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多拉菌素驱除绵羊痒螨的效果:药理学策略评估。

Doramectin efficacy against Psoroptes ovis in sheep: Evaluation of pharmacological strategies.

机构信息

Grupo de Salud Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), Modesta Victoria 4450, 8400, Bariloche, Argentina.

Laboratorio de Farmacología, Centro de Investigación Veterinaria de Tandil (CIVETAN) (UNCPBA-CICPBA-CONICET), Facultad de Ciencias Veterinarias, UNCPBA, Tandil, Argentina.

出版信息

Exp Parasitol. 2020 Nov;218:107998. doi: 10.1016/j.exppara.2020.107998. Epub 2020 Sep 15.

Abstract

The aims of this study were to evaluate the efficacy of two injectable formulations of doramectin (DRM) against Psoroptes ovis in sheep infested under controlled experimental conditions and to characterize the DRM plasma disposition kinetics in the infested animals. To this end, sheep were experimentally infested with a P. ovis strain from a farm with a history of treatment failure, and then treated either with DRM 1% (traditional preparation) on days 0 and 7 or with DRM 3.15% (long-acting formulation) on day 0. The efficacy of each treatment was calculated by counting live mites in skin scrapings. Plasma samples were obtained from each animal and DRM concentrations were measured by HPLC. After the two doses of DRM 1%, the maximum efficacy (98.8%) was reached on day 28, whereas after the single dose of DRM 3.15%, the maximum efficacy (100%) was reached on day 35 and ratified on day 42. The long-acting formulation allowed obtaining higher exposure and more sustained concentrations of DRM than the traditional preparation. Although both DRM formulations studied were effective according to international protocols, they did not reach 100% effectiveness in the time required for approved pharmaceutical products against sheep scab, according to Argentine regulations.

摘要

本研究的目的是评估两种不同剂型的多拉菌素(DRM)对受感染绵羊的嗜皮螨(Psoroptes ovis)的疗效,并对感染动物体内 DRM 的血浆处置动力学进行特征描述。为此,实验用来自一个曾有治疗失败史的农场的 P. ovis 株对绵羊进行人工感染,然后分别在第 0 天和第 7 天用 1%(传统制剂)的 DRM 或在第 0 天用 3.15%(长效制剂)的 DRM 进行治疗。通过对皮肤刮屑中活螨的计数来计算每种治疗的疗效。从每只动物获得血浆样本,并通过 HPLC 测量 DRM 浓度。在接受两剂 1%的 DRM 后,最大疗效(98.8%)在第 28 天达到,而在接受单剂 3.15%的 DRM 后,最大疗效(100%)在第 35 天达到,并在第 42 天得到确认。长效制剂允许获得比传统制剂更高的 DRM 暴露量和更持久的浓度。尽管根据国际协议,这两种 DRM 制剂都被证明是有效的,但根据阿根廷法规,它们在获得批准的治疗绵羊疥癣药物所需的时间内并未达到 100%的有效性。

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