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GadoSpin™ MRI agents GadoSpin™ MRI agents
FeraSpin™ MRI agents FeraSpin™ MRI agents
FeraTrack™ MRI contrast agent kits FeraTrack™ MRI contrast agent kits
ExiTron™ CT agents ExiTron™ CT agents
PolySon™ ultrasound agents PolySon™ ultrasound agents
NiraWave™ optical agents NiraWave™ optical agents
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FeraSpin™ Series XS-XXL, MRI contrast agents
Description
The FeraSpin Series is derived from FeraSpin R contrast agents, is a product family of six size-selected iron oxide particles with well-defined particle sizes from 10 to 100 nm. Their identical chemical composition and ultra-narrow size distribution allow for fine-tuning of the pharmacologic profile according to specific applications. FeraSpin nanoparticles are well suited for sequence development, MR physics and nanoparticle physiology studies.
Details
The FeraSpin Series comprises six superparamagnetic iron oxide (SPIO) and undltrasmall (USPIO) particles specifically formulated for pre-clinical magnetic resonance imaging (MRI): FeraSpin XS, FeraSpin S, FeraSpin M, FeraSpin L, FeraSpin XL, and FeraSpin XXL. Their well-defined sizes allow for MRI studies that rely on specific particle sizes.
FeraSpin XS to XXL are agents of high relaxivity and enhance the contrast in T1- as well as T2- and T2*-weighted MRI. The T2 effect increases with increasing particle size whereas the T1 effect increases with decreasing particle size. Upon accumulation in cells, the T1 effect diminishes and the T2 effect increases.

Upon intravenous injection, all agents of this series circulate in the bloodstream and are taken up by macrophages. They accumulate in the liver and spleen and are degraded within a few days. The iron is transferred into the physiological iron stores.
Uptake by macrophages depends on the particle size. Uptake by the Kupffer cells (macrophages of the liver) increases with particle size, thus leading to rapid accumulation in the liver and spleen and a short blood circulation time. With decreasing particle size, the uptake by the Kupffer cells is reduced, leading to a prolonged circulation time and increased uptake by other macrophages.

FeraSpin XS shows the longest blood circulation time among the FeraSpin products and therefore is particularly suited for vascular studies. This USPIO particle has the highest T1 effect and is specifically formulated for magnetc resonance angiography (MRA).
Disclaimer
For laboratory and animal research use only.
Warning: Not for human or animal therapeutic or diagnostic use.
Make sure to comply with all laws and regulations governing research on animals.
 
Figure 1
Characteristics of the FeraSpin™ Series in dependence of particle size.
Figure 2
Schematic diagram of small, medium, and large-sized nanoparticles of the FeraSpin™ Series.
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Details
Products
FeraSpin XS
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-140
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-141
Qty.:
 

FeraSpin S
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-166
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-167
Qty.:
 

FeraSpin M
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-168
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-169
Qty.:
 

FeraSpin L
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-170
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-171
Qty.:
 

FeraSpin XL
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-172
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-173
Qty.:
 

FeraSpin XXL
- 5 injections (1)
Components
- 1 vial
Download datasheet
130-095-174
Qty.:
 

- 25 injections (1)
Components
- 5 vials
Download datasheet
130-095-175
Qty.:
 

(1) One vial contains 850 μL of imaging agent, sufficient for 5 injections of the recommended volume of 100 μL (for a 20–30 g mouse).
Related products
FeraSpin™ R, MRI contrast agent
GadoSpin™ gadolinium chelate MRI agents
References
1. Lohrke et. al. (2008) Nanomedicine 3: 437–452.
2. Allkemper, T. et al. (2002) Radiology 223: 432–438.
3. Tsuda, N. et al. (2005) Invest. Radiol. 40: 676–681.
4. Metz, S. et al. (2004) Eur. Radiol. 14: 1851–1858.
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