Journal article
A 30 kDa polyethylene glycol-enfuvirtide complex enhances the exposure of enfuvirtide in lymphatic viral reservoirs in rats
LM Kaminskas, CC Williams, NJ Leong, LJ Chan, NJ Butcher, OM Feeney, CJH Porter, D Tyssen, G Tachedjian, DB Ascher
European Journal of Pharmaceutics and Biopharmaceutics | Published : 2019
Abstract
HIV therapy with anti-retroviral drugs is limited by the poor exposure of viral reservoirs, such as lymphoid tissue, to these small molecule drugs. We therefore investigated the effect of PEGylation on the anti-retroviral activity and subcutaneous lymphatic pharmacokinetics of the peptide-based fusion inhibitor enfuvirtide in thoracic lymph duct cannulated rats. Both the peptide and the PEG were quantified in plasma and lymph via ELISA. Conjugation to a single 5 kDa linear PEG decreased anti-HIV activity three-fold compared to enfuvirtide. Whilst plasma and lymphatic exposure to peptide mass was moderately increased, the loss of anti-viral activity led to an overall decrease in exposure to e..
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Awarded by Jack Brockhoff Foundation
Funding Acknowledgements
This work was supported by a National Health and Medical Research Council project grant. LMK is supported by an NHMRC Career Development fellowship. D.B.A. was supported by a Newton Fund RCUK-CONFAP Grant awarded by The Medical Research Council (MRC) and Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG) (MR/M026302/1, APQ-00828-15), a C.J. Martin Research Fellowship from the National Health and Medical Research Council of Australia (APP1072476) and the Jack Brockhoff Foundation (JBF 4186, 2016).