TY - JOUR
T1 - Gene delivery using layer-by-layer functionalized multi-walled carbon nanotubes
T2 - design, characterization, cell line evaluation
AU - Kumari, Monika
AU - Liu, Chi Hsien
AU - Wu, Wei Chi
AU - Wang, Chun Chao
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.
PY - 2021/4
Y1 - 2021/4
N2 - Multi-walled carbon nanotubes (MWCNTs) with special nanoneedle structure have emerged as new promising candidates for plasmid and drug delivery. However, the delivery is greatly limited by the high tendency of CNT to form aggregates, the “less dispersion problem,” and CNT cytotoxicity. Here, we described an extensive evaluation of the ability of layer-by-layer modification strategy to reduce CNT size and toxicity, and to shield CNT hydrophobic surfaces. The MWCNTs can be derivatized with carboxylate groups (cMWCNT) and sequentially functionalized with protein, cationic polyethylenimine (PEI), and polysaccharide. The protein coating, characterized by Fourier transform infrared and deconvolution methods, could serve as the hydrophilic, biocompatible matrix and scaffold for sequential conjugation. We found that coated PEI-enhanced electrostatic interactions between plasmid DNA and CNTs. The functionalized cMWCNTs were analyzed by thermogravimetric analysis, dynamic light scattering, and electron microscopy technologies. The conjugation of cMWCNTs–ovalbumin–PEI with oxidized pectin further promoted green fluorescence intensity by balancing the intracellular DNA release and were easier to disperse. Our in-depth study demonstrated that functionalized CNTs can be improved by fine-tuned process parameters of the protein–PEI–polysaccharide modification.
AB - Multi-walled carbon nanotubes (MWCNTs) with special nanoneedle structure have emerged as new promising candidates for plasmid and drug delivery. However, the delivery is greatly limited by the high tendency of CNT to form aggregates, the “less dispersion problem,” and CNT cytotoxicity. Here, we described an extensive evaluation of the ability of layer-by-layer modification strategy to reduce CNT size and toxicity, and to shield CNT hydrophobic surfaces. The MWCNTs can be derivatized with carboxylate groups (cMWCNT) and sequentially functionalized with protein, cationic polyethylenimine (PEI), and polysaccharide. The protein coating, characterized by Fourier transform infrared and deconvolution methods, could serve as the hydrophilic, biocompatible matrix and scaffold for sequential conjugation. We found that coated PEI-enhanced electrostatic interactions between plasmid DNA and CNTs. The functionalized cMWCNTs were analyzed by thermogravimetric analysis, dynamic light scattering, and electron microscopy technologies. The conjugation of cMWCNTs–ovalbumin–PEI with oxidized pectin further promoted green fluorescence intensity by balancing the intracellular DNA release and were easier to disperse. Our in-depth study demonstrated that functionalized CNTs can be improved by fine-tuned process parameters of the protein–PEI–polysaccharide modification.
UR - http://www.scopus.com/inward/record.url?scp=85100107362&partnerID=8YFLogxK
U2 - 10.1007/s10853-020-05648-6
DO - 10.1007/s10853-020-05648-6
M3 - 文章
AN - SCOPUS:85100107362
SN - 0022-2461
VL - 56
SP - 7022
EP - 7033
JO - Journal of Materials Science
JF - Journal of Materials Science
IS - 11
ER -