的药物四乙铵、对氨基马尿酸和甘露醇在幼龄大鼠(3至12日龄)中的吸收速度比老龄动物(18日龄、27日龄或成年)快约2倍。结果表明,3至12日龄大鼠的呼吸道膜比老龄动物的孔隙率更高。

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