Karbwang J, Molunto P, Na Bangchang K, Banmairuroi V, Bunnag D, Harinasuta T
Department of Clinical Tropical Medicine, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 1991 Dec;22(4):519-22.
The pharmacokinetics of the prophylactic dose of mefloquine (Lariam: 500 mg every 4 weeks, with a loading dose of 750 mg on the first week) was studied in six healthy Thai male volunteers. Mefloquine was well tolerated during the study period of 16 weeks. The only side-effects found were nausea and diarrhea in 2 volunteers after the first dose of mefloquine. The mean minimum concentration of mefloquine at steady state ranged from 290 to 460 ng/ml. The maximum concentration on week 16 after the last dose was 1558 +/- 48 ng/ml at the mean time of 38 +/- 19 hours. The other pharmacokinetic parameters obtained were: absorption half life = 6.6 +/- 3.0 hours; distribution = 5.1 +/- 3.1 days; terminal half life = 12.9 +/- 2.2 days; apparent volume of distribution = 10.5 +/- 2.3 l/kg; area under the concentration-time curve = 26.9 +/- 2.2 mg/dl. Although this prophylaxis regimen is ideal when considering the compliance, the minimum concentration obtained was much too low for optimum therapeutic concentration. We therefore suggest that weekly prophylaxis schedule should be a better regimen as the difference between minimum and maximum mefloquine concentration would be smaller.
在6名健康的泰国男性志愿者中研究了预防剂量甲氟喹(Lariam:每4周500mg,第1周给予750mg负荷剂量)的药代动力学。在16周的研究期间,甲氟喹耐受性良好。仅在2名志愿者首次服用甲氟喹后出现恶心和腹泻的副作用。稳态时甲氟喹的平均最低浓度范围为290至460ng/ml。末次给药后第16周的最高浓度在平均38±19小时时为1558±48ng/ml。获得的其他药代动力学参数为:吸收半衰期=6.6±3.0小时;分布=5.1±3.1天;终末半衰期=-12.9±2.2天;表观分布容积=10.5±2.3l/kg;浓度-时间曲线下面积=26.9±2.2mg/dl。虽然考虑到依从性,这种预防方案是理想的,但获得的最低浓度远低于最佳治疗浓度。因此,我们建议每周预防方案可能是更好的方案,因为甲氟喹最低浓度与最高浓度之间的差异会更小。