Levin V A, Csejtey J, Byrd D J
Cancer Chemother Pharmacol. 1983;10(3):196-9. doi: 10.1007/BF00255762.
We have determined the pharmacokinetic parameters for diffusion of alpha-[5-14C]-difluoromethylornithine (DFMO) from blood to brain, blood to cerebrospinal fluid (CSF), 9L rat brain tumor to adjacent brain, and blood to the subcutaneously-implanted 9L tumor in rats, and within the CSF of beagle dogs. DFMO diffusion across the blood-brain and blood-CSF barriers is quite restricted in both rats and dogs, but diffusion across the defective capillary system of both subcutaneous and intracerebral 9L tumors in rats is not. Under steady-state plasma conditions in rats, uptake of DFMO by the intracerebral 9L tumor and diffusion from tumor 5-6 mm into adjacent brain is not restricted; tissue/plasma ratios were approximately 1. Therapeutic efficacy will therefore not be limited by transport of DFMO into tumor or to the extracellular environment of tumor.
我们已经确定了α-[5-¹⁴C]-二氟甲基鸟氨酸(DFMO)从血液扩散至脑、从血液扩散至脑脊液(CSF)、从9L大鼠脑肿瘤扩散至邻近脑组织以及从血液扩散至大鼠皮下植入的9L肿瘤,以及在比格犬脑脊液中的药代动力学参数。在大鼠和犬中,DFMO跨血脑屏障和血脑脊液屏障的扩散都受到相当大的限制,但在大鼠皮下和脑内9L肿瘤的有缺陷毛细血管系统中的扩散则不受此限。在大鼠的稳态血浆条件下,脑内9L肿瘤对DFMO的摄取以及从肿瘤向邻近脑组织5-6毫米处的扩散不受限制;组织/血浆比率约为1。因此,治疗效果不会受到DFMO向肿瘤或肿瘤细胞外环境转运的限制。