Cellular pharmacokinetics of aclacinomycin A in cultured L1210 cells |
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Authors: | A. Zenebergh R. Baurain A. Trouet |
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Affiliation: | (1) Université of Louvain, Avenue Hippocrate 75, B-1200 Bruxelles, Belgium;(2) International Institute of Cellular and Molecular Pathology, Avenue Hippocrate, 75, B-1200 Bruxelles, Belgium |
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Abstract: | Summary 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. |
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