Marques, JoanaValle Delgado, Juan JoséUrbán, PatriciaBaró, ElisabetProhens López, RafaelMayor Aparicio, Alfredo GabrielCisteró, PauDelves, MichaelSinden, Robert E.Grandfils, ChristianPaz, José L. deGarcía Salcedo, José A.Fernàndez Busquets, Xavier2016-11-182016-11-182016-10-051549-9634https://hdl.handle.net/2445/103904The adaptation of existing antimalarial nanocarriers to new Plasmodium stages, drugs, targeting molecules, or encapsulating structures is a strategy that can provide new nanotechnology-based, cost-efficient therapies against malaria. We have explored the modification of different liposome prototypes that had been developed in our group for the targeted delivery of antimalarial drugs to Plasmodium-infected red blood cells (pRBCs). These new models include: (i) immunoliposome-mediated release of new lipid-based antimalarials; (ii) liposomes targeted to pRBCs with covalently linked heparin to reduce anticoagulation risks; (iii) adaptation of heparin to pRBC targeting of chitosan nanoparticles; (iv) use of heparin for the targeting of Plasmodium stages in the mosquito vector; and (v) use of the non-anticoagulant glycosaminoglycan chondroitin 4-sulfate as a heparin surrogate for pRBC targeting. The results presented indicate that the tuning of existing nanovessels to new malaria-related targets is a valid low-cost alternative to the de novo development of targeted nanosystems.12 p.application/pdfengcc by (c) Marques et al., 2016http://creativecommons.org/licenses/by/3.0/es/NanomedicinaMalàriaNanomedicineMalariainfo:eu-repo/semantics/article2016-11-16info:eu-repo/semantics/openAccess27720930