{"title":"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","authors":"Peijuan Zhang, Qifei Shen, Jianye Yang, Zhiqin Zhao, Anran Gao, Shuai Chen, Yan Zhang, Lingjie Meng, Dongfeng Dang","doi":"10.1016/j.matt.2024.09.001","DOIUrl":null,"url":null,"abstract":"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 <em>in vivo</em> 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.","PeriodicalId":17,"journal":{"name":"ACS Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":4.0000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Shuttle-like nanoassemblies by isomeric photosensitizers to enhance ROS generation and tumor penetration for photodynamic therapy\",\"authors\":\"Peijuan Zhang, Qifei Shen, Jianye Yang, Zhiqin Zhao, Anran Gao, Shuai Chen, Yan Zhang, Lingjie Meng, Dongfeng Dang\",\"doi\":\"10.1016/j.matt.2024.09.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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 <em>in vivo</em> 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.\",\"PeriodicalId\":17,\"journal\":{\"name\":\"ACS Infectious Diseases\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Infectious Diseases\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.matt.2024.09.001\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Infectious Diseases","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.matt.2024.09.001","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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.
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.