Suppr超能文献

氟诺昔康在老年受试者中的药代动力学。

Flunoxaprofen pharmacokinetics in elderly subjects.

作者信息

Segre G, Bianchi E, Mascaretti L, Quaglia G, Forgione A

出版信息

Int J Clin Pharmacol Res. 1987;7(4):243-50.

PMID:3596866
Abstract

Plasma kinetics and 24 h urinary elimination of flunoxaprofen, a nonsteroidal antiinflammatory drug, were studied in 23 elderly patients (mean age 69.9 years) and compared with the data obtained in four young volunteers. The drug was administered as a single oral 100 mg tablet and its plasma and urine concentrations were assayed by a high performance liquid chromatography method. Plasma kinetics fitted a 3-exponential equation with a mean half-life of 7.9 +/- 2.17 hours and a mean peak plasma of 8.5 +/- 2.97 micrograms/ml, which was observed at about the second hour. The values of the areas under the curves (AUC) and the values of total clearance (multiplied by the bioavailability) showed great variability, due to the large differences in the patients body weights; in fact the value of AUC was linearly correlated to the dose divided by the body weight. The mean residence time (MRT) of the drug in plasma was equal to 12.81 h. Low amounts of unmodified drug (about 10%) were found in 24 h urine sample, indicating a high degree of biotransformation. Small differences only were found in plasma kinetics of flunoxaprofen among the present group of elderly patients and the group of four young volunteers; the main difference corresponded to a slower rate of gastrointestinal absorption and to a longer mean residence time.

摘要

对23名老年患者(平均年龄69.9岁)进行了非甾体抗炎药氟诺洛芬的血浆动力学及24小时尿排泄研究,并与4名年轻志愿者的数据进行比较。药物以100毫克片剂单次口服给药,其血浆和尿液浓度采用高效液相色谱法测定。血浆动力学符合三指数方程,平均半衰期为7.9±2.17小时,平均血浆峰浓度为8.5±2.97微克/毫升,约在第二小时出现。由于患者体重差异较大,曲线下面积(AUC)值和总清除率(乘以生物利用度)值显示出很大的变异性;实际上,AUC值与剂量除以体重呈线性相关。药物在血浆中的平均驻留时间(MRT)为12.81小时。在24小时尿样中发现少量未修饰药物(约10%),表明生物转化程度较高。在本老年患者组和4名年轻志愿者组中,氟诺洛芬的血浆动力学仅存在微小差异;主要差异在于胃肠道吸收速率较慢和平均驻留时间较长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验