Merial GmbH, Kathrinenhof Research Center, 83101 Rohrdorf, Germany.
Merial Limited, Duluth, GA 30096, USA.
Vet Parasitol. 2014 Apr 28;202(1-2):34-9. doi: 10.1016/j.vetpar.2014.02.036.
The efficacy of a novel topical combination of fipronil 8.3% (w/v), (S)-methoprene 10% (w/v), eprinomectin 0.4% (w/v), and praziquantel 8.3% (w/v) (BROADLINE(®), Merial) was evaluated against adult and larval Toxocara cati in four controlled studies. All studies included experimentally infected, purpose-bred, short-haired cats. In two studies, 22 or 20 cats harbouring patent infections as confirmed by pre-treatment faecal examination, were included. Within each study, cats were allocated to one of two groups: control or treated. In a further two studies, 30 cats were included in each; cats were allocated to one of three groups: control, treated when T. cati were expected to be either migrating third and/or fourth-stage larvae, or treated when T. cati were expected to be fourth-stage larvae. Cats allocated to the treated groups received a single topical application of the combination product at 0.12 mL/kg bodyweight (10mg fipronil+12 mg (S)-methoprene+0.5mg eprinomectin+10mg praziquantel per kg). For parasite recovery and count, cats were euthanized humanely at different intervals after treatment. In the studies targeting adult T. cati, ascarids were recovered from all controls (range 1-150) while only two worms were isolated from one treated cat. Thus, the efficacy of the novel combination was 99.4% and 100% against adult T. cati. For studies targeting larval T. cati, up to 21 worms were recovered from each of seven or eight of the control cats per study. No T. cati were recovered from the treated cats in two studies, corresponding to 100% efficacy against both, migrating third and/or fourth-stage larvae and luminal fourth-stage larvae. All cats accepted the treatment well and no adverse experiences or other health problems were observed throughout the studies.
一种新型的氟虫腈 8.3%(w/v)、(S)-灭幼脲 10%(w/v)、埃普利诺菌素 0.4%(w/v)和吡喹酮 8.3%(w/v)(BROADLINE(®),梅里亚)的局部联合制剂对成年和幼虫期猫弓首蛔虫的疗效在四项对照研究中进行了评估。所有研究均纳入了经实验感染、专门饲养的短毛猫。在两项研究中,有 22 或 20 只猫在治疗前粪便检查确认存在现症感染。在每项研究中,猫被分配到两组之一:对照组或治疗组。在另外两项研究中,每组纳入 30 只猫;猫被分配到三组之一:对照组、当预期猫弓首蛔虫处于第三和/或第四期幼虫移行期时进行治疗,或当预期猫弓首蛔虫处于第四期幼虫期时进行治疗。治疗组猫接受单次局部应用联合制剂,剂量为 0.12 毫升/千克体重(10 毫克氟虫腈+12 毫克(S)-灭幼脲+0.5 毫克埃普利诺菌素+10 毫克吡喹酮/千克)。为了寄生虫回收和计数,猫在治疗后不同时间内被人道安乐死。在针对成年猫弓首蛔虫的研究中,所有对照组(范围 1-150)均回收了蛔虫,而仅从一只治疗猫中分离出两条蛔虫。因此,该新型联合制剂对成年猫弓首蛔虫的疗效为 99.4%和 100%。对于针对幼虫期猫弓首蛔虫的研究,每个研究中,7 或 8 只对照组猫中最多可回收 21 条蛔虫。在两项研究中,治疗组猫未回收猫弓首蛔虫,这对应于对移行的第三和/或第四期幼虫和腔道第四期幼虫的 100%疗效。所有猫均很好地接受了治疗,在整个研究过程中未观察到不良反应或其他健康问题。