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新型氟虫腈、(S)-灭幼脲、伊维菌素和吡喹酮局部联合制剂对猫体硬蜱属(Ixodes ricinus 和 Ixodes scapularis)的杀灭效果。

Efficacy of a novel topical combination of fipronil, (S)-methoprene, eprinomectin, and praziquantel, against the ticks, Ixodes ricinus and Ixodes scapularis, on cats.

机构信息

Merial SAS, Centre de Recherche de Saint-Vulbas, France.

Merial Limited, USA.

出版信息

Vet Parasitol. 2014 Apr 28;202(1-2):59-63. doi: 10.1016/j.vetpar.2014.02.041.

Abstract

Five controlled, blinded and randomized studies were conducted to examine the efficacy of a single topical application of a combination of fipronil, (S)-methoprene, eprinomectin, and praziquantel (BROADLINE(®), Merial) against induced infestations with Ixodes ticks on cats. Three studies investigated the efficacy against Ixodes ricinus and two against Ixodes scapularis. In each study, purpose-bred cats were assigned at random to an untreated group or to a treated group. For the studies using I. ricinus, cats were infested with 50 female ticks and a similar number of males 2 days before treatment application, and weekly afterwards on between four and six occasions. For the studies using I. scapularis, cats were infested with a total of 50 ticks (approximately 25 females and 25 males) according to the same schedule as for I. ricinus. Tick counts for the evaluation of efficacy were performed 48 h after treatment and 48 h after the subsequent weekly infestations. Weekly attachment rates to untreated cats of at least 29% for I. ricinus and at least 30% for I. scapularis demonstrated consistently that the ticks were vigorous and that the attachment rates were adequate for efficacy evaluation. In the I. ricinus studies, an efficacy of at least 93% was demonstrated for up to 37 days after the treatment. In the I. scapularis studies, the efficacy level was at least 95% 30 days after the treatment. The product was well tolerated and caused no adverse reaction.

摘要

五项对照、双盲、随机临床试验研究了一种新型复方体外驱虫药(氟虫腈、(S)-灭幼脲、依普菌素和吡喹酮,BROADLINE(®),梅里亚)单次给药驱除猫体寄生壁虱的效果。其中三项研究评估了该药驱除欧洲蓖子硬蜱(Ixodes ricinus)的效果,两项研究评估了该药驱除肩突硬蜱(Ixodes scapularis)的效果。每个研究中,选择特定品种的猫,随机分为未处理组和处理组。对于使用欧洲蓖子硬蜱的研究,在治疗前 2 天将 50 只雌性和 50 只雄性壁虱置于猫体,此后每周进行一次处理和感染。对于使用肩突硬蜱的研究,按照同样的时间表,在猫体放置总共 50 只壁虱(约 25 只雌性和 25 只雄性)。为评估疗效,在治疗后 48 小时和之后每周的感染后 48 小时进行蜱计数。对于欧洲蓖子硬蜱,未处理猫的每周附着率至少为 29%,肩突硬蜱至少为 30%,这表明壁虱活力良好,附着率足以进行疗效评估。在欧洲蓖子硬蜱的研究中,治疗后 37 天内,疗效至少为 93%。在肩突硬蜱的研究中,治疗后 30 天,疗效至少为 95%。该产品耐受性良好,无不良反应。

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