scholarly journals Multimodal Magnetic Resonance and Near-Infrared-Fluorescent Imaging of Intraperitoneal Ovarian Cancer Using a Dual-Mode-Dual-Gadolinium Liposomal Contrast Agent

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
M. K. Ravoori ◽  
S. Singh ◽  
R. Bhavane ◽  
A. K. Sood ◽  
B. Anvari ◽  
...  
2014 ◽  
Vol 50 (94) ◽  
pp. 14835-14838 ◽  
Author(s):  
Levi A. Ekanger ◽  
Meser M. Ali ◽  
Matthew J. Allen

An oxidation-responsive contrast agent for magnetic resonance imaging was synthesized using Eu2+ and liposomes.


Nanomedicine ◽  
2013 ◽  
Vol 8 (6) ◽  
pp. 875-890 ◽  
Author(s):  
Ian R Corbin ◽  
Kenneth K Ng ◽  
Lili Ding ◽  
Andrea Jurisicova ◽  
Gang Zheng

2019 ◽  
Author(s):  
Ziqing Du ◽  
Abhishek Gupta ◽  
Christian Clarke ◽  
Matt Cappadana ◽  
David Clases ◽  
...  

AbstractLanthanide ions doped upconversion nanoparticles (UCNPs) hold great promise as the imaging contrast agent for multimodal medical imaging techniques for diagnosis, including fluorescent bioimaging, magnetic resonance imaging, and computed tomography. However, the maximized signal values of fluorescence and MRI cannot be achieved simultaneously from the same upconversion nanoparticles structures because high specific surface areas can benefit the signal gaining of MRI while big size can induce brighter fluorescent imaging. In this work, we designed and fabricated novel core-porous shell structures for UCNPs with much-enhanced signal values for both fluorescent imaging and MRI. The core-porous shell UCNPs were synthesized via a post-treatment process after an inert shell was coated onto the core UCNPs. The formation mechanism was carefully investigated. The fluorescent and magnetic resonance properties have been detailed characterized and compared from core, core-shell and core-porous UCNPs. Large and bright UCNPs in fluorescence and MRI have been achieved and great potential as the dual-modal contrast agent.


2021 ◽  
Author(s):  
yunchao Zhang ◽  
Jingwen Wang ◽  
Yue Wu ◽  
Qing Tao ◽  
Feifei Wang ◽  
...  

Abstract BackgroundThe understanding of the engrafted cell behaviors such as the survival, growth and distribution is the prerequisite to optimize cell therapy, and a multimodal imaging at both anatomical and molecular levels is designed to achieve this goal. Methods and results We constructed a lentiviral vector carrying ferritin heavy chain 1 (FTH1), near-infrared fluorescent protein (iRFP) and enhanced green fluorescent protein (EGFP) via T2A linker, and established the induced pluripotent stem cells (iPSCs) culture stably expressing these three reporter genes. These iPSCs showed green and near-infrared fluorescence as well as the iron uptake capacity in vitro. After transplanted the labeled iPSCs into the rat brain, the engrafted cells could be in vivo imaged using magnetic resonance imaging (MRI) and near-infrared fluorescent imaging (NIF) up to 60 days at the anatomical level, moreover, these cells could be detected using EGFP immunostaining and Prussian blue stain at the cellular level. Conclusions Our study provides a novel tool to study the cellular behaviors of the transplanted cells in a multimodal way, which will be valuable for the effectiveness and safety evaluation of cell therapy.


PLoS ONE ◽  
2009 ◽  
Vol 4 (10) ◽  
pp. e7628 ◽  
Author(s):  
Ketan B. Ghaghada ◽  
Murali Ravoori ◽  
Divya Sabapathy ◽  
James Bankson ◽  
Vikas Kundra ◽  
...  

2021 ◽  
Author(s):  
Yunchao Zhang ◽  
Feifei Wang ◽  
Qing Tao ◽  
Nana Wang ◽  
Xingrui Gi ◽  
...  

Abstract Objectives The understanding of the engrafted cell behaviors is the prerequisite to optimize cell therapy, and a multimodal imaging at both anatomical and molecular levels is designed to achieve this goal. Results We constructed a lentiviral vector carrying ferritin heavy chain 1 (FTH1), near-infrared fluorescent protein (iRFP) and enhanced green fluorescent protein (EGFP) via T2A linker, and established the induced pluripotent stem cells (iPSCs) culture stably expressing these three reporter genes. These iPSCs showed green and near-infrared fluorescence as well as the iron uptake capacity in vitro. After transplanted the labeled iPSCs into the rat brain, the engrafted cells could be in vivo imaged using magnetic resonance imaging (MRI) and near-infrared fluorescent imaging (NIF) up to 60 days at the anatomical level, moreover, these cells could be detected using EGFP immunostaining and Prussian blue stain at the cellular level. Conclusions Our study provides a novel tool to study the cellular behaviors of the transplanted cells in a multimodal way, which will be valuable for the effectiveness and safety evaluation of cell therapy.


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