Abstract

Ivermectin (IVM) and moxidectin (MOX) are used extensively as parasiticides in veterinary medicine. Based on in vitro data, IVM has recently been proposed for the prevention and treatment of COVID-19 infection, a condition for which obesity is a major risk factor. In patients, IVM dosage is based on total body weight and there are no recommendations to adjust dosage in obese patients. The objective of this study was to establish, in a canine model, the influence of obesity on the clearance and steady-state volume of distribution of IVM, MOX, and a third analog, eprinomectin (EPR). An experimental model of obesity in dogs was based on a high calorie diet. IVM, MOX, and EPR were administered intravenously, in combination, to a single group of dogs in two circumstances, during a control period and when body weight had been increased by 50%. In obese dogs, clearance, expressed in absolute values (L/day), was not modified for MOX but was reduced for IVM and EPR, compared to the initial control state. However, when scaled by body weight (L/day/kg), plasma clearance was reduced by 55, 42, and 63%, for IVM, MOX and EPR, respectively. In contrast, the steady-state volume of distribution was markedly increased, in absolute values (L), by obesity. For IVM and MOX, this obese dog model suggests that the maintenance doses in the obese subject should be based on lean body weight rather than total weight. On the other hand, the loading dose, when required, should be based on the total body weight of the obese subject.

Highlights

  • IntroductionIvermectin (IVM) is a broad spectrum macrocyclic anti-parasitic drug, active against internal parasites (nematodes) and ectoparasites (arthropods) (Fox, 2006)

  • Ivermectin (IVM) is a broad spectrum macrocyclic anti-parasitic drug, active against internal parasites and ectoparasites (Fox, 2006)

  • For the three test articles, plasma clearance, expressed per kg BW, was significantly decreased during the obesity period. This was associated with large increases in mean residence time (MRT) (134, 164, and 91% for IVM, MOX, and EPR, respectively) and terminal halflife (76, 161, and 206% for IVM, MOX, and EPR, respectively) For volume of distribution, there was no significant difference for IVM, an increase for MOX (38%) and a decrease for EPR (29%)

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Summary

Introduction

Ivermectin (IVM) is a broad spectrum macrocyclic anti-parasitic drug, active against internal parasites (nematodes) and ectoparasites (arthropods) (Fox, 2006). It is used in both human and veterinary medicine. Mass drug administration of IVM is proposed as a complementary malaria vector control tool (The Ivermectin Roadmappers, 2020). The oral dosage of IVM is body-weight-based with a typical recommended anti-parasitic dose of 200 μg/kg (Anonymous, 2020b). This dose rate provides a wide margin of safety (Guzzo et al, 2002). A recent meta-analysis indicated that a dosage of 800 μg/kg was well-tolerated in patients with parasitic

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