Last Updated: 21/11/2014

Screening for a slow-release formulation of ivermectin for malaria vector control


Ivermectin (IVM) reduces mosquito survival in lab and field studies, potentially leading to a disruption in transmission. A key factor for interrupting transmission, however, would be the time IVM remains in blood above mosquito-killing levels. Current oral formulations can only maintain mosquitocidal concentrations for approximately 48 hours.

In this animal model, the aim was to find a safe implantable formulation capable of sustaining mosquito-killing levels of IVM for months.

Principal Investigators / Focal Persons

Carlos Chaccour

Partner Institutions

Cantonal Hospital Baselland

Rationale and Abstract

The prospect of eliminating malaria is challenged by emerging insecticide resistance and vectors with outdoor and/or crepuscular activity. Ivermectin can simultaneously tackle these issues by killing mosquitoes feeding on treated animals and humans. A single oral dose, however, confers only short-lived mosquitocidal plasma levels.

Three different slow-release formulations of ivermectin were screened for their capacity to sustain mosquito-killing levels of ivermectin for months. Thirty rabbits received a dose of one, two or three silicone implants containing different proportions of ivermectin, deoxycholate and sucrose. Animals were checked for toxicity and ivermectin was quantified periodically in blood. The potential impact of the corresponding long-lasting formulation was mathematically modelled.

All combinations of formulation and dose released ivermectin for more than 12 weeks; four combinations sustained plasma levels capable of killing 50% of Anopheles gambiae feeding on a treated subject for up to 24 weeks. No major adverse effects attributable to the drug were found. Modelling predicts a 98% reduction in infectious vector density by using an ivermectin formulation with a 12-week duration.

These results indicate that relatively stable mosquitocidal plasma levels of ivermectin can be safely sustained in rabbits for up to six months using a silicone-based subcutaneous formulation. Modifying the formulation of ivermectin promises to be a suitable strategy for malaria vector control.


Jan 2014 — Dec 2016

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