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单次口服炔诺酮和炔雌醇甲醚后血浆中炔诺酮的水平。

Plasma levels of norethindrone after single oral dose administration of norethindrone and lynestrenol.

作者信息

Odlind V, Weiner E, Victor A, Johansson E D

出版信息

Clin Endocrinol (Oxf). 1979 Jan;10(1):29-38. doi: 10.1111/j.1365-2265.1979.tb03030.x.

Abstract

Single oral doses of 0.3 mg, 0.5 mg and 5 mg Norethindrone (NET) and 0.5 mg and 5 mg Lynestrenol (lyn) were given to five women. Lynestrenol is probably metabolized through NET and exerts its main biological activity as NET. Plasma concentrations of NET were determined by a radioimmunoassay at different intervals after administration of the tablets. Peak concentrations of NET were found within two hours after intake of each table. The plasma half life of Net after NET and lyn administration for the period 8-24 h was 8-11 h. No significant difference was found between the half life of NET and the NET tablets and after the lyn tablets. When 5 mg NET was given the plasma half life of NET for the period 24-72 h was around 10 h and this was significantly shorter than the half-life of NET after 5 mg lyn, which was 16 1/2 h. The systemic availability of the drugs was estimated by calculating and comparing the areas under the plasma concentration versus time curve (AUC). 0-24 H. The AUC 0.24 after 0.3 MG NET was almost identical to the AUC 0.24 after 0.5 mg lyn. The AUC 0-24 after 0.5 mg NET was significantly larger than after 0.5 lyn. No difference was found between the AUC 0-24 after 5 mg lyn and 5 mg NET. This study supports the concept of a conversion from lyn to NET. It also shows that there were only minor pharmacokinetic differences between the drugs when all samples were measured as NET.

摘要

给五名女性单次口服0.3毫克、0.5毫克和5毫克炔诺酮(NET)以及0.5毫克和5毫克炔雌醇甲醚(lyn)。炔雌醇甲醚可能通过炔诺酮代谢,并作为炔诺酮发挥其主要生物活性。在服用片剂后的不同时间间隔,通过放射免疫测定法测定血浆中炔诺酮的浓度。每次服药后两小时内发现炔诺酮的峰值浓度。在8 - 24小时期间,服用炔诺酮和炔雌醇甲醚后炔诺酮的血浆半衰期为8 - 11小时。炔诺酮片和炔雌醇甲醚片给药后炔诺酮的半衰期之间未发现显著差异。给予5毫克炔诺酮时,24 - 72小时期间炔诺酮的血浆半衰期约为10小时,这明显短于服用5毫克炔雌醇甲醚后炔诺酮的半衰期,后者为16.5小时。通过计算和比较血浆浓度 - 时间曲线(AUC)下的面积来估计药物的全身可用性。0 - 24小时。0.3毫克炔诺酮后的AUC 0 - 24与0.5毫克炔雌醇甲醚后的AUC 0 - 24几乎相同。0.5毫克炔诺酮后的AUC 0 - 24显著大于0.5毫克炔雌醇甲醚后的AUC 0 - 24。5毫克炔雌醇甲醚和5毫克炔诺酮后的AUC 0 - 24之间未发现差异。这项研究支持了从炔雌醇甲醚转化为炔诺酮的概念。它还表明,当所有样本都作为炔诺酮测量时,这些药物之间只有微小的药代动力学差异。

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