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阿克拉霉素A在培养的L1210细胞中的细胞药代动力学。与柔红霉素和多柔比星的比较。

Cellular pharmacokinetics of aclacinomycin A in cultured L1210 cells. Comparison with daunorubicin and doxorubicin.

作者信息

Zenebergh A, Baurain R, Trouet A

出版信息

Cancer Chemother Pharmacol. 1982;8(2):243-9. doi: 10.1007/BF00255491.

Abstract

Aclacinomycin, which is more lipophilic than daunorubicin and doxorubicin, is taken up and released more rapidly and extensively by L1210 cells. After 5 h of incubation 91% of aclacinomycin is found in the nuclei of L1210 cells and the drug present in the post-nuclear fraction is distributed between the lysosomes and the cytosol. After an incubation of 5 h aclacinomycin decreases the density of the lysosomes. This effect is not observed either with doxorubicin or daunorubicin or when the cells are incubated with aclacinomycin for only 30 min.

摘要

阿克拉霉素比柔红霉素和多柔比星更具亲脂性,L1210细胞对其摄取和释放更为迅速和广泛。孵育5小时后,在L1210细胞核中发现91%的阿克拉霉素,核后组分中的药物分布于溶酶体和胞质溶胶之间。孵育5小时后,阿克拉霉素可降低溶酶体密度。柔红霉素、多柔比星或细胞仅与阿克拉霉素孵育30分钟时均未观察到这种效应。

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