Baraka O Z, Mahmoud B M, Marschke C K, Geary T G, Homeida M M, Williams J F
Department of Medicine, Faculty of Medicine, University of Khartoum, Sudan.
Eur J Clin Pharmacol. 1996;50(5):407-10. doi: 10.1007/s002280050131.
To determine the distribution of ivermectin in plasma and tissues of onchocerciasis patients following a single oral dose of 150 micrograms kg-1.
Medical Department at Soba University Hospital, Khartoum.
Twenty five patients and fourteen healthy volunteers.
Serial blood samples were obtained from both groups. Tissue samples were removed from various patients as full thickness skin punch biopsies or during nodulectomy. Ivermectin concentration was determined by radioimmunoassay.
The plasma pharmacokinetic variables for patients were; maximum plasma concentration 52.0 ng ml-1; time to achieve maximum concentration, 5.2 h.; elimination half life, 35.0 h; and the area under the plasma concentration curve versus time, 2852 ng.h.ml-1. In healthy volunteers, the plasma ivermectin distribution was similar to that in patients, and both groups showed a tendency for a second rise in plasma concentration of the drug suggestive of enterohepatic recirculation. Ivermectin was detected in tissues obtained from patients. Fat showed the highest and most persistent levels, whilst values for skin, nodular tissues, and worms were comparable. Subcutaneous fascia contained the lowest concentrations.
Infection with O. volvulus does not affect the pharmacokinetics of ivermectin, and filarial infected tissues and parasites themselves do take up the drug. There may be prolonged retention of ivermectin because of depot formation in fat tissue.
确定单剂量口服150微克/千克伊维菌素后,盘尾丝虫病患者血浆和组织中的药物分布情况。
喀土穆索巴大学医院医学部。
25例患者和14名健康志愿者。
两组均采集系列血样。从不同患者身上获取组织样本,包括全层皮肤打孔活检样本或在结节切除术中获取的样本。采用放射免疫分析法测定伊维菌素浓度。
患者的血浆药代动力学变量为:血浆最大浓度52.0纳克/毫升;达到最大浓度的时间为5.2小时;消除半衰期为35.0小时;血浆浓度-时间曲线下面积为2852纳克·小时/毫升。在健康志愿者中,血浆伊维菌素分布与患者相似,两组均显示该药物血浆浓度有再次升高的趋势,提示存在肠肝循环。在患者获取的组织中检测到了伊维菌素。脂肪中的药物水平最高且持续时间最长,而皮肤、结节组织和虫体中的药物水平相当。皮下筋膜中的浓度最低。
感染旋盘尾丝虫不影响伊维菌素的药代动力学,丝虫感染的组织和寄生虫本身确实会摄取该药物。由于在脂肪组织中形成储存库,伊维菌素的滞留时间可能会延长。