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    Porous Porphyrin-Based Organosilica Nanoparticles for NIR Two-Photon Photodynamic Therapy and Gene Delivery in Zebrafish

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    Type
    Article
    Authors
    Mauriello Jimenez, Chiara
    Aggad, Dina
    Croissant, Jonas G.
    Tresfield, Karen
    Laurencin, Danielle
    Berthomieu, Dorothée
    Cubedo, Nicolas
    Rossel, Mireille
    Alsaiari, Shahad K. cc
    Anjum, Dalaver H. cc
    Sougrat, Rachid cc
    Roldan-Gutierrez, Manuel
    Richeter, Sébastien
    Oliviero, Erwan
    Raehm, Laurence
    Charnay, Clarence
    Cattoën, Xavier
    Clément, Sébastien
    Wong Chi Man, Michel
    Maynadier, Marie
    Chaleix, Vincent
    Sol, Vincent
    Garcia, Marcel
    Gary-Bobo, Magali
    Khashab, Niveen M. cc
    Bettache, Nadir
    Durand, Jean-Olivier cc
    KAUST Department
    Advanced Membranes and Porous Materials Research Center
    Biological and Environmental Sciences and Engineering (BESE) Division
    Bioscience Program
    Chemical Science Program
    Electron Microscopy
    Imaging and Characterization Core Lab
    Physical Science and Engineering (PSE) Division
    Smart Hybrid Materials (SHMs) lab
    Date
    2018-03-30
    Online Publication Date
    2018-03-30
    Print Publication Date
    2018-05
    Permanent link to this record
    http://hdl.handle.net/10754/627633
    
    Metadata
    Show full item record
    Abstract
    Periodic mesoporous organosilica nanoparticles emerge as promising vectors for nanomedicine applications. Their properties are very different from those of well-known mesoporous silica nanoparticles as there is no silica source for their synthesis. So far, they have only been synthesized from small bis-silylated organic precursors. However, no studies employing large stimuli-responsive precursors have been reported on such hybrid systems yet. Here, the synthesis of porphyrin-based organosilica nanoparticles from a large octasilylated metalated porphyrin precursor is described for applications in near-infrared two-photon-triggered spatiotemporal theranostics. The nanoparticles display unique interconnected large cavities of 10-80 nm. The framework of the nanoparticles is constituted with J-aggregates of porphyrins, which endows them with two-photon sensitivity. The nanoparticle efficiency for intracellular tracking is first demonstrated by the in vitro near-infrared imaging of breast cancer cells. After functionalization of the nanoparticles with aminopropyltriethoxysilane, two-photon-excited photodynamic therapy in zebrafish is successfully achieved. Two-photon photochemical internalization in cancer cells of the nanoparticles loaded with siRNA is also performed for the first time. Furthermore, siRNA targeting green fluorescent protein complexed with the nanoparticles is delivered in vivo in zebrafish embryos, which demonstrates the versatility of the nanovectors for biomedical applications.
    Citation
    Mauriello Jimenez C, Aggad D, Croissant JG, Tresfield K, Laurencin D, et al. (2018) Porous Porphyrin-Based Organosilica Nanoparticles for NIR Two-Photon Photodynamic Therapy and Gene Delivery in Zebrafish. Advanced Functional Materials: 1800235. Available: http://dx.doi.org/10.1002/adfm.201800235.
    Sponsors
    C.M.J. and D.A. contributed equally to this work. The grant “Chercheur d'Avenir Languedoc-Roussillon” attributed to M.G.-B. and the ANR nanoptPDT are gratefully acknowledged. The authors thank L. Lichon for technical assistance. DFT calculations were performed using HPC resources from the CINES (projects x2016087394 and x2015087394), and from the CALMIP (Grant 2016-[P16042]). The authors thank MRI (Montpellier RIO Imaging platform) for confocal and multiphoton imaging facilities.
    Publisher
    Wiley
    Journal
    Advanced Functional Materials
    DOI
    10.1002/adfm.201800235
    10.1002/adfm.201870143
    Additional Links
    https://onlinelibrary.wiley.com/doi/abs/10.1002/adfm.201800235
    ae974a485f413a2113503eed53cd6c53
    10.1002/adfm.201800235
    Scopus Count
    Collections
    Articles; Biological and Environmental Science and Engineering (BESE) Division; Bioscience Program; Advanced Membranes and Porous Materials Research Center; Imaging and Characterization Core Lab; Physical Science and Engineering (PSE) Division; Chemical Science Program

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