Hsieh Chen-Hsi, Hou Mei-Ling, Wang Li-Ying, Tai Hung-Chi, Tsai Tung-Hu, Chen Yu-Jen
Division of Radiation Oncology, Department of Radiology, Far Eastern Memorial Hospital, Taipei, Taiwan.
Institute of Traditional Medicine, National Yang-Ming University, Taipei, Taiwan.
BMC Cancer. 2015 Apr 26;15:316. doi: 10.1186/s12885-015-1344-4.
5-fluorouracil (5-FU) is employed to enhance radiotherapy (RT) effect. Here, we evaluated the influence of whole-pelvic irradiation on the pharmacokinetics (PK) of 5-FU in plasma and lymphatic system of rats as the experimental model.
RT with 2 Gy was delivered to the whole pelvis of Sprague-Dawley rats. 5-FU at 100 mg/kg was intravenously infused 24 hours after radiation. The pharmacokinetics of 5-FU in plasma and lymphatic system were calculated.
RT at 2 Gy reduced the area under the plasma concentration vs. time curve and mean residence time of 5-FU by 21.5% and 31.5%, respectively compared with those of non-RT controls. By contrast, RT at 2 Gy increased drug clearances of 5-FU by 28.2% when compared with those of non-RT controls. There was no significant difference in T1/2, Cmax and Vss in plasma between both groups. Intriguingly, 5-Fu could be detected in the lymphatic system. In addition, the AUC in 5-FU without and with RT was 3.3-fold and 4.9-fold greater for lymph than for plasma, respectively. Compared with the non-RT group, the RT group showed increase in distribution of 5-FU in the lymphatic system (p = 0.001).
The local whole pelvic RT at 2 Gy could modulate systemic PK of 5-FU in plasma of rats and intravenous 5-FU passing into the lymphatic system was proved. The metabolism of 5-FU might be modulated by RT but the distribution of 5-FU from blood circulation to the lymphatic system might not be changed. The RT-PK phenomena in plasma provide references for adjustment of drug administration. Chemotherapy drugs entering the lymphatic system is worthy of further investigation.
5-氟尿嘧啶(5-FU)用于增强放射治疗(RT)效果。在此,我们以大鼠为实验模型,评估了全盆腔照射对5-FU在大鼠血浆和淋巴系统中药物动力学(PK)的影响。
对Sprague-Dawley大鼠的全盆腔给予2 Gy的放疗。放疗后24小时静脉输注100 mg/kg的5-FU。计算5-FU在血浆和淋巴系统中的药物动力学。
与未接受放疗的对照组相比,2 Gy的放疗分别使5-FU的血浆浓度-时间曲线下面积和平均驻留时间降低了21.5%和31.5%。相比之下,与未接受放疗的对照组相比,2 Gy的放疗使5-FU的药物清除率提高了28.2%。两组血浆中的半衰期、最大浓度和稳态分布容积无显著差异。有趣的是,在淋巴系统中可检测到5-氟尿嘧啶。此外,未接受放疗和接受放疗的5-FU在淋巴中的曲线下面积分别是血浆中的3.3倍和4.9倍。与未接受放疗组相比,接受放疗组5-FU在淋巴系统中的分布增加(p = 0.001)。
2 Gy的局部全盆腔放疗可调节大鼠血浆中5-FU的全身药物动力学,并证实静脉注射的5-FU可进入淋巴系统。5-FU的代谢可能受放疗调节,但5-FU从血液循环到淋巴系统的分布可能未改变。血浆中的放疗-药物动力学现象为调整给药提供了参考。化疗药物进入淋巴系统值得进一步研究。