Towards potential nanoparticle contrast agents: Synthesis of new functionalized PEG bisphosphonates

Scholarly Works

• Guedeney, N.; Deschamp, J.; Legigan, T.; Monteil, M.; Migianu-Griffoni, E.; Lecouvey, M. Synthesis of new alendronate analogs for bone-targeted drug delivery strategies. New Journal of Chemistry 2024, 48, 1436–1442. doi:10.1039/d3nj04980a
• Coutant, C.; Fischer, J.; Nun, P.; Coeffard, V. Synthesis of BODIPY Organophotocatalysts by Boron Functionalization with Quinine Derivatives and Applications in Asymmetric Photooxygenation. ChemistrySelect 2023, 8. doi:10.1002/slct.202303316
• Yılmaz, M.; Süer, N. C.; Eren, T.; Akar, A. Alendronic acid bearing acrylic monomer to produce heat resistant polyacrylonitrile copolymer and nanofibers. Polymer-Plastics Technology and Materials 2021, 60, 1833–1844. doi:10.1080/25740881.2021.1934015
• Karpati, S.; Hubert, V.; Hristovska, I.; Lerouge, F.; Chaput, F.; Bretonnière, Y.; Andraud, C.; Banyasz, A.; Micouin, G.; Monteil, M.; Lecouvey, M.; Mercey-Ressejac, M.; Dey, A. K.; Marche, P. N.; Lindgren, M.; Pascual, O.; Wiart, M.; Parola, S. Hybrid multimodal contrast agent for multiscale in vivo investigation of neuroinflammation. Nanoscale 2021, 13, 3767–3781. doi:10.1039/d0nr07026b
• Dussart, J.; Deschamp, J.; Migianu-Griffoni, E.; Lecouvey, M. From Industrial Method to the Use of Silylated P(III) Reagents for the Synthesis of Relevant Phosphonylated Molecules. Organic Process Research & Development 2020, 24, 637–651. doi:10.1021/acs.oprd.9b00490
• Boitard, C.; Curcio, A.; Rollet, A.-L.; Wilhelm, C.; Ménager, C.; Griffete, N. Biological Fate of Magnetic Protein-Specific Molecularly Imprinted Polymers: Toxicity and Degradation. ACS applied materials & interfaces 2019, 11, 35556–35565. doi:10.1021/acsami.9b11717
• Patsula, V.; Horák, D.; Kučka, J.; Macková, H.; Lobaz, V.; Francová, P.; Herynek, V.; Heizer, T.; Paral, P.; Šefc, L. Synthesis and modification of uniform PEG-neridronate-modified magnetic nanoparticles determines prolonged blood circulation and biodistribution in a mouse preclinical model. Scientific reports 2019, 9, 10765. doi:10.1038/s41598-019-47262-w
• Lobaz, V.; Konefał, R.; Pánek, J.; Vlk, M.; Kozempel, J.; Petřík, M.; Novy, Z.; Gurská, S.; Znojek, P.; Štěpánek, P.; Hrubý, M. In Situ In Vivo radiolabeling of polymer-coated hydroxyapatite nanoparticles to track their biodistribution in mice. Colloids and surfaces. B, Biointerfaces 2019, 179, 143–152. doi:10.1016/j.colsurfb.2019.03.057
• Fresnais, J.; Ma, Q.; Thai, L.; Porion, P.; Levitz, P.; Rollet, A.-L. NMR relaxivity of coated and non-coated size-sorted maghemite nanoparticles. Molecular Physics 2018, 117, 990–999. doi:10.1080/00268976.2018.1527410
• Sevrain, C. M.; Berchel, M.; Couthon, H.; Jaffrès, P.-A. Phosphonic acid: Preparation and applications. Beilstein journal of organic chemistry 2017, 13, 2186–2213. doi:10.3762/bjoc.13.219
• Khanal, A.; Fang, S. Solid Phase Stepwise Synthesis of Polyethylene Glycols. Chemistry (Weinheim an der Bergstrasse, Germany) 2017, 23, 15133–15142. doi:10.1002/chem.201703004
• Aufaure, R.; Buendia, R.; Motte, L.; Hardouin, J.; Lalatonne, Y.; Guénin, E. Versatile “click” synthesis of 1-hydroxy-1,1-methylenebisphosphonic acids with thioalkoxy substituents for the preparation of stable gold nanoparticles. New J. Chem. 2017, 41, 12153–12158. doi:10.1039/c7nj02773g
• Chmielewska, E.; Kafarski, P. Synthetic Procedures Leading towards Aminobisphosphonates. Molecules (Basel, Switzerland) 2016, 21, 1474. doi:10.3390/molecules21111474
• Khanal, A. Ph.D. Thesis, Michigan Technological University, . doi:10.37099/mtu.dc.etdr/594

Explore citations to this article at