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具有多种降解模式的光敏剂用于高效且术后安全的光动力疗法。

Photosensitizers with multiple degradation modes for efficient and postoperatively safe photodynamic therapy.

机构信息

Department of Chemistry, Institute of Molecular Aggregation Science, Tianjin University, Tianjin, 300072, PR China.

Department of Pharmacy, The Third Affiliated Hospital (The Affiliated Luohu Hospital) of Shenzhen University, Shenzhen, 518001, PR China.

出版信息

Biomaterials. 2023 Aug;299:122182. doi: 10.1016/j.biomaterials.2023.122182. Epub 2023 May 31.

Abstract

Photodynamic therapy (PDT) is emerging as a powerful tool for cancer treatment due to its unique advantages in terms of noninvasive and spatiotemporal selectivity. However, the residue of photosensitizers (PSs), which usually lead to thorny post-treatment side effects after photodynamic therapy (PDT), is one of bottlenecks for clinical translation. Herein, PSs with multiple degradation modes are developed to solve this issue. Upon 660 nm laser excitation, PSs can produce different types of reactive oxygen species (ROS), in which O and O could kill the cancer cells, while ·OH could oxide the PSs themselves for photodegradation. After PDT, the residual few number of PSs could be further oxidized by endogenous ROS for biodegradation, and the degradation products could be further excreted by urine. This process therefore solves the slow-metabolism issue of traditional PSs. Among them, SQSe demonstrates the highest killing efficiency with best degradation ability, as confirmed by both in vitro and in vivo results. The postoperative safety of SQSe is further verified by assessment on in vivo artificially induced post-operative side effects.

摘要

光动力疗法(PDT)由于其在非侵入性和时空选择性方面的独特优势,正在成为一种强大的癌症治疗工具。然而,光动力治疗(PDT)后残留的光敏剂(PS)通常会导致棘手的治疗后副作用,这是其临床转化的瓶颈之一。为此,开发了具有多种降解模式的 PS 以解决这个问题。在 660nm 激光激发下,PS 可以产生不同类型的活性氧(ROS),其中 O 和 O 可以杀死癌细胞,而·OH 可以将 PS 自身氧化进行光降解。PDT 后,残留的少数 PS 可以进一步被内源性 ROS 氧化进行生物降解,降解产物可以通过尿液进一步排出。这个过程解决了传统 PS 代谢缓慢的问题。其中,SQSe 表现出最高的杀伤效率和最佳的降解能力,这一点通过体外和体内结果得到了证实。SQSe 的术后安全性进一步通过评估体内人工诱导的术后副作用得到了验证。

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