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首页> 外文期刊>Photochemistry and Photobiology: An International Journal >Temperature effect on accumulation of protoporphyrin IX after topical application of 5-aminolevulinic acid and its methylester and hexylester derivatives in normal mouse skin
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Temperature effect on accumulation of protoporphyrin IX after topical application of 5-aminolevulinic acid and its methylester and hexylester derivatives in normal mouse skin

机译:在正常小鼠皮肤中局部应用5-氨基乙酰丙酸及其甲酯和己酸酯衍生物后,温度对原卟啉IX积累的影响

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摘要

Significant amounts of protoporphyrin IX (PpIX) are formed after 6 min of topical application of 5-aminolevulinic acid (ALA) and its hexylester derivative, whereas PpIX is formed after 10 min of topical application of ALA-methylester derivative in normal mouse skin at 37degreesC. Lowering the skin temperature to 28-32degreesC by the administration of the anesthetic Hypnorm-Dormicum reduces the PpIX fluorescence by a factor of 2-3. Practically no PpIX was formed as long as the skin temperature was kept at 12-18degreesC. At around 30degreesC PpIX fluorescence appears later after application of ALA-ester derivatives (14-20 min) than after application of ALA (8 min), indicating differences in their bioavailability (delayed penetration through the stratum corneum, cellular uptake, conversion to ALA, PpIX production) in mouse skin in vivo. The difference in lag time in the PpIX formation after application of ALA and ALA-esters may be partly related to deesterification of the ALA-ester molecules. The temperature dependence of PpIX production may be used for improvement of photodynamic therapy with ALA and ALA-ester derivatives, where accumulation of PpIX can be selectively enhanced by increasing the temperature of the target tissue. [References: 27]
机译:在37°C的正常小鼠皮肤中局部应用5-氨基乙酰丙酸(ALA)及其己酸酯衍生物6分钟后形成大量的原卟啉IX(PpIX),而PpIX在局部应用ALA-甲酯衍生物10分钟后形成。 。通过使用麻醉性Hypnorm-Dormicum将皮肤温度降低至28-32摄氏度,可使PpIX荧光降低2-3倍。只要将皮肤温度保持在12-18℃,实际上就不会形成PpIX。在约30摄氏度下,施用ALA-酯衍生物后(14-20分钟)比在施用ALA后(8分钟)更晚出现PpIX荧光,表明它们的生物利用度存在差异(穿过角质层的渗透,细胞摄取,转化为ALA, PpIX生产)在小鼠体内的皮肤。在施用ALA和ALA-酯后,PpIX形成中的滞后时间的差异可能部分与ALA-酯分子的脱酯作用有关。 PpIX产生的温度依赖性可用于改善ALA和ALA-酯衍生物的光动力疗法,其中PpIX的积累可通过提高靶组织的温度来选择性地提高。 [参考:27]

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