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Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides

INTRODUCTION: Encapsulation of biologically active molecules into nanoparticles (NPs), for site-specific delivery, is a fast growing area. These NPs must be biocompatible, non-toxic, and able to release their load in a controlled way. We have developed a series of NPs based on (bio)degradable and bi...

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Autores principales: Lepareur, Nicolas, Leal E Costa, Loleh, Bocqué, Maëva, Blondelle, Clément, Ruello, Clément, Desjulets, Marie, Noiret, Nicolas, Cammas-Marion, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559641/
https://www.ncbi.nlm.nih.gov/pubmed/26389121
http://dx.doi.org/10.3389/fmed.2015.00063
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author Lepareur, Nicolas
Leal E Costa, Loleh
Bocqué, Maëva
Blondelle, Clément
Ruello, Clément
Desjulets, Marie
Noiret, Nicolas
Cammas-Marion, Sandrine
author_facet Lepareur, Nicolas
Leal E Costa, Loleh
Bocqué, Maëva
Blondelle, Clément
Ruello, Clément
Desjulets, Marie
Noiret, Nicolas
Cammas-Marion, Sandrine
author_sort Lepareur, Nicolas
collection PubMed
description INTRODUCTION: Encapsulation of biologically active molecules into nanoparticles (NPs), for site-specific delivery, is a fast growing area. These NPs must be biocompatible, non-toxic, and able to release their load in a controlled way. We have developed a series of NPs based on (bio)degradable and biocompatible poly(malic acid) derivatives, poly(benzyl malate) (PMLABe), with its PEG-grafted stealth analog and target-specific biotin-PEG-b-PMLABe one. A lipophilic radiotracer has then been encapsulated into these NPs. METHODS: Monomers were synthesized from dl-aspartic acid. PEG(42)-b-PMLABe(73) and Biot-PEG(66)-b-PMLABe(73) block copolymers were obtained by anionic ring-opening polymerization of benzyl malolactonate in presence of α-methoxy-ω-carboxy-PEG(42) and α-biotin-ω-carboxy-PEG(66) as initiators. NPs were prepared by nanoprecipitation. Size, polydispersity, and zeta potential were measured by dynamic light scattering (DLS) and zetametry. (99m)Tc-SSS was prepared as previously described. Encapsulation efficacy was assessed by varying different parameters, such as encapsulation with preformed NPs or during their formation, influence of the solvent, and of the method to prepare the NPs. After decay, (99m)Tc-loaded NPs were also analyzed by DLS and zetametry. NPs’ morphology was assessed by transmission electron microscopy. RESULTS: (99m)Tc-SSS was added during nanoprecipitation, using two different methods, to ensure good encapsulation. Radiolabeled NPs present increased diameters, with identical low polydispersity indexes and negative zeta potentials in comparison to non-radiolabeled NPs. CONCLUSION: A radiotracer was successfully encapsulated, but some further optimization is still needed. The next step will be to modify these radiolabeled NPs with a hepatotrope peptide, and to replace (99m)Tc with (188)Re for therapy. Our team is also working on drugs’ encapsulation and grafting of a fluorescent probe. Combining these modalities is of interest for combined chemo-/radiotherapy, bimodal imaging, and/or theranostic approach.
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spelling pubmed-45596412015-09-18 Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides Lepareur, Nicolas Leal E Costa, Loleh Bocqué, Maëva Blondelle, Clément Ruello, Clément Desjulets, Marie Noiret, Nicolas Cammas-Marion, Sandrine Front Med (Lausanne) Medicine INTRODUCTION: Encapsulation of biologically active molecules into nanoparticles (NPs), for site-specific delivery, is a fast growing area. These NPs must be biocompatible, non-toxic, and able to release their load in a controlled way. We have developed a series of NPs based on (bio)degradable and biocompatible poly(malic acid) derivatives, poly(benzyl malate) (PMLABe), with its PEG-grafted stealth analog and target-specific biotin-PEG-b-PMLABe one. A lipophilic radiotracer has then been encapsulated into these NPs. METHODS: Monomers were synthesized from dl-aspartic acid. PEG(42)-b-PMLABe(73) and Biot-PEG(66)-b-PMLABe(73) block copolymers were obtained by anionic ring-opening polymerization of benzyl malolactonate in presence of α-methoxy-ω-carboxy-PEG(42) and α-biotin-ω-carboxy-PEG(66) as initiators. NPs were prepared by nanoprecipitation. Size, polydispersity, and zeta potential were measured by dynamic light scattering (DLS) and zetametry. (99m)Tc-SSS was prepared as previously described. Encapsulation efficacy was assessed by varying different parameters, such as encapsulation with preformed NPs or during their formation, influence of the solvent, and of the method to prepare the NPs. After decay, (99m)Tc-loaded NPs were also analyzed by DLS and zetametry. NPs’ morphology was assessed by transmission electron microscopy. RESULTS: (99m)Tc-SSS was added during nanoprecipitation, using two different methods, to ensure good encapsulation. Radiolabeled NPs present increased diameters, with identical low polydispersity indexes and negative zeta potentials in comparison to non-radiolabeled NPs. CONCLUSION: A radiotracer was successfully encapsulated, but some further optimization is still needed. The next step will be to modify these radiolabeled NPs with a hepatotrope peptide, and to replace (99m)Tc with (188)Re for therapy. Our team is also working on drugs’ encapsulation and grafting of a fluorescent probe. Combining these modalities is of interest for combined chemo-/radiotherapy, bimodal imaging, and/or theranostic approach. Frontiers Media S.A. 2015-09-04 /pmc/articles/PMC4559641/ /pubmed/26389121 http://dx.doi.org/10.3389/fmed.2015.00063 Text en Copyright © 2015 Lepareur, Leal E Costa, Bocqué, Blondelle, Ruello, Desjulets, Noiret and Cammas-Marion. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Lepareur, Nicolas
Leal E Costa, Loleh
Bocqué, Maëva
Blondelle, Clément
Ruello, Clément
Desjulets, Marie
Noiret, Nicolas
Cammas-Marion, Sandrine
Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title_full Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title_fullStr Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title_full_unstemmed Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title_short Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclides
title_sort development of biocompatible and functional polymeric nanoparticles for site-specific delivery of radionuclides
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559641/
https://www.ncbi.nlm.nih.gov/pubmed/26389121
http://dx.doi.org/10.3389/fmed.2015.00063
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