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基于载溴花菁-叶酸受体靶向 AgS 量子点的光声/光动力联合治疗增强的影像引导技术。

Image-Guided Enhanced PDT/PTT Combination Therapy Using Brominated Hemicyanine-Loaded Folate Receptor-Targeting AgS Quantum Dots.

机构信息

Department of Chemistry, Koç University, Rumelifeneri Yolu, Sariyer, Istanbul 34450, Turkey.

Nanofabrication and Nanocharacterization Centre for Scientific and Technological Advanced Research, Koç University, Istanbul 34450, Turkey.

出版信息

Bioconjug Chem. 2023 May 17;34(5):880-892. doi: 10.1021/acs.bioconjchem.3c00096. Epub 2023 Apr 20.

Abstract

Tumor-targeting nanoparticles and phototherapies are the two major trends in tumor-specific, local cancer therapy with minimal side effects. Organic photosensitizers (PSs) usually offer effective photodynamic therapy (PDT) but require enhanced solubility and tumor-targeting, which may be provided by a nanoparticle. Near-infrared (NIR)-emitting AgS quantum dots may act as a delivery vehicle for the PS, NIR tracking agent, and as a phototherapy (PTT) agent. A combination of the two provides luminescent dual-phototherapy agents with tumor-specificity and image-guided and enhanced cytotoxicity as a result of synergistic PDT and PTT. In this study, brominated hemicyanine (Hemi-Br), a photosensitizer, was loaded onto folic acid (FA)-tagged, glutathione (GSH)-coated AgS quantum dots (AS-GSH QDs) to provide enhanced phototoxicity via a photodynamic and mild photothermal effect in folate receptor(+) cancer cell lines at clinically relevant 640 nm irradiation. Final particles (AS-GSH-FA/Hemi-Br) had a hydrodynamic size of 75.5 nm, dual emission at both 705 and 910 nm, and a 93% light-to-heat conversion efficiency under 640 nm laser irradiation. cytotoxicity studies were conducted with folate receptor (FR)-positive HeLa and -negative A549 cell lines to differentiate receptor-mediated uptake. Enhanced phototoxicity on HeLa cells was observed with AS-GSH-FA/Hemi-Br compared to free Hemi-Br and AS-GSH-FA QDs due to increased uptake of the photosensitizer via active targeting and combination therapy, which is especially visible at the safe dose of single agents. Upon irradiation with a 640 nm (300 mW, 0.78 W/cm) laser for 5 min, the viability of the HeLa cells decreased from 64% to 42 and 25% when treated with free Hemi-Br, AS-GSH-FA, and AS-GSH-FA/Hemi-Br, respectively. Overall, AS-GSH-FA/Hemi-Br provides image-guided enhanced PDT/PTT, which may be adopted for different FR(+) tumors.

摘要

肿瘤靶向纳米粒子和光疗是具有最小副作用的肿瘤特异性局部癌症治疗的两个主要趋势。有机光敏剂 (PSs) 通常提供有效的光动力疗法 (PDT),但需要增强的溶解度和肿瘤靶向性,这可以通过纳米粒子提供。近红外 (NIR) 发射的 AgS 量子点可以作为 PS、NIR 示踪剂的递送载体,以及光疗 (PTT) 剂。两者的结合提供了具有肿瘤特异性、图像引导和增强细胞毒性的发光双重光疗剂,这是由于协同 PDT 和 PTT 的结果。在这项研究中,溴化半花青 (Hemi-Br),一种光敏剂,被装载到叶酸 (FA) 标记的、谷胱甘肽 (GSH) 包裹的 AgS 量子点 (AS-GSH QDs) 上,以提供通过光动力和温和光热效应在叶酸受体 (+) 癌细胞系中增强的光毒性在临床相关的 640nm 照射下。最终的粒子 (AS-GSH-FA/Hemi-Br) 的水动力尺寸为 75.5nm,在 705nm 和 910nm 处具有双重发射,在 640nm 激光照射下光热转换效率为 93%。使用叶酸受体 (FR) 阳性的 HeLa 和阴性的 A549 细胞系进行细胞毒性研究,以区分受体介导的摄取。与游离的 Hemi-Br 和 AS-GSH-FA QDs 相比,AS-GSH-FA/Hemi-Br 在 HeLa 细胞上观察到增强的光毒性,这是由于通过主动靶向和联合治疗增加了光敏剂的摄取,在单一药物的安全剂量下尤其明显。在用 640nm(300mW,0.78W/cm)激光照射 5 分钟后,当用游离的 Hemi-Br、AS-GSH-FA 和 AS-GSH-FA/Hemi-Br 处理时,HeLa 细胞的存活率分别从 64%下降到 42%和 25%。总的来说,AS-GSH-FA/Hemi-Br 提供了图像引导的增强 PDT/PTT,可用于不同的 FR(+)肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f4b/10197082/22304c76a40e/bc3c00096_0002.jpg

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