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β-环糊精通过主客体络合作用和静电相互作用形成的超分子纳米粒子共递送阿霉素和 p53 基因。

Codelivery of Doxorubicin and p53 Gene by β-Cyclodextrin-Based Supramolecular Nanoparticles Formed via Host-Guest Complexation and Electrostatic Interaction.

机构信息

Department of Biomedical Engineering, National University of Singapore, 15 Kent Ridge Crescent, Singapore 119276, Singapore.

NUS Environmental Research Institute (NERI), National University of Singapore, 5A Engineering Drive 1, Singapore 117411, Singapore.

出版信息

Biomacromolecules. 2024 May 13;25(5):2980-2989. doi: 10.1021/acs.biomac.4c00123. Epub 2024 Apr 8.


DOI:10.1021/acs.biomac.4c00123
PMID:38587905
Abstract

We developed a supramolecular system for codelivery of doxorubicin (Dox) and p53 gene based on a β-CD-containing star-shaped cationic polymer. First, a star-shaped cationic polymer consisting of a β-CD core and 3 arms of oligoethylenimine (OEI), named CD-OEI, was used to form a supramolecular inclusion complex with hydrophobic Dox. The CD-OEI/Dox complex was subsequently used to condense plasmid DNA via electrostatic interactions to form CD-OEI/Dox/DNA polyplex nanoparticles with positive surface charges that enhanced the cellular uptake of both Dox and DNA. This supramolecular drug and gene codelivery system showed high gene transfection efficiency and effective protein expression in cancer cells. The codelivery of Dox and DNA encoding the p53 gene resulted in reduced cell viability and enhanced antitumor effects at low Dox concentrations. With its enhanced cellular uptake and anticancer efficacy, the system holds promise as a delivery carrier for potential combination cancer therapies.

摘要

我们开发了一种基于含β-CD 的星形阳离子聚合物的阿霉素(Dox)和 p53 基因共递送的超分子系统。首先,使用由β-CD 核和 3 个支链聚乙二亚胺(OEI)组成的星形阳离子聚合物,命名为 CD-OEI,与疏水性 Dox 形成超分子包合物。然后,CD-OEI/Dox 复合物通过静电相互作用用于凝聚质粒 DNA,形成带正表面电荷的 CD-OEI/Dox/DNA 超分子聚合物纳米粒,增强了 Dox 和 DNA 的细胞摄取。该超分子药物和基因共递送系统在癌细胞中表现出高的基因转染效率和有效的蛋白表达。Dox 和编码 p53 基因的 DNA 的共递送导致在低 Dox 浓度下细胞活力降低和抗肿瘤作用增强。由于其增强的细胞摄取和抗癌功效,该系统有望成为潜在联合癌症治疗的递送载体。

相似文献

[1]
Codelivery of Doxorubicin and p53 Gene by β-Cyclodextrin-Based Supramolecular Nanoparticles Formed via Host-Guest Complexation and Electrostatic Interaction.

Biomacromolecules. 2024-5-13

[2]
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Int J Pharm. 2015-4-10

[3]
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[4]
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[5]
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J Colloid Interface Sci. 2017-12-7

[6]
Investigation of the Sequential Actions of Doxorubicin and p53 on Tumor Cell Growth Via Branched Polyethylenimine-β-cyclodextrin Conjugates.

Ann Biomed Eng. 2016-11

[7]
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Biomaterials. 2013-11-1

[8]
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Colloids Surf B Biointerfaces. 2015-4-1

[9]
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J Control Release. 2014-11-4

[10]
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Nanoscale. 2019-11-28

引用本文的文献

[1]
- Challenges and Perspectives in Polyelectrolytes.

Biomacromolecules. 2025-1-13

[2]
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J Agric Food Chem. 2024-8-31

[3]
Advances in Cyclodextrins and Their Derivatives in Nano-Delivery Systems.

Pharmaceutics. 2024-8-9

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