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用于细胞和细胞外囊泡成像的牛血清白蛋白包覆的金纳米材料。

Gold nanomaterials capped with bovine serum albumin for cell and extracellular vesicle imaging.

作者信息

Wu Re-Wen, Lin Yu-Han, Lu Cheng-Hsiu, Su Chia-Hao, Chen Yu-Shan, Wang Feng-Sheng, Lian Wei-Shiung

机构信息

Department of Orthopedic Surgery, College of Medicine Chang Gung University, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.

Center for Mitochondrial Research and Medicine, College of Medicine Chang Gung University, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.

出版信息

Nanotechnology. 2025 Jan 9;36(10). doi: 10.1088/1361-6528/ada3da.

Abstract

Bovine serum albumin-capped gold nanoclusters (AuNC@BSA) are ionic, ultra-small, and eco-friendly nanomaterials that exhibit red fluorescence emission. Upon modification, these nanomaterials can serve as imaging probes with multimodal functionality. Owing to their nanoscale properties, AuNC@BSA-based nanomaterials can be readily endocytosed by cells for imaging. With the increasing interest in cell therapy, extracellular vesicles (EVs) have attracted considerable attention from researchers; however, effective methods for imaging EVs remain limited. Although several studies have explored imaging strategies for cells and EVs using compounds, nuclear pharmaceuticals, nanoparticles, or genetic constructs, the use of AuNC@BSA-based nanomaterials for labeling EVs and their parental cells has rarely been discussed, with even less attention paid to their multimodal potential. To address this gap, we utilized three types of AuNC@BSA-based derivatives: AuNC@BSA, AuNC@BSA-Gd, and AuNC@BSA-Gd-I. Our findings demonstrate that these derivatives can effectively label both cells and EVs using a simple direct labeling approach, which is particularly notable for EVs, as they typically require more complex labeling procedures. Furthermore, the multimodal potential of labeled cells and EVs was evaluated, revealing their capabilities for multimodal imaging. In summary, this study presents an effective strategy for labeling EVs and their parental cells using multimodal nanomaterials. These findings will contribute to accelerating the development of drug delivery systems, cell- and EV-based therapies, and advanced imaging strategies.

摘要

牛血清白蛋白包覆的金纳米簇(AuNC@BSA)是具有离子性、超小尺寸且环保的纳米材料,可发出红色荧光。经过修饰后,这些纳米材料可作为具有多模态功能的成像探针。由于其纳米尺度特性,基于AuNC@BSA的纳米材料可被细胞轻易内吞用于成像。随着对细胞治疗的兴趣日益增加,细胞外囊泡(EVs)引起了研究人员的广泛关注;然而,用于EVs成像的有效方法仍然有限。尽管有几项研究探索了使用化合物、核药物、纳米颗粒或基因构建体对细胞和EVs进行成像的策略,但很少有人讨论使用基于AuNC@BSA的纳米材料标记EVs及其亲本细胞,对其多模态潜力的关注更少。为了填补这一空白,我们使用了三种基于AuNC@BSA的衍生物:AuNC@BSA、AuNC@BSA-Gd和AuNC@BSA-Gd-I。我们的研究结果表明,这些衍生物可以通过简单的直接标记方法有效地标记细胞和EVs,这对于EVs来说尤为显著,因为它们通常需要更复杂的标记程序。此外,还评估了标记细胞和EVs的多模态潜力,揭示了它们进行多模态成像的能力。总之,本研究提出了一种使用多模态纳米材料标记EVs及其亲本细胞的有效策略。这些发现将有助于加速药物递送系统、基于细胞和EVs的疗法以及先进成像策略的发展。

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