Porphyrin–phospholipid liposomes permeabilized by near-infrared light

K.A. Carter, S. Shao, M.I. Hoopes, D. Luo, B. Ahsan, V.M. Grigoryants, W. Song, Haoliang Huang, G. Zhang, R.K. Pandey, J. Geng, B.A. Pfeifer, C.P. Scholes, J. Ortega, M.E.J. Karttunen, J.F. Lovell

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The delivery of therapeutic compounds to target tissues is a central challenge in treating disease. Externally controlled drug release systems hold potential to selectively enhance localized delivery. Here we describe liposomes doped with porphyrin–phospholipid that are permeabilized directly by near-infrared light. Molecular dynamics simulations identified a novel light-absorbing monomer esterified from clinically approved components predicted and experimentally demonstrated to give rise to a more stable porphyrin bilayer. Light-induced membrane permeabilization is enabled with liposomal inclusion of 10 molar % porphyrin–phospholipid and occurs in the absence of bulk or nanoscale heating. Liposomes reseal following laser exposure and permeability is modulated by varying porphyrin–phospholipid doping, irradiation intensity or irradiation duration. Porphyrin–phospholipid liposomes demonstrate spatial control of release of entrapped gentamicin and temporal control of release of entrapped fluorophores following intratumoral injection. Following systemic administration, laser irradiation enhances deposition of actively loaded doxorubicin in mouse xenografts, enabling an effective single-treatment antitumour therapy.
Original languageEnglish
Article number3546
Number of pages11
JournalNature Communications
Publication statusPublished - 2014
Externally publishedYes


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