4.7 Article

Nano-carrier for gene delivery and bioimaging based on pentaetheylenehexamine modified carbon dots

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 639, 期 -, 页码 180-192

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2023.02.046

关键词

Carbon dots; Pentaethylenehexamine; Cellular uptake; Blood-brain barrier penetration; Nucleic acid; gene delivery

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Carbon dots (CDs) have attracted much attention due to their excellent properties and applications, especially as a non-viral vector for gene delivery. In this study, pentaethylenehexamine-derived CDs (PCDs) were prepared and characterized. Results showed that PCDs possessed amine groups, positive charge, low cytotoxicity, and high transfection efficiency. PCDs were also observed to cross the blood-brain barrier. These findings indicate that PCDs are a potential nucleic acid/gene vector for gene therapy and drug delivery for brain diseases.
Carbon dots (CDs) have attracted much attention due to their excellent properties and applications, especially the use for gene delivery. Considering the risks and concerns involved in the use of viral vectors for gene delivery in vivo, non-viral vectors such as CDs have gradually become an ideal alternative due to their biocompatibility and low toxicity. Therefore, in this study, the potential to apply CDs as a nonviral vector for gene delivery was investigated. The CDs were prepared using citric acid and pentaethylenehexamine (PEHA) as precursors via a one-step microwave-mediated approach. The optical, structural, and morphological properties of PEHA-derived CDs (PCDs) were characterized by ultraviolet spectroscopy (UV-vis), photoluminescence (PL), Fourier Transform Infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), zeta potential, circular dichroism spectrometry, atomic force (AFM) and transmission electron microscopies (TEM). The analysis demonstrated that the as-prepared PCDs were rich in amine groups and were positively charged. Subsequently, gel retardation assay showed that PCDs could non-covalently bind with DNA at a mass ratio of 2:1 (PCDs: DNA). Additionally, PCDs possessed a tremendously lower cytotoxicity compared with polyethylenimine (PEI), a popular precursor/dopant for many CDs preparations, and their plasmid composite showed a high transfection efficiency. Meanwhile, PCDs were also observed to cross the blood- brain barrier (BBB) by using a zebrafish model. In conclusion, these results significantly indicate that PCDs are a potential non-viral nucleic acid/gene vector to gene therapy. Also, PCDs can be utilized in drug delivery for treating brain diseases, such as Alzheimer's disease and brain tumors. (c) 2023 Elsevier Inc. All rights reserved.

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