Sarikabhuti B, Keschamrus N, Noeypatimanond S, Weidekamm E, Leimer R, Wernsdorfer W, Kölle E U
Department of Physiology, Faculty of Veterinary Medicine, Kasetsart University, Bangkok, Thailand.
Acta Trop. 1988 Sep;45(3):217-24.
The disposition of sulfadoxine was studied in the presence of pyrimethamine in 18 healthy Thai subjects who had been suffering from falciparum malaria in the 6 months prior to the study, and in 12 Thai patients with acute malaria. The volunteers were administered an oral dose of 500 mg sulfadoxine + 25 mg pyrimethamine (1 Fansidar tablet). They were classified retrospectively as responders (Group I, n = 8) or nonresponders (Group II, n = 10) according to previous response to treatment with Fansidar. The patients were treated with 3 Fansidar tablets corresponding to 1500 mg sulfadoxine and 75 mg pyrimethamine. Five of them were completely cured. Seven patients showed R I or R II resistance. In all cases blood samples were collected up to 288 h post dose. The resultant plasma was analyzed for active (i.e. unchanged) and total sulfadoxine using a modified Bratton-Marshall method. In the healthy volunteers the plasma concentration time course of total sulfadoxine was similar for responding and nonresponding subjects. However, in nonresponders active sulfadoxine tended to show shorter half-lives (harmonic means were 212 h vs 267 h, respectively). Furthermore, significantly higher amounts of metabolites (mainly N4-acetylsulfadoxine) were present in plasma of nonresponders. In contrast to these findings, in malaria patients, plasma concentrations of active and total sulfadoxine were even higher in nonresponders as compared to the subjects who could be successfully cured. Furthermore, in this case there was no increase of the amount of metabolites in plasma.(ABSTRACT TRUNCATED AT 250 WORDS)
在18名健康的泰国受试者和12名泰国急性疟疾患者中研究了乙胺嘧啶存在下磺胺多辛的处置情况。这些健康受试者在研究前6个月曾感染恶性疟原虫。志愿者口服500毫克磺胺多辛+25毫克乙胺嘧啶(1片Fansidar)。根据之前使用Fansidar治疗的反应,他们被回顾性地分为反应者(第一组,n = 8)或无反应者(第二组,n = 10)。患者接受3片Fansidar治疗,相当于1500毫克磺胺多辛和75毫克乙胺嘧啶。其中5人完全治愈。7名患者表现出R I或R II抗性。在所有情况下,给药后长达288小时采集血样。使用改良的Bratton-Marshall方法分析所得血浆中的活性(即未改变的)磺胺多辛和总磺胺多辛。在健康志愿者中,反应者和无反应者的总磺胺多辛血浆浓度-时间过程相似。然而,在无反应者中,活性磺胺多辛的半衰期往往较短(调和均值分别为212小时和267小时)。此外,无反应者血浆中存在的代谢物(主要是N4-乙酰磺胺多辛)量明显更高。与这些发现相反,在疟疾患者中,无反应者的活性和总磺胺多辛血浆浓度甚至高于可成功治愈的受试者。此外,在这种情况下,血浆中代谢物的量没有增加。(摘要截断于250字)