益母草多糖微波提取及在卷烟中的应用

采用微波辅助法对益母草多糖的提取工艺进行考察,并对益母草多糖进行了卷烟加香试验。以干燥益母草原料粒度（目数）、料液比、微波功率、提取时间为考察因素,益母草多糖得率为指标,采用单因素和正交试验法对益母草多糖提取工艺进行优化。确定了微波辅助提取的最佳工艺参数为：粒度（目数）80目（粒径约0.178 mm）,料液比1∶50（g/mL）,微波功率700 W,提取时间16min。按此优化条件,益母草多糖得率可达到3.20%。加香应用结果表明,益母草多糖能赋予卷烟特殊香韵调,保润并柔和细腻烟气,提高烟气舒适性。     

Maximizing the Retention of Ganoderic Acids and Water-Soluble Polysaccharides Content of Ganoderma lucidum Using Two-Stage Dehydration Method

Ganoderic acids and water-soluble polysaccharides are the main bioactive ingredients of Ganoderma lucidum and are heat sensitive. Hence, it is crucial to apply a suitable drying method for the drying of G. lucidum to minimize the loss of these bioactive ingredients. In this study, a two-stage drying method was applied to enhance the drying kinetics, as well as the retention of both ganoderic acids and water-soluble polysaccharides in dried G. lucidum fruiting bodies and slices compared to other single-stage-dried products. The results showed that two-stage drying enhanced the overall drying rate, which consequently shortened the total drying time up to 61 and 330% for fruiting bodies and slices, respectively, compared to single-stage drying methods. Furthermore, two-stage drying of Ganoderma fruiting bodies, which involves 18-h vacuum drying followed by 5-h heat pump drying, maximized the retention of ganoderic acids and water-soluble polysaccharides, with the retention of 97.90% of water-soluble polysaccharides and 4.2% more ganoderic acids than freeze-dried products. On the other hand, drying of Ganoderma slices within the shortest total drying time, which is 10-min heat pump drying followed by 50-min oven drying, also retained most of the ganoderic acids and water-soluble polysaccharides in the dried products; that is, about 80% of water-soluble polysaccharides and 11% more ganoderic acids than freeze-dried slices.     

Structural characterisation and determination of prebiotic activity of purified xylo-oligosaccharides obtained from Bengal gram husk (Cicer arietinum L.) and wheat bran (Triticum aestivum)

Water extractable polysaccharides (WEPs) were isolated from Bengal gram husk and wheat bran. These WEP were subjected to driselase enzyme hydrolysis to obtain oligosaccharide mixtures, which were purified successively on Biogel P-2 and high performance liquid chromatographies. The molecular weight and structural features of the purified oligosaccharides were deduced using ESI-MS and ¹H NMR, respectively. The prebiotic properties of these purified oligosaccharides were studied by using Bifidobacterium adolescentis NDRI 236. Increase in dry cell mass (0.7–0.9 mg/ml) and decrease in pH (<5.8) due to production of short chain fatty acid (SCFA) indicated oligosaccharide fermentation. Acetate was the chief SCFA produced and its amount varied from 97.2% to 100%. The activities of xylanase (257–470 mU/ml), xylopyranosidase (53–60 mU/ml) and arabinofuranosidase (60–70 mU/ml) in the culture broth indicated the breakdown of xylo-oligosaccharides and their subsequent utilisation by the bacterium for its growth.     

A simple preparative method for isolation and purification of polysaccharides from mulberry (Morus alba L.) leaves

An effective method for preparative extraction and purification of the polysaccharides from mulberry leaves was studied. Orthogonal experiment was carried out to get the optimal conditions (T = 70 °C, pH = 6, t = 60 min, D = 0.4 g g^?1 material) of activated carbon decolorisation. The staged, isocratic and multiple ethanol precipitation procedures were also investigated. Through the activated carbon decolorisation and 20% ethanol precipitation procedure, the polysaccharides yield reached 2.91%, and the content of neutral sugar and uronic acid were improved to 21.87% and 57.43% respectively. This process was superior to the macroporous resin adsorption and gel permeation chromatography (GPC) methods. The structure analysis indicated that the purified mulberry leaves polysaccharide (MLP) was composed of Man, GalA and Rha in the ratio of 1.0:7.2:20.0. The molecular weight measured using GPC was approximately 557 062 D. The IR and ¹H NMR spectra indicated that the MLP was mainly pectin, which was classified as high‐methoxyl pectin.     

Impact of the coating process on the molecular structure of starch‐based barrier coatings

Molecular analysis of starch structure can be used to explain and predict changes in physical properties, such as water vapor and oxygen barrier properties in packaging materials. Solution casting is a widely used technique to create films from starch formulations. This study compared the molecular properties of these standard films with those of experimental coatings applied to paper in laboratory‐scale and pilot‐scale trials, with all three techniques using the same starch formulation. The results revealed large differences in molecular structure, i.e., cross‐linking and hydrolysis, between films and coatings. The main differences were due to the shorter drying time allowed to laboratory‐scale coatings and the accelerated drying process in pilot trials owing to the high energy output of infrared dryers. Furthermore, surface morphology was highly affected by the coating technique used, with a rougher surface and many pinholes occurring in pilot‐scale coatings, giving lower water vapor permeability than laboratory‐scale coatings. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41190.     

Anticoagulant, Antioxidant and Antitumor Activities of Heterofucans from the Seaweed Dictyopteris delicatula

In the present study, six families of sulfated polysaccharides were obtained from seaweed Dictyopteris delicatula by proteolytic digestion, followed by acetone fractionation and molecular sieving on Sephadex G-100. Chemical analyses demonstrated that all polysaccharides contain heterofucans composed mainly of fucose, xylose, glucose, galactose, uronic acid, and sulfate. The fucans F0.5v and F0.7v at 1.0 mg/mL showed high ferric chelating activity (～45%), whereas fucans F1.3v (0.5 mg/mL) showed considerable reducing power, about 53.2% of the activity of vitamin C. The fucan F1.5v presented the most prominent anticoagulant activity. The best antiproliferative activity was found with fucans F1.3v and F0.7v. However, F1.3v activity was much higher than F0.7v inhibiting almost 100% of HeLa cell proliferation. These fucans have been selected for further studies on structural characterization as well as in vivo experiments, which are already in progress.     

Effects of extraction solvents,cooking procedures and storage conditions on the contents of ergothioneine and phenolic compounds and antioxidative capacity of the cultivated mushroom Flammulina velutipes

Edible mushrooms contain considerable amounts of the potent natural antioxidant 2‐thiol‐l ‐histidine‐betaine (l ‐ergothioneine, ESH). The objective of this study was to evaluate the effects of extraction solvents, common cooking methods and storage conditions on the ESH content, total phenols (TPs) and antioxidant capacity of the edible mushroom Flammulina velutipes fruiting body and its hot water extract that had been stored at different temperatures. Regarding cooking procedures, boiling in water resulted in the highest losses of antioxidant activity of both ESH and TPs. Most of the losses of ESH and TPs were detected in the cooking water. The ESH contents in the raw mushroom fruiting bodies significantly decreased after 8 days of refrigerated storage under both dark and fluorescent lighting conditions. However, the TP content in the raw mushroom stored under fluorescent lighting significantly increased during 10 days of refrigeration. In contrast, the ESH and TP contents as well as DPPH radical scavenging ability of the fruiting bodies remained unchanged for up to 15 days of frozen storage at ?18 °C. The same behaviour was obtained with the mushroom extract packed in plastic tubes. The correlation between DPPH radical scavenging activity and ESH contents was higher than that for TP compounds.     

Derivatized Polysaccharides: Preparation,Characterization, and Application as Bioadhesive Polymer for Drug Delivery

Derivatization of a natural polysaccharide, tamarind seed polysaccharide (TSP), was carried out. Both cationic and anionic derivatives of TSP were prepared, characterized, and their degree of substitution was determined. Films prepared using derivatives were evaluated for their swelling potential and bioadhesive strength. The carboxymethyl and sulfate derivatives were showed higher swelling index and required higher force of detachment compared to native gum thus, indicating that introduction of carboxymethyl, sulfate, and amine groups in TSP can increase the bioadhesive strength. The results suggested that anionic and cationic derivatives can be employed for formulation of bioadhesive drug delivery systems.