Giordani Raquel B, De Almeida Mauro V, Fernandes Ederson, França da Costa Cristiane, De Carli Geraldo A, Tasca Tiana, Zuanazzi José A S
Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga 2752, 90610-000 Porto Alegre, RS, Brazil.
Biomed Pharmacother. 2009 Sep;63(8):613-7. doi: 10.1016/j.biopha.2008.10.002. Epub 2008 Oct 31.
Taking in account the increased prevalence of metronidazole-resistant infections, alternative drugs are necessary for the treatment of trichomonosis. We report in this work the preparation and the in vitro anti-trichomonads activity of two diamines 1 and 2, and three different lipophilic amino alcohol derivatives 3, 4 and 5. These compounds were tested for in vitro activity against two isolates of Trichomonas vaginalis and displayed inhibition of the parasite growth. Five concentrations of each compound were tested. The butanediamine derivative 1, at a final concentration of 5.85 microM, presented a cytotoxic effect against 47% of T. vaginalis trophozoites. Furthermore, the cytotoxicity of 1 did not present statistically significant difference when compared to metronidazole in the same range of concentration (0.1-1.5 microg/mL).
考虑到甲硝唑耐药感染的患病率增加,治疗滴虫病需要使用替代药物。我们在这项工作中报告了两种二胺1和2以及三种不同的亲脂性氨基醇衍生物3、4和5的制备及其体外抗滴虫活性。测试了这些化合物对两种阴道毛滴虫分离株的体外活性,并显示出对寄生虫生长的抑制作用。对每种化合物的五个浓度进行了测试。丁二胺衍生物1在终浓度为5.85 microM时,对47%的阴道毛滴虫滋养体具有细胞毒性作用。此外,在相同浓度范围(0.1 - 1.5 microg/mL)内,与甲硝唑相比,1的细胞毒性没有统计学上的显著差异。