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一种用于局部治疗亚马逊利什曼原虫(利什曼原虫属)和巴西利什曼原虫(维安尼利什曼原虫属)感染的巴龙霉素亲水性制剂的活性。

Activity of a paromomycin hydrophilic formulation for topical treatment of infections by Leishmania (Leishmania) amazonensis and Leishmania (Viannia) braziliensis.

作者信息

Gonçalves Gisele Santos, Fernandes Ana Paula, Souza Renata Celi Carvalho, Cardoso Jarbas Eustáquio, de Oliveira-Silva Fernanda, Maciel Fabiana Cristina, Rabello Ana, Ferreira Lucas Antônio Miranda

机构信息

Department of Clinical and Toxicological Analysis, Faculty of Pharmacy, Federal University of Minas Gerais (UFMG), Av Antônio Carlos, 6627, CEP 31270-901, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Acta Trop. 2005 Feb;93(2):161-7. doi: 10.1016/j.actatropica.2004.10.007. Epub 2004 Dec 22.

Abstract

Studies on in vitro skin permeation and in vivo anti-leishmanial activity in mice experimentally infected with Leishmania (Leishmania) major pointed out to the potential of a new paromomycin (PA) formulation (hydrophilic gel) for treatment of cutaneous leishmaniasis (CL). In this study, the activity of this formulation was evaluated in animals experimentally infected by Leishmania species that prevail in the New World. PA gel activity was compared to antimony treatment, since it is still the first choice treatment to the different clinical forms of leishmaniasis. The topical treatment activity with 10% PA gel in BALB/c mice infected by Leishmania (Leishmania) amazonensis was higher than that observed for parenteral antimony treatment, while the efficacy of these two regimes in hamsters infected by Leishmania (Viannia) braziliensis was similar. These results suggest that this formulation could be suitable for clinical studies and may represent an alternative novel formulation for topical treatment of CL.

摘要

对实验感染硕大利什曼原虫(利什曼原虫属)的小鼠进行的体外皮肤渗透和体内抗利什曼活性研究表明,一种新的巴龙霉素(PA)制剂(亲水凝胶)具有治疗皮肤利什曼病(CL)的潜力。在本研究中,在实验感染新世界流行的利什曼原虫物种的动物中评估了该制剂的活性。将PA凝胶的活性与锑治疗进行了比较,因为锑仍然是治疗不同临床形式利什曼病的首选疗法。在感染亚马逊利什曼原虫(利什曼原虫属)的BALB/c小鼠中,10%PA凝胶的局部治疗活性高于肠胃外锑治疗,而这两种治疗方案在感染巴西利什曼原虫(维安尼亚利什曼原虫)的仓鼠中的疗效相似。这些结果表明,该制剂可能适合进行临床研究,并且可能代表一种用于CL局部治疗的新型替代制剂。

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