Journal
POLYMER CHEMISTRY
Volume 5, Issue 3, Pages 1037-1048Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3py01051a
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Funding
- PolyTherics
- IHR Biomedical Research Centre at Moorfields Hospital
- UCL Institute of Ophthalmology, Moorfields Special Trustees
- Helen Hamlyn Trust (in memory of Paul Hamlyn), Fight for Sight and Freemasons Grand Charity
- UK Engineering & Physical Sciences Research Council (EPSRC)
- EPSRC Centre
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Amphotericin B (AmB) is used to treat a neglected disease called visceral leishmaniasis (VL). We hypothesised that direct non-covalent association of AmB with poly(methacrylic acid) (PMAA) would replicate many of the properties of liposomal AmB (AmB-L), which is more efficacious than micellar AmB (AmB-D). Water-soluble AmB-PMAA complexes with AmB loadings ranging from similar to 20 to 45% were reproducibly prepared. The AmB in the PMAA complex displayed similar aggregation properties to the AmB within AmB-L. The AmB-PMAA complex displayed low heamolytic properties while maintaining in vitro activity against Leishmania donovani amastigotes with no macrophage toxicity observed at an IC50 of 0.043 (+/- 0.003) mu M. AmB-PMAA complexes were well tolerated in vivo at a total dose of 6 mg kg(-1) and both the complex (2.2 mg kg(-1) AmB) and AmB-L (2.5 mg kg(-1) AmB) achieved greater than 90% parasite inhibition in vivo after a single dose against L. donovani in HU3 infected BALB/c mice.
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