30 research outputs found

    A Monte Carlo simulation study to investigate the potential of diffraction enhanced breast imaging

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    Recent studies have demonstrated that image contrast in X-ray mammography could be enhanced by making use of both the transmitted and scattered radiation. At small angles coherently scattered photons undergo interference effects which can be used as a means of tissue characterisation. Several form factor data from X-ray diffraction measurements are now available. The authors implemented these data in the EGS4 code so as to use realistic breast tissues (both tumour and healthy tissue) for a Monte Carlo simulation. A breast imaging system which makes use of a combined scatter/transmission signal has been modelled. Results of the authors' simulation confirmed that the contrast between healthy and tumour tissue provided by small-angle scatter radiation is greater than that of primary image for object thicknesses of mammographic interest. Analysis of beam polychromaticity effects in coherent scattering showed that material discrimination is still possible with the conventional X-ray sources currently used. In the design of a diffraction enhanced breast imaging system signal-to-noise ratio performance must be considered in order to fully assess the increase in diagnostic capability effected by this approach

    A physical phantom for the calibration of three-dimensional X-ray microtomography examination

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    X-ray microtomography is rapidly gaining importance as a non-destructive investigation technique, especially in the three-dimensional examination of trabecular bone. Appropriate quantitative three-dimensional parameters describing the investigated structure were introduced, such as the model-independent thickness and the structure model index. The first parameter calculates a volume-based thickness of the structure in three dimensions independent of an assumed structure type. The second parameter estimates the characteristic form of which the structure is composed, i.e. whether it is more plate-like, rod-like or even sphere-like. These parameters are now experiencing a great diffusion and are rapidly growing in importance. To measure the accuracy of these three-dimensional parameters, a physical three-dimensional phantom containing different known geometries and thicknesses, resembling those of the examined structures, is needed. Unfortunately, such particular phantoms are not commonly available and neither does a consolidated standard exist. This work describes the realization of a calibration phantom for three-dimensional X-ray microtomography examination and reports an application example using an X-ray microtomography system. The calibration phantom (external size 13 mm diameter, 23 mm height) was based on various aluminium inserts embedded in a cylinder of polymethylmethacrylate. The inserts had known geometries (wires, foils, meshes and spheres) and thicknesses (ranging from 20 microm to 1 mm). The phantom was successfully applied to an X-ray microtomography device, providing imaging of the inserted structures and calculation of three-dimensional parameters such as the model-independent thickness and the structure model index. With the indications given in the present work it is possible to design a similar phantom in a histology laboratory and to adapt it to the requested applications

    Monosialylated biantennary N-glycoforms containing GalNAc-GlcNAc antennae predominate when human EPO is expressed in goat milk

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    Recently, our group reported the expression of recombinant human erythropoietin in goat milk (rhEPO-milk) as well as in the mammary epithelial cell line GMGE (EPO-GMGE) by cell culture using the adenoviral transduction system. N-Glycosylation characterization of rhEPO-milk by Normal-Phase HPLC profiling of the fluorophore, 4-aminobenzoic acid-labeled enzymatically released N-glycan pool from rhEPO-goat milk, combined with MALDI, ESI-MS and LC/MS, revealed that low branched, core-fucosylated, N-glycans predominate. The labeled N-glycans were separated into neutral and charged fractions by anion exchange chromatography and the charged N-glycans were found to be mostly a2,6-monosialylated with Neu5Ac or Neu5Gc in a ratio of 1:1. Unlike the N-glycans from rhEPO produced in CHO cells, where the glycans are multiantennary highly sialylated, core-fucosylated oligosaccahrides, or even in the goat mammary gland epithelial cell line cultured in vitro in which multiantennary, core- and outer-arm fucosylated, monosialylated Nglycans are the most abundant species, a large proportion of the N-glycans from rhEPO-milk were monosialylated, biantennary, antennae mostly terminating with the more unusual GalNAc–GlcNAc motive and without outer-arm fucosylation. These findings, emphasizing the difference in the N-glycan repertoire between the rhEPO-milk and EPO-GMGE, are consistent with the principle that glycosylation is cell-type dependent and that the cell environment is crucial as well

    Characterisation of the components of a prototype scanning intelligent imaging system for use in digital mammography: The I-ImaS system

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    The physical performance characteristics of a prototype scanning digital mammography (DM) system have been investigated. The I-ImaS system utilises CMOS MAPS technology promoting on-chip data processing; consequently statistical analysis is therefore achievable in real-time for the purpose of exposure modulation via a feedback mechanism during the image acquisition procedure. The imager employs a dual array of twenty CMOS APS sensing devices each individually coupled to a 100 μm thick thallium doped structured CsI scintillator. The x-ray performance of the sensors was characterised where the presampled modulation transfer function (MTF), normalised noise power spectrum (NNPS), and the detective quantum efficiency (DQE) was determined. The presampled MTF was measured utilising the slit technique and was found to be 0.1 at 6 lp/mm. The NNPS measured utilising a W/Al target/filter combination hardened with 38 mm PMMA was seen to decrease with increasing exposure as expected and the manifesting DQE was 0.30 at close to zero spatial frequency at an exposure of 1.75 mR. Preliminary image stitching of the individual steps acquired from the scanning system is presented. A conventionally acquired image that is without the implementation of beam modulation or off-line intelligence is compared and contrasted to an intelligently off-line processed image. Results indicate the implementation of real-time intelligence into the image acquisition phase of digital mammography is foreseeable. © 2006 IEEE

    Design and characterization of the I-ImaS multi-element X-ray detector system

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    I-ImaS (Intelligent Imaging Sensors) is a European project aiming to produce new, intelligent x-ray imaging systems using novel APS sensors to create optimal diagnostic images. Initial systems have been constructed for medical imaging; specifically mammography and dental encephalography. However, the I-ImaS system concept could be applied to all areas of x-ray imaging, including homeland security and industrial QA. The I-ImaS system intelligence is implemented by the use of APS technology and FPGAs, allowing real-time analysis of data during image acquisition. This gives the system the capability to perform as an on-the-fly adaptive imaging system, with the potential to create images with maximum diagnostic information within given dose constraints. The I-ImaS system uses a scanning linear array of scintillatorcoupled 1.5-D CMOS Active Pixel Sensors to create a full 2-D x-ray image of an object. This paper describes the parameters considered when choosing the scintillator elements of the detectors. A study of the positioning of the sensors to form a linear detector is also considered, along with a discussion of the potential losses in image quality associated with creating a linear sensor by tiling many smaller sensors. Preliminary results show that the detectors have sufficient performance to be used successfully in the initial mammographie and encephalographic I-ImaS systems that are currently under construction. © 2008 IEEE
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