scholarly journals Changes in MR relaxation times of the meniscal body with loading: an in vivo pilot study in knee osteoarthritis

2013 ◽  
Vol 21 ◽  
pp. S213
Author(s):  
K. Subburaj ◽  
R.B. Souza ◽  
B.T. Wyman ◽  
X. Li ◽  
T.M. Link ◽  
...  
2013 ◽  
Vol 41 (2) ◽  
pp. 536-543 ◽  
Author(s):  
Karupppasamy Subburaj ◽  
Richard B. Souza ◽  
Bradley T. Wyman ◽  
Marie-Pierre Hellio Le Graverand-Gastineau ◽  
Xiaojuan Li ◽  
...  

2015 ◽  
Vol 34 (2) ◽  
pp. 249-261 ◽  
Author(s):  
Nathaniel E. Calixto ◽  
Deepak Kumar ◽  
Karupppasamy Subburaj ◽  
Justin Singh ◽  
Joseph Schooler ◽  
...  

2006 ◽  
Vol 14 ◽  
pp. S154
Author(s):  
X. Li ◽  
S. Kazzaz ◽  
D. Castillo ◽  
G. Blumenkrantz ◽  
C.B. Ma ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-19 ◽  
Author(s):  
Nasim Hashempour Alamdari ◽  
Mahmood Alaei-Beirami ◽  
Seyed Ataollah Sadat Shandiz ◽  
Hadi Hejazinia ◽  
Rahimeh Rasouli ◽  
...  

Designing a unique theranostic biocompatible, biodegradable, and cost-effective agent which is easy to be synthesized as a biohybrid material was the aim of this study. In this matter, asparagine attached to anionic linear globular dendrimer G2 (as a biocompatible, biodegradable, and cost-effective agent which is negatively charged nanosized and water soluble polymer that outweighs other traditionally used dendrimers) and finally contrast agent (Gd3+) was loaded (which made complexes) in synthesized asparagine-dendrimer. Observations revealed that, in addition to successful colon cancer and brain targeting, Gd3+-dendrimer-asparagine, the proposed theranostic agent, could increase T1 MR relaxation times, decrease T2 MR relaxation times significantly, and improve contrast of image as well as illustrating good cellular uptake based on florescent microscopy/flow cytometry and ICP-mass data. In addition to that, it increased tumor growth inhibition percentage (TGI%) significantly compared to FDA approved contrast agent, Magnevist. Totally, Gd3+-anionic linear globular dendrimer G2-asparagine could be introduced to the cancer imaging/therapy (theranostics) protocols after in vivo MR and fluorescent analysis and passing clinical trials. Hence, this nanotheranostic agent would be a promising candidate for brain drug delivery and imaging in the future.


The Knee ◽  
2014 ◽  
Vol 21 (5) ◽  
pp. 881-885 ◽  
Author(s):  
Deepak Kumar ◽  
Abbas Kothari ◽  
Richard B. Souza ◽  
Samuel Wu ◽  
C. Benjamin Ma ◽  
...  

Author(s):  
Thomaz R. Mostardeiro ◽  
Ananya Panda ◽  
Robert J. Witte ◽  
Norbert G. Campeau ◽  
Kiaran P. McGee ◽  
...  

Abstract Purpose MR fingerprinting (MRF) is a MR technique that allows assessment of tissue relaxation times. The purpose of this study is to evaluate the clinical application of this technique in patients with meningioma. Materials and methods A whole-brain 3D isotropic 1mm3 acquisition under a 3.0T field strength was used to obtain MRF T1 and T2-based relaxometry values in 4:38 s. The accuracy of values was quantified by scanning a quantitative MR relaxometry phantom. In vivo evaluation was performed by applying the sequence to 20 subjects with 25 meningiomas. Regions of interest included the meningioma, caudate head, centrum semiovale, contralateral white matter and thalamus. For both phantom and subjects, mean values of both T1 and T2 estimates were obtained. Statistical significance of differences in mean values between the meningioma and other brain structures was tested using a Friedman’s ANOVA test. Results MR fingerprinting phantom data demonstrated a linear relationship between measured and reference relaxometry estimates for both T1 (r2 = 0.99) and T2 (r2 = 0.97). MRF T1 relaxation times were longer in meningioma (mean ± SD 1429 ± 202 ms) compared to thalamus (mean ± SD 1054 ± 58 ms; p = 0.004), centrum semiovale (mean ± SD 825 ± 42 ms; p < 0.001) and contralateral white matter (mean ± SD 799 ± 40 ms; p < 0.001). MRF T2 relaxation times were longer for meningioma (mean ± SD 69 ± 27 ms) as compared to thalamus (mean ± SD 27 ± 3 ms; p < 0.001), caudate head (mean ± SD 39 ± 5 ms; p < 0.001) and contralateral white matter (mean ± SD 35 ± 4 ms; p < 0.001) Conclusions Phantom measurements indicate that the proposed 3D-MRF sequence relaxometry estimations are valid and reproducible. For in vivo, entire brain coverage was obtained in clinically feasible time and allows quantitative assessment of meningioma in clinical practice.


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