Tumor-Homing Glycol Chitosan-Based Optical/PET Dual Imaging Nanoprobe for Cancer Diagnosis

Authors
Lee, SangminKang, Sun-WoongRyu, Ju HeeNa, Jin HeeLee, Dong-EunHan, Seung JinKang, Choong MoChoe, Yearn SeongLee, Kyo ChulLeary, James F.Choi, KuiwonLee, Kyung-HanKim, Kwangmeyung
Issue Date
2014-03
Publisher
AMER CHEMICAL SOC
Citation
BIOCONJUGATE CHEMISTRY, v.25, no.3, pp.601 - 610
Abstract
Imaging techniques including computed tomography, magnetic resonance imaging, and positron emission tomography (PET) offer many potential benefits to diagnosis and treatment of cancers. Each method has its own strong and weak points. Therefore, multimodal imaging techniques have been highlighted as an alternative method for overcoming the limitations of each respective imaging method. In this study, we fabricated PET/optical activatable imaging probe based on glycol chitosan nanoparticles (GNPs) for multimodal imaging. To prepare the dual PET/optical probes based on CNPs, both Cu-64 radiolabeled DOTA complex and activatable matrix metalloproteinase (MMP)-sensitive peptide were chemically conjugated onto azide-functionalized CNPs via bio-orthogonal click chemistry, which was a reaction between azide group and dibenzyl cyclooctyne. The PET/optical activatable imaging probes were visualized by PET and optical imaging system. Biodistribution of probes and activity of MNIP were successfully measured in tumor-bearing mice.
Keywords
FREE CLICK CHEMISTRY; MATRIX METALLOPROTEINASES; IN-VIVO; MULTIFUNCTIONAL NANOPARTICLES; CATHEPSIN-B; REAL-TIME; DELIVERY; THERAPY; PARTICLES; MICROPET; FREE CLICK CHEMISTRY; MATRIX METALLOPROTEINASES; IN-VIVO; MULTIFUNCTIONAL NANOPARTICLES; CATHEPSIN-B; REAL-TIME; DELIVERY; THERAPY; PARTICLES; MICROPET
ISSN
1043-1802
URI
https://pubs.kist.re.kr/handle/201004/127029
DOI
10.1021/bc500020g
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KIST Article > 2014
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