Dalmark M
Scand J Clin Lab Invest. 1981 Nov;41(7):633-9. doi: 10.3109/00365518109090508.
The doxorubicin (Adriamycin) transport was investigated by measuring the net efflux of dororubicin from loaded erythrocytes into doxorubicin-free media at 37 degree C. The doxorubicin concentration in the cell water was kept low (5-10 mumol/l). The doxorubicin transport increased with increasing pH. The approx. pKa of the doxorubicin amino group was 7.6(37 degree C, ionic strength 0.15). Phloretin, l-alcohols and local anaesthetics increased doxorubicin transport after the fashion of the effect of these drugs on membrane transport of lipophilic compounds. Several inhibitors of facilitated transport systems in erythrocytes did not affect doxorubicin transport. The calcium and magnesium concentration in the cell water (0-2 mmol/l) did not affect doxorubicin transport. It appears that doxorubicin transport in human erythrocytes takes place by free diffusion of the electrically uncharged (unprotonated) doxorubicin molecule through the lipid domain of the cell membrane.
通过在37℃下测量多柔比星从负载红细胞向无多柔比星培养基中的净流出量,研究了多柔比星(阿霉素)的转运。细胞内水相中多柔比星的浓度保持在较低水平(5-10μmol/L)。多柔比星的转运随pH升高而增加。多柔比星氨基的近似pKa为7.6(37℃,离子强度0.15)。根皮素、一元醇和局部麻醉药对多柔比星转运的影响,与这些药物对亲脂性化合物膜转运的影响方式相同。几种红细胞易化转运系统抑制剂对多柔比星转运无影响。细胞内水相中钙和镁的浓度(0-2mmol/L)对多柔比星转运无影响。看来,人红细胞中多柔比星的转运是通过电中性(未质子化)的多柔比星分子在细胞膜脂质区域的自由扩散进行的。