PubMed Health⌕ Search

PubMed · 11345267

BaSO4-loaded agarose: a construction material for multimodality imaging phantoms.

Abstract

RATIONALE AND OBJECTIVES: Phantom studies are an important part of the evaluation of imaging techniques; however, presently available phantom construction materials are not adequate for studies involving both magnetic resonance (MR) imaging and computed tomography (CT). The purpose of this study was to design a phantom construction material useful for multimodality imaging experiments. MATERIALS AND METHODS: Iodinated contrast agent or BaSO4 was added during the formation of agarose gels. Both CT and MR imaging were performed, and T1 and T2 values and CT numbers (in Hounsfield units) were obtained for multiple combinations of contrast material and agarose. Results. The T2 values of agarose gels span the range of those values found in biologic tissues. Phantoms containing iodinated contrast agent were not stable; contrast agent diffused across concentration gradients. BaSO4-loaded agarose phantoms were stable, however, and varying barium concentrations produced phantoms that spanned the range of CT numbers found in biologic tissues. Addition of BaSO4 did not substantially alter T1 or T2 values of agarose gels. Agarose concentration had only a small effect on the CT numbers of BaSO4 suspensions. CONCLUSION: BaSO4-loaded agarose is an effective material for construction of multimodality imaging phantoms. It provides adequate signal intensity for MR imaging and attenuation for CT, with independently variable contrast in both modalities.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

H I Litt, A S Brody. 2001. BaSO4-loaded agarose: a construction material for multimodality imaging phantoms.. https://doi.org/10.1016/s1076-6332(03)80544-5

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

KEEP EXPLORING

Related citations

Fabrication of agar-gelatin hybrid scaffolds using a novel entrapment method for in vitro tissue engineering applications.

Scaffolds of agar and gelatin were developed using a novel entrapment method where agar and gelatin molecules mutually entrapped one another forming stable cell adhesive matrices. Glutaraldehyde was used as a crosslinking agent for gelatin. Three types of hybrid matrices were prepared using agar and gelatin in different proportions in the weight ratio of 1:1, 2:1, and 3:1. Surface characterization of dry scaffolds was carried out by scanning electron microscope. Swelling studies were carried out in phosphate buffer saline (PBS) at physiological pH 7.4. The integral stability of the scaffolds was evaluated by estimating the released disintegrated gelatin from them in PBS at pH 7.4. The attachment kinetics of the cells was evaluated by culturing mouse fibroblast cell line NIH 3T3 on films. The cytocompatibility of these matrices was determined by studying growth kinetics of NIH 3T3 cells on them and morphology of cells was observed through optical photographs taken at various days of culture. It was found that the matrices containing agar and gelatin in 2:1 weight ratio exhibited best growth kinetics. The results obtained from these studies have suggested that the above-described method is a cheap and easy way to fabricate agar-gelatin hybrid scaffolds to grow cells which can be used in various in vitro tissue engineering applications like screening of drugs.

Agar↗

Interrelationships between colonies, biofilms, and planktonic cells of Pseudomonas aeruginosa.

Pseudomonas aeruginosa is a gram-negative bacterium and an opportunistic human pathogen that causes chronic infections in immunocompromised individuals. These infections are hard to treat, partly due to the high intrinsic resistance of the bacterium to clinically used antibiotics and partly due to the formation of antibiotic-tolerant biofilms. The three most common ways of growing bacteria in vitro are as planktonic cultures, colonies on agar plates, and biofilms in continuous-flow systems. Biofilms are known to express genes different from those of planktonic cells, and biofilm cells are generally believed to closely resemble planktonic cells in stationary phase. However, few, if any, studies have examined global gene expression in colonies. We used a proteomic approach to investigate the interrelationships between planktonic cells, colonies, and biofilms under comparable conditions. Our results show that protein profiles in colonies resemble those of planktonic cells. Furthermore, contrary to what has been reported previously, the protein profiles of biofilms were found to more closely resemble those of exponentially growing planktonic cells than those of planktonic cells in the stationary phase. These findings raise some intriguing questions about the true nature of biofilms.

Agar↗

Methods for additive hydration allowing observation of fully hydrated state of wet samples in environmental SEM.

Methods for additive hydration are presented that enable longtime observation of very wet biological specimens in an environmental scanning electron microscope. The changes of structure due to dehydration for specimens placed on a Peltier-cooled holder, put on a special agar base or embedded in it or blown over by water vapor are compared. The degree of dehydration damage of the observed specimen structures is evaluated and compared with the structure of a nondestructively dried specimen, prepared by the critical point drying method.

Agar↗