Biliary excretion
- 网络胆汁排泄
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Construction of determination of cefditoren and the investigation of mechanism of biliary excretion
头孢妥仑测定方法的建立及胆汁排泄机制研究
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Molecular Mechanism of Biliary Excretion of Cefditoren and the Effects of Cefditoren on the Expression Levels of Hepatic Transporters
头孢妥仑胆汁排泄的分子机制及其对肝脏转运蛋白调节作用的研究
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Mathematical expression of the model for liver and biliary excretion
肝-胆排泄模型的数学表达
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Biliary excretion of genistein and its metabolite at different doses in rats
不同剂量染料木黄酮及其代谢产物在大鼠胆汁中的排泄动力学
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Conclusion Hepatic uptake and biliary excretion function is closely related to the severity of liver damage and cholestasis .
结论肝摄取和排泄功能与肝细胞损害和胆汁淤积程度密切相关;
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Many researches indicate that CO generated by heme oxygenase controls the biliary excretion and increase in excretion of bile salts and phospholipids .
大量研究表明HO作用下产生的内源性的CO能调节肝胆汁分泌。
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Biliary excretion was also an important route of excretion . Normal rats excreted 57.7 % of the administered radioactivity in the bile in 48 hours , while only 20.2 % was in unchanged form .
静注后48小时,自胆汁排泄剂量的57.7%,其中原形药放射性占剂量的20.2%。
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The excretion of parent drug in urine amounted to only 0 09 % of the dosage and in feces to 42 9 % within 24 h after dosing . The biliary excretion were mainly metabolites and only 0 14 % of parent drug of the dosage within 12 h.
药后24h内尿和粪的排泄量分别占给药量的009%和429%,12h内胆汁排泄的主要为代谢产物,原型药物仅为给药量的014%。