Multifunctional gadolinium-based dendritic macromolecules as liver targeting imaging probes

被引:58
作者
Luo, Kui [1 ]
Liu, Gang [1 ]
He, Bin [1 ]
Wu, Yao [1 ]
Gong, Qingyong [2 ]
Song, Bin [2 ]
Ai, Hua [1 ,2 ]
Gu, Zhongwei [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Peoples R China
[2] Sichuan Univ, Dept Radiol, W China Hosp, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Dendritic macromolecules; Gadolinium; Contrast agent; MRI; Liver probes; MRI CONTRAST AGENTS; MODALITY MAGNETIC-RESONANCE; IN-VITRO; ANTISENSE OLIGONUCLEOTIDES; DENDRIMERS; DELIVERY; NANOPARTICLES; CLUSTERS; CORES; ACID;
D O I
10.1016/j.biomaterials.2010.12.049
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The quest for highly efficient and safe contrast agents has become the key factor for successful application of magnetic resonance imaging (MRI). The gadolinium (Gd) based dendritic macromolecules, with precise and tunable nanoscopic sizes, are excellent candidates as multivalent MRI probes. In this paper, a novel series of Gd-based multifunctional peptide dendritic probes (generation 2, 3, and 4) possessing highly controlled structures and single molecular weight were designed and prepared as liver MRI probes. These macromolecular Gd-ligand agents exhibited up to 3-fold increase in T-1 relaxivity comparing to Gd-DTPA complexes. No obvious in vitro cytotoxicity was observed from the measured concentrations. These dendritic probes were further functionalized with multiple galactosyl moieties and led to much higher cell uptake in vitro as demonstrated in T-1-weighted scans. During in vivo animal studies, the probes provided better signal intensity (SI) enhancement in mouse liver, especially at 60 min post-injection, with the most efficient enhancement from the galactosyl moiety decorated third generation dendrimer. The imaging results were verified with analysis of Gd content in liver tissues. The design strategy of multifunctional Gd-ligand peptide dendritic macromolecules in this study may be used for developing other sensitive MRI probes with targeting capability. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2575 / 2585
页数:11
相关论文
共 50 条
[11]   Dendrimer biocompatibility and toxicity [J].
Duncan, R ;
Izzo, L .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) :2215-2237
[12]  
Dykes GM, 2001, CHEM-EUR J, V7, P4730, DOI 10.1002/1521-3765(20011105)7:21<4730::AID-CHEM4730>3.0.CO
[13]  
2-A
[14]   Cascade polymeric MRI contrast media derived from poly(ethylene glycol) cores: Initial syntheses and characterizations [J].
Fu, Yanjun ;
Raatschen, Hans-Juergen ;
Nitecki, Danute E. ;
Wendland, Michael F. ;
Novikov, Viktor ;
Fournier, Laure S. ;
Cyran, Clemens ;
Rogut, Victor ;
Shames, David M. ;
Brasch, Robert C. .
BIOMACROMOLECULES, 2007, 8 (05) :1519-1529
[15]   Synthesis of cyclodextrin-based carbohydrate clusters by photoaddition reactions [J].
Fulton, DA ;
Stoddart, JF .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (25) :8309-8319
[16]   Neoglycoconjugates based on cyclodextrins and calixarenes [J].
Fulton, DA ;
Stoddart, JF .
BIOCONJUGATE CHEMISTRY, 2001, 12 (05) :655-672
[17]   Classification and basic properties of contrast agents for magnetic resonance imaging [J].
Geraldes, Carlos F. G. C. ;
Laurent, Sophie .
CONTRAST MEDIA & MOLECULAR IMAGING, 2009, 4 (01) :1-23
[18]   Targeted intracellular codelivery of chemotherapeutics and nucleic acid with a well-defined dendrimer-based nanoglobular carrier [J].
Kaneshiro, Todd L. ;
Lu, Zheng-Rong .
BIOMATERIALS, 2009, 30 (29) :5660-5666
[19]   Synthesis and Evaluation of Globular Gd-DOTA-Monoamide Conjugates with Precisely Controlled Nanosizes for Magnetic Resonance Angiography [J].
Kaneshiro, Todd Lyle ;
Jeong, Eun-Kee ;
Morrell, Glen ;
Parker, Dennis L. ;
Lu, Zheng-Rong .
BIOMACROMOLECULES, 2008, 9 (10) :2742-2748
[20]   A specific tumor-targeting magnetofluorescent nanoprobe for dual-modality molecular imaging [J].
Ke, Jyun-Han ;
Lin, Jia-Jyun ;
Carey, James R. ;
Chen, Jenn-Shing ;
Chen, Chiao-Yun ;
Wang, Li-Fang .
BIOMATERIALS, 2010, 31 (07) :1707-1715