异构光敏剂的穿梭式纳米组装可增强光动力疗法的 ROS 生成和肿瘤穿透力

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-09-26 DOI:10.1016/j.matt.2024.09.001
Peijuan Zhang, Qifei Shen, Jianye Yang, Zhiqin Zhao, Anran Gao, Shuai Chen, Yan Zhang, Lingjie Meng, Dongfeng Dang
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引用次数: 0

摘要

光动力疗法(PDT)迫切需要能产生大量活性氧(ROS)并具有良好肿瘤靶向性和穿透性的光敏剂,但在制备有机聚集体时,同时实现所有这些目标仍具有挑战性。特别是由异构光敏剂组装成的不同形状的纳米聚集体尚未见报道。因此,我们开发了 DTPA-2,5-BT-P 和 DTPA-5,2-BT-P 的异构光敏剂,DTPA-2,5-BT-P 可以产生有效的分子间相互作用,而 DTPA-5,2-BT-P 则会产生分子内相互作用。这导致 DTPA-2,5-BT-P 形成晶体状纳米梭(NSs),而 DTPA-5,2-BT-P 则形成无定形纳米球(NPs)。值得注意的是,DTPA-2,5-BT-P NSs 产生的 ROS 比 DTPA-5,2-BT-P NPs 高。此外,DTPA-2,5-BT-P NSs 还能实现更快的细胞内化、更好的肿瘤靶向性和穿透性,从而在体内实现高效的光导疗法,抑制率高达 81%。这表明,紧密堆积的DTPA-2,5-BT-P NSs是一种很有前景的光敏剂,可用于癌症治疗中的高效PDT。
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Shuttle-like nanoassemblies by isomeric photosensitizers to enhance ROS generation and tumor penetration for photodynamic therapy
Photosensitizers with high reactive oxygen species (ROS) generation and good tumor targeting and penetration are urgently needed for photodynamic therapy (PDT), but it is still challenging when preparing organic aggregates to achieve all these goals simultaneously. In particular, nanoaggregates assembled by isomeric photosensitizers but in different shapes have not been reported yet. Therefore, isomeric photosensitizers of DTPA-2,5-BT-P and DTPA-5,2-BT-P are developed, where an efficient intermolecular interaction can be obtained in DTPA-2,5-BT-P but an intramolecular interaction occurs in DTPA-5,2-BT-P. This results in the formation of crystalline nanoshuttles (NSs) for DTPA-2,5-BT-P but amorphous nanospheres (NPs) for DTPA-5,2-BT-P. Notably, higher ROS generation occurs in DTPA-2,5-BT-P NSs than in DTPA-5,2-BT-P NPs. Moreover, faster cellular internalization and better tumor targeting and penetration can be achieved in DTPA-2,5-BT-P NSs, leading to efficient PDT in vivo with an inhibition rate of 81%. This demonstrates that closely packed DTPA-2,5-BT-P NSs can be promising photosensitizers for high-performance PDT in cancer therapy.
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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