Zhang Weiyun, Cai Kai, Sun Zhiduo, Xiang Qin, Yuan Li, Fu Manli, Liu Xiaoming, Foda Mohamed Frahat Foda, Ye Zhichao, Huang Jinkun, Liu Huiyu, Han Heyou, Liang Huageng, Dong Haifeng, Zhang Xueji
Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering, Shenzhen University Medical School, Shenzhen 518060, China.
State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, P. R. China.
ACS Nano. 2023 Oct 10;17(19):18932-18941. doi: 10.1021/acsnano.3c04175. Epub 2023 Sep 28.
The second near-infrared (NIR-II) window laser-activated agents have attracted broad interest in an orthotopic cancer theranostic. However, developing NIR-II photothermal agents (PTAs) with advanced photothermal conversion efficiency (PTCE) and tumor-specific response elevation remains a crucial challenge. Herein, a hollow gold nanorod (AuHNR) with a strong localized surface plasmon resonance (LSPR) peak in the NIR-II window was coated with MnO and chitosan to obtain AuHNR@MnO@CS (termed AuMC) by a one-step method. Upon exposure to the tumor microenvironment (TME), the overexpressed GSH triggered degradation of the MnO layer to release Mn and resulted in the PTCE elevation owing to exposure of the AuHNR. Consequently, photoacoustic and magnetic resonance imaging for accurate diagnosis, Mn-mediated chemodynamic therapy, and AuHNR elevating PT therapy for precise treatment could be achieved. Both and experiments confirmed the good performance of the AuMC on an orthotopic bladder cancer precise theranostic. This study provided NIR-II activated, TME-response PT conversion efficiency enhanced PTAs and offered a tumor-selective theranostic agent for orthotopic bladder cancer in clinical application.
第二代近红外(NIR-II)窗口激光激活剂在原位癌症诊疗中引起了广泛关注。然而,开发具有先进光热转换效率(PTCE)和肿瘤特异性反应增强的NIR-II光热剂(PTA)仍然是一项关键挑战。在此,通过一步法用MnO和壳聚糖包覆在NIR-II窗口具有强烈局域表面等离子体共振(LSPR)峰的中空金纳米棒(AuHNR),以获得AuHNR@MnO@CS(称为AuMC)。暴露于肿瘤微环境(TME)时,过表达的谷胱甘肽(GSH)触发MnO层降解以释放Mn,并由于AuHNR的暴露导致PTCE升高。因此,可以实现用于精确诊断的光声和磁共振成像、Mn介导的化学动力学疗法以及AuHNR增强的光热疗法用于精确治疗。体内和体外实验均证实了AuMC在原位膀胱癌精确诊疗中的良好性能。本研究提供了NIR-II激活、TME响应的PT转换效率增强的PTA,并为原位膀胱癌临床应用提供了一种肿瘤选择性诊疗剂。