## Abstract ## Purpose: To demonstrate water‐ and fat‐suppressed proton projection MRI (WASPI) in a clinical scanner to visualize the solid bone matrix in animal and human subjects. ## Materials and Methods: Pig bone specimens and polymer pellets were used to optimize the WASPI method in terms o
Bone mineral imaged in vivo by 31P solid state MRI of human wrists
✍ Scribed by Yaotang Wu; Timothy G. Reese; Haihui Cao; Mirko I. Hrovat; Steven P. Toddes; Rostislav A. Lemdiasov; Jerome L. Ackerman
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 511 KB
- Volume
- 34
- Category
- Article
- ISSN
- 1053-1807
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Purpose:
To implement solid state ^31^P MRI (^31^P SMRI) in a clinical scanner to visualize bone mineral.
Materials and Methods:
Wrists of seven healthy volunteers were scanned. A quadrature wrist ^31^P transmit/receive coil provided strong B~1~ and good signal‐to‐noise ratio (SNR). A ^1^H‐^31^P frequency converter was constructed to enable detection of the ^31^P signal by means of the ^1^H channel. Data points lost in the receiver dead time were recovered by a second acquisition with longer dwell time and lower gradient strength.
Results:
Three‐dimensional ^31^P images, showing only bone mineral of the wrist, were obtained with a clinical 3 Tesla (T) scanner. In the best overall case an image with isotropic resolution of ∼5.1 mm and SNR of 30 was obtained in 37 min. ^31^P NMR properties (resonance line width 2 kHz and T~1~ 17–19 s) of in vivo human bone mineral were measured.
Conclusion:
In vivo ^31^P SMRI visualization of human wrist bone mineral with a clinical MR scanner is feasible with suitable modifications to circumvent the scanners' limitations in reception of short‐T~2~ signals. Frequency conversion methodology is useful for implementing ^31^P SMRI measurements on scanners which do not have multinuclear capability or for which the multinuclear receiver dead time is excessive. J. Magn. Reson. Imaging 2011;. © 2011 Wiley‐Liss, Inc.
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