TY - JOUR
T1 - Magnetic resonance and fluorescence imaging of doxorubicin-loaded nanoparticles using a novel in vivo model
AU - Erten, Ahmet
AU - Wrasidlo, Wolf
AU - Scadeng, Miriam
AU - Esener, Sadik
AU - Hoffman, Robert M.
AU - Bouvet, Michael
AU - Makale, Milan
PY - 2010/12
Y1 - 2010/12
N2 - We report here the in vivo combined-modality imaging of multifunctional drug delivery nanoparticles. These dextran core-based stealth liposomal nanoparticles (nanosomes) contained doxorubicin, iron oxide for magnetic resonance imaging (MRI) contrast, and BODIPY for fluorescence. The particles were long-lived in vivo because of surface decoration with polyethylene glycol and the incorporation of acetylated lipids that were ultraviolet cross-linked for physical stability. We developed a rodent dorsal skinfold window chamber that facilitated both MRI and non-invasive optical imaging of nanoparticle accumulation in the same tumors. Chamber tumors were genetically labeled with DsRed-2, which enabled co-localization of the MR images, the red fluorescence of the tumor, and the blue fluorescence of the nanoparticles. The nanoparticle design and MR imaging developed with the window chamber were then extended to orthotopic pancreatic tumors expressing DsRed-2. The tumors were MR-imaged using iron oxide-dextran liposomes and by fluorescence to demonstrate the deep imaging capability of these nanoparticles. From the Clinical Editor: In vivo combined-modality imaging of multifunctional drug delivery nanoparticles is discussed in this proof of principle paper.
AB - We report here the in vivo combined-modality imaging of multifunctional drug delivery nanoparticles. These dextran core-based stealth liposomal nanoparticles (nanosomes) contained doxorubicin, iron oxide for magnetic resonance imaging (MRI) contrast, and BODIPY for fluorescence. The particles were long-lived in vivo because of surface decoration with polyethylene glycol and the incorporation of acetylated lipids that were ultraviolet cross-linked for physical stability. We developed a rodent dorsal skinfold window chamber that facilitated both MRI and non-invasive optical imaging of nanoparticle accumulation in the same tumors. Chamber tumors were genetically labeled with DsRed-2, which enabled co-localization of the MR images, the red fluorescence of the tumor, and the blue fluorescence of the nanoparticles. The nanoparticle design and MR imaging developed with the window chamber were then extended to orthotopic pancreatic tumors expressing DsRed-2. The tumors were MR-imaged using iron oxide-dextran liposomes and by fluorescence to demonstrate the deep imaging capability of these nanoparticles. From the Clinical Editor: In vivo combined-modality imaging of multifunctional drug delivery nanoparticles is discussed in this proof of principle paper.
KW - Dorsal skinfold window chamber
KW - MRI
KW - Multifunctional nanoparticle
UR - http://www.scopus.com/inward/record.url?scp=78649844305&partnerID=8YFLogxK
U2 - 10.1016/j.nano.2010.06.005
DO - 10.1016/j.nano.2010.06.005
M3 - Article
C2 - 20599526
AN - SCOPUS:78649844305
SN - 1549-9634
VL - 6
SP - 797
EP - 807
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
IS - 6
ER -