The efficacy of aerosol treatment with non-ionic surfactant vesicles containing amphotericin B in rodent models of leishmaniasis and pulmonary aspergillosis infection

Alsaadi, Manal and Italia, Jagdishbhai Laxmanbhai and Mullen, Alexander and Kumar, M.N.V Ravi and Candlish, A.A. and Williams, Roderick and Shaw, C.D. and Al-Gawhari, Fatima and Coombs, Graham and Wiese, Martin and Thomson, Alison and Puig-Sellart, M. and Wallace, J. and Sharp, A and Wheeler, Lee and Warn, Peter and Carter, Katharine (2012) The efficacy of aerosol treatment with non-ionic surfactant vesicles containing amphotericin B in rodent models of leishmaniasis and pulmonary aspergillosis infection. Journal of Controlled Release, 160 (3). pp. 685-691. ISSN 0168-3659 (https://doi.org/10.1016/j.jconrel.2012.04.004)

Full text not available in this repository.Request a copy

Abstract

Amphotericin B (AMB) is used to treat both fungal and leishmanial infections, which are of major significance to human health. Clinical use of free AMB is limited by its nephrotoxicity, whereas liposomal AMB is costly and requires parenteral administration, thus development of novel formulations with enhanced efficacy, minimal toxicity and that can be applied via non-invasive routes is required. In this study we analysed the potential of non-ionic surfactant vesicles (NIV) given by nebulisation to deliver AMB to the lungs, liver and skin. Treatment with AMB-NIV resulted in significantly higher drug levels in the lungs and skin (p < 0.05) compared to similar treatment with AMB solution but significantly lower plasma levels (p < 0.05). Treatment with AMB-NIV resulted in a significant reduction in fungal lung burdens in a rat model of invasive pulmonary aspergillosis (p < 0.05) compared to treatment with the carrier alone. Treatment with AMB-NIV but not AMB solution significantly suppressed Leishmania donovani liver parasite burdens (p < 0.05) but could not inhibit the growth of cutaneous Leishmania major lesions. The results of this study indicate that aerosolised NIV enhanced pulmonary and hepatic delivery whilst minimising systemic exposure and toxicity.

ORCID iDs

Alsaadi, Manal, Italia, Jagdishbhai Laxmanbhai, Mullen, Alexander ORCID logoORCID: https://orcid.org/0000-0001-7475-5543, Kumar, M.N.V Ravi, Candlish, A.A., Williams, Roderick, Shaw, C.D., Al-Gawhari, Fatima, Coombs, Graham, Wiese, Martin ORCID logoORCID: https://orcid.org/0000-0003-4493-0835, Thomson, Alison ORCID logoORCID: https://orcid.org/0000-0002-2354-6116, Puig-Sellart, M., Wallace, J., Sharp, A, Wheeler, Lee ORCID logoORCID: https://orcid.org/0000-0002-9132-1875, Warn, Peter and Carter, Katharine;
CORE (COnnecting REpositories)