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通过受体介导递送系统的靶向光动力疗法。

Targeted photodynamic therapy via receptor mediated delivery systems.

作者信息

Sharman Wesley M, van Lier Johan E, Allen Cynthia M

机构信息

Department of Nuclear Medicine and Radiobiology, Faculty of Medicine, Université de Sherbrooke, Québec, Canada.

出版信息

Adv Drug Deliv Rev. 2004 Jan 13;56(1):53-76. doi: 10.1016/j.addr.2003.08.015.

Abstract

Targeted photodynamic therapy (PDT) offers the opportunity of enhancing photodynamic efficiency by directly targeting diseased cells and tissues. While antibody-conjugates have received the most attention, cellular transformations offer numerous other potent targets to exploit during the delivery of photosensitizers (PSs) for PDT. Alterations in receptor expression, increased levels of specific cell surface membrane lipids and proteins as well as changes in the cellular microenvironment all occur in diseased cells. Along with other biochemical and physiological changes that occur during diseased and malignant cell transformation, these factors have been utilized in order to improve the efficacy of PDT. Attempts have been made to either increase the uptake of the dye by the target cells and tissues or to improve subcellular localization so as to deliver the dye to photosensitive sites within the cells. This review discusses various PS bioconjugates that utilize these factors and summarizes the results obtained to date.

摘要

靶向光动力疗法(PDT)通过直接靶向病变细胞和组织,提供了提高光动力效率的机会。虽然抗体偶联物受到了最多关注,但细胞转化在为PDT递送光敏剂(PSs)的过程中提供了许多其他可利用的有效靶点。受体表达的改变、特定细胞表面膜脂质和蛋白质水平的增加以及细胞微环境的变化都发生在病变细胞中。连同病变和恶性细胞转化过程中发生的其他生化和生理变化,这些因素已被用于提高PDT的疗效。人们已尝试增加靶细胞和组织对染料的摄取,或改善亚细胞定位,以便将染料递送至细胞内的光敏位点。本文综述了利用这些因素的各种PS生物偶联物,并总结了迄今为止所获得的结果。

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