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深度学习增强型近红外二区成像及缺血性脑卒中的图像引导小干扰核糖核酸治疗

Deep Learning Enhanced Near Infrared-II Imaging and Image-Guided Small Interfering Ribonucleic Acid Therapy of Ischemic Stroke.

作者信息

Yu Kai, Fu Lidan, Chao Yu, Zeng Xiaodong, Zhang Yonggang, Chen Yuanyuan, Gao Jialu, Lu Binchun, Zhu Hua, Gu Lijuan, Xiong Xiaoxing, Hu Zhenhua, Hong Xuechuan, Xiao Yuling

机构信息

Department of Neurosurgery, Central Laboratory, Renmin Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.

Department of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430060, China.

出版信息

ACS Nano. 2025 Mar 18;19(10):10323-10336. doi: 10.1021/acsnano.4c18035. Epub 2025 Mar 5.

DOI:10.1021/acsnano.4c18035
PMID:40042964
Abstract

Small interfering RNA (siRNA) targeting the NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome has emerged as a promising therapeutic strategy to mitigate infarct volume and brain injury following ischemic stroke. However, the clinical translation of siRNA-based therapies is significantly hampered by the formidable blood-brain barrier (BBB), which restricts drug penetration into the central nervous system. To address this challenge, we have developed an innovative long-circulating near-infrared II (NIR-II) nanoparticle platform YWFC NPs, which is meticulously engineered to enhance BBB transcytosis and enable efficient delivery of siRNA targeting NLRP3 (siNLRP3@YWFC NPs) in preclinical models of ischemic stroke. Furthermore, we integrated advanced deep learning neural network algorithms to optimize NIR-II imaging of the cerebral infarct penumbra, achieving an improved signal-to-background ratio at 72 h poststroke. studies employing middle cerebral artery occlusion (MCAO) mouse models demonstrated that image-guided therapy with siNLRP3@YWFC NPs, guided by prolonged NIR-II imaging, resulted in significant therapeutic benefits.

摘要

靶向含NOD样受体家族吡咯结构域3(NLRP3)炎性小体的小干扰RNA(siRNA)已成为减轻缺血性中风后梗死体积和脑损伤的一种有前景的治疗策略。然而,基于siRNA的疗法的临床转化受到强大的血脑屏障(BBB)的显著阻碍,血脑屏障限制了药物向中枢神经系统的渗透。为应对这一挑战,我们开发了一种创新的长循环近红外II(NIR-II)纳米颗粒平台YWFC NPs,该平台经过精心设计,可增强血脑屏障转胞吞作用,并在缺血性中风的临床前模型中实现靶向NLRP3的siRNA(siNLRP3@YWFC NPs)的有效递送。此外,我们整合了先进的深度学习神经网络算法,以优化脑梗死半暗带的NIR-II成像,在中风后72小时实现了改善的信噪比。采用大脑中动脉闭塞(MCAO)小鼠模型的研究表明,在延长的NIR-II成像引导下,用siNLRP3@YWFC NPs进行图像引导治疗产生了显著的治疗效果。

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