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Layer-by-layer assembly of quercetin-loaded zein/γPGA/low-molecular-weight chitosan/fucoidan nanosystem for targeting inflamed blood vessels.

Authors :
Lu, Hsin-Ying
Mi, Fwu-Long
Chou, Chih-Ming
Lin, Chi
Chen, Yi-Yu
Chu, Cheng-Ying
Liu, Cheng-Yang
Lee, Yu-Lin Amy
Shih, Chun Che
Cheng, Chia-Hsiung
Source :
International Journal of Biological Macromolecules. May2024:Part 1, Vol. 267, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Chitosan acts as a versatile carrier in polymeric nanoparticle (NP) for diverse drug administration routes. Delivery of antioxidants, such as quercetin (Qu) showcases potent antioxidant and anti-inflammatory properties for reduction of various cardiovascular diseases, but low water solubility limits uptake. To address this, we developed a novel layer-by-layer zein/gamma-polyglutamic acid (γPGA)/low-molecular-weight chitosan (LC)/fucoidan NP for encapsulating Qu and targeting inflamed vessel endothelial cells. We used zein (Z) and γPGA (r) to encapsulate Qu (Qu-Zr NP) exhibited notably higher encapsulation efficiency compared to zein alone. Qu-Zr NP coated with LC (Qu-ZrLC2 NP) shows a lower particle size (193.2 ± 2.9 nm), and a higher zeta potential value (35.2 ± 0.4 mV) by zeta potential and transmission electron microscopy analysis. After coating Qu-ZrLC2 NP with fucoidan, Qu-ZrLC2Fa NP presented particle size (225.16 ± 0.92 nm), zeta potential (−25.66 ± 0.51 mV) and maintained antioxidant activity. Further analysis revealed that Qu-ZrLC2Fa NP were targeted and taken up by HUVEC cells and EA.hy926 endothelial cells. Notably, we observed Qu-ZrLC2Fa NP targeting zebrafish vessels and isoproterenol-induced inflamed vessels of rat. Our layer-by-layer formulated zein/γPGA/LC/fucoidan NP show promise as a targeted delivery system for water-insoluble drugs. Qu-ZrLC2Fa NP exhibit potential as an anti-inflammatory therapeutic for blood vessels. • Zein/gamma-polyglutamic acid/low-molecular-weight chitosan/fucoidan NPEncapsulated Quercetin (Qu-ZrLCF NP) • Qu-ZrLCF NP coated with fucoidan exhibited sustained antioxidant activity with uncoated NP. • Qu-ZrLCF NP demonstrated effective delivery to HUVEC and EA.hy926 endothelial cells and endothelial cells of zebrafish larvae. • Utilizing rat models successfully show in vivo targeting of Qu-ZrLCF NP into inflamed endothelial cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
267
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
177033449
Full Text :
https://doi.org/10.1016/j.ijbiomac.2024.131369