ライフサイエンスコーパス: ferumoxides

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1 um (50 mumol/kg) and then, 45 minutes later, ferumoxides (10 mumol/kg).

2 was virtually the same but was impaired with ferumoxides (-43%).

3 d Drug Administration (FDA)-approved agents, ferumoxides, a suspension of dextran-coated SPIO used as

4 56 mg of iron per kilogram of body weight of ferumoxides administered during 2 minutes (2 mL/min) or

5 (MR) imaging information was obtained after ferumoxides administration (P =.67).

6 tly improved by adding images obtained after ferumoxides administration to the images obtained before

7 n mesenchymal stem cells doubly labeled with ferumoxides and beta-galactosidase and injected intramyo

8 Three TAs were incubated with ferumoxides and MION-46L in cell culture medium at vario

9 etic labeling of mammalian cells with use of ferumoxides and TAs is possible and may enable cellular

10 superparamagnetic iron oxide nanoparticles (Ferumoxides) complexed to poly-L-Lysine (FE-PLL).

11 Various concentrations of ferumoxides (FE)-poly-l-lysine (PLL) complexes were used

12 PLL was incubated with ferumoxides for 60 minutes, incompletely coating the sup

13 Direct injection of ferumoxides has safety and effectiveness profiles simila

14 rther findings indicate that the addition of ferumoxides increases the sensitivity and specificity of

15 s after injection of syngeneic or xenogeneic ferumoxides-labeled stem cells (cardiac-derived stem cel

16 uptake was observed for cells incubated with ferumoxides or MION-46L alone.

17 EOB-DTPA [a hepatocyte-directed agent], and ferumoxides, or superpara-magnetic iron oxide particles

18 Administration of neither labeled MSCs nor ferumoxides-PLL complex had a significant effect on hema

19 les were stained with Prussian blue when the ferumoxides-PLL complex had magnetically labeled the hum

20 Magnetic cellular labeling with the ferumoxides-PLL complex had no short- or long-term toxic

21 ing cells that are magnetically labeled with ferumoxides-PLL complex into rats does not alter biochem

22 (group 2) received intravenous injections of ferumoxides-PLL complex only.

23 Cells were coincubated overnight with the ferumoxides-PLL complex, and iron uptake, cell viability

24 bin concentrations in the rats injected with ferumoxides-PLL complex, varied significantly during the

25 mouse Sca1+ cells were labeled in vitro with ferumoxides-poly-L-lysine complexes.

26 +) stem cells and other mammalian cells with ferumoxides-protamine sulfate complexes (FE-Pro), cellul

27 signal, for example, macrophages containing ferumoxides released from nonsurviving cells, has not be

28 Iron concentrations varied with ferumoxides-TA combinations and cells with a maximum of

29 When ferumoxides-TA or MION-46L-TA was used, intracytoplasmic

30 tic acid disodium was reduced (57%) but with ferumoxides was excellent (-55%).

31 cells labeled with a combination of TAs and ferumoxides were evaluated.

32 ment values with gadoxetic acid disodium and ferumoxides were excellent in the normal liver model (17

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