Genchi Marco, Geneteau Anne, Forget Patrick, Delcombel Romain, Genchi Claudio
Department of Veterinary Sciences, University of Parma, Parma, Italy.
Ceva Santé Animale, Libourne, France.
Parasitol Res. 2017 Jun;116(6):1723-1728. doi: 10.1007/s00436-017-5448-4. Epub 2017 Apr 22.
An exploratory study was carried out to assess the in vivo efficacy of different prototypes of subcutaneous implants containing ivermectin (IVM) for the prevention of canine Dirofilaria immitis infection. The implants consisted of an ethylcellulose matrix containing IVM (3.0, 4.5, and 6.0 mg/implant; from 0.29 to 0.63 mg/kg bw) as active ingredient designed to release approximately 0.1 ng of IVM/mL in the plasma for at least 12 months. Six dogs were implanted on day -365. On day -12, three heartworm-free dogs were included in the study as a control group. All nine dogs were examined on day -7 and day 0 for circulating D. immitis microfilariae and by an antigen ELISA kit to confirm that the dogs were heartworm-free. The dogs were artificially infected with 75 D. immitis infective larvae (L3) each on day 0. Dogs in the control group were humanely euthanized on day 153 to verify the infectivity of the larvae, while implanted dogs were further examined for circulating D. immitis microfilariae and antigen on days 153, 195, and 246. The treated dogs were not necropsied. The pharmacokinetic profile of the IVM implant was assessed in plasma samples taken on day -364, then at different times until the infection day, and again on days, 15, 30, 60, 90, 120, and 153. Throughout the study, body weights were measured during clinical examination on days 0, 30, 60, 90, 120, and 153. At necropsy, all control dogs were found infected, each with 10-11 adult heartworms. Implanted dogs were negative at both microfilaria and D. immitis antigen examinations until day 246 (8 months from the infection). IVM plasma levels ranged 0.06-0.16 ng/mL on day 0 and remained stable until day 60, afterward they gradually decreased under the limit of quantification of the method. Throughout the study, no side effect was observed. On the basis of these results, it was possible to conclude that the different prototypes of implants were able to protect the dogs from D. immitis artificial infection for at least 12 months.
开展了一项探索性研究,以评估含伊维菌素(IVM)的不同皮下植入剂原型预防犬恶丝虫感染的体内疗效。植入剂由含IVM(每植入剂3.0、4.5和6.0毫克;相当于0.29至0.63毫克/千克体重)的乙基纤维素基质组成,设计为在血浆中至少12个月释放约0.1纳克IVM/毫升。在第-365天对6只犬进行植入。在第-12天,将3只无犬恶丝虫的犬纳入研究作为对照组。所有9只犬在第-7天和第0天检查循环中的犬恶丝虫微丝蚴,并通过抗原ELISA试剂盒确认犬无犬恶丝虫。在第0天,每只犬人工感染75条犬恶丝虫感染性幼虫(L3)。对照组的犬在第153天实施安乐死以验证幼虫的感染性,而植入植入剂的犬在第153天、195天和246天进一步检查循环中的犬恶丝虫微丝蚴和抗原。未对接受治疗的犬进行尸检。在第-364天采集血浆样本评估IVM植入剂的药代动力学特征,然后在感染日前的不同时间以及在第15天、30天、60天、90天、120天和153天再次评估。在整个研究过程中,在第0天、30天、60天、90天、120天和153天的临床检查期间测量体重。尸检时,发现所有对照犬均被感染,每只犬有10 - 11条成年犬恶丝虫。植入植入剂的犬在微丝蚴和犬恶丝虫抗原检查中均为阴性,直至第246天(感染后8个月)。第0天IVM血浆水平为0.06 - 0.16纳克/毫升,并在第60天前保持稳定,此后逐渐降至该方法的定量下限以下。在整个研究过程中,未观察到副作用。基于这些结果,可以得出结论,不同原型的植入剂能够保护犬免受犬恶丝虫人工感染至少12个月。