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去铁胺增强 5-氨基酮戊酸诱导的原卟啉 IX 积累和增生性瘢痕的治疗效果。

Desferrioxamine Enhances 5-Aminolaevulinic Acid- Induced Protoporphyrin IX Accumulation and Therapeutic Efficacy for Hypertrophic Scar.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, University Town, Guangzhou, 510006, PR China.

School of Pharmaceutical Sciences, Sun Yat-sen University, University Town, Guangzhou, 510006, PR China; School of Pharmaceutical Sciences, Hainan University, Haikou, 570228, PR China.

出版信息

J Pharm Sci. 2023 Jun;112(6):1635-1643. doi: 10.1016/j.xphs.2023.01.015. Epub 2023 Jan 20.

Abstract

Hypertrophic scar is a common problem after skin burns or trauma which brings physical, psychological, and cosmetic problems to patients. Photodynamic therapy with 5-aminolevulinic acid (5-ALA) is a promising therapy for hypertrophic scar. However, clinical applications of 5-ALA are limited because of the low permeability of 5-ALA in the skin stratum corneum and the rapid binding of protoporphyrin IX (PpIX) with iron ions, which lead to insufficient PpIX production in target tissues. Herein, a mixture of 5-ALA and DFO (deferoxamine, a special iron chelator) was applied for the treatment of hypertrophic scar. 5-ALA/DFO could efficiently block the biotransformation of PpIX to heme, thus realizing a significant accumulation of photosensitizer. In addition, injection locally into the lesion was applied, which combined with enhanced photodynamic therapy to destroy hypertrophic scar fibroblasts. In vitro experiments showed that 5-ALA/DFO could increase more ROS generation by increasing the accumulation of PpIX, resulting in the apoptosis of hypertrophic scar fibroblasts. Furthermore, 5-ALA/DFO inhibited the proliferation and migration of hypertrophic scar fibroblasts. In vivo study showed that 5-ALA/DFO could effectively inhibit the formation of proliferative scar. Therefore, 5-ALA/DFO has the potential to enhance the photodynamic therapy of 5-ALA and provides a new treatment strategy for hypertrophic scar.

摘要

增生性瘢痕是皮肤烧伤或创伤后常见的问题,给患者带来身体、心理和美容方面的问题。5-氨基酮戊酸(5-ALA)光动力疗法是治疗增生性瘢痕的一种有前途的疗法。然而,由于 5-ALA 在皮肤角质层中的低渗透性和原卟啉 IX(PpIX)与铁离子的快速结合,导致靶组织中产生的 PpIX 不足,因此 5-ALA 的临床应用受到限制。在此,我们将 5-ALA 与 DFO(去铁胺,一种特殊的铁螯合剂)混合应用于增生性瘢痕的治疗。5-ALA/DFO 可以有效地阻止 PpIX 向血红素的生物转化,从而实现光敏剂的显著积累。此外,还应用了局部注射到病变部位,结合增强光动力疗法来破坏增生性瘢痕成纤维细胞。体外实验表明,5-ALA/DFO 通过增加 PpIX 的积累来增加更多的 ROS 生成,导致增生性瘢痕成纤维细胞凋亡。此外,5-ALA/DFO 抑制增生性瘢痕成纤维细胞的增殖和迁移。体内研究表明,5-ALA/DFO 可以有效地抑制增殖性瘢痕的形成。因此,5-ALA/DFO 有可能增强 5-ALA 的光动力疗法,并为增生性瘢痕提供新的治疗策略。

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