乌贼墨多糖提取物的制备及其对B16F10细胞的影响

为了探索乌贼墨多糖(SIP)对体外培养的B16F10细胞的生物学效应,以乌贼墨为原材料,对SIP进行提取分离,并研究SIP提取物对B16F10细胞活力、细胞内酪氨酸酶活性及黑色素合成等的影响。结果表明,SIP提取的最优条件为提取温度40℃,料液比1∶3,提取时间4h,提取次数3次,在此条件下SIP得率为14.12 mg·g~(-1)。SIP提取物对B16F10细胞形态有一定影响,对细胞活性、酪氨酸酶活性和黑色素合成均有一定抑制作用,且呈现一定剂量效应。综上可知,SIP提取物能抑制黑色素合成,具有作为美白剂的发展前景,这为乌贼墨合理利用提供了一定科学依据。     

欧李多酚提取纯化及抗氧化性研究

欧李富含钙素和多酚类物质,具有提高人体免疫力等保健功能,近年来在中国得到了大力发展。欧李多酚提取、纯化及其抗氧化功能,为欧李开发利用提供理论依据。该研究采用单因素及响应面优化试验研究了欧李多酚超声辅助酶解提取工艺,采用大孔树脂纯化多酚粗提物,利用高效液相色谱法测定酚类物质的种类,利用分光光度法测定欧李多酚类物质总还原力和对自由基·OH、DPPH·、ABTS·的清除作用。试验得出欧李多酚提取最优工艺参数为：超声波功率105 W、酶解温度50 ℃、酶解时间80 min、液料比30∶1 mL/g,多酚提取量为42.63 mg/g。经大孔树脂纯化后纯化物中欧李总多酚含量为73.42 mg/g,从欧李果实中检测出6种多酚类物质,其含量顺序为绿原酸>没食子儿茶素没食子酸酯>咖啡因>对羟基苯甲酸>原儿茶酸>没食子酸。欧李多酚的总还原力与维生素C相当,对·OH、DPPH·、ABTS·等自由基清除作用显著。     

祁白术多酚酶法提取工艺优化及其抗氧化、抑制黑色素合成活性

为考察祁白术多酚(polyphenols from Atractylodes macrocephala Koidz grown in Qimen, AMP)的可利用性,采用响应面分析法优化酶法提取工艺,并研究AMP的抗氧化、抑制黑色素合成活性。结果表明,在料液比1:30 g·mL^-1、酶解时间20 min的条件下,当纤维素酶添加量为1.35%、酶解温度为44℃、pH值为4.7、搅拌转速为670 r·min^-1时,AMP提取量最高,为26.58±0.23 mg·g^-1。统计学分析显示,所选响应面模型拟合较好,优化后的提取工艺条件合理可行。AMP具有较好的抗氧化活性,其总还原力、对1,1-二苯基-2-三硝基苯肼(DPPH)和2,2-联氮-二(3-乙基-苯并噻唑-6-磺酸)二铵盐(ABTS)自由基清除作用随其浓度的增加而增强。当AMP浓度为0~0.02 mg·mL^-1时,对B16细胞无毒性作用。与α-MSH模型组相比,AMP显著下调了细胞内酪氨酸酶活性(P<0.05),并呈浓度依赖性地抑制细胞内黑色素的合成(P<0.05);当AMP浓度为0.02 mg·mL^-1时,对细胞内酪氨酸酶活性及黑色素合成抑制率分别为30.11%、43.35%,阳性对照熊果苷(0.1 mg·mL^-1)对细胞内酪氨酸酶活性及黑色素合成的抑制率分别为22.03%、39.77%,表明AMP对黑色素生成的抑制效果强于熊果苷。本研究结果为祁白术多酚的综合开发利用提供了依据。     

低共熔溶剂提取核桃青皮多酚工艺优化及其抑菌活性

为了充分利用核桃副产物,减少环境污染,该研究以核桃青皮为研究对象,分别采用不同pH值（3、7、10）水溶液、50%乙醇溶液和低共熔溶剂（尿素/氯化胆碱：DES-UC,草酸/氯化胆碱：DES-OC）提取多酚。首先在温度80 ℃、液料比25 mL/g、低共熔溶剂（Deep Eutectic Solvents, DESs）配位剂摩尔比1.0的条件下提取60 min筛选出DES-OC提取效果较好;随后在单因素试验考察的基础上,采用响应面分析法确定了DES-OC提取核桃青皮多酚的优化工艺参数：草酸/氯化胆碱摩尔比1.0、温度85 ℃、时间62 min、液料比50 mL/g,在此条件下多酚提取量为50.87 mg/g。另外,通过对核桃青皮多酚提取混合溶剂抑菌活性试验的研究,发现DES-OC与核桃青皮多酚混合后对大肠杆菌（E.coli）的抑菌效果较佳,金黄色葡萄球菌（S.aureus）次之,最后为黄青霉（P.chrysogenum）。以上试验结果可为研究开发天然抑菌剂、保鲜剂等提供理论基础,拓宽核桃青皮加工利用途径的同时也为提取农产品副产物中生物活性成分提供新思路。     

超声波辅助提取木薯皮活性物质工艺

木薯皮乙醇提取物同时具有抗乙酰胆碱酯酶（AChE）和抗丁酰胆碱酯酶（BuChE）的活性,为了能充分提取和利用其抗胆碱酯酶活性物质,研究了超声波提取木薯皮活性物质的工艺。通过单因素试验和Box-Behnken Design法设计的响应面优化试验确定了超声波辅助乙醇提取木薯皮中抗胆碱酯酶活性物质的最优工艺条件,并比较了超声波提取与传统溶剂浸提的提取效果。试验结果表明：超声波辅助乙醇提取木薯皮中抗胆碱酯酶活性物质的最优工艺条件为：乙醇体积分数为95%,超声波功率550W,提取时间90min,提取温度60℃,液料比12mL/g,在此工艺条件下,木薯皮活性物质的平均得率为8.97%,质量浓度为0.5mg/mL时的AChE抑制率为54.62%,BuChE抑制率为45.7%;影响木薯皮活性物质得率的4个主要因素的显著程度排列顺序为：超声波提取功率＞提取温度＞提取时间＞液料比;与传统溶剂浸提法相比,超声波提取法具有提取速度快,得率高,提取物活性好,溶剂用量少等明显优势。     

红松种子壳多酚物质的提取及抗氧化特性

该文选取超声波辅助提取法,采用单因素试验及响应面设计,研究了超声波提取时间、温度、乙醇浓度及料液比对红松种子壳中多酚类化合物提取的影响。并利用Fenton体系、1,1-二苯基-2-苦苯肼(DPPH·)体系及邻苯三酚体系测定其提取成分的抗氧化活性。结果表明,松壳中多酚成分提取的最佳工艺条件为:超声提取时间2.80h、料液比1∶26.36(g/mL)、乙醇浓度42.86%、提取温度80℃,多酚得率7.96mg/g。在此优化条件下,红松种子壳提取物对羟自由基(甲基紫法)、DPPH·自由基及超氧阴离子均具有较强清除作用,半数抑制浓度分别为6.67×10-4、2.34×10-2、3.97mg/mL。     

番茄茎叶活性成分杀虫试验

探索了番茄茎叶活性成分杀虫能力。通过不同溶剂提取的活性成分杀虫试验、不同浓度活性成分杀虫试验、不同萃取溶剂杀虫试验、石油醚不同浓度的杀虫试验,得出采用溶剂乙醇提取、活性物质杀虫的半致死浓度LC50为10.40 mg/mL、石油醚为萃取溶剂、萃取物杀虫的半致死浓度LC50为6.58 mg/mL。为番茄茎叶活性成分的应用作提供理论参考。     

仙人掌皮黄酮提取工艺优化(简报)

仙人掌皮黄酮提取可提高废弃物的资源利用和活性成分的开发。采用响应面分析法对乙醇体积分数、提取温度、提取时间和剂料比等提取条件进行了优化。结果表明,曲面回归方程拟合性好;优化工艺为乙醇体积分数67%、提取温度76℃、提取时间5.7 h、剂料比21.4 mL/g时,仙人掌皮黄酮得率为6.45 %。经鉴定仙人掌皮中主要黄酮为异鼠李素-3-O-[2-O,6-O-双-?-L-鼠李糖基]-?-L-葡萄糖苷、异鼠李素-3-O-（6?-鼠李糖）葡萄糖苷。     

仙人掌皮黄酮提取工艺优化

仙人掌皮黄酮提取可提高废弁物的资源利用和活性成分的开发.采用响应面分析法对乙醇体积分数、提取温度、提取时间和剂料比等提取条件进行了优化.结果表明,曲面回归方程拟合性好;优化工艺为乙醇体积分数67%、提取温度76°C、提取时间5.7 h、剂料比21.4 mL/g时,仙人掌皮黄酮得率为6.45%.经鉴定仙人掌皮中主要黄酮为异鼠李素-3-O-[2-O,6-O-双-α-L-鼠李糖基]-α-L葡萄糖苷、异鼠李素-3-O-(6'-鼠李糖) 葡萄糖苷.     

甘油水溶液提取米糠多酚绿色工艺优化及多酚种类鉴定

为探究甘油作为绿色溶剂提取米糠多酚的可行性,该文选取提取温度、甘油体积分数、液料比和提取时间4个因素,采用单因素结合响应面试验进行米糠多酚提取工艺优化。同时,分析了甘油提取液的黏度特性,并利用超高效液相色谱串联三重四级杆飞行时间质谱(UPLC-Triple-TOF/MS)方法进行多酚鉴定。结果表明,甘油提取米糠多酚最优条件为提取温度67℃,甘油体积分数19%,液料比33 mL/g,提取时间固定为80 min,获得的最大多酚得率为700.35 mg/(100 g)。甘油对米糠多酚的提取效率和甘油的黏度有显著的负相关性。此外,UPLC-Triple-TOF/MS分析表明,最优条件下甘油提取得到13种米糠多酚,其中酚酸质量分数如下:对羟基苯甲酸48.53μg/g,香草酸69.64μg/g,丁香酸33.63μg/g,4-香豆酸361.18μg/g,阿魏酸392.17μg/g,水杨酸34.67μg/g。研究结果表明,甘油可以作为从米糠中提取多酚的绿色溶剂。     

Rapid reversed phase ultra-performance liquid chromatography analysis of the major cocoa polyphenols and inter-relationships of their concentrations in chocolate

Chocolate and other cocoa-containing products are a rich source of polyphenols. This paper describes an ultra-performance liquid chromatography (UPLC) method that can separate and quantify in 3 min six of the major chocolate polyphenols: catechin; epicatechin; B2 (epicatechin-4beta-8-epicatechin); B5 (epicatechin-4beta-6-epicatechin); C1 (epicatechin-4beta-8-epicatechin-4beta-8-epicatechin); and tetramer D (epicatechin-4beta-8-epicatechin-4beta-8-epicatechin-4beta-8-epicatechin). A survey of 68 chocolate samples indicated that there was a strongly predictive relationship between epicatechin and the other individual polyphenols, especially procyanidin B2 (R 2 = 0.989), even though the chocolates came from varied sources and manufacturers. The relationship was less strong with catechin, and so further work to explore the reasons for this difference was performed. Chiral analysis on a subset of 23 chocolates showed that (-)-epicatechin had a predictive relationship with (+)-catechin in line with the other polyphenols, but not with (-)-catechin (the predominant form). This indicates that (-)-catechin is the most affected by manufacturing conditions, possibly formed through epimerization from (-)-epicatechin during processing. The results show that epicatechin concentrations can be used to predict the content of other polyphenols, especially B2 and C1, and total polyphenols content. Finally, the (-)-catechin content is not predictable from the epicatechin content, and it is concluded that this is the main form of polyphenol that varies according to manufacturing conditions and cocoa origin.     

Procyanidin trimers to pentamers fractionated from apple inhibit melanogenesis in B16 mouse melanoma cells

The effects of apple polyphenols on melanogenesis in B16 mouse melanoma cells were investigated. The inhibitory effect of apple polyphenols was stronger than that of arbutin or kojic acid. Three polyphenol fractions (phenolic acid derivatives, procyanidins and other flavonoids) were isolated, and the procyanidins were fractionated according to the degree of polymerization using normal-phase chromatography. The procyanidin trimer-to-pentamer fractions were found to have the most pronounced effect on melanogenesis. Furthermore, each procyanidin fraction inhibited mushroom tyrosinase. No correlation between the degree of procyanidin polymerization and tyrosinase inhibitory activity was observed. Nevertheless, these observations suggest that procyanidins are effective inhibitors of tyrosinase.     

杏仁种皮酚类物质的低共熔溶剂提取及其抗氧化能力

为了探讨低共熔溶剂（Deep Eutectic Solvents, DESs）对杏仁种皮酚类物质的提取率及其提取物抗氧化能力,以4种传统溶剂和5种低共熔溶剂为提取溶剂,比较评价了低共熔溶剂对杏仁种皮酚类物质的提取效果,并采用DPPH、ABTS自由基清除法和氧自由基吸收能力（Oxygen Radical Absorption Capacity, ORAC）分析杏仁种皮低共熔溶剂提取物的抗氧化能力。结果表明,低共熔溶剂对杏仁种皮酚类物质的提取效果更佳,其中氯化胆碱-草酸（DESs2）和氯化胆碱-苹果酸（DESs3）两组低共熔溶剂对杏仁种皮酚类的提取率分别为酸化甲醇的2.18和1.84倍;与酸化甲醇的杏仁种皮提取物相比,DESs2和DESs3杏仁种皮提取物的DPPH自由基清除能力分别提高了26.89%和73.13%,ABTS自由基清除能力分别提高了33.18%和114.81%,氧自由基吸收能力分别提高了14.92和17.73 μmol/g。HPLC结果表明传统溶剂的杏仁种皮提取液中酚类物质组成较复杂,而氯化胆碱-草酸（DESs2）、氯化胆碱-苹果酸（DESs3）和氯化胆碱-苹果酸-脯氨酸（DESs5）的杏仁种皮提取液中酚类物质组成较为单一,说明低共熔溶剂在提取酚类物质时具有很强的专一性。     

Phenolic composition of kiwifruit juice

Phenolic compounds in kiwifruit pulp were separated and characterized by reversed-phase HPLC, and the effect of juice processing on the phenolic composition was studied. Fractionation of phenolic compounds was achieved through selective elution from C-18 cartridges prior to preconcentration and subsequent separation by HPLC. Strongly acidic compounds were identified as derivatives of coumaric and caffeic acids, including chlorogenic acid, protocatechuic acid, and a derivative of 3,4-dihydroxybenzoic acid. The weakly acidic fraction contained epicatechin, catechin, and procyanidins (B3, B2, or B4 and oligomers). Flavonols were present as the glycosides of quercetin (glucoside, rhamnoside, and rutinoside) and kaempferol (rhamnoside and rutinoside). Phenolic compounds were present, at levels of <1-7 mg/L, in clarified juice. The concentration of phenolics was highest after high-temperature short-time treatment (HTST) of juice. Hydrolysis of hydroxycinnamic acids occurred after enzyme addition and HTST treatment. The flavonol glycoside composition is the best identifier of kiwifruit juice.     

trans-Resveratrol, quercetin, (+)-catechin, and (-)-epicatechin content in south Italian monovarietal wines: relationship with maceration time and marc pressing during winemaking

The concentrations of trans-resveratrol, (+)-catechin, (-)-epicatechin, and quercetin were evaluated by means of high-performance liquid chromatography-diode array detection in red wines obtained from Aglianico, Piedirosso, and Nerello Mascalese grapes. The trans-resveratrol and epicatechin concentrations did not differ significantly between experimental wines. The concentration of quercetin in Nerello Mascalese wines was more than twice that observed in Aglianico and Piedirosso wines. Nerello Mascalese wines also significantly differed from other wines in the (+)-catechin content, which was significantly higher than those found in the other two wines. During maceration, the maximum extraction of trans-resveratrol was reached after 12 days for Aglianico and Piedirosso, after which a decline was observed. On the contrary, in the case of Nerello Mascalese, the concentration of trans-resveratrol increased steadily throughout the whole maceration process. After 2 days of maceration, the maximum concentration of quercetin was observed in Aglianico must, whereas the maximum quercetin extraction was reached after 12 days for Piedirosso and 17 days for Nerello Mascalese. The maximum levels of (+)-catechin and (-)-epicatechin were generally observed after 12 days of maceration for all wines, although a decline of (-)-epicatechin occurred after maximum extraction in Aglianico and Piedirosso wines. Following marc pressing, a significant increase in the concentration of trans-resveratrol for Aglianico, (+)-catechin and (-)-epicatechin for Piedirosso, and (-)-epicatechin for Nerello Mascalese was observed.     

Phenolic profile of Asturian (Spain) natural cider

The polyphenolic composition of natural ciders from the Asturian community (Spain), during 2 consecutive years, was analyzed by RP-HPLC and the photodiode-array detection system, without previous extraction (direct injection). A total of 16 phenolic compounds (catechol, tyrosol, protocatechuic acid, hydrocaffeic acid, chlorogenic acid, hydrocoumaric acid, ferulic acid, (-)-epicatechin, (+)-catechin, procyanidins B2 and B5, phloretin-2'-xyloglucoside, phloridzin, hyperin, avicularin, and quercitrin) were identified and quantified. A fourth quercetin derivative, one dihydrochalcone-related compound, two unknown procyanidins, three hydroxycinnamic derivatives, and two unknown compounds were also found. Among the low-molecular-mass polyphenols analyzed, hydrocaffeic acid was the most abundant compound, representing more than 80% of the total polyphenolic acids. Procyanidins were the most important family among the flavonoid compounds. Discriminant analysis was allowed to correctly classify more than 93% of the ciders, according to the harvest year; the most discriminant variables were an unknown procyanidin and quercitrin.     

Purification and characterization of polyphenols from chestnut astringent skin

Polyphenolic compounds from chestnut astringent skin (CAS) were purified by dialysis, using Diaion HP-20 and Sephadex LH-20 columns. During purification, specific α-amylase inhibitory activities were increased about 3.4-fold, and the 50% inhibition value was 5.71 μg/mL in the Sephadex LH-20 fraction (SE-fraction). The SE-fraction contained about 67% of the total polyphenols, 57.3% of the flavanol-type tannins, and 51.3% of the procyanidins. Strong antioxidant activity was observed in the SE-fraction. Oral administration of the SE-fraction in rats fed corn starch significantly suppressed an increase in blood glucose levels. The SE-fraction contained gallic acid and ellagic acid. The MALDI-TOF spectrum showed a peak series exhibiting a mass increment of 288 Da, reflecting the variation in the number of catechin/epicatechin units. Our results suggest CAS contains polyphenols with strong α-amylase inhibitory activity. The data also suggest CAS polyphenols might be oligomeric proanthocyanidins with gallic acid and ellagic acid.