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戊二醛处理的载甲氨蝶呤载体红细胞在犬体内的肝脏药代动力学

Hepatic pharmacokinetics of glutaraldehyde-treated methotrexate-loaded carrier erythrocytes in dogs.

作者信息

DeLoach J R, Tangner C H, Barton C

出版信息

Res Exp Med (Berl). 1983;183(3):167-75. doi: 10.1007/BF01855639.

Abstract

Methotrexate-loaded glutaraldehyde-treated canine carrier erythrocytes were used to deliver a 1.6-mg/kg dosage of drug. About 90% of the drug-loaded cells disappeared from circulation within 1 h. Approximately 11 mg of drug reached the liver, and a substantial portion of the methotrexate entered the enterohepatic bile salt circulation. Biochemical tests of liver function, such as alkaline phosphatase and serum glutamine pyruvate transaminase, indicated mild hepatocellular necrosis which was attributed to the action of methotrexate on the hepatocytes. Bilirubin levels were unchanged during and following drug treatment. The plasma half-life of the drug was extended 2.4-fold in the first 24 h following injection.

摘要

负载甲氨蝶呤的戊二醛处理犬载体红细胞用于递送1.6毫克/千克剂量的药物。约90%负载药物的细胞在1小时内从循环中消失。约11毫克药物到达肝脏,并且大部分甲氨蝶呤进入肠肝胆汁盐循环。肝功能生化检测,如碱性磷酸酶和血清谷丙转氨酶,表明存在轻度肝细胞坏死,这归因于甲氨蝶呤对肝细胞的作用。药物治疗期间及之后胆红素水平未发生变化。注射后的前24小时内,药物的血浆半衰期延长了2.4倍。

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