Delmonte Camila, Cruz Paula Barroso, Zeringóta Viviane, de Mello Valéria, Ferreira Felipe, Amaral Maria da Penha Henriques, Daemon Erik
Programa de Pós Graduação em Ciências Biológicas - Comportamento e Biologia Animal, Universidade Federal de Juiz de Fora UFJF, Juiz de Fora, Minas Gerais, Brazil.
Programa de Pós Graduação em Ciências Veterinárias, Departamento de Parasitologia Animal, Universidade Federal Rural do Rio de Janeiro, UFRRJ, Seropédica,, Rio de Janeiro, Brazil.
Parasitol Res. 2017 Nov;116(11):2957-2964. doi: 10.1007/s00436-017-5604-x. Epub 2017 Sep 5.
The objective of this study was to assess, for the first time, the in vitro acaricidal activity of two topical formulations containing thymol, on immature stages of Rhipicephalus sanguineus sensu lato. For this purpose, two base formulations were prepared: an oil-in-water (O/W) emulsion and a hydroalcoholic solution, containing different thymol concentrations (0.5 to 20 mg/mL). We used the larval packet test for non-engorged larvae and nymphs, and the immersion test for engorged larvae and nymphs. For emulsion, a mortality rate of 94.2% was achieved at 0.75 mg/mL in non-engorged larvae. For engorged larvae, there was 95.0% mortality at 5.0 mg/mL. Non-engorged nymphs showed 83.3% mortality at 2.5 mg/mL, and for engorged nymphs, 86.0% mortality was verified at 5.0 mg/mL. For the hydroalcoholic solution, the mortality found for non-engorged larvae was 88.1% at 2.5 mg/mL. For engorged larvae, the highest mortality was 25.0% at 20 mg/mL; non-engorged nymphs had 91.0% mortality at 1.0 mg/mL and for engorged nymphs; the maximum value verified was 18.3% mortality at 20 mg/mL. Preliminary stability tests were carried, and the hydroalcoholic solution remained stable under all the conditions analyzed. The O/W emulsion showed signs of early instability at the concentration of 5.0 mg/mL. The results obtained indicate that the acaricidal activity of thymol, when included in the proposed formulations, was enhanced against non-engorged larvae with topical treatment in comparison with data in the literature. Although there were variations in toxicity between the different stages, these formulations are promising for future therapeutic use.
本研究的目的是首次评估两种含百里酚的局部用制剂对血红扇头蜱狭义亚种未成熟阶段的体外杀螨活性。为此,制备了两种基础制剂:水包油(O/W)乳剂和含不同百里酚浓度(0.5至20mg/mL)的水醇溶液。对于未饱血幼虫和若虫,我们使用幼虫包囊试验;对于饱血幼虫和若虫,我们使用浸泡试验。对于乳剂,在未饱血幼虫中,0.75mg/mL时死亡率达到94.2%。对于饱血幼虫,5.0mg/mL时死亡率为95.0%。未饱血若虫在2.5mg/mL时死亡率为83.3%,对于饱血若虫,5.0mg/mL时死亡率为86.0%。对于水醇溶液,未饱血幼虫在2.5mg/mL时死亡率为88.1%。对于饱血幼虫,20mg/mL时最高死亡率为25.0%;未饱血若虫在1.0mg/mL时死亡率为91.0%,对于饱血若虫,20mg/mL时验证的最高死亡率为18.3%。进行了初步稳定性试验,水醇溶液在所有分析条件下均保持稳定。O/W乳剂在5.0mg/mL浓度时显示出早期不稳定的迹象。所得结果表明,与文献数据相比,当百里酚包含在所提出的制剂中时,通过局部治疗对未饱血幼虫的杀螨活性增强。尽管不同阶段的毒性存在差异,但这些制剂在未来治疗应用方面很有前景。