2019
DOI: 10.1016/j.aca.2019.03.054
|View full text |Cite
|
Sign up to set email alerts
|

Multifunctional iron oxide-carbon hybrid nanoparticles for targeted fluorescent/MR dual-modal imaging and detection of breast cancer cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
27
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 45 publications
(27 citation statements)
references
References 54 publications
0
27
0
Order By: Relevance
“…Up to the present time, different sensors and platforms were developed to detect CD44-expressing cells. This includes quartz crystal microbalance-based sensor 5 and magnetic-fluorescent iron oxide–carbon hybrid nanoparticles 6 and colorimetric nanobiosensor 7 for the detection of CD44 + breast cancer cells, functionalized interdigitated electrodes for prostate cancer cells expressing CD44 8 , functionalized stainless steel wire to capture breast CSC 9 among others.…”
Section: Introductionmentioning
confidence: 99%
“…Up to the present time, different sensors and platforms were developed to detect CD44-expressing cells. This includes quartz crystal microbalance-based sensor 5 and magnetic-fluorescent iron oxide–carbon hybrid nanoparticles 6 and colorimetric nanobiosensor 7 for the detection of CD44 + breast cancer cells, functionalized interdigitated electrodes for prostate cancer cells expressing CD44 8 , functionalized stainless steel wire to capture breast CSC 9 among others.…”
Section: Introductionmentioning
confidence: 99%
“…Particularly in the biomedical field, when designed to be injected intravenously, the particles will face the recognition and capture by the macrophages of the immune system [5,6], hence the need to make them biomimetic by coating with, for instance, poly(ethylene glycol) (PEG) [7], dextran [8] or chitosan [9]. Of comparable importance is their transformation into specific-targeting vehicles designed to approach diseased cells and not healthy ones [10]; as examples, we can cite the conjugation with CD44 monoclonal antibodies for specific binding to 4T1 breast cancer cells [11], and the overexpression of folate or biotin receptors in some tumor cells, suggesting the use of folic acid or biotin on the particles for preferential (rarely, exclusive) linkage to cancer cells. The number of possible ligands is certainly large, as has been summarized by Loomis et al [12].…”
Section: Introductionmentioning
confidence: 99%
“…From these results, specifically by the MRI data from our transgenic HER-2 mouse model, it shows persistence of signal enhancement out to 24 h after initial injection, similar to earlier time points at 4 and 8 h after injection for both CT and MRI. Though imaging agents have proved to be an invaluable tool, circulation time and biodistribution of these agents are concerns [38,39]. This is because increasing circulation times and extending the signal enhancement window, usually results in imaging agents being retained in untargeted organs.…”
Section: Discussionmentioning
confidence: 99%