Antioxidant activity of Sophora exigua and liposome development of its powerful extract.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY Drug Discoveries and Therapeutics Pub Date : 2024-07-09 Epub Date: 2024-05-22 DOI:10.5582/ddt.2024.01018
Soraya Rodwattanagul, Mathurada Sasarom, Pornthida Riangjanapatee, Songyot Anuchapreeda, Siriporn Okonogi
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Abstract

Sophora exigua (SE) was sequentially extracted using hexane, ethyl acetate, and ethanol. The obtained extracts were tested for antioxidant activity. Among them, the fractionated ethyl acetate extract (SE-EA) showed the highest potential in free radical scavenging and ferric-reducing properties. The chemical analysis identified sophoraflavanone G as one of the active ingredients in SE-EA. According to SE-EA solubility, SE-EA liposomes were developed using a sonication-assisted thin film method. Cholesterol and phospholipids were used as the main compositions of the liposomes. The obtained liposomes were spherical with different nano-size ranges, size distribution, and zeta potential depending on SE-EA and total lipid concentrations. SE-EA liposomes were slightly bigger than their empty liposomes. All liposomes exhibited a phospholipid crystalline structure. Cholesterol and SE-EA existed in the liposomes as an amorphous state. SE-EA liposomes with high total lipid content exhibited high entrapment efficiency and sustained release behavior. Whereas liposomes with low total lipid content showed low entrapment efficiency and fast-release behavior. All SE-EA liposomes showed stronger antioxidant activity than the non-entrapped SE-EA. In conclusion, SE-EA is a natural source of potent antioxidants. The developed SE-EA liposomes are a promising pharmaceutical formulation to efficiently deliver the active ingredients of SE-EA and are suitable for further study in vivo.

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国槐的抗氧化活性及其强效提取物的脂质体开发
Sophora exigua(SE)依次用正己烷、乙酸乙酯和乙醇提取。对获得的提取物进行了抗氧化活性测试。其中,分馏乙酸乙酯提取物(SE-EA)在清除自由基和还原铁元素方面表现出最高的潜力。化学分析确定槐黄烷酮 G 是 SE-EA 的活性成分之一。根据 SE-EA 的溶解性,采用超声辅助薄膜法开发了 SE-EA 脂质体。脂质体的主要成分是胆固醇和磷脂。所获得的脂质体呈球形,其纳米尺寸范围、尺寸分布和 Zeta 电位因 SE-EA 和总脂质浓度的不同而不同。SE-EA 脂质体比空脂质体略大。所有脂质体都呈现磷脂结晶结构。胆固醇和SE-EA以无定形状态存在于脂质体中。总脂质含量高的 SE-EA 脂质体具有较高的包载效率和持续释放特性。而总脂质含量低的脂质体则表现出较低的夹带效率和快速释放特性。与未包封的 SE-EA 相比,所有 SE-EA 脂质体都表现出更强的抗氧化活性。总之,SE-EA 是一种天然的强效抗氧化剂。所开发的 SE-EA 脂质体是一种很有前景的药物制剂,能有效地传递 SE-EA 的活性成分,适合在体内进行进一步研究。
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来源期刊
Drug Discoveries and Therapeutics
Drug Discoveries and Therapeutics PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
3.20%
发文量
51
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