Graphene Quantum Dots prepared by Electron Beam Irradiation for Safe Fluorescence Imaging of Tumor.

Q1 Pharmacology, Toxicology and Pharmaceutics Nanotheranostics Pub Date : 2022-01-01 DOI:10.7150/ntno.67070
Honghong Cao, Wei Qi, Xudong Gao, Qiang Wu, Longlong Tian, Wangsuo Wu
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Abstract

Graphene quantum dots (GQD) have attracted much attention due to their unique properties in biomedical application, such as biosensing, imaging, and drug delivering. However, scale preparing red luminescing GQD is still challenging now. Herein, with the help of electron beam irradiation, a simple, rapid, and efficient up-to-down strategy was developed to synthesize GQD with size of 2.75 nm emitting 610 nm luminescence. GQD were further functionalized with polyethylene glycol (PEG) and exhibited good solubility and biocompatibility. The potential in vivo toxicity of PEGylated GQD could completely be eliminated by the clinic cholesterol-lowering drug simvastatin. PEGylated GQD could selectively accumulate in tumor after intravenous injection as a security, reliable and sensitive tumor fluorescence imaging agent. Therefore, this work presented a new method preparing red luminescing GQD for biomedical application.

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利用电子束辐照制备石墨烯量子点,用于肿瘤的安全荧光成像。
石墨烯量子点(GQD)因其在生物传感、成像和给药等生物医学应用中的独特性能而备受关注。然而,规模化制备红色发光 GQD 目前仍具有挑战性。本文利用电子束辐照技术,开发了一种简单、快速、高效的 "从上到下 "合成策略,合成了尺寸为 2.75 nm 的 GQD,可发出 610 nm 的荧光。GQD 与聚乙二醇(PEG)进一步官能化,表现出良好的溶解性和生物相容性。临床降胆固醇药物辛伐他汀可完全消除 PEG 化 GQD 的潜在体内毒性。PEG 化的 GQD 经静脉注射后可选择性地在肿瘤内蓄积,是一种安全、可靠、灵敏的肿瘤荧光成像剂。因此,本研究提出了一种制备生物医学用红色发光 GQD 的新方法。
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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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