Bogliolo G, Muzzulini C, Lerza R, Pannacciulli I
Cancer Treat Rep. 1986 Nov;70(11):1275-81.
Compared with free doxorubicin, doxorubicin linked to poly-L-aspartic acid shows a reduction in overall toxicity, without loss of its antitumor activity. In this study, the toxicity of the new anthracycline conjugate on hematopoietic precursor cells of normal DBA/2NCrlBR mice was investigated by assays of bone marrow and spleen CFUs and CFUc (colony-forming units in spleen and culture). In vivo dose- and time-survival curves were determined. Results showed that the conjugate is three to ten times less hematotoxic than doxorubicin. Differences in susceptibility between bone marrow and spleen hematopoietic precursor cells to doxorubicin or the conjugate were observed, suggesting further studies on the pharmacokinetics of the new conjugate.
与游离阿霉素相比,与聚-L-天冬氨酸连接的阿霉素总体毒性降低,且不丧失其抗肿瘤活性。在本研究中,通过骨髓和脾脏集落形成单位(CFU)及脾集落形成细胞(CFUc)测定,研究了这种新型蒽环类缀合物对正常DBA/2NCrlBR小鼠造血前体细胞的毒性。测定了体内剂量-存活曲线和时间-存活曲线。结果表明,该缀合物的血液毒性比阿霉素低三至十倍。观察到骨髓和脾脏造血前体细胞对阿霉素或该缀合物的敏感性存在差异,提示需进一步研究这种新型缀合物的药代动力学。