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In vitro and in vivo activities of dicationic diguanidino compounds against Echinococcus multilocularis metacestodes.

机译:双胍盐类化合物对多棘棘球meta球菌的体外和体内活性。

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摘要

Alveolar echinococcosis (AE) is a disease predominantly affecting the liver, with metacestodes (larvae) of the tapeworm Echinococcus multilocularis proliferating and exhibiting tumor-like infiltrative growth. For many years, chemotherapeutical treatment against alveolar echinococcosis has relied on the benzimidazoles albendazole and mebendazole, which require long treatment durations and exhibit parasitostatic rather than parasiticidal efficacy. Although benzimidazoles have been and still are beneficial for the patients, there is clearly a demand for alternative and more efficient treatment options. Aromatic dications, more precisely a small panel of di-N-aryl-diguanidino compounds, were screened for efficacy against E. multilocularis metacestodes in vitro. Only those with a thiophene core group were active against metacestodes, while furans were not. The most active compound, DB1127, was further investigated in terms of in vivo efficacy in mice experimentally infected with E. multilocularis metacestodes. This diguanidino compound was effective against AE when administered intraperitoneally but not when applied orally. Thus, thiophene-diguanidino derivatives with improved bioavailability when administered orally could lead to treatment options against AE.
机译:肺泡棘球co病(AE)是一种主要影响肝脏的疾病,the虫棘球E球菌的子囊(幼虫)正在增殖并表现出肿瘤样浸润性生长。多年来,针对肺泡棘球菌病的化学疗法治疗依赖于苯并咪唑类阿苯达唑和甲苯达唑,它们需要较长的治疗时间,并且具有抑寄生作用而不是杀寄生虫功效。尽管苯并咪唑已经并且仍然对患者有益,但是显然仍需要替代和更有效的治疗选择。筛选了芳香族药物,更确切地说是一小组的二-N-芳基-双胍基化合物,以在体外对抗多叶大肠杆菌的代谢。只有那些具有噻吩核心基团的化合物才具有抗灭肠活性,而呋喃则没有。就在实验上感染多叶大肠杆菌的小鼠的体内功效方面,进一步研究了活性最高的化合物DB1127。当腹膜内给药时该双胍基化合物对AE有效,但口服时无效。因此,口服时具有改善的生物利用度的噻吩-双胍基衍生物可导致针对AE的治疗选择。

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