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吲哚美辛缓释制剂在老年人中的药代动力学。

Pharmacokinetics of a sustained-release product of indomethacin in the elderly.

作者信息

Bruguerolle B, Barbeau G, Bélanger P M, Labrecque G

出版信息

Gerontology. 1986;32(5):277-85. doi: 10.1159/000212802.

Abstract

The pharmacokinetics of indomethacin (Indo) was studied in 10 healthy elderly male volunteers (age 67-81 years) following the oral administration of a single 75-mg dose of a sustained release form of Indo. The total and free plasma and erythrocyte concentrations of Indo were determined by a specific high-pressure liquid chromatographic method. A maximum concentration (Cmax) of 4.28 +/- (SE) 0.43 micrograms/ml was reached after 1.85 +/- 0.22 h. The area under the plasma concentration versus time curve (AUC) was 22.83 +/- 2.70 micrograms ml-1 h and the plasma elimination half-life was 4.34 +/- 0.64 h. The maximum concentration of Indo in the red blood cells was 0.123 +/- 0.013 microgram/ml and was obtained at 1.95 +/- 0.14 h after drug administration. The erythrocyte concentrations of Indo represented 2.4% of the total plasma levels of Indo whereas only 1.3% of the drug was unbound to plasma proteins. The Cmax and AUC values determined in the elderly were approximately double the values reported in young adults for the same dose.

摘要

在10名健康老年男性志愿者(年龄67 - 81岁)口服单剂量75毫克缓释型吲哚美辛(Indo)后,对其药代动力学进行了研究。采用特定的高压液相色谱法测定Indo的总血浆、游离血浆及红细胞浓度。给药后1.85±0.22小时达到最大浓度(Cmax)4.28±(标准误)0.43微克/毫升。血浆浓度-时间曲线下面积(AUC)为22.83±2.70微克·毫升⁻¹·小时,血浆消除半衰期为4.34±0.64小时。红细胞中Indo的最大浓度为0.123±0.013微克/毫升,于给药后1.95±0.14小时测得。Indo的红细胞浓度占Indo血浆总水平的2.4%,而仅有1.3%的药物未与血浆蛋白结合。在老年人中测定的Cmax和AUC值约为相同剂量年轻成年人报道值的两倍。

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