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首页> 外文期刊>Lasers in surgery and medicine >Intense pulse light and 5-ALA PDT: phototoxic effects in vitro depend on the spectral overlap with protoporphyrine IX but do not match cut-off filter notations.
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Intense pulse light and 5-ALA PDT: phototoxic effects in vitro depend on the spectral overlap with protoporphyrine IX but do not match cut-off filter notations.

机译:强脉冲光和5-ALA PDT:光毒性的影响体外取决于光谱重叠第九protoporphyrine但不匹配截止过滤符号。

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BACKGROUND AND OBJECTIVES: Successful photodynamic therapy (PDT) requires a light source by which light is absorbed by the photosensitizer. Such absorption is achieved by adapting the emission spectrum of the lamp to the absorption-spectrum of the photosensitizer. Intense pulsed light sources (IPLs) are widely used in dermatology, but a standardized protocol for IPL-PDT is not available. Five different IPLs were chosen to evaluate their efficacy for PDT in vitro and the possibility for developing a standard protocol for PDT. MATERIALS AND METHODS: Emission-spectra of IPLs were measured with an optical spectrograph and compared with the absorption spectrum of protoporphyrine IX (PpIX). Keratinocytes were incubated with 5-ALA and illuminated with the IPLs. Cell viability was determined for radiant exposures ranging from 0 to 504 J/cm(2) and pulse durations from 8 to 100 milliseconds. A standard LED light source was used as a reference. RESULTS: Cell viability is less effectively reduced by 5-ALA-PDT with IPLs than by a LED light source. Radiant exposures of the five IPLs ranged between 80 and 311 J/cm(2) to achieve the EC(50) value. This value correlated with the spectral overlap of the respective IPL and the absorption-spectrum of PpIX but not with the cut-off filter notations supplied by the manufacturer. CONCLUSIONS: All IPLs assessed emit different spectra because of different filter technologies. Different radiant exposures (J/cm(2) ) were necessary to achieve a photodynamic effect with 5-ALA in vitro depending on these spectra similar to the photodynamic effect of the standard LED light source. IPLs may be applicable in clinical PDT but radiant exposure protocols must be separately evaluated for each single IPL despite similar cut-off filter specifications. Such protocols are highly important for clinical practice to avoid a potential mismatch of excitation wavelengths and to prevent photothermal side effects when light intensities of up to hundreds of W/cm(2) are applied.
机译:背景和目标:成功的光能治疗(PDT)需要的光源光吸收的光敏剂。吸收是通过调整发射灯的光谱吸收光谱光敏剂。来源(ipl)广泛应用于皮肤,但IPL-PDT不是标准化的协议可用。评价体外和PDT的功效开发一种标准协议可能性PDT。的ipl和光学测量摄谱仪并与吸收光谱protoporphyrine第九(PpIX)。角化细胞和5-ALA和孵化与ipl照亮。确定了辐射暴露从0504 J /厘米(2)和脉冲持续时间从8到100年毫秒。用作参考。更有效地减少5-ALA-PDT ipl比由LED光源。五ipl介于80和311之间J /厘米(2)实现电子商务(50)值。相关的光谱重叠各自的IPL的吸收光谱PpIX但不是截止滤光片的符号由制造商提供的。ipl发出不同的光谱,因为评估不同的过滤技术。曝光(J /厘米(2))实现是必要的光动力效应与5-ALA体外不同在这些光谱与光动力相似标准的LED光源的效果。适用于临床PDT但辐射接触协议必须单独评估为每个单独的IPL尽管类似截止过滤器规格。避免重要的临床实践潜在的激发波长和不匹配为了防止当光光照的副作用强度的数以百计的W / cm (2)应用。

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