Benckhuijsen C, Kroon B B, van Geel A N, Wieberdink J
The Netherlands Cancer Institute (Antoni van Leeuwenhoek Huis), Amsterdam.
Eur J Surg Oncol. 1988 Apr;14(2):157-63.
The time course of tissue levels of melphalan during normothermic isolated limb perfusion, and the overall tissue levels per 60 min of perfusion, were estimated from the known pharmacokinetic parameters for a fixed dose of drug per liter of tissue (Benckhuijsen et al., J. Pharmacol Exp Ther 1986; 237: 583-8). The application of differing total doses of drug resulted in varying concentrations in the perfusate plasma. Above a certain plasma level, uptake into the bulk of the tissues did not increase with the area under the plasma concentration vs time curve or its beta-phase. Similar tissue levels were found after perfusion of regions of less than three and a half liter with 13 mg/l as in regions of 5 to 16 liter after perfusion with 10 mg of melphalan per liter. It cannot be predicted from the available data whether the extent of uptake of melphalan into the tumour tissue is equal to or greater than that into the bulk of the tissues. The estimated uptake of drug into the tissues confirms the validity of the dose calculation per liter of tissue. On the basis of the present results, a refined dosimetric formula will be obtainable that includes the desired area under the plasma concentration vs time curve as a determinant for an optimal dose.
根据每升组织中固定剂量药物的已知药代动力学参数(Benckhuijsen等人,《药理学与实验治疗学杂志》1986年;237:583 - 588),估算了在常温离体肢体灌注过程中美法仑的组织水平随时间的变化过程,以及每60分钟灌注的总体组织水平。应用不同的药物总剂量会导致灌注液血浆中浓度不同。在高于一定血浆水平时,大部分组织的摄取量不会随血浆浓度-时间曲线下面积或其β相增加。在用每升13毫克美法仑灌注不到3.5升区域后,发现的组织水平与在用每升10毫克美法仑灌注5至16升区域后相似。根据现有数据无法预测美法仑在肿瘤组织中的摄取程度是否等于或大于在大部分组织中的摄取程度。估计的药物在组织中的摄取量证实了每升组织剂量计算的有效性。根据目前的结果,将可获得一个改进的剂量计算公式,该公式将所需的血浆浓度-时间曲线下面积作为最佳剂量的决定因素。