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新型伊维菌素鼻腔喷雾剂在猪模型中的安全性和药代动力学评估。

Safety and Pharmacokinetic Assessments of a Novel Ivermectin Nasal Spray Formulation in a Pig Model.

机构信息

Cátedra de Farmacología Básica, General y Farmacodinamia, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, La Plata, Argentina; INCAM S.A, Cañuelas, Argentina.

Laboratorio de Farmacología, Centro de Investigación Veterinarias de Tandil (CIVETAN), CONICET-CICPBA-UNCPBA, Facultad de Ciencias Veterinarias, Universidad Nacional Del Centro de La Provincia de Buenos Aires, Tandil, Argentina.

出版信息

J Pharm Sci. 2021 Jun;110(6):2501-2507. doi: 10.1016/j.xphs.2021.01.017. Epub 2021 Jan 23.

Abstract

Recently published data indicates that high ivermectin (IVM) concentrations suppress in vitro SARS-CoV-2 replication. Nasal IVM spray administration may contribute to attaining high drug concentrations in nasopharyngeal tissue, a primary site of virus entrance/replication. The safety and pharmacokinetic performances of a novel IVM spray formulation were assessed in a pig model. Piglets received IVM either orally (0.2 mg/kg) or by one or two nasal spray doses. The overall safety, and histopathology of the IVM-spray application site tissues, were assessed. The IVM concentration profiles measured in plasma and respiratory tract tissues after the nasal spray were compared with those achieved after the oral administration. Animals tolerated well the nasal spray formulation. No local/systemic adverse events were observed. After nasal administration, the highest IVM concentrations were measured in nasopharyngeal and lung tissues. The nasal/oral IVM concentration ratios in nasopharyngeal and lung tissues markedly increased by repeating (12 h apart) the spray application. The fast attainment of high and persistent IVM concentrations in nasopharyngeal tissue is the main advantage of the nasal over the oral route. These original results support the undertaking of future clinical trials to evaluate the safety/efficacy of the nasal IVM spray application in the prevention and/or treatment of COVID-19.

摘要

最近发表的数据表明,高浓度伊维菌素(IVM)可抑制体外 SARS-CoV-2 复制。鼻腔 IVM 喷雾剂给药可能有助于在鼻咽组织中达到高药物浓度,鼻咽组织是病毒进入/复制的主要部位。在猪模型中评估了一种新型 IVM 喷雾剂配方的安全性和药代动力学性能。小猪经口(0.2mg/kg)或经一次或两次鼻腔喷雾给药接受 IVM。评估了 IVM 喷雾应用部位组织的整体安全性和组织病理学。比较了鼻腔喷雾后测量的血浆和呼吸道组织中的 IVM 浓度曲线与口服后获得的浓度曲线。动物耐受良好的鼻腔喷雾制剂。未观察到局部/全身不良事件。经鼻腔给药后,在鼻咽和肺部组织中测量到的 IVM 浓度最高。通过重复(间隔 12 小时)喷雾应用,鼻咽和肺部组织中的鼻腔/口服 IVM 浓度比值显著增加。在鼻咽组织中快速达到高且持续的 IVM 浓度是鼻腔途径优于口服途径的主要优势。这些原始结果支持开展未来的临床试验,以评估鼻腔 IVM 喷雾应用在预防和/或治疗 COVID-19 中的安全性/疗效。

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