McCully C L, Balis F M, Bacher J, Phillips J, Poplack D G
Pediatric Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Lab Anim Sci. 1990 Sep;40(5):520-5.
A new rhesus monkey model with two intraventricular catheter systems was developed to examine the pharmacokinetics and neurotoxicity of chemotherapeutic agents administered by continuous intraventricular infusion. A lateral ventricular catheter system implanted in the lateral ventricle and attached to a subcutaneous access port on the animal's back is used for infusion of drugs into the ventricle. A Pudenz catheter implanted in the fourth ventricle and connected to a subcutaneous Ommaya reservoir permits repetitive CSF sampling in unanesthetized animals. The model was evaluated in five animals for over 12 months for catheter patency, surgical complications, and utility in studying the pharmacokinetics of continuous intraventricular infusion of methotrexate. There were no perioperative complications. Three of the five monkeys maintained both systems successfully. The other two animals developed staphylococcal ventriculitis, one at 7 days as a result of manipulation of the incision by the animal leading to cellulitis around the catheter site and subsequent ventriculitis, the other at 5 months. Both animals were treated successfully with antibiotics and catheter removal. An infusion of 0.05 mg of methotrexate over 24 hours maintained ventricular drug concentrations of 1 mol/L without evidence of neurotoxicity. This new model has applications both for the development of continuous intraventricular infusion as a therapeutic approach for the treatment of meningeal cancers in humans and as a research tool to study the distribution and elimination of drugs from the CSF.
为了研究通过持续脑室内输注给予化疗药物的药代动力学和神经毒性,开发了一种具有两个脑室内导管系统的恒河猴新模型。植入侧脑室并连接到动物背部皮下接入端口的侧脑室导管系统用于将药物输注到脑室内。植入第四脑室并连接到皮下奥马亚贮液器的普登兹导管允许在未麻醉的动物中重复采集脑脊液。对五只动物进行了超过12个月的模型评估,以观察导管通畅情况、手术并发症以及在研究甲氨蝶呤持续脑室内输注药代动力学方面的实用性。没有围手术期并发症。五只猴子中有三只成功维持了两个系统。另外两只动物发生了葡萄球菌性脑室炎,一只在7天时因动物对切口的操作导致导管部位周围蜂窝织炎及随后的脑室炎,另一只在5个月时发生。两只动物均通过抗生素治疗和拔除导管成功治愈。在24小时内输注0.05毫克甲氨蝶呤可使脑室内药物浓度维持在1微摩尔/升,且无神经毒性迹象。这种新模型既适用于开发持续脑室内输注作为治疗人类脑膜癌的一种治疗方法,也适用于作为研究脑脊液中药物分布和消除的研究工具。