首页|期刊导航|黑龙江农业科学|Box-Behnken法优化锦灯笼总黄酮提取工艺及多产地质量评价

Box-Behnken法优化锦灯笼总黄酮提取工艺及多产地质量评价OA

Optimization of Extraction Process of Total Flavonoids from Physalis alkekengi and Quality Evaluation of Multi-Producing Arear by Box-Behnken Design

中文摘要英文摘要

为促进锦灯笼资源开发利用及质量控制,以锦灯笼为试验材料,采用超声波辅助提取技术提取总黄酮,选取提取时间(A)、乙醇体积分数(B)、料液比(C)进行单因素试验,Box-Behnken响应面法研究锦灯笼总黄酮的最佳提取工艺.选取10个产地的锦灯笼进行性状鉴别、显微鉴别、薄层色谱鉴别、水分含量、醇溶性浸出物含量及总黄酮含量测定,对比评价不同产地锦灯笼质量.结果表明,响应面试验中各因素对锦灯笼全果总黄酮得率的影响大小为B>A>C,最佳提取工艺参数为提取时间40.823 min、乙醇浓度79.378%、料液比1∶30.704,此时锦灯笼总黄酮的得率为0.567%.显微鉴别中吉林省的锦灯笼粉末的薄壁组织中橙红色颗粒多且大,分布较均匀.薄层鉴别中,10个不同产地的锦灯笼、锦灯笼对照药材与酸浆苦味素L斑点清晰,分离度较好.水分含量测定结果均符合中国药典标准.醇溶性浸出物含量由高到低的顺序为吉林>内蒙古>四川>辽宁>浙江>河北>黑龙江>河南>湖北>山东.总黄酮含量测定结果可知吉林、四川产地锦灯笼总黄酮含量接近,且总黄酮含量最高.综上,采用Box-Behnken法构建多因素协同作用模型,可优化锦灯笼提取工艺,对比分析不同产地锦灯笼质量.

In order to promote the development and utilization of the resources of Physalis alkekengi L.and its quality control,using P.alkekengi L.as the raw material,total flavonoids are extracted from it by ultrasonic-assisted extraction technology.Single-factor experiments were conducted to investigate the effects of three variables,i.e.,extraction time(A),ethanol volume fraction(B),and solid-liquid ratio(C),on the yield of total flavonoids.Subsequently,Box-Behnken response surface methodology(RSM)was employed to optimize the extraction process of TFs from P.alkekengi L.Samples of P.alkekengi L.collected from ten producing areas were subjected to macroscopic identification,microscopic identification,thin-layer chromatography(TLC)identification,as well as determinations of moisture content,ethanol-soluble extract content,and TF content,so as to comparatively evaluate the quality of P.alkekengi L.from different producing areas.The results demonstrated that response surface analysis revealed the order of influence of each factor on the TF yield from the whole fruit of P.alkekengi L.was B>A>C.The optimal extraction process parameters were an extraction time of 40.823 min,an ethanol concentration of 79.378%,and a solid-liquid ratio of l:30.704.Under these parameters,the yield of total flavonoids(TFs)from P.alkekengi L.was 0.567%.Microscopic identification showed that the parenchyma tissue of P.alkekengi L.powder from Jilin Province contained abundant large orange-red particles with uniform distribution.TLC identification indicated that the spots of P.alkekengi L.samples from 10 different producing areas,the reference crude drug of P.alkekengi L.,and physalin L were clear with good resolution.All determined moisture contents complied with the specifications of the Chinese Pharmacopoeia(ChP).The order of ethanol-soluble extract content from high to low was,Jilin>Inner Mongolia>Sichuan>Liaoning>Zhejiang>Hebei>Heilongjiang>Henan>Hubei>Shandong.TF content determination results showed that the contents in samples from Jilin and Sichuan were similar and the highest among all tested samples.In conclusion,the Box-Behnken method was used to construct a multi-factor interaction model to optimize the extraction process of P.alkekengi and compare the quality of P.alkekengi from different origins.

马铭泽;李楠;洪泽辉;李冰;崔佳;宋欢

长春科技学院 医药学院,吉林 长春 130600长春科技学院 医药学院,吉林 长春 130600长春科技学院 医药学院,吉林 长春 130600长春科技学院 医药学院,吉林 长春 130600长春科技学院 医药学院,吉林 长春 130600长春科技学院 医药学院,吉林 长春 130600

锦灯笼Box-Behnken法总黄酮质量标准

Physalis alkekengi L.Box-Behnken designtotal flavonoidsquality standard

《黑龙江农业科学》 2026 (4)

36-45,10

长春科技学院2024年度科研基金项目(CCKJXY2024KJ18).

10.11942/j.issn1002-2767.2026.04.0036

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