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中国精品科技期刊2020
张晴晴,张梦娇,马翊铭,等. 亚临界水萃取薄荷黄酮工艺优化及神经保护活性研究[J]. 食品工业科技,2024,45(10):17−24. doi: 10.13386/j.issn1002-0306.2023100088.
引用本文: 张晴晴,张梦娇,马翊铭,等. 亚临界水萃取薄荷黄酮工艺优化及神经保护活性研究[J]. 食品工业科技,2024,45(10):17−24. doi: 10.13386/j.issn1002-0306.2023100088.
ZHANG Qingqing, ZHANG Mengjiao, MA Yiming, et al. Optimization of Extraction Process and Neuroprotective Activities of Flavonoids from Mentha haplocalyx Briq. with Subcritical Water[J]. Science and Technology of Food Industry, 2024, 45(10): 17−24. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023100088.
Citation: ZHANG Qingqing, ZHANG Mengjiao, MA Yiming, et al. Optimization of Extraction Process and Neuroprotective Activities of Flavonoids from Mentha haplocalyx Briq. with Subcritical Water[J]. Science and Technology of Food Industry, 2024, 45(10): 17−24. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023100088.

亚临界水萃取薄荷黄酮工艺优化及神经保护活性研究

Optimization of Extraction Process and Neuroprotective Activities of Flavonoids from Mentha haplocalyx Briq. with Subcritical Water

  • 摘要: 目的:优化亚临界水萃取薄荷黄酮提取工艺,探究薄荷黄酮对H2O2诱导的大鼠肾上腺嗜铬细胞瘤(PC12细胞)损伤的缓解作用。方法:采用单因素实验、Box-Behnken响应面试验优化亚临界水萃取薄荷黄酮工艺,并与回流提取法、超声波辅助提取法、超临界CO2萃取法进行比较。体外培养PC12细胞,建立H2O2诱导的PC12细胞损伤模型,噻唑蓝(methyl thiazolye tetrazolium,MTT)法考察薄荷黄酮对PC12细胞存活力的影响,分析神经保护活性。结果:最佳提取工艺为提取温度142 ℃、提取时间38 min、液料比21:1 mL/g,在此条件下得到薄荷黄酮得率为14.07%±0.23%,比回流提取法提高了334%,比超声波辅助提取法提高了75%,比超临界CO2萃取法提高了173%,显著高于以上3种提取方法的得率(P<0.001)。与H2O2组比较,薄荷黄酮在1~100 µg/mL浓度范围内,使PC12细胞存活率从53.61%±0.64%显著(P<0.001)提高到78.49%±0.84%,表明薄荷黄酮能明显缓解细胞氧化损伤。结论:建立了一套绿色、高效、可靠的亚临界水萃取薄荷黄酮的工艺,萃取的薄荷黄酮对H2O2诱导的PC12细胞损伤具有极显著的保护作用(P<0.01)。

     

    Abstract: Objective: This study aims to optimize the subcritical water extraction process for flavonoids from Mentha haplocalyx Briq. (mint) and assess the mitigating effects of peppermint flavonoids on H2O2-induced adrenal pheochromocytoma (PC12 cell) injury in rats. Methods: The subcritical water extraction process for mint flavonoids was optimized using single-factor and Box-Behnken response surface tests. A comparison was made with reflux extraction, ultrasonic-assisted extraction, and supercritical CO2 extraction methods. In vitro cell culture of PC12 cells was employed to establish an H2O2-induced PC12 cell injury model. The neuroprotective activity of mint flavonoids was analyzed using the MTT (methyl thiazolye tetrazolium, MTT) method. Results: The optimized extraction conditions were determined to be 142 ℃, 38 min, and 21:1 mL/g, resulting in a mint flavonoid yield of 14.07%±0.23%. This yield was significantly higher (P<0.001) than that of reflux extraction (334% increase), ultrasonic-assisted extraction (75% increase), and supercritical CO2 extraction (173% increase). Mint flavonoids, within the concentration range of 1~100 μg/mL, significantly enhanced the survival rate of PC12 cells from 53.61%±0.64% to 78.49%±0.84% compared to the H2O2 group (P<0.001), indicating substantial alleviation of cellular oxidative injury. Conclusion: The study established an environmentally friendly, efficient, and reliable subcritical water extraction process for mint flavonoids. The extracted mint flavonoids demonstrated significant protective effects against H2O2-induced PC12 cell injury (P<0.01).

     

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