Baek Suhyeon, Bae Ji-Eun, Miao Yu, Kim Gahyeon, Ryu Bomi, Lee Byung-Hoo, Lee Sanggil
Department of Smart Green Technology Engineering, Pukyong National University, Busan 48513, Republic of Korea.
Department of Food Science and Nutrition, Pukyong National University, Busan 48513, Republic of Korea.
Mar Drugs. 2024 Dec 2;22(12):543. doi: 10.3390/md22120543.
Sargahydroquinoic acid (SHQA), a bioactive compound found in certain species, exhibits significant health benefits. This study optimized the extraction of SHQA from using response surface methodology (RSM) and evaluated its antioxidant effects through in vitro and in vivo assays. A Box-Behnken design (BBD) was effectively employed to investigate the effects of incubation temperature, time, and ethanol concentration on SHQA yield, achieving a high coefficient of determination (R = 0.961). Analysis of variance (ANOVA) validated the model's reliability ( = 13.86, = 0.005) and highlighted ethanol concentration as a highly significant factor ( < 0.001). Optimal extraction conditions were identified as 52.8 °C, 8.3 h, and 74.1% ethanol. The SHQA-maximized extract (SME) contained 67.8 ± 0.6 mg SHQA/g and 25.00 ± 1.01 mg phloroglucinol equivalent/g. SME exhibited antioxidant capacity of 26.45 ± 0.66 mg and 28.74 ± 2.30 mg vitamin C equivalent/g in ABTS and DPPH assays, respectively, and 0.29 ± 0.02 mM FeSO equivalent/g in the FRAP assay. Additionally, SME at 50 µg/mL and SHQA at 1 µg/mL inhibited reactive oxygen species (ROS) generation in an HO-induced zebrafish model. This study presents the first optimization of SHQA extraction using RSM and demonstrates SHQA's ROS inhibition in a zebrafish model.
萨嘎氢醌酸(SHQA)是在某些物种中发现的一种生物活性化合物,具有显著的健康益处。本研究采用响应面法(RSM)优化了从[具体来源未提及]中提取SHQA的工艺,并通过体外和体内试验评估了其抗氧化作用。有效地采用Box-Behnken设计(BBD)来研究孵育温度、时间和乙醇浓度对SHQA产量的影响,获得了较高的决定系数(R = 0.961)。方差分析(ANOVA)验证了模型的可靠性(F = 13.86,p = 0.005),并突出显示乙醇浓度是一个高度显著的因素(p < 0.001)。确定的最佳提取条件为52.8℃、8.3小时和74.1%乙醇。SHQA最大化提取物(SME)含有67.8±0.6毫克SHQA/克和25.00±1.01毫克间苯三酚当量/克。在ABTS和DPPH试验中,SME的抗氧化能力分别为26.45±0.66毫克和28.74±2.30毫克维生素C当量/克,在FRAP试验中为0.29±0.02毫摩尔硫酸亚铁当量/克。此外,在HO诱导的斑马鱼模型中,50微克/毫升的SME和1微克/毫升的SHQA抑制了活性氧(ROS)的产生。本研究首次采用RSM对SHQA提取进行了优化,并在斑马鱼模型中证明了SHQA对ROS的抑制作用。