Abstract:An x-ray fluorescence measurement system has been developed with an 125I source to detect arsenic in superficial layers of phantoms and tissue. Based on in vivo measurements, in conjunction with Monte Carlo simulations, the detection limit for arsenic in skin ranges between 2.6+/-0.5 and 5.7+/-1.1 microg g(-1), depending on skin thickness and assuming that arsenic is uniformly distributed in the skin. The effect of skin arsenic distribution was also examined.
“…1). Since the mean free path of the most energetic characteristic x-rays under consideration in this study (K α x-rays from As at 10.5 keV) is only E2 mm in rice (Studinski et al, 2005), this geometry ensured that the XRF signal was not influenced by differences between samples in factors such as height, density, or moisture content. The column had a Kapton window at its base, which was placed directly against the XRF beam window for the duration of the measurement.…”
“…1). Since the mean free path of the most energetic characteristic x-rays under consideration in this study (K α x-rays from As at 10.5 keV) is only E2 mm in rice (Studinski et al, 2005), this geometry ensured that the XRF signal was not influenced by differences between samples in factors such as height, density, or moisture content. The column had a Kapton window at its base, which was placed directly against the XRF beam window for the duration of the measurement.…”
“…95–97 This technique is also applicable to the study of a variety of biological samples 95–109 to investigate metal toxicity 95–96, 109 , the uptake and distribution of metallopharmacueticals 99 , and intracellullar elemental distributions. 95–99, 106–109 In addition, in vivo studies have been performed to non-invasively determine the lead concentration in the bones of children and young adults, 100–101 arsenic in human skin, 110–111 and iodine in the thyroid 112 .…”
X-rays have been used for non-invasive high-resolution imaging of thick biological specimens since their discovery in 1895. They are widely used for structural imaging of bone, metal implants, and cavities in soft tissue. Recently, a number of new contrast methodologies have emerged which are expanding X-ray’s biomedical applications to functional as well as structural imaging. These techniques are promising to dramatically improve our ability to study in situ biochemistry and disease pathology. In this review, we discuss how X-ray absorption, X-ray fluorescence, and X-ray excited optical luminescence can be used for physiological, elemental, and molecular imaging of vasculature, tumours, pharmaceutical distribution, and the surface of implants. Imaging of endogenous elements, exogenous labels, and analytes detected with optical indicators will be discussed.
“…A final example of a toxic measurement is arsenic, where the preferred site of measurement is skin. Development work has been performed by Studinski et al [12] and also by Gherase and Fleming [13]. This brief listing is not comprehensive, but it should provide an impression of the range of elements for which X-ray fluorescence measurement systems have been developed.…”
Section: Elements Measured In Vivo By X-ray Fluorescencementioning
X-ray fluorescence has been used to measure several elements noninvasively within living human subjects. Some description is given of the constraints imposed by this rather unusual form of analysis together with a brief listing indicating the range of elements for which such analyses have been developed. Measurements of two elements are then presented in more detail. Lead is measured in bone and has become a well-established tool in continuing research into the long term effects of lead. Strontium is also measured in bone and, although presently not in widespread use, offers the potential for essential information in the study of the reported benefits of strontium supplementation.
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