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用于红光下肿瘤光动力治疗的硅(IV)-一氧化氮供体酞菁共轭物自组装纳米颗粒

Self-Assembled Nanoparticles of Silicon (IV)-NO Donor Phthalocyanine Conjugate for Tumor Photodynamic Therapy in Red Light.

作者信息

Aikelamu Kadireya, Bai Jingya, Zhang Qian, Huang Jiamin, Wang Mei, Zhong Chunhong

机构信息

Xinjiang Key Laboratory of Natural Medicines Active Components and Drug Release Technology, Ministry of Education, Engineering Research Center of Xinjiang and Central Asian Medicine Resources, College of Pharmacy, Xinjiang Medical University, Urumqi 830017, China.

出版信息

Pharmaceutics. 2024 Sep 4;16(9):1166. doi: 10.3390/pharmaceutics16091166.

Abstract

The combination of photodynamic therapy (PDT) and pneumatotherapy is emerging as one of the most effective strategies for increasing cancer treatment efficacy while minimizing side effects. Photodynamic forces affect nitric oxide (NO) levels as activated photosensitizers produce NO, and NO levels in the tumor and microenvironment directly impact tumor cell responsiveness to PDT. In this paper, 3-benzenesulfonyl-4-(1-hydroxy ether)-1,2,5-oxadiazole-2-oxide NO donor-silicon phthalocyanine coupling (SiPc-NO) was designed and prepared into self-assembled nanoparticles (SiPc-NO@NPs) by precipitation method. By further introducing arginyl-glycyl-aspartic acid (RGD) on the surface of nanoparticles, NO-photosensitizer delivery systems (SiPc-NO@RGD NPs) with photo-responsive and tumor-targeting properties were finally prepared and preliminarily evaluated in terms of their formulation properties, NO release, and photosensitizing effects. Furthermore, high reactive oxygen species (ROS) generation efficiency and high PDT efficiency in two breast cancer cell lines (human MCF-7 and mouse 4T1) under irradiation were also demonstrated. The novel SiPc-NO@RGD NPs show great potential for application in NO delivery and two-photon bioimaging-guided photodynamic tumor therapy.

摘要

光动力疗法(PDT)与气体疗法相结合正成为提高癌症治疗效果同时将副作用降至最低的最有效策略之一。光动力作用会影响一氧化氮(NO)水平,因为活化的光敏剂会产生NO,而肿瘤和微环境中的NO水平直接影响肿瘤细胞对PDT的反应性。本文设计并通过沉淀法将3-苯磺酰基-4-(1-羟基醚)-1,2,5-恶二唑-2-氧化物NO供体-硅酞菁偶联物(SiPc-NO)制备成自组装纳米颗粒(SiPc-NO@NPs)。通过在纳米颗粒表面进一步引入精氨酰-甘氨酰-天冬氨酸(RGD),最终制备出具有光响应和肿瘤靶向特性的NO-光敏剂递送系统(SiPc-NO@RGD NPs),并对其制剂性质、NO释放和光敏效果进行了初步评估。此外,还证明了在照射下两种乳腺癌细胞系(人MCF-7和小鼠4T1)中具有高活性氧(ROS)生成效率和高PDT效率。新型SiPc-NO@RGD NPs在NO递送和双光子生物成像引导的光动力肿瘤治疗中显示出巨大的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c60/11435187/ebadc9f62324/pharmaceutics-16-01166-g001.jpg

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