大桑菊合剂的提取工艺研究

目的：大桑菊舍刺为医院制剂,由桑叶、菊花、薄荷、连翘、鱼腥草等中药经乙醇提取制成,为完善大桑菊合剂的制备工艺,对该制剂的制备工艺进行初步的研究。方法：①实验设计：以加水量、提取时间、提取次数和醇沉浓度为考察因素,各因素均取3水平,采用正交试验L4（3^4）优选制备工艺。②含量测定方法：以大桑菊饮合剂中总黄酮的含量为指标,以芦丁为标准品,利用紫外分光光度计于503nm下测定吸光值,计算样品中总黄酮的含量,以此作为筛选大桑菊合剂最佳制备工艺的重要指标。结果：最佳制备工艺为不浸泡,加8倍水,提取3次,每次1小时。结论：经正交设计优化的大桑菊合剂的中药制备工艺合理、可行。     

葛根总黄酮提取工艺的研究

目的:筛选提取葛根总黄酮的最佳工艺条件。方法:采用单因素和正交试验对提取葛根总黄酮的工艺条件进行优化;利用紫外可见分光光度计测量葛根总黄酮的含量;利用高效液相色谱仪测量葛根素的含量;分别以葛根素和葛根总黄酮的含量为指标进行最优工艺的评价。结果:最佳工艺条件是以9倍量的30%乙醇提取3次,每次1h。结论:该提取工艺简单,成本低,适合于生产应用。     

苏州荠苧总黄酮的提取工艺研究

目的:研究苏州荠苧总黄酮的提取工艺.方法:选择乙醇浓度(A)、溶媒倍数(B)、提取时间(C)等为考察因素,以总黄酮含量为考察指标,采用正交试验设计考察提取工艺.结果:乙醇浓度和提取时间对总黄酮含量影响显著,应加以控制.结论:最佳提取工艺为A1B1C3,即加8倍量的浓度为70%的乙醇回流提取6 h,总黄酮得率最高.     

正交设计优选贯叶连翘中总黄酮提取工艺

本文采用正交设计实验,对影响贯叶连翘总黄酮提取工艺的因素进行了系统考察。结果发现,以总黄酮得率作为考察指标,影响贯叶连翘总黄酮提取的主次因素为:溶媒种类>提取时间>提取次数>溶剂用量,其中溶媒种类、提取时间、提取次数均对总黄酮的提取有显著性影响;贯叶连翘中总黄酮的最佳提取工艺条件为:用10倍量80%乙醇提取3次,每次1h。建立了以UV法测定贯叶连翘中总黄酮的含量方法。     

超声波法优选苦豆子中总黄酮的提取工艺研究

目的:超声波法优选苦豆子中总黄酮的提取工艺。方法:以超声波为提取方法,以总黄酮提取率为考察指标,选取乙醇浓度(体积分数)、加溶剂倍量和超声时间为考察因素,采用均匀实验和正交实验,优选苦豆子中总黄酮的提取工艺。结果:影响总黄酮提取率各因素主次为:ACB,确定最佳提取工艺为A2B3C3,即70%乙醇,加溶剂40倍量,超声提取75 min。结论:采用该工艺提取苦豆子中总黄酮,提取率较高且稳定,说明该工艺合理可行。     

天花粉中总黄酮提取工艺研究

本研究优化了天花粉中总黄酮的提取工艺,采用Al(NO3)3-Na NO2比色法测定了天花粉中总黄酮的含量。在单因素试验的基础上,采用L9(34)正交试验,以天花粉中总黄酮提取率为指标,探讨了甲醇体积分数、料液比、提取温度、提取时间对天花粉中总黄酮提取率的影响。结果表明最佳提取工艺参数为:甲醇体积分数50%、料液比1∶15、提取温度70℃、提取时间90 min。在最佳工艺条件下测得天花粉中总黄酮平均含量为0.1184 mg/g。该方法操作简单,稳定性和重复性好,本实验首次测定了天花粉中总黄酮含量,为天花粉药材质量控制提供了依据。     

红枣总黄酮提取工艺

目的：采用分光光度法,以芦丁为标准品测定红枣中的总黄酮含量。方法：在提取过程中通过单因素实验分析了乙醇浓度、溶媒量、提取时间三个主要因素对提取率的影响。在单因素实验的基础上通过正交设计法进行实验,优化红枣总黄酮提取工艺条件。结果：以总黄酮含量作为考察指标,影响红枣总黄酮提取的主次因素为：乙醇浓度〉溶媒量〉提取时间,红枣中总黄酮的最佳提取工艺条件为：50%乙醇、35倍量、提取时间100min。     

最优化制备沙棘膏工艺研究

沙棘果为制备沙棘膏的原料,以沙棘膏中总黄酮含量为考察影响工艺因素的指标,通过单因素试验和正交试验,确定最优化制取沙棘膏工艺为:料液比1∶20(g/mL),温度75℃,提取溶剂为80%乙醇,综合考虑成本因素,提取时间4 h。按照该工艺沙棘膏中总黄酮的得率为15.64%。     

扁蓄总黄酮提取方法的比较研究

目的:筛选扁蓄总黄酮的最佳提取方法和提取工艺.方法:以扁蓄总黄酮的提取率为指标,分别采用乙醇回流法、超声波法和微波法提取扁蓄总黄酮,通过正交试验对提取工艺中的温度、固液比、提取功率及时间等技术参数进行考察,使用分光光度法测定扁蓄总黄酮含量.结果:回流提取扁蓄总黄酮提取率为1.09%,超声波提取扁蓄总黄酮的最佳条件为温度80℃,固液比1:10,功率700 W,提取2次,每次20 min,提取率为1.67%,微波法提取扁蓄总黄酮的最佳条件为温度100℃,功率700 W,固液比1:20,提取2次,每次10min,提取率为1.98%.结论:微波提取法提取扁蓄总黄酮具有高效、省时、节能等优点,在中药提取中有良好的应用前景.     

新疆菊苣籽中总黄酮提取工艺研究

目的:以芦丁为标准品,采用分光光度法测定菊苣籽中总黄酮含量 .方法:在提取过程中通 过单因素实验,分析了乙醇浓度、回流温度、提取时间及料液比等四个因素对提取 率的影响.在单因素实验的基础上建立正交实验,优化菊苣籽总黄酮提取工艺条件.结果: 在最佳吸收波长512nm处,菊苣籽最佳提取工艺条件为乙醇浓度70%,料液比1∶50, 回流温 度70℃,提取时间2h,最佳黄酮含量C为3.80%.结论:以芦丁为对照品 ,用紫外可见分光光度法测定菊苣籽中总黄酮含量,方法简单,准确度较高.     

Ultrasonication assistance increases the efficiency of isoflavones extraction from kudzu (Pueraria lobata Ohwi) roots waste

This study assesses the use of ultrasonication to improve the extraction process of classical solvent extraction methods for extracting isoflavones from the kudzu roots waste. The kudzu roots waste was produced after squeezing fresh kudzu roots to make juice. The effects of extraction time, extraction temperature, ultrasonic power, and ethanol concentration in ethanol/water mixtures were investigated. The extraction yield was found to increase with extraction time and temperature. The application of ultrasonication-assisted extraction (UAE) increased the extraction yield of water/ethanol mixture (20:80) at 25°C 3 fold. A maximum amount (7.28 g) of isoflavone was obtained from 100 g of dried kudzu roots waste by UAE with water/ethanol mixture (20:80) for 6 h at 80°C. Combining the use of ultrasonication with conventional vacuum evaporation method also reduced the concentration time for extracts from 45 to 24 min.     

正交-满意度函数优化灵芝多糖及三萜共提取条件及其清除自由基活性

灵芝Ganoderma lingzhi是我国的一种著名珍稀药用真菌,多糖及三萜类化合物是其主要活性成分提。取乙时醇间水4h溶和液料为液提比取1:剂40,,以多灵糖芝和多三糖萜及的三提萜取提率取分率别为达响到应1值.13,=%正?和交k0-.4满6意%。度优函化数条优件化下乙提醇取含的量多、糖提和取三温萜,前者DPPH自由基清除活性高于热水法提取多糖,后者与乙醇浸提法提取三萜有相近的DPPH自由基清除活性。     

Preparation of reminiscent aroma mixture of Japanese soy sauce

To prepare an aroma mixture of Japanese soy sauce by fewest components, the aroma concentrate of good sensory attributes was prepared by polyethylene membrane extraction, which could extract only the volatiles with diethyl ether. GC-MS-Olfactometry was done with the aroma concentrate, and 28 odor-active compounds were detected. Application of aroma extract dilution analysis to the separated fraction revealed high flavor dilution factors with respect to acetic acid, 4-hydroxy-2(or5)-ethyl-5(or2)-methyl-3(2H)-furanone (HEMF), 3-methyl-1-butanol (isoamyl alcohol), and 3-(methylsulfanyl)propanal (methional). A model aroma mixture containing above four odorants showed a good similarity with the aroma of the soy sauce itself. Consequently, the reminiscent aroma mixture of soy sauce was prepared in water. The ratio of acetic acid, HEMF, isoamyl alcohol, and methional was 2500:300:100:1.     

Lipid Extraction from <Emphasis Type="Italic">Tetraselmis</Emphasis> sp. Microalgae for Biodiesel Production Using Hexane-based Solvent Mixtures

Lipid extraction is a critical step in the downstream processing of biodiesel production from microalgae. Solvent extraction using mixtures of non-polar and polar solvents is one of the most well-known processes for this purpose. Hexane is the most common solvent of choice for large-scale lipid extractions due to its technical and economic advantages, especially its high selectivity toward lipids and low cost. In this study, extractions using mixtures of hexane and polar solvents were evaluated for their performance in order to develop a more efficient method for large-scale lipid extraction from microalgae. The combination of hexane and methanol resulted in the highest fatty acid methyl ester (FAME) yield for lipids from Tetraselmis sp. The effects of extraction conditions, including proportions of methanol to hexane, ratios of total solvent volume to dry biomass, and extraction time, on extraction yields were evaluated to determine optimum conditions providing higher lipid and FAME yields. The optimal conditions were as follows: proportion of hexane to methanol of 1:1, ratio of total solvent volume to dry biomass of 10 mL/g, and extraction time of 120 min. Finally, the selected solvent mixture and optimal conditions were applied to larger scale extraction experiments with scale-up factors of 10, 50, and 100. FAME yields of large-scale extractions were almost completely consistent with increasing scale-up factors. The results of this study suggest that a hexane and methanol mixture is a promising solvent for large-scale lipid extraction from microalgae.     

A novel high-pressure liquid-liquid extraction process for downstream processing in biotechnology: extraction of cardiac glycosides

This investigation examines phase equilibrium phenomena that can be used to create two water-like solvents for liquid-liquid extraction in downstream processing in biotechnology: a completely miscible, binary liquid mixture of water and a hydrophilic organic solvent (e. g., an alcohol) reveals a liquid phase split, when it is pressurized with a "near-critical" gas (i.e., a substance which at ambient conditions is a gas, near its critical temperature). This phase split results in two hydrophilic liquid phases. Making use of this phenomenon in process development first requires research on the phase split phenomenon and, second, research on the feasibility of biomolecule extraction and separation. In this study, basic fluid phase equilibrium phenomena are briefly described. Then, experimental results are reported for the partitioning of small amounts of cardiac glycosides (digitoxin and digoxin) on coexisting liquid phases in the high-pressure, three-phase, vapor-liquid-liquid equilibrium of the ternary system of "near critical" CO(2) + water + 1-propanol, at 313 K and 333 K. Finally, a process for extraction and separation of the aforementioned glycosides by means of the high-pressure phase equilibrium phenomenon is discussed.     

芦荟凝胶中海藻糖的提取与检测

从芦荟提取多糖后的“废液”——上清液经过浓缩、脱色后冷冻干燥,得到单糖和寡糖的混合物。经质谱检测证明,该混合糖含有二糖,可能有海藻糖成分;利用高效液相色谱证实其中含有海藻糖、葡萄糖和果糖,含量比为1：62：21。该结果为芦荟强保水能力提供理论依据,而且“废液”的再利用,可以提高芦荟叶片的利用率,充分利用资源,为综合开发利用芦荟开辟一条新路。     

微波辅助提取灰树花多糖工艺研究

采用提取时间、微波功率、液料比的单因素试验和正交试验法优化微波辅助提取灰树花多糖条件.结果表明,以净多糖得率为指标,影响微波辅助提取灰树花多糖的主次因素为:提取时间＞微波功率＞液料比,并且提取时间和微波功率的影响达到了极显著水平.灰树花多糖最佳提取工艺条件为:提取时间为10 min,微波功率为80%(全功率为800 W),液料比为25∶1.创立了一种用苯酚-硫酸法测定多糖时排除蛋白质干扰的方法.     

A Rapid Method,Combining Microwave-Assisted Extraction and Gas Chromatography-Mass Spectrometry with a Database,for Determining Organochlorine Pesticides and Polycyclic Aromatic Hydrocarbons in Soils and Sediments

A rapid method for determining organochlorine pesticides and polycyclic aromatic hydrocarbons in soils and sediments was developed to allow pollution surveys to be performed in emergencies. The method involves microwave-assisted extraction and uses an automated identification/quantification system with a gas chromatography mass spectrometry database. A sample (3 g) is extracted with a 3:2 v/v hexane:water mixture (10 mL) for 30 min using a microwave-assisted extraction system at 120°C. The hexane extract is then cleaned using silica gel, then analyzed by gas chromatography mass spectrometry. The total analysis time is approximately 4 h. The precision of the quantitative results and accuracy of the analyte identification were determined. The total analyte concentrations were generally comparable to (61%–110% of) the concentrations determined using a Soxhlet extraction method, but the concentrations of individual high-molecular-weight polycyclic aromatic hydrocarbons were unacceptably low compared with the concentrations determined using the Soxhlet method. However, these compounds (e.g., benzo(ghi)perylene and indeno(1,2,3-cd)pyrene) were subsequently efficiently extracted using a hexane:water:ethanol mixture. The accuracy of identification was evaluated using accurate masses determined by gas chromatography time-of-flight mass spectrometry, and the mass error was 2 ppm for 21 of the 22 compounds identified using the new method.     

Decrease of lipid extractability of chloroform-methanol upon water addition to human erythrocytes

The yield of lipids extractable by chloroform-methanol 2:1 from human erythrocytes decreases as a function of the relative amount of water added to--or present in--the erythrocyte pellet prior to the lipid extraction. Only slight modifications are observed as long as the volume of water does not exceed that of the red blood cell pellet. As the volume of added water increases, the phosphatidylserine recovery drops dramatically and tends to zero while the yield of the other phospholipids remains unchanged. This phenomenon is not observed when the lipids are extracted by a mixture of isopropanol-chloroform.