提高纳米技术介导的光动力治疗效果的策略。

IF 3.9
Nanomedicine (London, England) Pub Date : 2025-10-01 Epub Date: 2025-08-28 DOI:10.1080/17435889.2025.2550233
Yanhan Mo, Xu Liu, Jian You, Lihua Luo
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引用次数: 0

摘要

光动力疗法(PDT)是一种无创治疗方法,在肿瘤治疗中特别有效。PDT利用光敏剂(ps)吸收特定波长的光,将光子能量转化为化学能,随后产生细胞毒性活性氧(ROS)。这些ROS通过凋亡、坏死和自噬相关途径触发细胞死亡。与传统疗法相比,PDT具有高选择性、可重复性、安全性增强、副作用小、耐药低、与放疗或化疗兼容等显著优势。然而,由于光的组织穿透深度有限,PDT治疗深部肿瘤的效果不理想。此外,光敏剂的靶向性差、肿瘤微环境中的不利因素等局限性极大地限制了PDT的治疗效果和临床适用性。为了提高PDT的有效性,人们探索了各种策略,其中纳米技术已成为研究的重点。本文综述了增强纳米技术介导的PDT的多种方法,重点是实现光敏剂(组织、细胞和细胞器水平)的靶向递送,提高光敏剂的性能和调节肿瘤微环境。这些见解为开发新型高效PDT纳米平台提供了理论指导和实践参考。我们在PubMed、Elsevier ScienceDirect、Web of Science、Wiley和Scopus(2004 - 2025)进行了文献检索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strategies to enhance the effects of nanotechnology-mediated photodynamic therapy.

Photodynamic therapy (PDT) is a noninvasive therapeutic approach, particularly effective in tumor treatment. PDT utilizes photosensitizers (PSs) to absorb light at specific wavelengths, converting photon energy into chemical energy and subsequently generating cytotoxic reactive oxygen species (ROS). These ROS trigger cell death through apoptosis, necrosis and autophagy-related pathways. Compared with conventional therapies, PDT exhibits significant advantages, including high selectivity, repeatability, enhanced safety, minimal side effects, low drug resistance, and compatibility with radiotherapy or chemotherapy. However, due to the limited tissue penetration depth of light, PDT demonstrates suboptimal efficacy in treating deep tumors. Additionally, limitations such as poor targeting of photosensitizers and unfavorable factors in the tumor microenvironment greatly restrict PDT's therapeutic efficacy and clinical applicability. To enhance PDT efficacy, various strategies have been explored, among which nanotechnology has emerged as a key research focus. This review summarizes multiple approaches to augmenting nanotechnology-mediated PDT, with emphasis on achieving targeted delivery of photosensitizers (tissue, cell, and organelle-level), improving the performance of photosensitizers and modulating the tumor microenvironment. These insights provide theoretical guidance and practical references for developing novel and efficient PDT nanoplatforms. We conducted the literature search in PubMed, Elsevier ScienceDirect, Web of Science, Wiley and Scopus (from 2004 to 2025).

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