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在光动力疗法中进行预处理以增强原卟啉IX的积累。

Pretreatment to enhance protoporphyrin IX accumulation in photodynamic therapy.

作者信息

Gerritsen M J P, Smits T, Kleinpenning M M, van de Kerkhof P C M, van Erp P E J

机构信息

Department of Dermatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

Dermatology. 2009;218(3):193-202. doi: 10.1159/000183753. Epub 2008 Dec 11.

Abstract

The response rates of photodynamic therapy (PDT) vary widely. Limited uptake of topically applied 5-aminolaevulinic acid (ALA), or its methyl ester (MAL), and suboptimal production of protoporphyrin IX (PpIX) may account for these differences. Recently, we demonstrated that hyperkeratosis is an important negative factor in ALA uptake. This review has its focus on pretreatment of the skin in order to improve the clinical outcome of ALA/MAL PDT. Pretreatment of hyperkeratosis can be achieved with keratolytics, curettage/debulking, tape stripping, microdermabrasion or laser ablation. Penetration enhancers may alter the composition or organization of the intercellular lipids of the stratum corneum. Several studies have been performed on the use of dimethyl sulfoxide, azone, glycolic acid, oleic acid and iontophoresis to increase the penetration of ALA. As PpIX production is also dominated by temperature-dependent processes, elevating skin temperature during ALA application may also improve treatment results. Another approach is the use of additives that interact with the heme biosynthetic pathway, e.g. by removing ferrous iron with iron-chelating substances such as: ethylenediaminetetraacetic acid; 3-hydroxypyridin-4-ones; 1,2-diethyl-3-hydroxypyridin-4-one-hydrochloride; and desferrioxamine. In conclusion, simple pretreatments or additions to the regular practice of PDT, aimed to optimize intralesional PpIX content, improve the clinical outcome.

摘要

光动力疗法(PDT)的有效率差异很大。局部应用5-氨基酮戊酸(ALA)或其甲酯(MAL)摄取受限,以及原卟啉IX(PpIX)生成欠佳可能是造成这些差异的原因。最近,我们证明角化过度是ALA摄取的一个重要负面因素。本综述重点关注皮肤预处理,以改善ALA/MAL PDT的临床疗效。可通过角质剥脱剂、刮除/清除、胶带剥离、微晶磨皮或激光消融来预处理角化过度。渗透促进剂可能会改变角质层细胞间脂质的组成或结构。已开展多项关于使用二甲亚砜、氮酮、乙醇酸、油酸和离子电渗疗法来增加ALA渗透的研究。由于PpIX的生成也受温度依赖性过程主导,在应用ALA期间提高皮肤温度也可能改善治疗效果。另一种方法是使用与血红素生物合成途径相互作用的添加剂,例如用铁螯合剂(如乙二胺四乙酸、3-羟基吡啶-4-酮、1,2-二乙基-3-羟基吡啶-4-酮盐酸盐和去铁胺)去除亚铁离子。总之,旨在优化皮损内PpIX含量而对PDT常规操作进行的简单预处理或添加物可改善临床疗效。

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