近红外触发的氮氧化物生成与光动力疗法相结合治疗肿瘤

IF 3.1 3区 医学 Q2 ONCOLOGY Photodiagnosis and Photodynamic Therapy Pub Date : 2024-08-20 DOI:10.1016/j.pdpdt.2024.104241
Zhiyuan Lin , Tao Zhu , Xiaoqin Zhong
{"title":"近红外触发的氮氧化物生成与光动力疗法相结合治疗肿瘤","authors":"Zhiyuan Lin ,&nbsp;Tao Zhu ,&nbsp;Xiaoqin Zhong","doi":"10.1016/j.pdpdt.2024.104241","DOIUrl":null,"url":null,"abstract":"<div><p>Photodynamic therapy (PDT), as one of the most promising cancer therapy methods, is still limited by several drawbacks, such as tissue hypoxia and shallow light penetration of blue-violet light (200–450 nm), and red light (750 nm) is more penetrating to tissues than blue-violet light, but still lower than near-red light (750–1350 nm). Therefore, we proposed a synergistic therapy system by combining the near-infrared light-triggered PDT with nitric oxide (NO)-based gas therapy to enhance the anti-tumor effects. Upconversion nanoparticles (UCNPs) were loaded with the photosensitizers of ZnPc and the NO donors of l-arginine (L-Arg) to obtain the nanocomposites of UCN@mSiO<sub>2</sub>@ZnPc@L-Arg. Under 980 nm laser irradiation, reactive oxygen species (ROS) could be produced for PDT and react with l-Arg to produce NO, which is previously reported to have a greater killing effect on tumor cells than ROS and also plays an important role in promoting PDT in our study. Both the in vitro and in vivo tests demonstrated that the combined therapy of PDT with NO therapy could enhance the tumor killing effect significantly compared with the unique application of PDT. The UCNPs-based nanocomposites are expected to be widely used in biomedicine for tumor inhibition.</p></div>","PeriodicalId":20141,"journal":{"name":"Photodiagnosis and Photodynamic Therapy","volume":"49 ","pages":"Article 104241"},"PeriodicalIF":3.1000,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1572100024002783/pdfft?md5=6afdc83138dd57166f45257127206835&pid=1-s2.0-S1572100024002783-main.pdf","citationCount":"0","resultStr":"{\"title\":\"NIR-triggered NO production combined with photodynamic therapy for tumor treatment\",\"authors\":\"Zhiyuan Lin ,&nbsp;Tao Zhu ,&nbsp;Xiaoqin Zhong\",\"doi\":\"10.1016/j.pdpdt.2024.104241\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Photodynamic therapy (PDT), as one of the most promising cancer therapy methods, is still limited by several drawbacks, such as tissue hypoxia and shallow light penetration of blue-violet light (200–450 nm), and red light (750 nm) is more penetrating to tissues than blue-violet light, but still lower than near-red light (750–1350 nm). Therefore, we proposed a synergistic therapy system by combining the near-infrared light-triggered PDT with nitric oxide (NO)-based gas therapy to enhance the anti-tumor effects. Upconversion nanoparticles (UCNPs) were loaded with the photosensitizers of ZnPc and the NO donors of l-arginine (L-Arg) to obtain the nanocomposites of UCN@mSiO<sub>2</sub>@ZnPc@L-Arg. Under 980 nm laser irradiation, reactive oxygen species (ROS) could be produced for PDT and react with l-Arg to produce NO, which is previously reported to have a greater killing effect on tumor cells than ROS and also plays an important role in promoting PDT in our study. Both the in vitro and in vivo tests demonstrated that the combined therapy of PDT with NO therapy could enhance the tumor killing effect significantly compared with the unique application of PDT. The UCNPs-based nanocomposites are expected to be widely used in biomedicine for tumor inhibition.</p></div>\",\"PeriodicalId\":20141,\"journal\":{\"name\":\"Photodiagnosis and Photodynamic Therapy\",\"volume\":\"49 \",\"pages\":\"Article 104241\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1572100024002783/pdfft?md5=6afdc83138dd57166f45257127206835&pid=1-s2.0-S1572100024002783-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Photodiagnosis and Photodynamic Therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1572100024002783\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Photodiagnosis and Photodynamic Therapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572100024002783","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

光动力疗法(PDT)是最有前景的癌症治疗方法之一,但仍受限于组织缺氧和蓝紫光(200-450 nm)光穿透力浅等缺点,而红光(750 nm)对组织的穿透力高于蓝紫光,但仍低于近红光(750-1350 nm)。因此,我们提出了一种协同治疗系统,将近红外光触发的光动力疗法与基于一氧化氮(NO)的气体疗法相结合,以增强抗肿瘤效果。在上转换纳米颗粒(UCNPs)中添加光敏剂ZnPc和一氧化氮供体精氨酸(L-Arg),得到UCN@mSiO2@ZnPc@L-Arg纳米复合材料。在980 nm激光照射下,活性氧(ROS)可产生PDT,并与l-Arg反应生成NO,而NO对肿瘤细胞的杀伤作用比ROS更大,在我们的研究中,NO也在促进PDT中发挥了重要作用。体外和体内试验均表明,与单独应用 PDT 相比,PDT 与 NO 联合治疗可显著提高杀灭肿瘤的效果。基于 UCNPs 的纳米复合材料有望广泛应用于生物医学的肿瘤抑制领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
NIR-triggered NO production combined with photodynamic therapy for tumor treatment

Photodynamic therapy (PDT), as one of the most promising cancer therapy methods, is still limited by several drawbacks, such as tissue hypoxia and shallow light penetration of blue-violet light (200–450 nm), and red light (750 nm) is more penetrating to tissues than blue-violet light, but still lower than near-red light (750–1350 nm). Therefore, we proposed a synergistic therapy system by combining the near-infrared light-triggered PDT with nitric oxide (NO)-based gas therapy to enhance the anti-tumor effects. Upconversion nanoparticles (UCNPs) were loaded with the photosensitizers of ZnPc and the NO donors of l-arginine (L-Arg) to obtain the nanocomposites of UCN@mSiO2@ZnPc@L-Arg. Under 980 nm laser irradiation, reactive oxygen species (ROS) could be produced for PDT and react with l-Arg to produce NO, which is previously reported to have a greater killing effect on tumor cells than ROS and also plays an important role in promoting PDT in our study. Both the in vitro and in vivo tests demonstrated that the combined therapy of PDT with NO therapy could enhance the tumor killing effect significantly compared with the unique application of PDT. The UCNPs-based nanocomposites are expected to be widely used in biomedicine for tumor inhibition.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.80
自引率
24.20%
发文量
509
审稿时长
50 days
期刊介绍: Photodiagnosis and Photodynamic Therapy is an international journal for the dissemination of scientific knowledge and clinical developments of Photodiagnosis and Photodynamic Therapy in all medical specialties. The journal publishes original articles, review articles, case presentations, "how-to-do-it" articles, Letters to the Editor, short communications and relevant images with short descriptions. All submitted material is subject to a strict peer-review process.
期刊最新文献
The ability of changes in oct angiography values to predict visual field and retinal nerve layer tomography progression in patients with glaucoma progression: A prospective study The effect of antimicrobial photodynamic therapy using different concentrations of phycocyanin against Streptococcus mutans Posterior corneal elevation after small incision lenticule extraction (SMILE) in eyes of different myopia severity Comparative analysis of central corneal thickness in ocular hypertension and healthy individuals Development and validation of polymer-based porphyrin-incorporated reference materials for calibration of quantitative light-induced fluorescence device
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1