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采用双重光照方案对无毛小鼠皮肤进行局部5-氨基酮戊酸光动力治疗:原卟啉IX荧光动力学、光漂白及生物学效应

Topical 5-aminolevulinic acid-photodynamic therapy of hairless mouse skin using two-fold illumination schemes: PpIX fluorescence kinetics, photobleaching and biological effect.

作者信息

Robinson D J, de Bruijn H S, de Wolf W J, Sterenborg H J, Star W M

机构信息

Photodynamic Therapy and Optical Spectroscopy Research Program, Subdivision of Clinical Physics, Department of Radiation Oncology, Daniel den Hoed Cancer Centre, University Hospital Rotterdam, Rotterdam, The Netherlands.

出版信息

Photochem Photobiol. 2000 Dec;72(6):794-802. doi: 10.1562/0031-8655(2000)072<0794:TAAPTO>2.0.CO;2.

Abstract

Light fractionation with dark periods of the order of hours has been shown to considerably increase the efficacy of 5-aminolevulinic acid-photodynamic therapy (ALA-PDT). Recent investigations have suggested that this increase may be due to the resynthesis of protoporphyrin IX (PpIX) during the dark period following the first illumination that is then utilized in the second light fraction. We have investigated the kinetics of PpIX fluorescence and PDT-induced damage during PDT in the normal skin of the SKH1 HR hairless mouse. A single illumination (514 nm), with light fluences of 5, 10 and 50 J cm-2 was performed 4 h after the application of 20% ALA, to determine the effect of PDT on the synthesis of PpIX. Results show that the kinetics of PpIX fluorescence after illumination are dependent on the fluence delivered; the resynthesis of PpIX is progressively inhibited following fluences above 10 J cm-2. In order to determine the influence of the PpIX fluorescence intensity at the time of the second illumination on the visual skin damage, 5 + 95 and 50 + 50 J cm-2 (when significantly less PpIX fluorescence is present before the second illumination), were delivered with a dark interval of 2 h between light fractions. Each scheme was compared to illumination with 100 J cm-2 in a single fraction delivered 4 or 6 h after the application of ALA. As we have shown previously greater skin damage results when an equal light fluence is delivered in two fractions. However, significantly more damage results when 5 J cm-2 is delivered in the first light fraction. Also, delivering 5 J cm-2 at 5 mW cm-2 + 95 J cm-2 at 50 mW cm-2 results in a reduction in visual skin damage from that obtained with 5 + 95 J cm-2 at 50 mW cm-2. A similar reduction in damage is observed if 5 + 45 J cm-2 are delivered at 50 mW cm-2. PpIX photoproducts are formed during illumination and subsequently photobleached. PpIX photoproducts do not dissipate in the 2 h dark interval between illuminations.

摘要

已证明,进行时长为几小时的暗期光分割可显著提高5-氨基酮戊酸光动力疗法(ALA-PDT)的疗效。最近的研究表明,这种疗效提高可能是由于在首次光照后的暗期内原卟啉IX(PpIX)重新合成,然后在第二次光分割中被利用。我们研究了SKH1 HR无毛小鼠正常皮肤在光动力疗法期间PpIX荧光和光动力疗法诱导损伤的动力学。在涂抹20%ALA后4小时,进行单次光照(514 nm),光通量分别为5、10和50 J/cm²,以确定光动力疗法对PpIX合成的影响。结果表明,光照后PpIX荧光的动力学取决于所传递的光通量;光通量高于10 J/cm²后,PpIX的重新合成逐渐受到抑制。为了确定第二次光照时PpIX荧光强度对肉眼可见皮肤损伤的影响,分别以5 + 95和50 + 50 J/cm²(第二次光照前PpIX荧光明显较少时)进行光照,两次光分割之间的暗间隔为2小时。每种方案都与在涂抹ALA后4或6小时单次给予100 J/cm²光照进行比较。正如我们之前所表明的,当等量的光通量分两次给予时,会导致更大的皮肤损伤。然而,当第一次光分割给予5 J/cm²时,会导致明显更多的损伤。此外,以5 mW/cm²给予5 J/cm² + 以50 mW/cm²给予95 J/cm²,与以50 mW/cm²给予5 + 95 J/cm²相比,肉眼可见的皮肤损伤有所减少。如果以50 mW/cm²给予5 + 45 J/cm²,也会观察到类似的损伤减少。PpIX光产物在光照期间形成,随后发生光漂白。PpIX光产物不会在两次光照之间的2小时暗间隔中消散。

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