8 research outputs found

    Deepening subwavelength acoustic resonance via metamaterials with universal broadband elliptical microstructure

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    Slow sound is a frequently exploited phenomenon that metamaterials can induce in order to permit wave energy compression, redirection, imaging, sound absorption, and other special functionalities. Generally, however, such slow sound structures have a poor impedance match to air, particularly at low frequencies and consequently exhibit strong transmission only in narrow frequency ranges. This therefore strongly restricts their application in wave manipulation devices. In this work, we design a slow sound medium that halves the effective speed of sound in air over a wide range of low frequencies (hence our referral to the microstructure as “broadband”), whilst simultaneously maintaining a near impedance match to air. This is achieved with a rectangular array of acoustically rigid cylinders of elliptical cross section, a microstructure that is motivated by combining transformation acoustics with homogenization. Microstructural parameters are optimized in order to provide the required anisotropic material properties as well as near impedance matching. We then employ this microstructure in order to halve the size of a quarter-wavelength resonator (QWR) or equivalently to halve the resonant frequency of a QWR of a given size. This provides significant space savings in the context of low-frequency tonal noise attenuation in confined environments where the absorbing material is adjacent to the region in which sound propagates, such as in a duct. We employ the term “universal” since we envisage that this microstructure may be employed in a number of diverse applications involving sound manipulation.EPSRC Grant EP/K033208/I and EP/R014604/

    Influence of Nucleoshuttling of the ATM Protein in the Healthy Tissues Response to Radiation Therapy: Toward a Molecular Classification of Human Radiosensitivity.

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    PURPOSE: Whereas post-radiation therapy overreactions (OR) represent a clinical and societal issue, there is still no consensual radiobiological endpoint to predict clinical radiosensitivity. Since 2003, skin biopsy specimens have been collected from patients treated by radiation therapy against different tumor localizations and showing a wide range of OR. Here, we aimed to establish quantitative links between radiobiological factors and OR severity grades that would be relevant to radioresistant and genetic hyperradiosensitive cases. METHODS AND MATERIALS: Immunofluorescence experiments were performed on a collection of skin fibroblasts from 12 radioresistant, 5 hyperradiosensitive, and 100 OR patients irradiated at 2 Gy. The numbers of micronuclei, γH2AX, and pATM foci that reflect different steps of DNA double-strand breaks (DSB) recognition and repair were assessed from 10 minutes to 24 hours after irradiation and plotted against the severity grades established by the Common Terminology Criteria for Adverse Events and the Radiation Therapy Oncology Group. RESULTS: OR patients did not necessarily show a gross DSB repair defect but a systematic delay in the nucleoshuttling of the ATM protein required for complete DSB recognition. Among the radiobiological factors, the maximal number of pATM foci provided the best discrimination among OR patients and a significant correlation with each OR severity grade, independently of tumor localization and of the early or late nature of reactions. CONCLUSIONS: Our results are consistent with a general classification of human radiosensitivity based on 3 groups: radioresistance (group I); moderate radiosensitivity caused by delay of nucleoshuttling of ATM, which includes OR patients (group II); and hyperradiosensitivity caused by a gross DSB repair defect, which includes fatal cases (group III)

    Zweibasische Säuren (Dicarbonsäuren)

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