Polymeric liposomes-coated superparamagnetic iron oxide nanoparticles as contrast agent for targeted magnetic resonance imaging of cancer cells

The purpose of this study was to use polymeric liposomes (PLs) with a targeting ligand (folate) to coat superparamagnetic iron oxide nanoparticles (SPIONs) and transfer the magnetic nanoparticles from organic phases to aqueous solutions, and further evaluate their efficacy as a magnetic resonance im...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 27(2011), 6 vom: 15. März, Seite 3100-5
1. Verfasser: Liao, Zhenyu (VerfasserIn)
Weitere Verfasser: Wang, Hanjie, Lv, Ruichun, Zhao, Peiqi, Sun, Xuezeng, Wang, Sheng, Su, Wenya, Niu, Ruifang, Chang, Jin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Contrast Media Liposomes Magnetite Nanoparticles Polymers
LEADER 01000naa a22002652 4500
001 NLM206061188
003 DE-627
005 20231223235125.0
007 cr uuu---uuuuu
008 231223s2011 xx |||||o 00| ||eng c
024 7 |a 10.1021/la1050157  |2 doi 
028 5 2 |a pubmed24n0687.xml 
035 |a (DE-627)NLM206061188 
035 |a (NLM)21341768 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Liao, Zhenyu  |e verfasserin  |4 aut 
245 1 0 |a Polymeric liposomes-coated superparamagnetic iron oxide nanoparticles as contrast agent for targeted magnetic resonance imaging of cancer cells 
264 1 |c 2011 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 21.10.2014 
500 |a Date Revised 19.11.2015 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a The purpose of this study was to use polymeric liposomes (PLs) with a targeting ligand (folate) to coat superparamagnetic iron oxide nanoparticles (SPIONs) and transfer the magnetic nanoparticles from organic phases to aqueous solutions, and further evaluate their efficacy as a magnetic resonance imaging (MRI) contrast agent. The formed nanoparticles exhibited a narrow range of size dispersity (core size of the particles is about 8-10 nm) and relatively high T2 relaxivities (r2 = 164.14 s(-1) mM(-1) for folate-PLs-coated SPIONs). The in vitro tumor cell targeting efficacy of the folate functionalized and PLs-coated SPIONs was evaluated upon observing cellular uptake of magnetite liposomes by HeLa cells, which overexpresses surface receptors for folic acid. In the Prussian blue staining experiments, cells incubated with folate-PLs-coated SPIONs showed much higher intracellular iron density than did the cells incubated with the folate-free PLs-coated SPIONs. Meanwhile, the MTT assay explains the negligible cell cytotoxicity of SPIONs and folate-PLs-coated SPIONs. In HeLa cells, the in vitro MRI study also indicates the better T2-weighted images in folate-PLs-coated SPIONs than in folate-free PLs-coated SPIONs 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Contrast Media  |2 NLM 
650 7 |a Liposomes  |2 NLM 
650 7 |a Magnetite Nanoparticles  |2 NLM 
650 7 |a Polymers  |2 NLM 
700 1 |a Wang, Hanjie  |e verfasserin  |4 aut 
700 1 |a Lv, Ruichun  |e verfasserin  |4 aut 
700 1 |a Zhao, Peiqi  |e verfasserin  |4 aut 
700 1 |a Sun, Xuezeng  |e verfasserin  |4 aut 
700 1 |a Wang, Sheng  |e verfasserin  |4 aut 
700 1 |a Su, Wenya  |e verfasserin  |4 aut 
700 1 |a Niu, Ruifang  |e verfasserin  |4 aut 
700 1 |a Chang, Jin  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1992  |g 27(2011), 6 vom: 15. März, Seite 3100-5  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:27  |g year:2011  |g number:6  |g day:15  |g month:03  |g pages:3100-5 
856 4 0 |u http://dx.doi.org/10.1021/la1050157  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |d 27  |j 2011  |e 6  |b 15  |c 03  |h 3100-5