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阿苯达唑砜对映异构体的体外分析表明,(+)-(R)-阿苯达唑砜是对抗猪带绦虫的活性对映异构体。

In vitro analysis of albendazole sulfoxide enantiomers shows that (+)-(R)-albendazole sulfoxide is the active enantiomer against Taenia solium.

机构信息

Laboratorio de Inmunopatología en Neurocisticercosis, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Perú

出版信息

Antimicrob Agents Chemother. 2013 Feb;57(2):944-9. doi: 10.1128/AAC.01465-12. Epub 2012 Dec 10.

Abstract

Albendazole is an anthelmintic drug widely used in the treatment of neurocysticercosis (NCC), an infection of the brain with Taenia solium cysts. However, drug levels of its active metabolite, albendazole sulfoxide (ABZSO), are erratic, likely resulting in decreased efficacy and suboptimal cure rates in NCC. Racemic albendazole sulfoxide is composed of ABZSO (+)-(R)- and (-)-(S) enantiomers that have been shown to differ in pharmacokinetics and activity against other helminths. The antiparasitic activities of racemic ABZSO and its (+)-(R)- and (-)-(S) enantiomers against T. solium cysts were evaluated in vitro. Parasites were collected from naturally infected pigs, cultured, and exposed to the racemic mixture or to each enantiomer (range, 10 to 500 ng/ml) or to praziquantel as a reference drug. The activity of each compound against cysts was assayed by measuring the ability to evaginate and inhibition of alkaline phosphatase (AP) and parasite antigen release. (+)-(R)-ABZSO was significantly more active than (-)-(S)-ABZSO in suppressing the release of AP and antigen into the supernatant in a dose- and time-dependent manner, indicating that most of the activity of ABZSO resides in the (+)-(R) enantiomer. Use of this enantiomer alone may lead to increased efficacy and/or less toxicity compared to albendazole.

摘要

阿苯达唑是一种驱虫药物,广泛用于治疗脑囊虫病(NCC),这是一种由猪带绦虫囊虫引起的感染。然而,其活性代谢物阿苯达唑亚砜(ABZSO)的药物水平不稳定,可能导致 NCC 的疗效降低和治愈率不理想。消旋阿苯达唑亚砜由 ABZSO 的 (+)-(R)-和 (-)-(S)对映异构体组成,这两种对映异构体在药代动力学和对其他寄生虫的活性方面存在差异。本研究评估了消旋 ABZSO 及其 (+)-(R)-和 (-)-(S)对映异构体对猪带绦虫囊虫的体外驱虫活性。寄生虫从自然感染的猪中采集,培养并暴露于消旋混合物或每个对映异构体(范围为 10 至 500 ng/ml)或吡喹酮(作为参考药物)。通过测量囊虫逸出能力以及碱性磷酸酶(AP)和寄生虫抗原释放的抑制作用来测定每种化合物对囊虫的活性。(+)-(R)-ABZSO 以剂量和时间依赖的方式显著比(-)-(S)-ABZSO 更能抑制 AP 和抗原释放到上清液中,表明 ABZSO 的大部分活性存在于(+)-(R)对映异构体中。与阿苯达唑相比,单独使用这种对映异构体可能会提高疗效和/或降低毒性。

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