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人基因重组红细胞生成素在大鼠和人体的药物动力学研究 被引量:1

Pharmacokinetics of recombinant human erythropoietin in rats and human
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摘要 正常SD大鼠皮下注射rHuEPO(人基因重组红细胞生成素)的F参数(相对生物利用度)显著高于腹腔注射.单次皮下注射100U/kg时,正常人、尿毒症未透析和腹透组t1/2β(消除相半衰期)分别为15.4±0.9、16.6±6.9和9.2±2.7h.在尿毒症未透析组,皮下注射后血药浓度下降缓慢,F为(41±17)%,用药48h后仍为基础浓度的3倍左右。表明rHuFPO以皮下用药更为合适。 The mean biovailability(F) after s.c. injection of rHuEPO was signincantly higher than that after i.p. injection in healthy SD rats. The mean t1/2β after a s.c.dose of 100U/kg in normal human volunteers, pre-dialysis and peritoneal dialysis uremic patients were 15.4 ± 0.9, 16.6 ± 6.9 and 9.2 ± 2.7 h respectively. In pre-dialysis patients, the mean F after a s.c. dose was 41 ± 17%. Serum rHuEPO concentrations after a s.c. dose decreased slowly and were over three times of baseline 48 hours later. It is concluded that s.c. administration is the optical route for rHuEPO.
出处 《核技术》 CAS CSCD 北大核心 1994年第11期680-683,共4页 Nuclear Techniques
关键词 红细胞生成素 药物动力学 大鼠 尿毒症 人体 Erythropoietin, Pharmacokinetics, Rat, Uremia
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