1. The document discusses various nanoparticles (NPs) and their applications in medical imaging techniques such as X-ray CT, PET, and MRI. Gold NPs and iron oxide NPs are highlighted. 2. For MRI, iron oxide NPs can act as contrast agents by enhancing the relaxation of water protons. Superparamagnetic iron oxide NPs consisting of a magnetite or maghemite core coated with dextran or polymers are promising MRI contrast agents. 3. The formation methods of various NPs are described, including controlling size and coating to influence properties like plasma half-life. Cationic liposome coated magnetite NPs have also been investigated for their cell membrane interaction and uptake.

1. 1
Multifunctional NP for Imaging

2. Imaging techniques and related contrast agents
X-ray  Iodinated contrast materials
Au
MRI  Gadolinium-based
Fe-based
19F-based
PET  Radioactively labelled agents (11C, 18F)

3. X-ray CT
CT is ubiquitous in the clinical setting as. The increasing use and
development of micro-CT and hybrid systems that with PET,
MRI.
The most investigated NPs in this field are gold NPs, since they
have large absorption coefficients against the x-ray source used
for CT imaging and may increase the signal-to-noise ratio of the
technique.
To date, different types of gold NPs have been tested in a
preclinical setting as contrast agents for molecular imaging:
nanospheres, nanocages, nanorods and nanoshells. Gold NPs
formulations as an injectable imaging agent have been utilized to
study the distribution in rodent brain ex vivo

4. nanocage
nanosphere
nanorod
nanoshell
Size 4-40 nm

5. PET
The strategy utilized is consisting in incorporating PET emitters
within the components of the NP, or entrapping them within the
core.
brain cancer
Oku et al (2011), Int. J. Pharm. 403 :170–177

6. MRI
MRI relies upon the enhancement of local water proton relaxation in the
presence of a contrast agent (CA). CA are compounds that catalytically shorten
the relaxation times of bulk water protons.
T1 (longitudinal relaxation– in simple terms, the time taken for the protons to
realign with the external magnetic field) Positive CA (Gd)
T2 (transverse relaxation –in simple terms, the time taken for the protons to
exchange energy with other nuclei) Negative CA (Iron oxide agents )

7. Gd-based NP
several nanotechnological approaches have been devised, based on
2 ideas:
-carrying many Gd chelates;
-slow down the rotation of the complex
Examples include liposomes micelles dendrimers fullerenes.
However, this approach has not yet achieved clinical applications.

8. 8
Magnetic Nanoparticles
magnetic NPs (MNPs) are of considerable interest because they
may behave either as contrast agents or carriers for drug
delivery. Among these, the most promising and developed NP
system is represented by superparamagnetic iron oxide agents

9. 9
Types of Magnets
• Ferromagnetic materials: the magnetic moments of
neighboring atoms align resulting in a net magnetic moment.
• Paramagnetic materials are randomly oriented due to Brownian
motion, except in the presence of external magnetic field.
• Superparamagnetic Combination of paramagnetic and ferromagnetic
properties. Made of nano-sized ferrous magnetic particles, but
affected by Brownian Motion. They will align in the presence of an
external magnetic field.

10. The most promising and developed NP system is
represented by superparamagnetic iron oxide
agents, consisting of a magnetite (Fe3O4) and/or
maghemite (Fe2O3) crystalline core surrounded by a
low molecular weight carbohydrate (usually dextran
or carboxydextran) or polymer coat.
. Iron oxide NPs can be classified according to their
core structure, such as Monocrystalline (MION;
10–30 nm diameter), or according to their size as
ultra-small superparamagnetic (USPIO) (20–50 nm
diameter), superparamagnetic (SPIO) (60–250 nm).

11. J Lodhia et al. Biomed Imaging Interv J 2010; 6(2):e12

12. Polymer Coated Magnetite Nanoparticles
Dextran, silane, poly-lactic acid, PEG, dextran, chitosan,
gelatin, ethylcellulose…

13. 13
Formation of Nanoparticles
• Solution of Dextran, FeCl3.6H2O and FeCl2.4H2O (acidic
solution)
– Less Dextran Larger Particles
• Drip in Ammonium hydroxide (basic) at ~2oC
• Stirred at 75oC for 75 min.
• Purified by washing and
ultra-centrifugation
• Resulting Size ~ 10-20 nm
• Plasma half-life: 200 min

14. Variation of Formation
• Change Coating Material
• Crosslinking coating material
– Increases plasma half-life
– Same Particle Size
Lee H et al. J. AM. CHEM. SOC. 2007,129, 1273-12745

15. • Why Cationic?
– Interaction between + liposome and – cell
– membrane results in 10x uptake.
Magnetite Cationic Liposomes (MCL)
Fe3O4

16. Formation of MCL
• magnetite NP dispersed in distilled water
• N-(a-trimethyl-amminoacetyl)-didodecyl-D-glutamate
chloride (TMAG) Dilauroylphosphatidylcholine (DLPC)
Dioleoylphosphatidyl-ethanolamine (DOPE) added to
dispersion at ratio of 1:2:2
• Stirred and sonicated for 15 min
• pH raised to 7.4 by NaCl and Na phosphate buffered and
then sonicated
DLPC
DOPE