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局部外用5-氨基酮戊酸诱导的荧光在紫外线B照射小鼠皮肤中的光动力治疗期间的光漂白及光动力治疗后的荧光重现

Photobleaching during and re-appearance after photodynamic therapy of topical ALA-induced fluorescence in UVB-treated mouse skin.

作者信息

Van der Veen N, De Bruijn H S, Star W M

机构信息

Department of Clinical Physics, Dr. Daniel den Hoed Cancer Centre, Rotterdam, The Netherlands.

出版信息

Int J Cancer. 1997 Jul 3;72(1):110-8. doi: 10.1002/(sici)1097-0215(19970703)72:1<110::aid-ijc16>3.0.co;2-n.

Abstract

Photodynamic therapy (PDT) using protoporphyrin IX (PpIX) induced by topically applied 5-aminolevulinic acid (ALA) seems a promising alternative for the treatment of superficial non-melanoma skin cancer and actinic keratosis. In this study, the kinetics of new PpIX fluorescence arising after a PDT treatment that had photobleached the original fluorescence were determined. Our purpose was to examine the feasibility of multiple irradiations, following a single topical ALA application, to increase PDT efficacy. In addition, photobleaching during PDT and the fluorescence spectra during and after PDT were studied. As a model we used hairless mice with and without UVB-induced skin lesions. ALA was applied to the skin for 4 hr. An illumination was delivered either immediately after application or 6 hr after the end of the application (at interval of maximum fluorescence). During PDT, the fluorescence of normal skin decreased at a faster rate than the fluorescence of the skin lesions. In the fluorescence study after PDT, the areas treated immediately post-application showed a fluorescence increase over time similar to that in non-treated areas on the same mice. A remarkable result was that the fluorescence of areas treated at maximum fluorescence increased, whereas the fluorescence of non-treated areas did not increase over time. With both treatment intervals the new fluorescence showed a characteristic PpIX spectrum. Our results demonstrate that a second illumination, when new PpIX fluorescence has been formed, may increase PDT efficacy after topical ALA application. This finding has been demonstrated previously for systemic ALA administration.

摘要

使用局部应用5-氨基酮戊酸(ALA)诱导产生的原卟啉IX(PpIX)进行光动力疗法(PDT)似乎是治疗浅表性非黑素瘤皮肤癌和光化性角化病的一种有前景的替代方法。在本研究中,测定了在一次光动力疗法治疗使原始荧光发生光漂白后新产生的PpIX荧光的动力学。我们的目的是研究在单次局部应用ALA后进行多次照射以提高光动力疗法疗效的可行性。此外,还研究了光动力疗法期间的光漂白以及光动力疗法期间和之后的荧光光谱。我们使用有和没有紫外线B(UVB)诱导皮肤损伤的无毛小鼠作为模型。将ALA应用于皮肤4小时。在应用后立即或应用结束后6小时(在最大荧光间隔时)进行照射。在光动力疗法期间,正常皮肤的荧光下降速度比皮肤损伤部位的荧光下降速度更快。在光动力疗法后的荧光研究中,应用后立即治疗的区域随着时间的推移荧光增加,类似于同一只小鼠未治疗区域的荧光增加情况。一个显著的结果是,在最大荧光时治疗的区域的荧光增加,而未治疗区域的荧光并未随时间增加。两种治疗间隔下新产生的荧光均显示出特征性的PpIX光谱。我们的结果表明,当新的PpIX荧光形成后进行第二次照射,可能会提高局部应用ALA后的光动力疗法疗效。这一发现先前已在全身应用ALA时得到证实。

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