TY - GEN
T1 - Targeted MRI and optical molecular imaging using gadolinium loaded small unilamellar vesicles
AU - Iqbal, Umar
AU - Albaghdadi, Homam
AU - Nieh, Mu Ping
AU - Tuor, Ursula I.
AU - Mester, Zoltan
AU - Stanimirovic, Danica
AU - Katsaras, John
AU - Abulrob, Abedelnasser
N1 - Publisher Copyright:
© (2011) by AIChE All rights reserved.
PY - 2011
Y1 - 2011
N2 - Noninvasive investigation of cellular and molecular processes becomes possible through the novel techniques, one of which is molecular imaging, where enhanced sensitivity is a key component for clinic translation of the technique. In this presentation, spontaneously forming, small unilamellar vesicles (ULVs) (30 nm in diameter) were used as a platform to build a bi-modal [i.e., optical and Magnetic Resonance Imaging (MRI)] targeted contrast agent for the molecular imaging of brain tumors. Small ULVs were loaded with a gadolinium (Gd) chelated lipid (Gd-DPTA-BOA), functionalized with targeting antibodies (anti-EGFR monoclonal and anti-IGFBP7 single domain), and incorporated a near infrared dye (Cy5.5). The resultant ULVs were characterized in vitro using small angle neutron scattering (SANS), in phantom MRI and dynamic light scattering (DLS). Targeted (with antibodies) and nontargeted-Gd loaded sULVs labeled with Cy5.5 were assessed in vivo in a mice brain tumor model using both optical imaging and MRI. The results demonstrated that a spontaneously forming, nanosized ULV loaded with a high payload of Gd can selectively target and image, using MR and optical imaging, brain tumor vessels when functionalized with antibodies. The unique features of these targeting ULVs make them promising molecular MRI contrast agents.
AB - Noninvasive investigation of cellular and molecular processes becomes possible through the novel techniques, one of which is molecular imaging, where enhanced sensitivity is a key component for clinic translation of the technique. In this presentation, spontaneously forming, small unilamellar vesicles (ULVs) (30 nm in diameter) were used as a platform to build a bi-modal [i.e., optical and Magnetic Resonance Imaging (MRI)] targeted contrast agent for the molecular imaging of brain tumors. Small ULVs were loaded with a gadolinium (Gd) chelated lipid (Gd-DPTA-BOA), functionalized with targeting antibodies (anti-EGFR monoclonal and anti-IGFBP7 single domain), and incorporated a near infrared dye (Cy5.5). The resultant ULVs were characterized in vitro using small angle neutron scattering (SANS), in phantom MRI and dynamic light scattering (DLS). Targeted (with antibodies) and nontargeted-Gd loaded sULVs labeled with Cy5.5 were assessed in vivo in a mice brain tumor model using both optical imaging and MRI. The results demonstrated that a spontaneously forming, nanosized ULV loaded with a high payload of Gd can selectively target and image, using MR and optical imaging, brain tumor vessels when functionalized with antibodies. The unique features of these targeting ULVs make them promising molecular MRI contrast agents.
UR - http://www.scopus.com/inward/record.url?scp=85054613506&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:85054613506
SN - 9781618397416
T3 - Nanoscale Science and Engineering Forum - Core Programming Topic at the 2011 AIChE Annual Meeting
SP - 245
EP - 253
BT - Nanoscale Science and Engineering Forum - Core Programming Topic at the 2011 AIChE Annual Meeting
PB - AIChE
T2 - Nanoscale Science and Engineering Forum - Core Programming Topic at the 2011 AIChE Annual Meeting
Y2 - 16 October 2011 through 21 October 2011
ER -