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量子点的细胞内递呈方法。

Methods for Intracellular Delivery of Quantum Dots.

机构信息

Departamento de Biofísica e Radiobiologia, Universidade Federal de Pernambuco, CB, UFPE, Av. Prof. Moraes Rego, S/N, Recife, PE, 50670-901, Brazil.

Moleculaire Biofysica, Zernike Instituut, Rijksuniversiteit Groningen, Groningen, The Netherlands.

出版信息

Top Curr Chem (Cham). 2021 Jan 5;379(1):1. doi: 10.1007/s41061-020-00313-7.

DOI:10.1007/s41061-020-00313-7
PMID:33398442
Abstract

Quantum dots (QDs) have attracted considerable attention as fluorescent probes for life sciences. The advantages of using QDs in fluorescence-based studies include high brilliance, a narrow emission band allowing multicolor labeling, a chemically active surface for conjugation, and especially, high photostability. Despite these advantageous features, the size of the QDs prevents their free transport across the plasma membrane, limiting their use for specific labeling of intracellular structures. Over the years, various methods have been evaluated to overcome this issue to explore the full potential of the QDs. Thus, in this review, we focused our attention on physical and biochemical QD delivery methods-electroporation, microinjection, cell-penetrating peptides, molecular coatings, and liposomes-discussing the benefits and drawbacks of each strategy, as well as presenting recent studies in the field. We hope that this review can be a useful reference source for researches that already work or intend to work in this area. Strategies for the intracellular delivery of quantum dots discussed in this review (electroporation, microinjection, cell-penetrating peptides, molecular coatings, and liposomes).

摘要

量子点 (QDs) 作为荧光探针在生命科学中引起了广泛关注。在基于荧光的研究中使用 QDs 的优点包括高亮度、允许多色标记的窄发射带、用于缀合的化学活性表面,特别是高光稳定性。尽管具有这些有利的特点,但 QDs 的尺寸阻止了它们自由穿过质膜的运输,限制了它们用于特定标记细胞内结构的用途。多年来,已经评估了各种方法来克服这个问题,以探索 QDs 的全部潜力。因此,在这篇综述中,我们将注意力集中在物理和生化 QD 传递方法上 - 电穿孔、显微注射、细胞穿透肽、分子涂层和脂质体 - 讨论每种策略的优缺点,并介绍该领域的最新研究。我们希望这篇综述可以成为已经在该领域工作或打算在该领域工作的研究人员的有用参考资料。本文讨论了用于细胞内量子点传递的策略(电穿孔、显微注射、细胞穿透肽、分子涂层和脂质体)。

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本文引用的文献

1
Red blood cell membrane-mediated fusion of hydrophobic quantum dots with living cell membranes for cell imaging.红细胞膜介导疏水性量子点与活细胞膜融合用于细胞成像。
J Mater Chem B. 2016 Jun 21;4(23):4191-4197. doi: 10.1039/c6tb01067a. Epub 2016 May 26.
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Electroporation for nanomedicine: a review.用于纳米医学的电穿孔:综述
J Mater Chem B. 2017 Apr 21;5(15):2726-2738. doi: 10.1039/c7tb00038c. Epub 2017 Mar 15.
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Studies on intracellular delivery of carboxyl-coated CdTe quantum dots mediated by fusogenic liposomes.关于融合脂质体介导的羧基包被碲化镉量子点细胞内递送的研究。
Microsyst Nanoeng. 2023 Nov 17;9:145. doi: 10.1038/s41378-023-00608-x. eCollection 2023.
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Recent trends in macromolecule-conjugated hybrid quantum dots for cancer theranostic applications.用于癌症诊疗应用的大分子共轭杂化量子点的最新趋势。
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5
Density functional theory computation of the intermolecular interactions of Al@C and Al@MgO semiconducting quantum dots conjugated with the glycine tripeptide.与甘氨酸三肽共轭的Al@C和Al@MgO半导体量子点分子间相互作用的密度泛函理论计算。
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6
Peptide nano 'bead-grafting' for SDT-facilitated immune checkpoints blocking.用于声动力疗法促进免疫检查点阻断的肽纳米“珠接枝”
Chem Sci. 2022 Nov 23;13(47):14052-14062. doi: 10.1039/d2sc02728c. eCollection 2022 Dec 7.
7
Examining the Cellular Transport Pathway of Fusogenic Quantum Dots Conjugated With Tat Peptide.研究与Tat肽偶联的融合性量子点的细胞运输途径。
Front Bioeng Biotechnol. 2022 May 27;10:831379. doi: 10.3389/fbioe.2022.831379. eCollection 2022.
8
Design and Application of Near-Infrared Nanomaterial-Liposome Hybrid Nanocarriers for Cancer Photothermal Therapy.用于癌症光热治疗的近红外纳米材料-脂质体混合纳米载体的设计与应用
Pharmaceutics. 2021 Dec 3;13(12):2070. doi: 10.3390/pharmaceutics13122070.
J Mater Chem B. 2013 Sep 14;1(34):4297-4305. doi: 10.1039/c3tb20245c. Epub 2013 Jul 16.
4
Liposomes of Quantum Dots Configured for Passive and Active Delivery to Tumor Tissue.量子点脂质体经被动和主动递送至肿瘤组织的构建。
Nano Lett. 2019 Sep 11;19(9):5844-5852. doi: 10.1021/acs.nanolett.9b01027. Epub 2019 Aug 22.
5
In Vivo Imaging of Single Tumor Cells in Fast-Flowing Bloodstream Using Near-Infrared Quantum Dots and Time-Gated Imaging.利用近红外量子点和时间门控成像技术在快速血流中对单个肿瘤细胞进行体内成像。
ACS Nano. 2019 Mar 26;13(3):3125-3131. doi: 10.1021/acsnano.8b08463. Epub 2019 Mar 11.
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Diselenolane-Mediated Cellular Uptake: Efficient Cytosolic Delivery of Probes, Peptides, Proteins, Artificial Metalloenzymes and Protein-Coated Quantum Dots.二硒醚介导的细胞摄取:探针、肽、蛋白质、人工金属酶和蛋白包覆量子点的有效细胞内递送。
Chemistry. 2019 Mar 15;25(16):4047-4051. doi: 10.1002/chem.201805900. Epub 2019 Feb 28.
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Enhanced Uptake of Luminescent Quantum Dots by Live Cells Mediated by a Membrane-Active Peptide.膜活性肽介导活细胞对发光量子点的摄取增强
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Highly Efficient Protein-free Membrane Fusion: A Giant Vesicle Study.高效无蛋白膜融合:巨囊泡研究。
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