scholarly journals Dye-Doped Fluorescent Nanoparticles in Molecular Imaging: A Review of Recent Advances and Future Opportunities

2014 ◽  
Vol 11 (2) ◽  
pp. 102-113 ◽  
Author(s):  
Yadollahpour Ali ◽  
Rezaee Zohre ◽  
Jalilifar Mostafa ◽  
Rashidi Samaneh

Molecular imaging (MI) is an in vivo assessment of characterization and quantitatively measurement of biological processes at the molecular level. Determination of pathologies of malfunctioned tissues without invasive biopsies or surgical procedures, early detection, monitoring of treatment process and visualization of cell trafficking are advantages of this approach. One example of basic requirement of MI is high affinity molecular probe that acts as the source of image contrast. Recent advances in nanotechnology have developed the use of nanoparticles as MI probe. Optical molecular imaging is one of the main categories of molecular imaging with great potentials for in vivo cell trafficking. Fluorescent nanoparticles are a major group of nanoparticles in optical molecular imaging. Dye-doped, quantum dots and up conversion particles are three classes of fluorescent nanoparticles. This paper reviews the basic principles of molecular imaging based on nanoparticles focusing on the optical molecular imaging. The characteristics of dye-doped nanoparticles, their as well as of that are reviewed in this paper.


2009 ◽  
Vol 4 (7) ◽  
pp. 535-546 ◽  
Author(s):  
Mikako Ogawa ◽  
Nobuyuki Kosaka ◽  
Peter L. Choyke ◽  
Hisataka Kobayashi




2019 ◽  
Vol 20 (3) ◽  
pp. 471 ◽  
Author(s):  
Shriya S. Srinivasan ◽  
Rajesh Seenivasan ◽  
Allison Condie ◽  
Stanton L. Gerson ◽  
Yanming Wang ◽  
...  

Chemotherapeutic dosing, is largely based on the tolerance levels of toxicity today. Molecular imaging strategies can be leveraged to quantify DNA cytotoxicity and thereby serve as a theranostic tool to improve the efficacy of treatments. Methoxyamine-modified cyanine-7 (Cy7MX) is a molecular probe which binds to apurinic/apyrimidinic (AP)-sites, inhibiting DNA-repair mechanisms implicated by cytotoxic chemotherapies. Herein, we loaded (Cy7MX) onto polyethylene glycol-coated gold nanoparticles (AuNP) to selectively and stably deliver the molecular probe intravenously to tumors. We optimized the properties of Cy7MX-loaded AuNPs using optical spectroscopy and tested the delivery mechanism and binding affinity using the DLD1 colon cancer cell line in vitro. A 10:1 ratio of Cy7MX-AuNPs demonstrated a strong AP site-specific binding and the cumulative release profile demonstrated 97% release within 12 min from a polar to a nonpolar environment. We further demonstrated targeted delivery using imaging and biodistribution studies in vivo in an xenografted mouse model. This work lays a foundation for the development of real-time molecular imaging techniques that are poised to yield quantitative measures of the efficacy and temporal profile of cytotoxic chemotherapies.



2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Senthilkumar Kalimuthu ◽  
Ji Min Oh ◽  
Prakash Gangadaran ◽  
Liya Zhu ◽  
Ho Won Lee ◽  
...  



MedChemComm ◽  
2015 ◽  
Vol 6 (3) ◽  
pp. 391-402 ◽  
Author(s):  
Masahiro Ono ◽  
Hideo Saji

We review recent advances in our development of molecular imaging probes for PET, SPECT, and optical imaging for in vivo detection of β-amyloid plaques in the brain.



2012 ◽  
Vol 11 (5) ◽  
pp. 7290.2012.00003 ◽  
Author(s):  
Rahul A. Sheth ◽  
Alexandra Kunin ◽  
Lars Stangenberg ◽  
Mark Sinnamon ◽  
Kenneth E. Hung ◽  
...  


2015 ◽  
Vol 3 (2) ◽  
pp. 118-128
Author(s):  
Yingfeng Tu ◽  
Lei Jiang ◽  
Ruiping Zhang ◽  
Baozhong Shen ◽  
Zhen Cheng




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