Research Topics
| Zibo LiSummaryAffiliation: University of Southern California Country: USA Publications
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Detail Information
Publications
Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probesZibo Li
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles 90033, USA
Chem Commun (Camb) 46:8043-5. 2010..The reaction proceeds with exceptionally fast rates, making it an effective conjugation method within seconds at low micromolar concentrations...
Rapid aqueous [18F]-labeling of a bodipy dye for positron emission tomography/fluorescence dual modality imagingZibo Li
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles 90033, USA
Chem Commun (Camb) 47:9324-6. 2011..This radiolabeled dye, whose biodistribution and clearance has been studied in mice, is stable in vivo and can be used as a positron emission tomography/fluorescence dual modality imaging agent...
Evaluation of copper-64 labeled AmBaSar conjugated cyclic RGD peptide for improved microPET imaging of integrin alphavbeta3 expressionHancheng Cai
Molecular Imaging Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA
Bioconjug Chem 21:1417-24. 2010..The AmBaSar chelator will also have general applications for (64)Cu labeling of various bioactive molecules in high radiochemical yield and high in vivo stability...
Design, synthesis and validation of integrin α2β1-targeted probe for microPET imaging of prostate cancerChiun Wei Huang
Department of Radiology, University of Southern California, 1510 San Pablo Street, Los Angeles, CA 90033, USA
Eur J Nucl Med Mol Imaging 38:1313-22. 2011..In this study, (64)Cu-labeled integrin α(2)β(1)-targeted PET probes were designed and evaluated for the imaging of prostate cancer...
Novel α(2)β(1) integrin-targeted peptide probes for prostate cancer imagingChiun Wei Huang
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles, CA 90033, USA
Mol Imaging 10:284-94. 2011..In vitro and in vivo localization demonstrated the potential of this agent to identify tumor subtypes amenable to anti-α(2)β(1) integrin treatment and potentially provide prognostic information regarding tumor progression...
Efficient construction of PET/fluorescence probe based on sarcophagine cage: an opportunity to integrate diagnosis with treatmentShuanglong Liu
Department of Radiology, Keck School of Medicine, Molecular Imaging Center, University of Southern California, Los Angeles, CA 90033, USA
Mol Imaging Biol 14:718-24. 2012....
In vivo near-infrared fluorescence imaging of integrin α2β1 in prostate cancer with cell-penetrating-peptide-conjugated DGEA probeChiun Wei Huang
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles, California 90033, USA
J Nucl Med 52:1979-86. 2011..Here, we aimed to further improve the targeting efficacy of this peptide by incorporating a series of cell-penetrating peptides (CPPs) into the DGEA sequence...
Targeting the EphB4 receptor for cancer diagnosis and therapy monitoringDan Li
Department of Radiology, Molecular Imaging Center, University of Southern California, Los Angeles, California 90033, United States
Mol Pharm 10:329-36. 2013....
Biological stability evaluation of the α2β1 receptor imaging agents: diamsar and DOTA conjugated DGEA peptideChiun Wei Huang
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles, California 90033, United States
Bioconjug Chem 22:256-63. 2011..Free carboxyl groups may naturally compete with DOTA for (64)Cu(2+) binding and therefore reduce the complex stability...
The efficient synthesis and biological evaluation of novel bi-functionalized sarcophagine for (64)cu radiopharmaceuticalsShuanglong Liu
1 Department of Radiology, Keck School of Medicine, Molecular Imaging Center, University of Southern California, Los Angeles, CA 90033, USA
Theranostics 2:589-96. 2012..Conclusion Three novel chelators with two functional groups have been developed based on Sarcophagine cage. The platform developed in this study could have broad applications in the design and synthesis of( 64)Cu-radiopharmaceuticals...
The improved syntheses of 5-substituted 2'-[18F]fluoro-2'-deoxy-arabinofuranosyluracil derivatives ([18F]FAU, [18F]FEAU, [18F]FFAU, [18F]FCAU, [18F]FBAU and [18F]FIAU) using a multistep one-pot strategyHancheng Cai
Department of Radiology, Molecular Imaging Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA
Nucl Med Biol 38:659-66. 2011..In this study, we studied the feasibility of radiosynthesizing [(18)F]FAU, [(18)F]FEAU, [(18)F]FFAU, [(18)F]FCAU, [(18)F]FBAU and [(18)F]FIAU using this newly developed method...
(64)Cu labeled AmBaSar-RGD2 for micro-PET imaging of integrin αvβ3 expressionHancheng Cai
Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, California 90033, USA
Curr Radiopharm 4:68-74. 2011..Therefore, the new tracer 64Cu-AmBaSar- RGD2 exhibited better tumor-targeting efficacy and more favorable in vivo pharmacokinetics than the 64Cu labeled RGD monomer due to the polyvalency effect...
Trackable and Targeted Phage as Positron Emission Tomography (PET) Agent for Cancer ImagingZibo Li
1 Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles 90033, USA
Theranostics 1:371-80. 2011....
[18F]-2'-Fluoro-5-methyl-1-beta-D-arabinofuranosyluracil (18F-FMAU) in prostate cancer: initial preclinical observationsHossein Jadvar
Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA
Mol Imaging 11:426-32. 2012..Our initial preclinical observations suggest that there may be an association between androgen signaling and thymidine metabolism and that (18)F-FMAU PET may be useful in prostate tumor characterization...
An improved synthesis and biological evaluation of a new cage-like bifunctional chelator, 4-((8-amino-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane-1-ylamino)methyl)benzoic acid, for 64Cu radiopharmaceuticalsHancheng Cai
Molecular Imaging Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA
Nucl Med Biol 37:57-65. 2010..Here we report the improved synthesis of AmBaSar, (64)Cu(2+) labeling conditions and its biological evaluation compared with the known BFC 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid (DOTA)...
Radioactive smart probe for potential corrected matrix metalloproteinase imagingChiun Wei Huang
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles, CA 90033, USA
Bioconjug Chem 23:2159-67. 2012..This approach provides an attractive new strategy for accurate imaging of MMP activity, which may also be applied for other protease imaging...
Microwave-assisted one-pot radiosynthesis of 2'-deoxy-2'-[18F]fluoro-5-methyl-1-β-d-arabinofuranosyluracil ([18F]-FMAU)Kai Chen
Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033 9061, USA
Nucl Med Biol 39:1019-25. 2012..In this study, we investigated the efficiency of microwave-assisted radiosynthesis of [(18)F]-FMAU in comparison with conventional thermal conditions...
Improved synthesis of 2'-deoxy-2'-[18F]fluoro-5-methyl-1-β-D-arabinofuranosyluracil ([18F]FMAU)Zibo Li
Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA
Curr Radiopharm 4:24-30. 2011..In this study, we report the use of Friedel-Crafts catalysts for an improved synthesis of [18F]FMAU, which also includes a significantly simplified one-pot reaction condition...
Automated synthesis of 2'-deoxy-2'-[18F]fluoro-5-methyl-1-β-D-arabinofuranosyluracil ([18F]-FMAU) using a one reactor radiosynthesis moduleZibo Li
Department of Radiology, Keck School of Medicine, Molecular Imaging Center, University of Southern California, Los Angeles, CA 90033, USA
Nucl Med Biol 38:201-6. 2011..The overall reaction time was about 150 min from the end of bombardment and the radiochemical purity was >99%. This automated synthesis should also be suitable for the production of other 5-substituted thymidine analogues...
Radiopharmaceutical chemistry for positron emission tomographyZibo Li
Molecular Imaging Center, Department of Radiology, University of Southern California, Los Angeles, CA 90033, United States
Adv Drug Deliv Rev 62:1031-51. 2010..4min), ¹³N (t₁(/)₂=9.9min), ¹⁵O (t₁(/)₂=2min), ⁶⁸Ga (t₁(/)₂=68min), ¹⁸F (t₁(/)₂=109.8min), ⁶⁴Cu (t₁(/)₂=12.7h), and ¹²⁴I (t₁(/)₂=4.12d)...
