The distribution of biologically effective UV spectral irradiances received on a manikin face that cause erythema and skin cancer.

The distribution of biologically effective UV spectral irradiances received on a manikin face that cause erythema and skin cancer.
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人体模型面部收到的生物有效紫外线光谱辐照度的分布,会导致红斑和皮肤癌。

DOI:
10.1016/j.jphotobiol.2014.08.004
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发表时间:
2014
期刊:
Journal of photochemistry and photobiology. B, Biology
影响因子:
--
通讯作者:
Yang Liu
Yang Liu
中科院分区:
--
文献类型:
--
作者:
F. Wang;Tiantian Ge;Q. Gao;Liwen Hu;Jiaming Yu;Yang Liu

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太阳紫外线(UV)辐射是人类红斑和皮肤癌的主要原因,面部是风险最高的部位之一。生物有效的紫外线辐射(UVBE)是波长依赖性的,风险评估已被证明是基于接收到的紫外线辐射值。因此,本研究使用分光辐射计和头部人体模型测量面部皮肤暴露于UV光谱辐照度,通过作用光谱对其进行加权,以计算引起红斑(UVBEery)、非黑色素瘤(UVBEnon-mel)、人鳞状细胞癌(UVBEh-SCC)和DNA损伤(UVBEDNA-d)的UVBE。结果表明,在晴天,生物有效UVB和UVA辐射分别在65-73° SEA(8-9 UVI)和55-68° SEA(6-7 UVI)处有峰值。在10-30° SEA范围内,高度皮肤损伤波长均在300 nm处观察到。然而,在30-60°、60-81°和10-81° SEA范围内,对于UVBEery,高度皮肤损伤波长分别为300 nm、304 nm和300 nm;对于UVBEnon-mel,高度皮肤损伤波长分别为304 nm、306 nm和304 nm;对于UVBEh-SCC,高度皮肤损伤波长均为305 nm,对于UVBEDNA-d,高度皮肤损伤波长分别为302 nm和312 nm。
Solar ultraviolet (UV) radiation is a major cause of erythema and skin cancer in humans and the face is one of the highest risk sites. Biologically effective UV irradiation (UVBE) is wavelength-dependent, and risk assessment has been demonstrated based on the value of the received UV radiation. Therefore, this study measured the face skin exposure to UV spectral irradiance using a spectroradiometer and a head manikin, which were weighted by action spectra to calculate the UVBE that causes erythema (UVBEery), non-melanoma (UVBEnon-mel), human squamous cell cancer (UVBEh-SCC), and DNA damage (UVBEDNA-d). We determined that the biologically effective UVB and UVA irradiances on clear sky days had peak values at 65–73° SEA (8–9 UVI) and 55–68° SEA (6–7 UVI), respectively. In the 10–30° SEA range, the highly skin-damaging wavelengths were all observed at 300 nm. However, in the 30–60°, 60–81°, and 10–81° SEA ranges, the highly skin damaging wavelengths were 300 nm, 304 nm and 300 nm for UVBEery, respectively; 304 nm, 306 nm and 304 nm for UVBEnon-mel, respectively; all 305 nm for UVBEh-SCC, and two small peaks at 302 nm and 312 nm for UVBEDNA-d.
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