木犀草素
异核单量子相干光谱
异核分子
化学
聚合
生物利用度
细胞毒性
类黄酮
核化学
二维核磁共振波谱
碳-13核磁共振
核磁共振波谱
有机化学
立体化学
生物化学
聚合物
体外
药理学
医学
抗氧化剂
作者
Parichat Tawornchat,Thitiporn Pattarakankul,Tanapat Palaga,Varol Intasanta,Supason Wanichwecharungruang
出处
期刊:ACS omega
[American Chemical Society]
日期:2021-01-19
卷期号:6 (4): 2846-2855
被引量:18
标识
DOI:10.1021/acsomega.0c05142
摘要
Luteolin is an anti-inflammatory flavonoid commonly found in many edible plants. The compound is popularly consumed as a supplement regardless of its poor water solubility (27.8 μg/mL at 25 °C) and low bioavailability. Here, mild one-pot polymerization of luteolin into water-dispersible nanospheres, with an average dry size of 234.8 ± 101.6 nm, an aqueous size distribution of 379.1 ± 220.5 nm (PDI = 0.338), an average ζ-potential of −36.2 ± 0.2 mV, and an 89.3 ± 4.8% yield, is described. The nanospheres consist of polymerized luteolin (polyluteolin) with a weight-average molecular mass of around 410000 Da. The chemical structure of polyluteolin is identified through 1H–1H correlated spectroscopy (COSY), 1H–13C heteronuclear single-quantum coherence (HSQC), and 1H–13C heteronuclear multiple-bond correlation (HMBC) NMR spectroscopic analyses of the oligomers, and a polymerization mechanism is proposed. Unlike luteolin that showed both dose-dependent anti-inflammatory activity and cytotoxicity when tested in lipopolysaccharide-stimulated macrophages, the polyluteolin nanoparticles possess dose-dependent anti-inflammatory activity without causing cell death even at high concentrations.
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