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5th EuropEan MolEcular IMagIng MEEtIng - ESMI

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<strong>5th</strong> <strong>EuropEan</strong> <strong>MolEcular</strong> <strong>IMagIng</strong> <strong>MEEtIng</strong> – EMIM2010<br />

Lanthanide-based in vivo luminescence imaging<br />

Petoud S. .<br />

CNRS, France<br />

spetoud@pitt.edu<br />

Introduction: Fluorescence and luminescence<br />

are detection techniques that possess important<br />

advantages for bioanalytical applications and<br />

biologic imaging: high sensitivity, versatility and<br />

low costs of instrumentation. A common characteristic<br />

of biologic analytes is their presence in<br />

small quantities among complex matrices such as<br />

blood, cells, tissue and organs. These matrices<br />

emit significant background fluorescence (autofluorescence),<br />

limiting detection sensitivity.<br />

The luminescence of lanthanide cations has several<br />

complementary advantages over the fluorescence<br />

of organic fluorophores and semiconductor<br />

nanocrystals, such as sharp emission bands for<br />

spectral discrimination from background emission,<br />

long luminescence lifetimes for temporal<br />

discrimination and strong resistance to photobleaching.<br />

In addition, several lanthanides emit<br />

near-infrared (NIR) photons that can cross deeply<br />

into tissues for non-invasive investigations and<br />

that result in improved detection sensitivity due<br />

to the absence of native NIR luminescence from<br />

tissues and cells. The main requirement to obtain<br />

lanthanide emission is to sensitize them with an<br />

appropriate chromophore.<br />

Methods: An innovative concept for such sensitization<br />

of lanthanide cations is proposed herein;<br />

the current limitation of low quantum yields<br />

experienced by most mononuclear lanthanide<br />

complexes is compensated for by using larger<br />

numbers of lanthanide cations and by maximizing<br />

the absorption of each discrete molecule,<br />

thereby increasing the number of emitted photons<br />

per unit of volume and the overall sensitivity<br />

of the measurement. To apply this concept, we<br />

are developing a family of dendrimer-naphthalimide<br />

ligands that are able to incorporate several<br />

lanthanide cations. Polyamidoamine (PAMAM)<br />

dendrimers have been chosen as a basis for these<br />

complexes because the oxygen atoms of the amido<br />

groups located along their branches can bind<br />

and protect the lanthanide cations inside the<br />

dendrimer core.1,2 Derivatives of naphthalimide<br />

groups, required for the sensitization of the lanthanide<br />

cations, are located at the branch termini.<br />

Our synthetic approach allows facile modification<br />

of the dendrimer complex for control over<br />

photophysical properties and solubility. It also<br />

provides for the attachment of different types<br />

of targeting agents such as peptides, oligonucleotides<br />

or proteins, as well as other sensing agents,<br />

to provide functionality to these compounds in a<br />

broad range of applications.<br />

Results: In this paper, we will describe several<br />

examples of luminescent polymetallic lanthanide<br />

complexes based on dendrimers. We will also<br />

present examples of their applications as reporters<br />

and sensors for biologic imaging in living cells<br />

and small animals.<br />

References:<br />

1. J. P. Cross, M. Lauz, P. D. Badger, S. Petoud, Journal of<br />

the American Chemical Society, 2004, 126, 16278.<br />

2. D. R. Kauffman, C. M. Shade, H. Uh, A. Star and S. Petoud,<br />

Nature Chemistry 2009, 1, 500.<br />

<strong>EuropEan</strong> SocIEty for <strong>MolEcular</strong> <strong>IMagIng</strong> – <strong>ESMI</strong><br />

day1<br />

Parallel Session 4: PROBES - supported by COST

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