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在动物体内重组人生长激素 1-84 的药代动力学、组织分布和排泄。

Pharmacokinetics, tissue distribution and excretion of recombinant human parathyroid hormone 1-84 in animals.

机构信息

Department of Endocrinology, First Affiliated Hospital of the General Hospital of PLA, Beijing, 100048, China.

出版信息

Cell Biochem Biophys. 2013 Jun;66(2):379-87. doi: 10.1007/s12013-012-9477-4.

Abstract

To study the plasma pharmacokinetics and accumulation of the recombinant human parathyroid hormone (rhPTH) (1-84) in rhesus monkeys, and the tissue distribution and excretion profiles of (125)I-rhPTH (1-84) in rats. The concentration of rhPTH (1-84) in plasma samples were determined by an enzyme immunoassay (EIA) method after subcutaneous and intravenous bolus injection. The tissue distribution and urinary, fecal and biliary excretion patterns of (125)I-rhPTH (1-84) were investigated by trichloroacetic acid (TCA) precipitation method. Following subcutaneous (sc) administration rhPTH (1-84) in rhesus monkeys, rhPTH (1-84) exhibited rapid absorption and elimination and had no accumulated tendency after successive sc administration. Following sc administration (125)I-rhPTH (1-84) in rats, the TCA-precipitated radioactivity was widely distributed and rapidly diminished in most tissues. Approximately 83.9 and 6.8 % of the total radioactivity was recovered in urine and feces by 72 h postdosing, respectively; whereas 4.1 % excreted into bile up to 24 h postdosing. The pharmacokinetics of rhPTH (1-84) complied with linear kinetics within the examined dose range following a single sc administration had no accumulated tendency following multiple sc administration in rhesus monkeys. The accumulation of (125)I-rhPTH (1-84) in tissues/organs examined, appeared to be low in rats. The major elimination route was by urinary excretion.

摘要

目的

研究重组人生长激素(rhPTH)(1-84)在恒河猴体内的药代动力学和蓄积情况,以及(125)I-rhPTH(1-84)在大鼠体内的组织分布和排泄特征。方法:采用酶联免疫吸附法(EIA)测定皮下和静脉推注后血浆中 rhPTH(1-84)的浓度。采用三氯乙酸(TCA)沉淀法研究(125)I-rhPTH(1-84)在组织中的分布以及尿、粪和胆汁中的排泄模式。结果:恒河猴皮下给予 rhPTH(1-84)后,rhPTH(1-84)表现出快速吸收和消除的特点,连续皮下给药后无蓄积倾向。大鼠皮下给予(125)I-rhPTH(1-84)后,TCA 沉淀放射性在大多数组织中广泛分布并迅速减少。给药后 72 小时,尿和粪便中分别有 83.9%和 6.8%的总放射性被回收,而在 24 小时内有 4.1%的放射性排泄到胆汁中。rhPTH(1-84)在单次皮下给药范围内的药代动力学符合线性动力学,连续皮下给药后无蓄积倾向。在大鼠中,(125)I-rhPTH(1-84)在检测的组织/器官中的蓄积似乎较低,主要的消除途径是通过尿液排泄。

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