Slice-selective pulses

Closer examination of equation B 1,14,3 reveals that, after the slice selection pulse, the spin isocln-omats at different positions in the gradient direction are not in phase. Rather they are rotated by i exp jyC. )tind... 

Another approach to obtain spatially selective chemical shift information is, instead of obtaining the entire image, to select only the voxel of interest of the sample and record a spectrum. This method called Volume Selective spectroscopY (VOSY) is a ID NMR method and is accordingly fast compared with a 3D sequence such as the CSI method displayed in Figure 1.25(a). In Figure 1.25(b), a VOSY sequence based on a stimulated echo sequence is displayed, where three slice selective pulses excite coherences only inside the voxel of interest. The offset frequency of the slice selective pulse defines the location of the voxel. Along the receiver axis (rx) all echoes created by a stimulated echo sequence are displayed. The echoes V2, VI, L2 and L3 can be utilized, where such multiple echoes can be employed for signal accumulation. 

Fig. 14. MBEST-EPI (a) slice-selective pulse sequence and (b) corresponding k-space raster.

A closely related technique can be used for multi-slice imaging (Fig. 6.2.7) [Fral]. The scheme of Fig. 6.2.5(c) is appended by further slice-selective 90° pulses with different centre frequencies, so that the magnetization of other slices is selected [Fral]. In this way, the otherwise necessary recycle delay can effectively be used for acquisition of additional slices. However, the contrast in each slice is affected by a different Ty weight, because is different for each slice. The technique can readily be adapted to line-scan imaging by applying successive slice-selective pulses in orthogonal gradients [Finl]. 

---