Nebulized ivermectin for COVID-19 and other respiratory diseases, a proof of concept, dose-ranging study in rats.
Administration, Inhalation
Animals
Antiparasitic Agents
/ pharmacokinetics
Behavior, Animal
/ drug effects
COVID-19
Coronavirus Infections
/ drug therapy
Dose-Response Relationship, Drug
Female
Half-Life
Ivermectin
/ pharmacokinetics
Lung
/ metabolism
Male
Necrosis
Pandemics
Pneumonia, Viral
/ drug therapy
Proof of Concept Study
Rats
Rats, Sprague-Dawley
Respiration Disorders
/ drug therapy
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
13 10 2020
13 10 2020
Historique:
received:
13
07
2020
accepted:
25
09
2020
entrez:
14
10
2020
pubmed:
15
10
2020
medline:
29
10
2020
Statut:
epublish
Résumé
Ivermectin is a widely used antiparasitic drug with known efficacy against several single-strain RNA viruses. Recent data shows significant reduction of SARS-CoV-2 replication in vitro by ivermectin concentrations not achievable with safe doses orally. Inhaled therapy has been used with success for other antiparasitics. An ethanol-based ivermectin formulation was administered once to 14 rats using a nebulizer capable of delivering particles with alveolar deposition. Rats were randomly assigned into three target dosing groups, lower dose (80-90 mg/kg), higher dose (110-140 mg/kg) or ethanol vehicle only. A toxicology profile including behavioral and weight monitoring, full blood count, biochemistry, necropsy and histological examination of the lungs was conducted. The pharmacokinetic profile of ivermectin in plasma and lungs was determined in all animals. There were no relevant changes in behavior or body weight. There was a delayed elevation in muscle enzymes compatible with rhabdomyolysis, that was also seen in the control group and has been attributed to the ethanol dose which was up to 11 g/kg in some animals. There were no histological anomalies in the lungs of any rat. Male animals received a higher ivermectin dose adjusted by adipose weight and reached higher plasma concentrations than females in the same dosing group (mean C
Identifiants
pubmed: 33051517
doi: 10.1038/s41598-020-74084-y
pii: 10.1038/s41598-020-74084-y
pmc: PMC7555481
doi:
Substances chimiques
Antiparasitic Agents
0
Ivermectin
70288-86-7
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
17073Références
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