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首页> 外文期刊>Photochemistry and Photobiology: An International Journal >Topical application of 5-aminolevulinic acid hexyl eater and 5-aminolevulinic acid to normal nude mouse skin: Differences in protoporphyrin IX fluorescence kinetics and the role of the stratum corneum
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Topical application of 5-aminolevulinic acid hexyl eater and 5-aminolevulinic acid to normal nude mouse skin: Differences in protoporphyrin IX fluorescence kinetics and the role of the stratum corneum

机译:5-氨基乙酰丙酸己基和5-氨基乙酰丙酸在正常裸鼠皮肤上的局部应用:原卟啉IX荧光动力学和角质层作用的差异

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摘要

An important limitation of topical 5-aminolevulinic acid (ALA)-based photodetection and photodynamic therapy is that the amount of the fluorescing and photosensitizing product protoporphyrin IX (PpIX) formed is limited. The reason for this Is probably the limited diffusion of ALA through the stratum corneum, A solution to this problem might be found in the use of ALA derivatives, as these compounds are more lipophilic and therefore might have better penetration properties than ALA itself. Previous studies have shown that ALA hexyl ester (ALA-HE) is more successful than ALA for photodetection of early (pre)malignant lesions in the bladder. However, ALA pentyl ester slightly increased the in vivo PpIX fluorescence in early (pre)malignant lesions in hairless mouse skin compared to ALA. The Increased PpIX fluorescence is located in the stratum corneum and not in the dysplastic epidermal layer. In the present study, ALA- and ALAHE-induced PpIX fluorescence kinetics are compared in the normal nude mouse skin, of which the permeability properties differ from the bladder. Application times and ALA(HE) concentrations were varied, the effect of a penetration enhancer and the effect of tape stripping the skin before or after application were investigated. Only during application for 24 h, did ALAHE induce slightly more PpIX fluorescence than ALA, After application times ranging from I to 60 min, ALA-induced PpIX fluorescence was higher than ALAHE-induced PpIX fluorescence. ALA also induced higher PpIX production than ALAHE after 10 min of application with concentrations ranging from 0.5 to 40%. The results of experiments with the penetration enhancer and tape stripping indicated that the stratum corneum acts a barrier against ALA and ALAHE, Use of penetration enhancer or tape stripping enhanced the PpIX production more in the case of ALAHE application than in the case of ALA application. This, together with the results from the different application times and concentrations indicates that ALAHE diffuses more slowly across the stratum corneum than ALA. [References: 39]
机译:基于局部5-氨基乙酰丙酸(ALA)的光检测和光动力疗法的一个重要限制是,形成的荧光和光敏产品原卟啉IX(PpIX)的数量受到限制。其原因可能是ALA在角质层中的扩散有限。使用ALA衍生物可以找到解决该问题的方法,因为这些化合物具有更高的亲脂性,因此比ALA本身具有更好的渗透性能。以前的研究表明,ALA己酸酯(ALA-HE)在早期检测膀胱癌前(恶性)病变方面比ALA更成功。但是,与ALA相比,ALA戊酯在无毛小鼠皮肤的早期(恶性)早期病变中略微增加了体内PpIX荧光。 PpIX荧光增加位于角质层,而不位于发育不良的表皮层。在本研究中,在正常裸鼠皮肤中比较了ALA和ALAHE诱导的PpIX荧光动力学,其渗透性不同于膀胱。改变施用时间和ALA(HE)浓度,研究渗透促进剂的作用以及在施用之前或之后用胶带剥离皮肤的作用。仅在施用24小时期间,ALAHE诱导的PpIX荧光要比ALA略多。施用时间为1至60分钟后,ALA诱导的PpIX荧光要高于ALAHE诱导的PpIX荧光。施用10分钟后,ALA的PpIX产量也高于ALAHE,浓度为0.5%至40%。使用渗透促进剂和胶带剥离的实验结果表明,角质层对ALA和ALAHE起到了屏障作用。使用渗透促进剂或胶带剥离在ALAHE的情况下比在ALA的情况下提高了PpIX的产量。这与来自不同施用时间和浓度的结果一起表明,ALAHE在角质层中的扩散比ALA慢。 [参考:39]

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