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  4. Carbonization of quercetin into nanogels: a leap in anticoagulant development
 
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Carbonization of quercetin into nanogels: a leap in anticoagulant development

Journal
Journal of Materials Chemistry B
Journal Volume
12
Journal Issue
22
Start Page
5391
End Page
5404
ISSN
2050-750X
2050-7518
Date Issued
2024
Author(s)
Han-Wei Chu
Wan-Jyun Chen
Ko-Hsin Liu
Ju-Yi Mao
Scott G. Harroun
Binesh Unnikrishnan
Han-Jia Lin
Yunn-Hwa Ma
HUAN-TSUNG CHANG  
Chih-Ching Huang
DOI
10.1039/d4tb00228h
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/719852
Abstract
Quercetin, a flavonoid abundantly found in onions, fruits, and vegetables, is recognized for its pharmacological potential, especially for its anticoagulant properties that work by inhibiting thrombin and coagulation factor Xa. However, its clinical application is limited due to poor water solubility and bioavailability. To address these limitations, we engineered carbonized nanogels derived from quercetin (CNGsQur) using controlled pyrolysis and polymerization techniques. This led to substantial improvements in its anticoagulation efficacy, water solubility, and biocompatibility. We generated a range of CNGsQur by subjecting quercetin to varying pyrolytic temperatures and then assessed their anticoagulation capacities both in vitro and in vivo. Coagulation metrics, including thrombin clotting time (TCT), activated partial thromboplastin time (aPTT), and prothrombin time (PT), along with a rat tail bleeding assay, were utilized to gauge the efficacy. CNGsQur showed a pronounced extension of coagulation time compared to uncarbonized quercetin. Specifically, CNGsQur synthesized at 270 °C (CNGsQur270) exhibited the most significant enhancement in TCT, with a binding affinity to thrombin exceeding 400 times that of quercetin. Moreover, variants synthesized at 310 °C (CNGsQur310) and 290 °C (CNGsQur290) showed the most substantial delays in PT and aPTT, respectively. Our findings indicate that the degree of carbonization significantly influences the transformation of quercetin into various CNGsQur forms, each affecting distinct coagulation pathways. Additionally, both intravenous and oral administrations of CNGsQur were found to extend rat tail bleeding times by up to fivefold. Our studies also demonstrate that CNGsQur270 effectively delays and even prevents FeCl3-induced vascular occlusion in a dose-dependent manner in mice. Thus, controlled pyrolysis offers an innovative approach for generating quercetin-derived CNGs with enhanced anticoagulation properties and water solubility, revealing the potential for synthesizing self-functional carbonized nanomaterials from other flavonoids for diverse biomedical applications.
SDGs

[SDGs]SDG2

Publisher
Royal Society of Chemistry (RSC)
Type
journal article

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