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1.
采用高效液相色谱法（HPLC）对 4 种黔引迷迭香的多酚成分进行定性和定量分析,并利用 DPPH、ABTS自由基清除能力和铁离子还原能力（FRAP）3 种方法评价多酚成分的抗氧化能力。结果显示 4 种材料均富含类黄酮、酚酸和二萜酚等多酚类化合物,总酚含量介于 4 345.5~5 673.0 mg/100 g 。其中槲皮素、迷迭香酸、阿魏酸、绿原酸和鼠尾草酸是迷迭香最主要的酚类物质。黔引迷迭香 4 号的抗氧化活性最高,利用 DPPH、ABTS 和 FRAP等 3 种方法检测的结果依次为 184.4、290.0、155.6 μmol/g。相关性分析表明,总酚与总抗氧化活性能力显著相关,迷迭香酸对总抗氧化活性能力贡献最大,其次为鼠尾草酸、槲皮素和水杨酸。本研究对于了解黔引迷迭香抗氧化活性成分,以及资源的进一步开发利用具有重要指导意义。  相似文献   

2.
本文建立了采用高效液相色谱法同时检测火麻籽油中10种酚类物质的方法,10种单体酚检出限为0.05～0.12μg/mL,线性相关系数为0.9970～0.9998,回收率为85%～108%。检测了8份不同产地火麻籽油的总酚、总黄酮含量及体外抗氧化活性指标（DPPH、FRAP、ABTS+·）。总酚含量为1.20～17.35mg对香豆酸/100g,总黄酮含量为7.61～51.72mg柚皮苷/100g。DPPH清除能力为9.03～19.71mmol TE/100g,FRAP还原能力为13.12～30.09mmol TE/100g,ABTS+•清除能力为29.40～358.37mmol TE/100g。相关性分析表明,总酚含量与DPPH、ABTS+•清除能力和FRAP还原能力呈显著正相关;总黄酮含量与DPPH清除能力、FRAP的还原能力呈显著正相关。  相似文献   

3.
不同品种桑葚叶总酚含量及其抗氧化活性比较   总被引：1，自引：0，他引：1  
为了研究不同品种桑葚叶的总酚含量差异及应用价值,以收集引种的40个品种桑葚叶为研究对象,采用超声波辅助提取桑葚叶中酚类物质,以总酚提取率为指标,利用单因素试验和正交试验考察各因素对超声辅助提取桑葚叶总酚提取率的影响;采用DPPH自由基清除能力评价不同品种桑葚叶提取物的抗氧化能力,同时对不同品种桑葚叶中总酚含量及其抗氧化能力进行相关性分析。结果表明：超声辅助提取桑葚叶总酚的最佳工艺条件为：超声温度65 ℃、超声时间30 min、固液比1∶45（g/mL）、乙醇浓度60%,4个因素对桑葚叶总酚提取率影响大小顺序为：超声温度>超声时间>固液比>乙醇浓度。不同品种桑葚叶总酚含量差异较大,其中‘条桑五号’总酚含量最高,为（26.35 ± 0.29）mg/g,‘滇桑’总酚含量最低,为（20.44 ± 0.15）mg/g;不同品种桑葚叶抗氧化活性也存在差异,且趋势与总酚含量基本一致,‘条桑五号’桑葚叶抗氧化活性最强,清除DPPH自由基能力IC50为（77.64 ± 0.34）mg/L,总抗氧化能力（FRAP）TEAC值为（2.58 ± 0.11）mmol/g;‘滇桑’桑葚叶抗氧化活性最弱,清除DPPH自由基能力IC50为（210.30 ± 0.19）mg/L,总抗氧化能力（FRAP）TEAC值为（0.73 ± 0.04）mmol/g。桑葚叶总酚含量与其提取物抗氧化能力呈正相关,选择总酚含量高的桑葚品种栽培,可提高桑葚的综合附加值。  相似文献   

4.
以柑橘杂交品种葡萄柚、茂谷橘橙果皮为材料,研究超声波和微波对柑橘果皮提取物中酚类物质及其抗氧化活性的影响。结果表明:葡萄柚果皮中含有丰富的柚皮苷、芦丁、橙皮素等酚类物质,茂谷橘橙果皮中含有丰富的槲皮素、川陈皮素、橙皮素等酚类物质。葡萄柚果皮提取液的抗氧化活性高于茂谷橘橙。葡萄柚果皮超声波提取液中酚类物质的含量和抗氧化活性高于微波提取液。柑橘果皮提取物中酚类物质的含量与其DPPH自由基和羟自由基清除能力呈正相关。此结果说明超声波提取法可提高葡萄柚果皮中酚类物质的提取率和提取液抗氧化能力。  相似文献   

5.
本研究采用高效液相色谱、酶标检测技术,确定可可豆加工过程中黄烷醇类物质组成变化趋势,分析抗氧化活性。在发酵及焙炒阶段检测黄烷醇物质儿茶素（C）、表儿茶素（EC）、表没食子儿茶素（EGC）、表儿茶素没食子酸酯（ECG）、原花青素B1（PC B1）、原花青素B2（PC B2）。结果表明：经7 d发酵各成分含量分别为EGC（8.521~ 3.017 mg/g）、C（15.521~6.633 mg/g）、EC（19.615~3.142 mg/g）、ECG（0.236~0.084 mg/g）、PC B1（19.152~10.774 mg/g）、PC B2（4.254~2.083 mg/g）,发酵使得可可豆中儿茶素及低聚物含量大量减少;135 ℃不同时间焙炒下,各物质含量分别为EGC（3.079~2.221 mg/g）、C（8.611~5.143 mg/g）、EC（3.956~0.982 mg/g）、ECG（0.111~0.070 mg/g）、PC B1（10.987~ 8.223 mg/g）、PC B2（2.385~1.534 mg/g）。可可豆在高温焙炒时,DPPH、ABTS自由基清除率呈下降趋势,降低了可可抗氧化活性。研究结果为可可加工提供相关保健功能性的依据。  相似文献   

6.
荔枝采后果皮变色分子机理研究   总被引：1，自引：0，他引：1  
以不同处理荔枝在贮藏过程中冻干果皮为研究对象,采用高效液相色谱分析鉴定,通过对荔枝贮藏过程中果皮中有机物分子含量变化的研究,得出果皮中一种称为类黄酮的酚类物质即水溶性花色素苷含量的变化是引起荔枝果皮变色的一个重要原因,而果皮中的其他有机物如黄烷醇类物质和黄酮醇类物质对水容性花色素苷含量的变化有着重要的影响。不同保鲜处理的荔枝贮藏结果表明:冰水处理的荔枝果皮比热水处理的荔枝果皮中的花色素苷降解速度慢,本实验可以为研究荔枝采后褐变机理、果皮着色变化与酚类物质的关系提供理论指导及相应的操作工艺。  相似文献   

7.
分析了我国不同产区不同品种亚麻籽的组成及体外抗氧化特性。结果表明,除基本组成成分外,不同品种亚麻籽主要活性组分含量和体外抗氧化活性具有显著差异。α-亚麻酸、木酚素、总酚酸、黄酮、生育酚、植物甾醇含量范围分别为33.42%~59.74%,120~918 mg/100g,209~491 mg/100g,33.04~75.63 mg/100g,8.68~20.75 mg/100g,340~596 mg/100g。亚麻籽提取物DPPH值和FRAP值分别为4 357~8 146 μmol Trolox/100g, 8 289~15058 μmol Trolox/100g。此外,不同品种亚麻籽抗营养因子生氰糖苷含量差异较为显著(5.57~11.34 mg HCN/100g)。相关性分析结果表明,亚麻籽提取物体外抗氧化活性与木酚素、总酚酸和黄酮含量具有显著相关性（p<0.05）。主成分分析和聚类分析结果表明,亚麻籽主要酚类化合物及其抗氧化活性主要依赖于亚麻籽品种特性,而非种植区域。  相似文献   

8.
椰子种皮油提取物的抗氧化活性研究   总被引：1，自引：0，他引：1  
测定椰子种皮油提取物中的总酚含量,对羟基自由基、DPPH（1,1-二苯基-2-三硝基苯肼）自由基、ABTS（2,2连氮-双-（3-乙基苯并噻咪唑-6-磺酸）自由基清除能力和总抗氧化能力等抗氧化活性指标。结果表明,椰子种皮油提取物中含有较高的总酚含量（68 mg/g）,提取物浓度为0.1 mg/mL时对羟基自由基的清除率为56.89％,对DPPH自由基的清除率为71.0％,对ABTS自由基的清除率为96.4％,表明椰子种皮油提取物具有很好的抗氧化活性。  相似文献   

9.
以广东的红叶1号、红叶2号、丹妃和云南紫娟4种红紫芽品种（系）为供试材料,以英红九号绿芽品种为对照,通过分析酶活性研究了红紫芽茶花青素合成关键酶活性变化规律,并揭示了其与花青素、茶多酚、儿茶素组分等重要酚类物质含量的相互关系。结果表明,红紫芽茶花青素合成过程中,同一季节不同品种（系）类黄酮-3-O-糖基转移酶（UFGT）活性与茶多酚总量和花青素含量均显著正相关,为花青素合成的关键酶;而苯丙氨酸解氨酶（PAL）、查尔酮合成酶（CHS）、类黄酮-3-羟化酶（F3H）、二氢黄酮醇-4-还原酶（DFR）、黄酮醇合成酶（FLS）、花青素合成酶（ANS）和花青素还原酶（ANR）等活性能力与花青素含量变化趋势不存在密切的相关性;春季各样品儿茶素（C）含量与PAL酶活性显著正相关,表儿茶素没食子酸酯（ECG）含量与DFR酶活性存在显著正相关;同一季节不同品种（系）CHS、F3H、ANS以及ANR酶活性与酚类物质含量无显著相关性。  相似文献   

10.
为了筛选出有利于荔枝贮藏的复合保鲜剂,以‘井岗红糯’荔枝果实为试验材料,通过正交试验研究了不同浓度的油菜素内酯（brassinolide, BL）和曲酸（kojic acid, KA）配比对采后荔枝果实的保鲜效果。结果表明,在25 ℃贮藏条件下,对荔枝果实的最佳保鲜配方为：油菜素内酯40 μmol/L、曲酸35 mmol/L,浸泡时间为3 min,该复合保鲜剂配方能较好地抑制荔枝果实褐变和腐烂,降低果皮相对电导率、果皮pH和果皮丙二醛（malonaldehyde, MDA）含量,延缓果肉总可溶性固形物（total soluble solids, TSS）和维生素C（vitamin C, VC）含量的下降,维持较高的果皮色度L *值、a *值、C *值和花色苷含量,抑制了多酚氧化酶（polyphenol oxidase, PPO）、过氧化物酶（peroxidase, POD）及漆酶（laccase, Lac）的活性。  相似文献   

11.
Chickpea (Cicer arietinum L.) genotypes, nine kabuli from Mexico and 9 desi from other countries, were investigated for their phenolic profiles and antioxidant activity (AA). Phenolics in methanol extracts (ME) were analyzed by ultra-performance liquid chromatography coupled to diode array detection and mass spectrometry (UPLC-DAD-MS), whereas the AA was measured as Trolox equivalents (TE) by ABTS, DPPH and FRAP methods. Twenty phenolic compounds were identified in the ME and their levels showed a great variability among the chickpea genotypes. Phenolic acids and flavonoids were the most abundant compounds in kabuli and desi genotypes, respectively. The AA values (μmol TE/ 100 g dw) by ABTS (278–2417), DPPH (52–1650), and FRAP (41–1181) were mainly associated with the content of sinapic acid hexoside, gallic acid, myricetin, quercetin, catechin, and isorhamnetin, suggesting they are the main compounds responsible for the AA. The sum of the AA obtained for standards of these compounds evaluated at the concentration found in the extracts accounted for 34.3, 69.8, and 47.0% of the AA in the extract by ABTS, DPPH, and FRAP, respectively. In the AA by DPPH, most of the mixtures of these compounds resulted in synergistic interactions. Three desi genotypes with black seeds (ICC 4418, ICC 6306, and ICC 3761) showed the highest AA and flavonoids content, whereas the most promising kabuli genotypes were Surutato 77, Bco. Sin. 92, and Blanoro that showed the highest values of phenolic acids. These genotypes represent good sources of antioxidants for the improvement of nutraceutical properties in chickpea.  相似文献   

12.
In this work, α-amylase was used to treat oat flour with the intent to release phenolic compounds with known antioxidant properties. After methanol extraction, the amounts of nine beneficial phenolic compounds were measured using HPLC. The antioxidant activities of the extracts were assessed using 2,2′-azinobis (3- ethylbenzothiazoline-6-sulfonic acid) (ABTS)，2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and protein oxidative damage protection assays. Compared with heating-only treated oat flour, that treated with α-amylase showed significant increase of extractable total phenolic content (0.46–1.35 μmol gallic acid equivalents per gram oat), total antioxidant capacity, and an increased ability on the protection of protein from oxidative damage. Heating-only increased caffeic acid and vanillin content by 17 (0.03 vs 0.54 μg/g oat) and 1.8 (0.62 vs 1.11 μg/g oat) folds, but slightly increased the content of other phenols. Excluding heating effect, α-amylase treatment increased gallic acid content by 2.6 folds (0.38 vs 1.38 μg/g oat), caffeic acid content by 2.4 (0.54 vs 1.82 μg/g oat) folds, and other phenols by 1.0–1.8 folds. In conclusion, α-amylase treatment can yield oat products containing more extractable phenolic compounds with increased antioxidant capacity.  相似文献   

13.
Chestnut (Castanea sativa) shell and eucalyptus (Eucalyptus globulus) bark, waste products of the food and wood industries, respectively, were analysed as potential sources of antioxidant compounds. The extraction yield, the antioxidant activity and total phenols content of the extracts were greater in chestnut shell than in eucalyptus bark for most of the extraction conditions essayed. Extraction of chestnut shell with a 2.5% Na2SO3 aqueous solution led to the highest extraction yield, 25.6%, total phenols, 13.4 g gallic acid equivalent/100 g oven-dried shell, and FRAP antioxidant activity, 80.7 mmol ascorbic acid equivalent/100 g oven-dried shell. Extraction with methanol:water (50:50, v/v) provided the best results for eucalyptus bark. The antioxidant activity and the total phenols content of the extracts had a positive linear correlation. FTIR spectroscopy confirmed the higher content of phenolic compounds in chestnut shell extracts compared to eucalyptus bark extracts. Chestnut shell extracts were characterized by the presence of high molecular weight species whereas lower molecular weight species were predominant in eucalyptus bark extracts.  相似文献   

14.
The chestnut bur, a forest waste product from chestnut processing in the food industry, was studied as a potential source of natural antioxidants. Extractions were performed using aqueous solutions of methanol or ethanol. Experiments were planned according to an incomplete 33 factorial design to study the influence of temperature (25-75 °C), time (30-120 min) and solvent concentration (50-90%) on extraction yield and on extract properties: total phenols content, antioxidant activity (using the FRAP, DPPH and ABTS methods) and average molecular weights. All dependent variables were influenced by temperature and solvent concentration whereas the influence of time was almost negligible. Using the response surface methodology the optimal extraction conditions were selected: the highest temperature assayed (75 °C), the lowest solvent concentration (50%) and an extraction time of 75 min for the methanolic extractions and of 30 min for the ethanolic ones. Under those conditions the values predicted for extraction yield and total phenols content were 18.95% and 36.32 g GAE/100 g extract for the methanolic extract and 17.95% and 26.11 g GAE/100 g extract for the ethanolic ones. Methanolic extracts showed superior total phenols content and antioxidant properties and slightly higher extraction yields than ethanolic extracts; however, ethanol is recommended for food applications due to its GRAS (Generally Recognized as Safe) qualification. Gallic acid esters of glucose, ellagic acid and small proportions of quercetin-3-β-d-glucoside, phenolic compounds with demonstrated antioxidant properties, were identified in chestnut bur extracts by RP-HPLC-ESI-TOF.  相似文献   

15.
Aqueous acetone extracts prepared from five Indigofera species of Burkina Faso, namely Indigofera colutea (Burm.) Murril., I. macrocalyx Guilld et Perr., I. nigritana Hook f., I. pulchra willd. and I. tinctoria L., were investigated for their phytochemical composition and their antioxidant activities. Standard methods and TLC were used to screen the phytochemical composition. The total phenolic and flavonoid content of extracts were assessed by Folin-Ciocalteu and AlCl3 methods, respectively. These extracts were also evaluated for their antioxidant potentials using ferric reducing antioxidant power (FRAP), 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azinobis(3-ethylbenzothiazoline-6-sulphonate) (ABTS) assays. Flavonoids, saponins, quinones, sterols/triterpenes and tannins were present in all these species except for I. pulchra where quinones were not found. Gallic acid, caffeic acid, rutin and myricetin in I. colutea; gallic acid, quercitrin, myricetin in I. tinctoria; galangin and myricetin in I. macrocalyx were identified by thin layer chromatography. Among these, I. colutea, I. tinctoria, I. nigritana and I. macrocalyx, which had the highest phenolic content, were also found to possess the best antioxidant activities. The results indicated a good correlation between antioxidant activities and total phenolic content (p<0.05 for FRAP/DPPH and DPPH/ABTS and p<0.01 for FRAP/ABTS). These plants represent promising sources of natural antioxidants and these findings give scientific bases to their ethnopharmacological uses.  相似文献   

16.
The bioactivity of two kiwifruit’s cultivars growing under organic and conventional conditions were studied and compared. The bioactive compounds were extracted with water and ethanol using similar conditions which are applied in pharmaceutical applications and for daily fruit consumption such as tea drink. Antioxidant radical scavenging assays [ferric-reducing/antioxidant power (FRAP); cupric reducing antioxidant capacity (CUPRAC); 2, 2-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) (ABTS)], fourier transform infrared (FT-IR) and ultraviolet spectroscopy, two (2D-FL) and three-dimensional (3D-FL) fluorometry were used for the detection of biologically active metabolites derived from kiwifruits (total phenols, flavonoids, chlorophylls, carotenoids and ascorbic acid). The correlation between the total phenol content (TPC) and other bioactive compounds, and their total antioxidant capacities (TAC) was calculated for studied kiwifruit’s extracts. The interaction between drugs and human serum albumin (HSA) plays an important role in the distribution and metabolism of drugs. The properties of kiwifruit’s phenol extracts showed their ability to quench HSA, forming the complexes similar to the ones between the proteins and pure flavonoids such as quercetin. The cultivar ‘Bidan’ exhibited significantly higher TAC than the classic ‘Hayward’. In conclusion, for the first time ‘Bidan’ organic kiwifruit was analyzed and compared with widely consumed ‘Hayward’, using its bioactive and fluorescence properties. The influence of physiologically active kiwifruit’s compounds on human health, through our investigations in vitro and scientifically proven information, was explained. Relatively high content of bioactive compounds, high antioxidant and fluorescence properties of kiwifruit justify its use as a source of valuable antioxidants.  相似文献   

17.
To investigate the relationship between reducing sugars and phenolic retention of brown rice after enzymatic extrusion, reducing sugars, total phenolic content, total antioxidant activity, and individual phenolic acids of brown rice extruded with different α-amylase concentrations (0.1%, 0.5%, 1%, w/w) were evaluated. Reducing sugars were produced during enzymatic extrusion and significantly increased with the increasing enzyme concentration. Compared with traditional extrusion, the enzymatic extrusion with 1% amylase significantly increased the phenolic retention, DPPH value, FRAP value, and ABTS value by 22.4%, 19.5%, 14.7%, and 41.5%, respectively. The retention of most free phenolic acids was also increased with the increasing enzyme concentration. Besides, the correlation analysis indicated that the content of reducing sugars was positively correlated with total phenolic content (r = 0.915), DPPH value (r = 0.882), FRAP value (r = 0.861), ABTS value (r = 0.867) and free individual phenolic acids (r = 0.595–0.943) of treated brown rice. These results suggested that reducing sugars might protect phenolic compounds during enzymatic extrusion.  相似文献   

18.
The effects of three independent variables: solvent polarity, temperature and extraction time on the antioxidant capacity, total phenolic content and phenolic acid composition in extracts obtained from sunflower shells before and after enzymatic treatment were studied. Response surface methodology based on three-level, three-variable Box-Behnken design was used for optimization of extraction parameters and evaluation of their effect on antioxidant capacity and total phenolic content in shell extracts.The average antioxidant capacities of extracts from sunflower shells without enzymatic treatment (368.1-1574.4 μmol TE/100 g) were higher than those for cellulolytic and pectolytic enzymes-treated shells (222.7-1419.0 and 270.7-1570.7 μmol TE/100 g, respectively). The content of total phenolic compounds ranged between 58.2-341.2 mg CGA/100 g, 26.7-277.3 mg CGA/100 g and 51.4-301.5 mg CGA/100 g for extracts obtained from shells without enzyme and treated with cellulolytic and pectolytic enzymes, respectively. Total phenolic content (TPC) in the studied shell extracts correlated significantly (p < 0.0001) positively with their antioxidant capacity determined by the ferric reducing antioxidant power (FRAP) method (r = 0.9275). Results of FRAP, TPC and phenolic acid composition in the studied shell extracts depend on the extraction conditions (solvent polarity, temperature, time), but they are independent on the addition of enzyme solutions. The antioxidant capacity and total phenolic content in the resulting extracts increased with a line in extraction temperature and solvent polarity.  相似文献   

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