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体内评价阿苯达唑微球治疗犬蛔虫幼虫移行症。

In vivo evaluation of albendazole microspheres for the treatment of Toxocara canis larva migrans.

机构信息

Departamento Farmacia, Universidad Nacional de Rosario, Rosario, Argentina.

出版信息

Eur J Pharm Biopharm. 2010 Aug;75(3):451-4. doi: 10.1016/j.ejpb.2010.03.017. Epub 2010 Mar 27.

Abstract

Albendazole is a benzimidazole derivative with proven efficacy against many parasites such as intestinal helminths. Toxocariasis is one of the important parasitic diseases in humans and animals caused by Toxocara canis. It is well known that T. canis larvae migrate in paratenic hosts, including humans where it may cause visceral larva migrans. Thus, the present research was carried out using in vivo experiments with the aim of finding whether novel albendazole microparticles would be active against migrating larvae of the parasite. Albendazole-chitosan microparticles were prepared by ionotropic gelation with sodium lauryl sulphate or by a liquid-liquid phase separation with sodium hydroxide. Mice were infected with T. canis and then treated with both albendazole-chitosan microparticles. After treatment (28days post-infection), it was examined the anthelmintic effect in mice after oral administration of microparticulate preparations. The number of larvae recovered from mice treated with albendazole formulations were compared with placebo. The results showed that albendazole microparticles were easily prepared in high yield using both aqueous solutions of sodium lauryl sulphate or sodium hydroxide. In vivo evaluation of larva migration showed that albendazole microparticles exhibited a greater anthelmintic effect in the brain (0 larva/mouse). In addition, it was also found that liver and lung showed a significant decrease in the number of larvae. Therefore, these data suggest that albendazole-chitosan microparticles are effective formulations for the treatment of toxocariasis infection by reducing the number of larvae in liver and lung. Particularly, these polymeric preparations were able to totally prevent migration of larvae to the mice brain.

摘要

阿苯达唑是一种苯并咪唑衍生物,已被证明对许多寄生虫有效,如肠道蠕虫。旋毛虫病是由犬旋毛虫引起的人类和动物的重要寄生虫病之一。众所周知,犬旋毛虫幼虫在中间宿主中迁移,包括人类,在那里它可能引起内脏幼虫移行症。因此,本研究采用体内实验进行,目的是寻找新型阿苯达唑微球是否对寄生虫迁移幼虫有活性。阿苯达唑-壳聚糖微球通过离子凝胶作用用十二烷基硫酸钠或通过液-液相分离用氢氧化钠制备。用犬旋毛虫感染小鼠,然后用阿苯达唑-壳聚糖微球处理。感染后(感染后 28 天),检查经口给予微粒制剂后小鼠的驱虫效果。用阿苯达唑制剂治疗的小鼠中回收的幼虫数量与安慰剂进行比较。结果表明,使用十二烷基硫酸钠或氢氧化钠的水溶液,很容易以高产率制备阿苯达唑微球。体内幼虫迁移评估表明,阿苯达唑微球在大脑(0 条幼虫/只小鼠)中表现出更强的驱虫作用。此外,还发现肝脏和肺部的幼虫数量明显减少。因此,这些数据表明,阿苯达唑-壳聚糖微球是治疗旋毛虫病感染的有效制剂,可减少肝脏和肺部的幼虫数量。特别是,这些聚合制剂能够完全阻止幼虫向小鼠大脑迁移。

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