Overbosch D, van de Nes J C, Groll E, Diekmann H W, Polderman A M, Mattie H
Department of Infectious Diseases, University Hospital, Leiden, The Netherlands.
Eur J Clin Pharmacol. 1987;33(3):287-92. doi: 10.1007/BF00637564.
Two patients with cysticercosis received praziquantel (PZQ) 75 mg/kg/day orally together with 30 mg prednisone daily for 3 weeks. The first patient presented with grand-mal seizures, a pyramidal tract syndrome and subcutaneous cysticerci, and the other had internal hydrocephalus necessitating drainage. Serial plasma samples were taken after the first dose of PZQ. Lumbar CSF was obtained from the first patient and ventricular CSF from the second. Subcutaneous cysticerci were removed from the first patient. PZQ in the specimens was assayed by GLC. For distribution between plasma and CSF a rate constant of 4.9 h-1 for free PZQ, corresponding to a t1/2 of 8 min or less for the non-protein bound fraction was calculated for Patient 1. In the second patient the distribution was so rapid that the rate constant could not be calculated. The difference in distribution rate might have been due to use of different sampling times or to a time lag in the entry of PZQ between the ventricles and the lumbar sac. The rate constant for distribution of the drug between plasma and parasites was 1.4 h-1, corresponding to a t1/2 of 30 min or less. Thus PZQ penetrates rapidly into the CSF. It enters the parasite more slowly, although still more rapidly than the plasma half-life of PZQ (1-1 1/2 h).
两名囊尾蚴病患者口服吡喹酮(PZQ),剂量为75mg/kg/天,并每日服用30mg泼尼松,持续3周。第一名患者出现癫痫大发作、锥体束综合征和皮下囊尾蚴,另一名患者有需要引流的脑积水。在首次服用PZQ后采集系列血浆样本。从第一名患者获取腰椎脑脊液,从第二名患者获取脑室脑脊液。从第一名患者身上取出皮下囊尾蚴。通过气相色谱法测定样本中的PZQ。对于血浆和脑脊液之间的分布,计算出第一名患者游离PZQ的速率常数为4.9h-1,对应于非蛋白结合部分的半衰期为8分钟或更短。在第二名患者中,分布非常迅速,以至于无法计算速率常数。分布速率的差异可能是由于采样时间不同或PZQ进入脑室和腰骶部之间存在时间滞后。药物在血浆和寄生虫之间的分布速率常数为1.4h-1,对应于半衰期为30分钟或更短。因此,PZQ能迅速穿透进入脑脊液。它进入寄生虫的速度较慢,尽管仍然比PZQ的血浆半衰期(1-1.5小时)快。