MAGfect: a novel liposome formulation for MRI labelling and visualization of cells

被引:35
作者
Oliver, Morag
Ahmad, Ayesha
Kamaly, Nazila
Perouzel, Eric
Caussin, Annabelle
Keller, Michael
Herlihy, Amy
Bell, Jimmy
Miller, Andrew D.
Jorgensen, Michael R.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Imperial Coll Genet Therapies Ctr, Dept Chem, London SW7 2AZ, England
[2] IC Vec Ltd, London SW7 1NA, England
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Mol Imaging Grp, Imaging Sci Dept,MRC Clin Sci Ctr, London W12 0HS, England
[4] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Biol Imaging Ctr, Imaging Sci Dept,MRC Clin Sci Ctr, London W12 0HS, England
基金
英国医学研究理事会;
关键词
D O I
10.1039/b605394g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cellular entry of imaging probes, such as contrast agents for magnetic resonance imaging (MRI), is a key requirement for many molecular imaging studies, particularly imaging intracellular events and cell tracking. Here, we describe the successful development and in vitro analysis of MAGfect, a novel liposome formulation containing a lipidic gadolinium contrast agent for MRI, Gd-DOTA-Chol 1, designed to enter and label cells. Liposome formulation and cell incubation time were optimised for maximum cellular uptake of the imaging probe in a variety of cell lines. MRI analysis of cells incubated with MAGfect showed them to be highly MRI active. This formulation was examined further for cytotoxicity, cell viability and mechanism of cell labelling. One of the key advantages of using MAGfect as a labelling vehicle arises from its potential for additional functions, such as concomitant drug or gene delivery and fluorescent labelling. The gadolinium liposome was found to be an effective vehicle for transport of plasmid DNA (pDNA) into cells and expression levels were comparable to the commercial transfection agent Trojene(TM).
引用
收藏
页码:3489 / 3497
页数:9
相关论文
共 41 条
[1]   In situ stem cell therapy:: novel targets, familiar challenges [J].
Agrawal, S ;
Schaffer, DV .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (02) :78-83
[2]   Cellular delivery of MRI contrast agents [J].
Allen, MJ ;
MacRenaris, KW ;
Venkatasubramanian, PN ;
Meade, TJ .
CHEMISTRY & BIOLOGY, 2004, 11 (03) :301-307
[3]   Synthesis and visualization of a membrane-permeable MRI contrast agent [J].
Allen, MJ ;
Meade, TJ .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2003, 8 (07) :746-750
[4]  
Bendszus M, 2003, J NEUROSCI, V23, P10892
[5]   Macrocyclic chelators with paramagnetic cations are internalized into mammalian cells via a HIV-tat derived membrane translocation peptide [J].
Bhorade, R ;
Weissleder, R ;
Nakakoshi, T ;
Moore, A ;
Tung, CH .
BIOCONJUGATE CHEMISTRY, 2000, 11 (03) :301-305
[6]   Neurotransplantation of magnetically labeled oligodendrocyte progenitors: Magnetic resonance tracking of cell migration and myelination [J].
Bulte, JWM ;
Zhang, SC ;
van Gelderen, P ;
Herynek, V ;
Jordan, EK ;
Duncan, ID ;
Frank, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15256-15261
[7]   Cell therapy for bone disease: A review of current status [J].
Cancedda, R ;
Bianchi, G ;
Derubeis, A ;
Quarto, R .
STEM CELLS, 2003, 21 (05) :610-619
[8]   DOTAP/DOPE and DC-Chol/DOPE lipoplexes for gene delivery: zeta potential measurements and electron spin resonance spectra [J].
Ciani, L ;
Ristori, S ;
Calamai, L ;
Martini, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1664 (01) :70-79
[9]   Improving lipoplex-mediated gene transfer into C6 glioma cells and primary neurons [J].
da Cruz, MTG ;
Simoes, S ;
de Lima, MCP .
EXPERIMENTAL NEUROLOGY, 2004, 187 (01) :65-75
[10]   Stem cell therapy of the liver - Fusion or fiction? [J].
Dahlke, MH ;
Popp, FC ;
Larsen, S ;
Schlitt, H ;
Rasko, JEJ .
LIVER TRANSPLANTATION, 2004, 10 (04) :471-479