PubMed HealthSearch

PubMed · 8316065

Magnetization transfer effects in multislice MR imaging.

Abstract

A theoretical model is presented which describes the effects of magnetization transfer in multislice MR imaging of a tissue-mimicking phantom composed of cross-linked agar gel. The model is successful in explaining differences between single and multislice image signal intensities observed for the agar gel but not seen in a simple aqueous solution. Magnetization transfer leads to a reduction in the image signal intensity of a slice of interest due to off-resonance RF irradiation arising from 90 degrees and 180 degrees pulses intended for neighboring slices. The contribution of magnetization transfer to multislice MR imaging depends on the amount of off-resonance RF irradiation during the imaging sequence repetition interval. For the tissue-mimicking agar gel, conventional spin-echo multislice imaging gave rise to a negligible image signal intensity reduction (< or = 2%); however, fast spin-echo (FSE) imaging, which employs up to 16 times as many RF pulses per slice, exhibited as much as a 13% reduction in image signal intensity (13 slices). The reduction in multislice image signal intensity due to magnetization transfer is sample specific and is shown to be more dramatic for in vivo human leg muscle (10% for conventional spin echo, 40% for FSE) where magnetization transfer rates are greater than in the cross-linked agar gel.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

G E Santyr. 1993. Magnetization transfer effects in multislice MR imaging.. https://doi.org/10.1016/0730-725x(93)90471-o

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Is the direct quantitation of antibiotics in agar by high-performance liquid chromatography useful?

The direct quantification of antibiotics in agar allows one to study the quality of the agar matrix, the kinetics of diffusion and the bacteria-antibiotic interaction. Mueller-Hinton agar (MHA) plates from three manufacturers were tested using HPLC and the disc diffusion test of ceftazidime (CAZ). Notable differences in the chromatographic profiles of MHA plate extracts from OXOID, DID and Becton Dickinson (BD) were shown, with a higher CAZ concentration after 24 h a 6 mm in BD P. aeruginosa inoculated plates (5.1 +/- 1.7 micrograms/ml, n = 6) vs. OXOID and DID (1.6 +/- 0.3 micrograms/ml, n = 12). BD plates gave also a different inhibition zone diameter (26 +/- 0.5 mm, n = 3) with respect to DID and OXOID (29 +/- 0.5 mm, n = 3).

Agar

Transduction of the SkBr3 breast carcinoma cell line with the HOXB7 gene induces bFGF expression, increases cell proliferation and reduces growth factor dependence.

Several melanomas, carcinomas, glioblastomas and leukemias showed coordinated expression of HOXB7 and bFGF with exception of the SkBr3 mammary carcinoma that was negative for both. Transduction of HOXB7 gene into SkBr3 cells, induced bFGF expression, increased growth rate, independence from serum withdrawal and ability to form colonies in semisolid medium. ELISA assay showed that most of bFGF was associated to cell lysate when cells were cultured at 1% serum whereas in cells kept to 10% serum bFGF was detected both within cell lysate or secreted into cell supernatants. Antisense oligos to bFGF inhibited the growth of cells cultured in 1%, indicating that beside the possible activation of additional genes other than bFGF by HOXB7 transduction, only bFGF induction accounts for the observed results. Moreover, since inhibition of cell proliferation occurred in cells kept in 1% but not 10% serum, a bFGF intracrine loop appears operative in serum starved SkBr3/HOXB7 cells. Also, these results further indicate bFGF as target of HOXB7.

Agar

Growth of Salmonella enteritidis and S. pullorum on Hektoen agar and the expression of lipopolysaccharide or flagella.

Growth of strains of Salmonella enteritidis and Salmonella pullorum on Hektoen agar has been reported to influence the expression of long-chain lipopolysaccharide and motility respectively. In this study we used a panel of strains of S. enteritidis and S. pullorum to investigate these phenomena. Culture on Hektoen agar did not cause rough strains of S. enteritidis to express long-chain lipopolysaccharide or strains of S. pullorum to become motile. It was concluded that growth of strains of S. enteritidis and S. pullorum on Hektoen agar would not normally affect the expression of somatic or flagellar antigens, and would not influence the interpretation of the Kauffman-White typing scheme.

Agar