Cummings J
J Chromatogr. 1985 Jun 14;341(2):401-9. doi: 10.1016/s0378-4347(00)84053-0.
4'-Deoxydoxorubicin (4'-DOX) is a new and structurally similar analogue of the anti-cancer drug adriamycin (ADR). Based on known pathways of metabolism of ADR a high-performance liquid chromatographic method for the separation and identification of 4'-DOX and five possible metabolites was developed. Sensitivity for serum is 10 ng/ml for 4'-DOX and its alcoholic product 4'-deoxydoxorubicinol (4'-DOL) and 2 ng/ml for four of its aglycone products with coefficients of variation in k' of less than 5% throughout the day. An extraction step with better than 80% recovery of 4'-DOX and five reference metabolites from serum is described. Analysis of patient sera identified two metabolite peaks. These co-eluted with the reference metabolites of 4'-DOL and the 7-deoxyaglycone of 4'-DOX. Pharmacokinetics of the parent drug followed a two-compartment model. Both the metabolites were produced quickly and disappeared quickly.
4'-脱氧阿霉素(4'-DOX)是抗癌药物阿霉素(ADR)的一种新型结构类似物。基于已知的阿霉素代谢途径,开发了一种高效液相色谱法,用于分离和鉴定4'-DOX及其五种可能的代谢产物。血清中4'-DOX及其醇类产物4'-脱氧阿霉素醇(4'-DOL)的检测灵敏度为10 ng/ml,其四种苷元产物的检测灵敏度为2 ng/ml,全天k'的变异系数小于5%。描述了一种从血清中提取4'-DOX和五种参考代谢产物的方法,回收率优于80%。对患者血清的分析鉴定出两个代谢物峰。这些峰与4'-DOL的参考代谢产物和4'-DOX的7-脱氧苷元共洗脱。母体药物的药代动力学遵循二室模型。两种代谢产物均产生迅速且消失迅速。