Easy and effective method to produce functionalized particles for cellular uptake |
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Authors: | Floraine Collette Régis Delatouche Christophe Blanquart Fabien Gueugnon Marc Grégoire Philippe Bertrand Valérie Héroguez |
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Affiliation: | 1. Laboratoire de Chimie des Polymères Organiques, UMR CNRS 5629‐IPB‐ENSCBP‐Université Bordeaux 1, 16 avenue Pey‐Berland, F‐33607 Pessac cedex, France;2. Laboratoire Synthèse et Réactivité des Substances Naturelles, UMR CNRS 6514, 40 Avenue du Recteur Pineau, 86022, Poitiers cedex, France;3. INSERM, U892, Institut de Recherche Thérapeutique, Centre de Recherche en Cancérologie Nantes‐Angers‐8 Quai Moncousu, BP 70721, 44007 Nantes cedex 1, France |
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Abstract: | In this contribution, a versatile approach for the synthesis of functionalized particles for drug delivery is presented, using two nonaggressive standardized procedures. The first procedure considered is the functionalization of an azido‐terminated α‐norbornenyl poly(ethylene oxide) (PEO) macromonomer with an alkyne‐containing active molecule via the copper catalyzed azide alkyne cycloaddition, click type reaction. The functionalized macromonomer is then polymerized by Ring‐Opening Metathesis Polymerization (ROMP) in dispersion to form functionalized particles. The second procedure consists in synthesizing particles by ROMP in dispersed media of norbornene with azido‐terminated α‐norbornenyl PEO macromonomer. The ROMP was initiated by the first generation Grubbs catalyst. Such functionalized core‐shell particles have stealthy properties due to their PEO shell and can be viewed as universal nanocarriers on which any alkyne‐modified active molecule can be grafted by click chemistry. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 |
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Keywords: | biocompatibility click chemistry core‐shell particles poly(ethylene oxide) polynorbornene ROMP |
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