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Article Dans Une Revue Journal of Liposome Research Année : 2014

Carrier-inside-carrier: polyelectrolyte microcapsules as reservoir for drug-loaded liposomes

Résumé

Conventional liposomes have a short life-time in blood, unless they are protected by a polymer envelope, most often polyethylene glycol. However, these stabilizing polymers frequently interfere with cellular uptake, impede liposome-membrane fusion and inhibit escape of liposome content from endosomes. To overcome such drawbacks, polymer-based systems as carriers for liposomes are currently developed. Conforming to this approach, we propose a new and convenient method for embedding small size liposomes, 30–100 nm, inside porous calcium carbonate microparticles. These microparticles served as templates for deposition of various polyelectrolytes to form a protective shell. The carbonate particles were then dissolved to yield hollow polyelectrolyte microcapsules. The main advantage of using this method for liposome encapsulation is that carbonate particles can serve as a sacrificial template for deposition of virtually any polyelectrolyte. By carefully choosing the shell composition, bioavailability of the liposomes and of the encapsulated drug can be modulated to respond to biological requirements and to improve drug delivery to the cytoplasm and avoid endosomal escape.
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Dates et versions

hal-01142690 , version 1 (15-04-2015)

Identifiants

  • HAL Id : hal-01142690 , version 1

Citer

O. Maniti, S. Rebaud, J. Sarkis, Y Jia, J Zhao, et al.. Carrier-inside-carrier: polyelectrolyte microcapsules as reservoir for drug-loaded liposomes. Journal of Liposome Research, 2014, 25 (2), pp.122-130. ⟨hal-01142690⟩
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