Home
This Title All WIREs
WIREs RSS Feed
How to cite this WIREs title:
WIREs Nanomed Nanobiotechnol
Impact Factor: 4.761

Two decades of dendrimers as versatile MRI agents: a tale with and without metals

Full article on Wiley Online Library:   HTML PDF

Can't access this content? Tell your librarian.

Dendrimers or dendritic polymers are a class of compounds with great potential for nanomedical use. Some of their properties, including their rigidity, low polydispersity and the ease with which their surfaces can be modified make them particularly well suited for use as MRI diagnostic or theranostic agents. For the past 20 years, researchers have recognized this potential and refined dendrimer formulations to optimize these nanocarriers for a host of MRI applications, including blood pool imaging agents, lymph node imaging agents, tumor‐targeted theranostic agents and cell tracking agents. This review summarizes the various types of dendrimers according to the type of MR contrast they can provide. This includes the metallic T1, T2 and paraCEST imaging agents, and the non‐metallic diaCEST and fluorinated (19F) heteronuclear imaging agents.

The first dendrimer platform used as MR contrast agent. (a) General structure of PAMAM‐Gd‐DOTA dendrimers showing a G = 3 PAMAM dendrimer and Gd‐DOTA with linker. (b) The first image acquired with PAMAM Gd‐DOTA dendrimers as MR contrast agent. A Gd‐DOTA‐conjugated G = 6 PAMAM dendrimer, having a half‐life of approximately 200 min, was injected in the left rat at 0.005 mmol Gd kg−1. A clear vascular enhancement can be seen compared with the uninjected rat on the right. (Reprinted with permission from Ref Copyright 1994 John Wiley & Sons, Inc.)
[ Normal View | Magnified View ]
Chronological representation of milestone publications on dendrimer development and their (green) use as MRI agents (red).
[ Normal View | Magnified View ]
Available topologies for synthesizing dendrimers. Shown are representative core and building block topologies (top row), the topology for Generations 1–4 for one core and one building block as present in polyaminoamine (PAMAM) and poly‐L‐lysine (PLL) dendrimers (middle row), and a topology for a dendron, a generalized Janus dendrimer with two dendrons presenting different terminal groups which are grafted to a single core, a Janus dendrimer suitable for self‐assembly into MR dendrisomes, and an MR dendrisome (bottom row).
[ Normal View | Magnified View ]
Building blocks that have been used for production of commercially available dendrimers. These include poly‐L‐lysine (PLL), polyaminoamine (PAMAM), polypropylimine [PPI, also known as diaminobutane (DAB)], 2,2‐bis‐methylolpropionic acid (bis‐MPA), and phenoxymethyl(methylhydrazone) (PMMH).
[ Normal View | Magnified View ]
Two decades of (a) publications and (b) citations on dendrimer MRI agents (Source: ISI Web of Science).
[ Normal View | Magnified View ]
(a) General structure of PAMAM‐SA‐Ac dendrimers showing a G = 3 PAMAM dendrimer, salicylic acid (SA) with linker, and acetyl termination. (B–E) In vivo images of salicylic acid methyl ester (SAME) G = 5 PAMAM dendrimer conjugates infused into a mouse carrying a glioblastoma xenograft. Shown are (b) T2w (arrow highlights tumor) and CEST MR images obtained (c) pre‐ and (d) 30 and (e) 60 min postinjection of a 500 μM solution of diaCEST dendrimer. (Reprinted with permission from Ref Copyright 2016 American Chemical Society)
[ Normal View | Magnified View ]
Structure of magnetodendrimers. Shown is a schematic representation of the stabilization of maghemite nanoparticles by G = 4.5 carboxyl‐terminated PAMAM dendrimers. (Reprinted with permission from Ref Copyright 2001 American Chemical Society)
[ Normal View | Magnified View ]
Variable field relaxometry of a Dy‐DOTA‐conjugated G = 5 PAMAM dendrimer and single Dy(III) chelates. Shown are the T2 relaxivities of (a) Dy‐DOTA‐PAMAM G = 5 dendrimers, (b) Dy‐DOTA single chelates, and (c) Dy‐DTPA single chelates as a function of magnetic field strength. Data are shown at 3 (), 10 (), 20 (), and 37°C (+). Solid lines represent quadratic fits to the equation 1/T2 = a + bB0, with B0 being the external magnetic field strength. For comparison, the T1 relaxivities are negligible, shown as dashed lines at 3 () and 37 C (·). (Reprinted with permission form Ref Copyright 1998 Wolters Kluwer Health)
[ Normal View | Magnified View ]

Browse by Topic

Diagnostic Tools > In Vivo Nanodiagnostics and Imaging
Implantable Materials and Surgical Technologies > Nanomaterials and Implants

Access to this WIREs title is by subscription only.

Recommend to Your
Librarian Now!

The latest WIREs articles in your inbox

Sign Up for Article Alerts

In the Spotlight

Mauro Ferrari

Mauro Ferrari

started out in mechanical engineering and became interested in nanotechnology with his studies on nanomechanics and nanofluidics. His research work and involvement with setting up some of the premier nano centers and alliances in the world, bringing together universities, hospitals, and federal agencies, showcases interdisciplinarity at work.

Learn More