Zenebergh A, Baurain R, Trouet A
Cancer Chemother Pharmacol. 1982;8(2):243-9. doi: 10.1007/BF00255491.
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.
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。