Photon-triggered polymersome rupture under temporal, spatial and spectral control
PEYRET, Ariane
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
IBARBOURE, Emmanuel
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
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Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
PEYRET, Ariane
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
IBARBOURE, Emmanuel
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
BEAUTÉ, Louis
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
SANDRE, Olivier
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
LECOMMANDOUX, Sebastien
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
< Réduire
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 3 LCPO : Polymer Self-Assembly & Life Sciences
Langue
en
Article de revue
Ce document a été publié dans
Journal of Controlled Release. 2017, vol. 259, p. e8-e9
Elsevier
Résumé en anglais
Polymersomes are robust self-assembled vesicular structures that are widely studied in a variety of domains from nanomedicine to artificial cell design [1]. Control over their membrane diffusion properties and structural ...Lire la suite >
Polymersomes are robust self-assembled vesicular structures that are widely studied in a variety of domains from nanomedicine to artificial cell design [1]. Control over their membrane diffusion properties and structural integrity is crucial for their future development [2]. In particular, a high level of control is mandatory in drug delivery applications where species have to be released at the right place and time. Here, we present a high precision method allowing programmed vesicle rupture with full control in time, space and excitation wavelength for selective cargo-release.We designed an easy and tunable protocol for light-driven specific polymersome rupture controlled in time and space, which combines the advantages of utilizing light as a trigger and the fast release of components from bursting vesicles. Our system is based on laser excitation of hydrophilic dyes loaded in the lumen of distinct giant poly(butadiene)-b-poly(ethylene oxide) polymersomes. Upon excitation, the fast generation of reactive oxygen species leads to an increase of the internal osmotic pressure that can not be compensated fast enough, resulting in subsequent vesicle rupture (Fig. 1). This process allows for a precise and fast release of entrapped species from different compartments. Additionally, such a selective mechanism allows discrimination between two types of vesicles within a group of many and successive triggered release of their content without altering the remaining vesicles. This unique mechanism is shown to selectively rupture polymersomes with high precision, and even to deliver small polymersomes and liposomes.< Réduire
Mots clés en anglais
targeted delivery
diethylstilbestrol
cancer hormone therapy
triggered rupture
polymersomes
cargo-release
self-assembly
light stimulus
reactive oxygen species
Project ANR
Développement de cellule synthétique comme micro-réacteur pour l'étude de l'activité enzymatique des NO-synthases et la compréhension de leur fonctionnement en conditions physiologiques - ANR-14-CE16-0015
Origine
Importé de halUnités de recherche