Sugar/gadolinium-loaded gold nanoparticles for labelling and imaging cells by magnetic resonance imaging

被引:42
作者
Irure, Ainhoa [1 ]
Marradi, Marco [1 ,2 ]
Arnaiz, Blanca [1 ]
Genicio, Nuria [1 ]
Padro, Daniel [3 ]
Penades, Soledad [1 ,2 ]
机构
[1] CIC biomaGUNE, Biofunct Nanomat Unit, Lab Glyconanotechnol, San Sebastian 20009, Spain
[2] Biomed Res Networking Ctr Bioengn Biomat & Nanome, San Sebastian 20009, Spain
[3] CIC biomaGUNE, Mol Imaging Unit, San Sebastian 20009, Spain
关键词
MRI CONTRAST AGENTS; IN-VIVO; DC-SIGN; GADOLINIUM; GLYCONANOPARTICLES; BINDING; DELIVERY; CANCER; T-1; METABOLISM;
D O I
10.1039/c3bm60032g
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Targeted magnetic resonance imaging (MRI) probes for selective cell labelling and tracking are highly desired. We here present biocompatible sugar-coated paramagnetic Gd-based gold nanoparticles (Gd-GNPs) and test them as MRI T-1 reporters in different cellular lines at a high magnetic field (11.7 T). With an average number of 20 Gd atoms per nanoparticle, Gd-GNPs show relaxivity values r(1) ranging from 7 to 18 mM(-1) s(-1) at 1.41 T. The multivalent presentation of carbohydrates on the Gd-GNPs enhances the avidity of sugars for carbohydrate-binding receptors at the cell surface and increases the local concentration of the probes. A large reduction in longitudinal relaxation times T1 is achieved with both fixed cells and live cells. Differences in cellular labelling are obtained by changing the type of sugar on the gold surface, indicating that simple monosaccharides and disaccharides are able to modulate the cellular uptake. These results stress the benefits of using sugars to produce nanoparticles for cellular labelling. To the best of our knowledge this is the first report on labelling and imaging cells with Gd-based gold nanoparticles which use simple sugars as receptor reporters.
引用
收藏
页码:658 / 668
页数:11
相关论文
共 78 条
[41]   CARBOHYDRATE-PROTEIN INTERACTIONS - BASIS OF GLYCOBIOLOGY [J].
LEE, YC ;
LEE, RT .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (08) :321-327
[42]   Paramagnetic gold nanostructures for dual modal bioimaging and phototherapy of cancer cells [J].
Lim, Yong Taik ;
Cho, Mi Young ;
Choi, Bang Sil ;
Lee, Jung Min ;
Chung, Bong Hyun .
CHEMICAL COMMUNICATIONS, 2008, (40) :4930-4932
[43]   Lectins: Carbohydrate-specific proteins that mediate cellular recognition [J].
Lis, H ;
Sharon, N .
CHEMICAL REVIEWS, 1998, 98 (02) :637-674
[44]   HEPATIC RECEPTOR OF AVIAN ORIGIN CAPABLE OF BINDING SPECIFICALLY MODIFIED GLYCOPROTEINS [J].
LUNNEY, J ;
ASHWELL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (02) :341-343
[45]   Bioresponsive, Cell-Penetrating, and Multimeric MR Contrast Agents [J].
Major, Jody L. ;
Meade, Thomas J. .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (07) :893-903
[46]   Glyconanoparticles as multifunctional and multimodal carbohydrate systems [J].
Marradi, Marco ;
Chiodo, Fabrizio ;
Garcia, Isabel ;
Penades, Soledad .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (11) :4728-4745
[47]   GLYCONANOPARTICLES: POLYVALENT TOOLS TO STUDY CARBOHYDRATE-BASED INTERACTIONS [J].
Marradi, Marco ;
Martin-Lomas, Manuel ;
Penades, Soledad .
ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY, VOL 64, 2010, 64 :211-290
[48]   Paramagnetic Gd-based gold glyconanoparticles as probes for MRI: tuning relaxivities with sugars [J].
Marradi, Marco ;
Alcantara, David ;
Martinez de la Fuente, Jesus ;
Luisa Garcia-Martin, Maria ;
Cerdan, Sebastian ;
Penades, Soledad .
CHEMICAL COMMUNICATIONS, 2009, (26) :3922-3924
[49]   Gold Manno-Glyconanoparticies: Multivalent Systems to Block HIV-1 gp120 Binding to the Lectin DC-SIGN [J].
Martinez-Avila, Olga ;
Hijazi, Karolin ;
Marradi, Marco ;
Clavel, Caroline ;
Campion, Colin ;
Kelly, Charles ;
Penades, Soledad .
CHEMISTRY-A EUROPEAN JOURNAL, 2009, 15 (38) :9874-9888
[50]   Cellular Response of Polyvalent Oligonucleotide-Gold Nanoparticle Conjugates [J].
Massich, Matthew D. ;
Giljohann, David A. ;
Schmucker, Abrin L. ;
Patel, Pinal C. ;
Mirkin, Chad A. .
ACS NANO, 2010, 4 (10) :5641-5646