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Near-infrared optical imaging of nucleic acid nanocarriers in vivo.

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  • معلومة اضافية
    • Contributors:
      ANTE-INSERM U836, équipe 5, Neuroimagerie fonctionnelle et perfusion cérébrale; Institut d'oncologie/développement Albert Bonniot de Grenoble (INSERM U823); Université Joseph Fourier - Grenoble 1 (UJF)-Centre Hospitalier Universitaire CHU Grenoble (CHUGA)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Joseph Fourier - Grenoble 1 (UJF)-Centre Hospitalier Universitaire CHU Grenoble (CHUGA)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM); Commissariat à l'énergie atomique et aux énergies alternatives - Laboratoire d'Electronique et de Technologie de l'Information (CEA-LETI); Direction de Recherche Technologique (CEA) (DRT (CEA)); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA); Ingénierie de la vectorisation particulaire; Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM); Centre de recherche en Biologie Cellulaire (CRBM); Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS); Recherche In Vivo; Université Louis Pasteur - Strasbourg I-Polyplus-transfection SA; Université Joseph Fourier - Grenoble 1 (UJF)-Centre Hospitalier Universitaire CHU Grenoble (CHUGA)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM); Université Joseph Fourier
    • بيانات النشر:
      HAL CCSD
      Humana Press
      Humana Press/Springer Imprint
    • الموضوع:
      2013
    • Collection:
      Université de Montpellier: HAL
    • نبذة مختصرة :
      International audience ; Noninvasive, real-time optical imaging methods are well suited to follow the in vivo distribution of nucleic acid nanocarriers, their dissociation, and the resulting gene expression or inhibition. Indeed, most small animal imaging devices perform bioluminescence and fluorescence measurements without moving the animal, allowing a simple, rapid, and cost-effective method of investigation of several parameters at a time, in longitudinal experiments that can last for days or weeks.Here we help the reader in choosing adapted near-infrared (NIR) fluorophores or pairs of fluorophores for Förster resonance energy transfer assays, imaging of reporter genes, as well as nanocarriers for in vivo gene and siRNA delivery. In addition, we present the labeling methods of these macromolecules and of their payload and the protocols to detect them using bioluminescence and NIR fluorescence imaging in mice.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/23070763; inserm-00874399; https://inserm.hal.science/inserm-00874399; https://inserm.hal.science/inserm-00874399/document; https://inserm.hal.science/inserm-00874399/file/ROME_2013_Near-infrared_optical_imaging_AA.pdf; PUBMED: 23070763; PUBMEDCENTRAL: PMC5116057
    • الرقم المعرف:
      10.1007/978-1-62703-140-0_5
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.58B19DE0