In vivo tumor targeting and biodistribution evaluation of paramagnetic solid lipid nanoparticles for magnetic resonance imaging

2017 ◽  
Vol 13 (2) ◽  
pp. 693-700 ◽  
Author(s):  
Simona Ghiani ◽  
Martina Capozza ◽  
Claudia Cabella ◽  
Alessandra Coppo ◽  
Luigi Miragoli ◽  
...  
2013 ◽  
Vol 24 (9) ◽  
pp. 1455-1467 ◽  
Author(s):  
Erica Andreozzi ◽  
Peter Wang ◽  
Anthony Valenzuela ◽  
Chuqiao Tu ◽  
Fredric Gorin ◽  
...  

2018 ◽  
Vol 6 (1) ◽  
pp. 207-215 ◽  
Author(s):  
Wen Xu ◽  
Jinghua Sun ◽  
Liping Li ◽  
Xiaoyang Peng ◽  
Ruiping Zhang ◽  
...  

A magnetic resonance imaging contrast agent, based on Mn2+-chelating melanin nanoparticles, that has ultrahigh efficient clearance in vivo for tumor-targeted imaging.


2021 ◽  
Vol 9 (14) ◽  
pp. 3161-3167
Author(s):  
Bo Song ◽  
Xinyi Wen ◽  
Xinyue Zhang ◽  
Qi Liu ◽  
Hua Ma ◽  
...  

Multifunctional bioconjugates of lanthanide complexes for tumor-targeting time-gated luminescence and magnetic resonance imaging in vitro and in vivo.


2021 ◽  
Author(s):  
Shu Yao ◽  
Li Li ◽  
Chang Liu ◽  
Ziying Wang ◽  
Hong Liu ◽  
...  

Abstract Background: The high incidence and mortality rates of cervical cancer pose a serious threat to women's health. Traditional chemotherapy has inevitable drawbacks of nonspecific tumor targeting, high toxicity, and poor therapeutic efficiency. In order to overcome these shortcomings, a novel multifunctional magnetic nanoparticles drug delivery system with tumor targeting and magnetic resonance imaging was developed to achieve precise diagnosis and targeted tumor killing effects.Methods: Transmission electron microscopy, dynamic light scatting and ultraviolet methods were used to characterize the nanoparticles in vitro. Cell function tests were performed by scratch, transwell and flow cytometry assays. MTT was used to detect the toxicity of the nanoparticles. The motion trajectory, drug release and uptake studies were carried out in vitro. The in vivo pharmacokinetic and drug distribution studies were verified by high performance liquid chromatography methods. Attenuation of the MRI signal by the nanoparticles and their enhanced antitumor efficiency were examined in vivo in mouse cervical cancer models. Sequencing and proteomics were used to detect the key antitumor molecules of the nanoparticles.Results: Multifunctional magnetic nanoparticles coated with ferric oxide nanoparticles and doxorubicin hydrochloride (DOX-Fe3O4-PEG-PLA-NPs) was prepared successfully. No toxicity was detected of PEG-PLA-NP, however, the tumor killing effect was enhanced under the alternating magnetic field significantly. The drug-release study showed that the cumulative release rates of NP groups were much less than free DOX group, while the drug release rate increased under acidic condition. In addition, DOX-Fe3O4-PEG-PLA-NPs showed improved internalized into carcinoma cells under magnetic field significantly. In vivo studies demonstrated that the combined therapy under an alternating magnetic field displayed improved therapeutic effect when compared with individual therapies as documented by the delayed tumor growth, inhibition of metastasis, and prolonged survival. The in vitro and in vivo MRI results showed that the multifunctional magnetic nanomaterial had a better MRI signal reduction effect and a higher T2 relaxation rate.Conclusions: We developed an cervical cancer targeting nano-carrier drug delivery system successfully, which showed perfect excellent T2 contrast magnetic resonance imaging, chemotherapy-sensitizing, tumor targeting , and anti-tumor effect, thus have the potential to be a new theranostic strategy for ovarian cancer patients.


2019 ◽  
Vol 15 (7) ◽  
pp. 1384-1400 ◽  
Author(s):  
Yang Wang ◽  
Yan Dai ◽  
Qiang Luo ◽  
Xiaoli Wei ◽  
Xueyang Xiao ◽  
...  

Branched macromolecules have been used as carriers for imaging probes and drug delivery systems because of their tunable molecular structures, as well as their regular nanoscale structures and dimensions. We designed and synthesized two tumor environment-responsive branched and gadolinium (Gd)-based glycopolymer conjugates and investigated their potency as highly effective and safe magnetic resonance imaging (MRI) contrast agents. These branched macromolecules were prepared by one-pot reversible addition fragmentation chain transfer (RAFT) polymerization and conjugating chemistry. A biodegradable GFLG oligopeptide was used to successfully link the branch-chains of the branched macromolecules, finally a conjugate of this branched macromolecule and DOTA-Gd (HB-pGAEMA-Gd) with a molecular weight (MW) of 124 kDa was produced. Meanwhile, to improve the ability of tumor-targeting, we conjugated a tumor-targeting cRGDyK cyclic peptide to the branched molecule to prepare a tumor-targeted branched macromoleculeDOTA-Gd conjugate (HB-pGAEMA-RGD-Gd) with a MW of 136 kDa. The prepared branched macromolecules had a nanoscale hydrodynamic particle size and could be degraded into lower MW fragments with the cathepsin B. The aqueous phase relaxation efficiency of HB-pGAEMA-RGD-Gd (12.3 mM–1s–1 and HB-pGAEMA-Gd (13.2 mM–1s–1 was four times higher than that of DTPA-Gd (2.9 mM–1s–1), a clinically used contrast agent. In comparison with DTPA-Gd, the branched macromolecular contrast agents significantly enhanced the MRI signal intensity at the tumor site in vivo, and the enhancement of MRI signal intensity was up to 6 times that of the DTPA-Gd owing to their high relaxation efficiencies and accumulation at the tumor site. In addition, in vitro and in vivo toxicity studies indicated that the degradable macromolecular contrast agents had no significant toxicity.


2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Maiju Soikkeli ◽  
Mikko I. Kettunen ◽  
Riikka Nivajärvi ◽  
Venla Olsson ◽  
Seppo Rönkkö ◽  
...  

Magnetic resonance imaging examinations are frequently carried out using contrast agents to improve the image quality. Practically all clinically used contrast agents are based on paramagnetic metals and lack in selectivity and specificity. A group of stable organic radicals, nitroxides, has raised interest as new metal-free contrast agents for MRI. Their structures can easily be modified to incorporate different functionalities. In the present study, a stable nitroxide TEEPO (2,2,6,6-tetraethylpiperidin-1-oxyl) was linked to a glucose moiety (Glc) to construct a water-soluble, potentially tumor-targeting compound with contrast-enhancing ability. The ability was assessed with in vivo MRI experiments. The constructed TEEPO-Glc agent proved to shorten the T1 relaxation time in tumor, while the T1 time in healthy brain tissue remained the same. The results indicate the potential of TEEPO-Glc as a valuable addition to the growing field of metal-free contrast enhancement in MRI-based diagnostics.


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