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    • 6. 发明申请
    • ULTRAVIOLET PROTECTION EFFECT EVALUATION METHOD, EVALUATION APPARATUS, AND RECORDING MEDIUM
    • 超声波保护效应评估方法,评估装置和记录介质
    • US20130169951A1
    • 2013-07-04
    • US13823438
    • 2011-07-13
    • Yoshimasa MiuraMasato Hatao
    • Yoshimasa MiuraMasato Hatao
    • G01N21/59
    • G01N21/59G01N17/004G01N21/33
    • An evaluation method for evaluating the ultraviolet protection effect of a measurement sample applied on a substrate includes a first step of measuring, at predetermined wavelength intervals, a change over time of a spectral transmission spectrum of the measurement sample within a predetermined wavelength range by irradiating light from a light source that includes ultraviolet light, visible light, and infrared light under a predetermined irradiation condition; a second step of establishing, based on the change over time of the spectral transmission spectrum, a correlation between a light irradiation time and an erythema effective dose per unit time, which is obtained by dividing an erythema effective dose of the measurement sample by an erythema effective dose per 1 MED; and a third step of calculating an in vitro rSPF predictive value for the measurement sample on the basis of a time until a cumulative erythema effective dose, which is obtained through time integration based on the correlation, reaches 1 MED.
    • 用于评估施加在基板上的测量样品的紫外线保护效果的评估方法包括:第一步骤,以预定波长间隔,通过照射光来测量在预定波长范围内的测量样品的光谱透射光谱随时间的变化 从包含紫外光,可见光和红外光的光源在预定的照射条件下; 基于光谱透射光谱随时间的变化建立光照射时间和每单位时间的红斑有效剂量之间的相关性的第二步骤,其通过将测量样品的红斑有效剂量除以红斑 每1 MED有效剂量; 以及基于通过基于相关性的时间积分获得的累积红斑有效剂量之间的时间达到1 MED的时间来计算测量样品的体外rSPF预测值的第三步骤。
    • 8. 发明申请
    • METHOD, APPARATUS, PROGRAM, AND RECORDING MEDIUM FOR EVALUATING ULTRAVIOLET RADIATION PROTECTION EFFECT
    • 用于评估超紫外线辐射防护效果的方法,装置,程序和记录介质
    • US20100256924A1
    • 2010-10-07
    • US12682286
    • 2008-10-17
    • Yoshimasa MiuraMasato Hatao
    • Yoshimasa MiuraMasato Hatao
    • G01N21/84G01N21/25G06F19/00
    • G01N21/33
    • An evaluating method for evaluating an ultraviolet radiation protection effect in a measurement sample includes a first step of measuring a temporal change of the spectral transmission spectrum in the measurement sample within a predetermined wavelength range at predetermined wavelength intervals by irradiating with light including ultraviolet radiation from a light source under a predetermined light irradiating condition, a second step of setting a correlation between a light irradiating time and minimal erythema doses by predetermined time intervals based on the temporal change of the spectral transmission spectrum obtained in the first step, and a third step of calculating a predicted in vitro SPF in the measurement sample using a time until an accumulated minimal erythema dose that is obtained as a time integration of the minimal erythema doses based on the correlation obtained in the second step reaches 1 MED.
    • 用于评价测定试样的紫外线防护效果的评价方法包括:第一步骤,通过用包含紫外线辐射的光进行照射,以规定的波长间隔测定预定波长范围内的测定样品中的光谱透射光谱的时间变化 光源,在第一步骤中获得的光谱透射光谱的时间变化的第二步骤,将光照射时间和最小红斑剂量之间的相关性设定预定时间间隔;第三步骤, 使用一段时间计算测量样品中预测的体外SPF,直到基于在第二步骤中获得的相关性的最小红斑剂量的时间积分获得的累积最小红斑剂量达到1 MED。