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1.
Ann N Y Acad Sci ; 904: 263-6, 2000 May.
Artículo en Inglés | MEDLINE | ID: mdl-10865752

RESUMEN

A noninvasive in vivo method has been developed and optimized for measuring platinum concentrations in the kidneys of patients receiving chemotherapy. The method is based on polarizing the X-ray beam from an orthovoltage radiotherapy treatment unit, the Pantak DXT-300, and using the beam to produce emission of the characteristic platinum X-rays from the kidney. The platinum is derived from platinum-based chemotherapy drugs, such as cisplatin and its analogues (carboplatin and iproplatin), used to treat cancer patients. The clinical motivation for measuring the platinum concentration in both the kidneys and the tumor is to optimize the treatment by establishing the relationships between the accumulation of the drug at those sites. Such clinical information could be valuable in maximizing the therapeutic ratio toward the tumor tissue and limiting the hazards to the kidney. The performance of the system was experimentally optimized with respect to the applied X-ray tube voltage, filter material, and polarizer. Additionally, the MCNP-4B Monte-Carlo computer code was used to estimate the optimum shielding materials, the thickness surrounding the X-ray tube, and the arrangement of collimators, to protect patients from the hazards of the scattering radiation. Clinical measurements can be made with a combination of a bilayer of copper and silicon as polarizer, a 0.25-mm tin filter introduced in the path between the X-ray beam and the polarizer, and an operating voltage of 220 kV. The minimum detection limit achieved with this arrangement is 16 ppm, for a kidney depth of 3 x 3 cm, with a skin dose of 1.6 mGy and measurement time of 2,000 seconds.


Asunto(s)
Riñón/metabolismo , Platino (Metal)/análisis , Espectrometría por Rayos X/métodos , Antineoplásicos/farmacocinética , Antineoplásicos/uso terapéutico , Carboplatino/farmacocinética , Carboplatino/uso terapéutico , Cisplatino/farmacocinética , Cisplatino/uso terapéutico , Humanos , Riñón/química , Neoplasias/tratamiento farmacológico , Compuestos Organoplatinos/farmacocinética , Compuestos Organoplatinos/uso terapéutico , Fotones , Platino (Metal)/farmacocinética , Dispersión de Radiación , Sensibilidad y Especificidad
2.
Phys Med Biol ; 43(8): 2337-45, 1998 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-9725608

RESUMEN

A plane polarized x-ray fluorescence system based on an orthovoltage radiotherapy treatment unit, the Pantak DXT-300, has been developed and optimized to measure tumour platinum concentration. The platinum derives from platinum based chemotherapy agents, such as cisplatin and carboplatin used to treat tumours in the head and neck region. Photons from an x-ray tube are polarized by scattering through 90 degrees, and used to stimulate the emission of characteristic platinum x-rays from the tumour. Information about the drug in the tumour could be of use in establishing dose-response relationships, in order to optimize the treatment and reduce the toxicity of the drug. The performance of the system was optimized with respect to the applied x-ray tube voltage, the current and the filter material; the effect on the minimum detection limit (MDL) of the thickness of the overlying tissue surrounding the tumour was investigated in detail. The lowest MDL is achieved using 0.25 mm of tin filter and x-ray tube voltage of 220 kV. This is 5.6 ppm for a tumour surrounded with 20 mm of overlying tissue, a measurement time of 2000 s and an estimated skin dose of 3.0 mGy. This represents the most sensitive in vivo XRF system to date. We have embarked on a clinical pilot study to measure the platinum concentration in tumours of the head and neck, and expect initial results to be available in the near future.


Asunto(s)
Neoplasias de Cabeza y Cuello/diagnóstico por imagen , Platino (Metal)/análisis , Espectrometría por Rayos X/instrumentación , Espectrometría por Rayos X/métodos , Cisplatino/análogos & derivados , Cisplatino/farmacocinética , Cisplatino/uso terapéutico , Diseño de Equipo , Neoplasias de Cabeza y Cuello/tratamiento farmacológico , Humanos , Radiografía , Sensibilidad y Especificidad
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