玻璃海鞘不同极性提取物体外抗氧化活性的研究

通过对DPPH自由基、脂质过氧化及总抗氧化能力的测定,从而探求玻璃海鞘不同极性提取物的抗氧化能力。结果表明,玻璃海鞘不同极性提取物均具有一定的抗氧化能力,但均低于VC的抗氧化能力。用IC50衡量清除自由基的能力,正丁醇萃取物清除DPPH自由基能力最强,为(1218.03±4.79)mg/L,其次是石油醚萃取物,乙酸乙酯萃取物最弱;乙酸乙酯萃取物对脂质过氧化的抑制作用最强,为(2325.17±3.80)mg/L,石油醚萃取物次之,正丁醇萃取物最弱;在一定浓度下,总抗氧化能力从强到弱排列顺序依次为石油醚萃取物>乙酸乙酯萃取物>正丁醇萃取物。      

人心果叶不同极性组分的抗氧化与抗菌活性

通过体外DPPH自由基、ABTS自由基清除能力和总抗氧化能力评价人心果叶不同极性萃取物(石油醚相、乙酸乙酯相、正丁醇相、水相)的抗氧化活性,并探究各极性组分对金黄色葡萄球菌、枯草芽孢杆菌和大肠杆菌的抑制能力.结果表明:乙酸乙酯组分的体外抗氧化活性最强,清除DPPH自由基能力IC50值为(0.019±0.010)mg/m...     

火棘果不同极性部位提取物体外抗氧化研究

目的:系统地评价火棘果粗分体系抗氧化活性,同时探究抗氧化能力与总多酚含量之间的关系。方法:用75%乙醇冷浸提取火棘果,分别用石油醚、乙酸乙酯、正丁醇和水分为四个不同极性部位,然后测定了各部位萃取物对DPPH自由基、ABTS+自由基的清除能力,并且测定了总还原力、FRAP值和总多酚含量,同时考察总酚含量与抗氧化活性的关系。结果:火棘果提取物的不同极性部位均有抗氧化活性,其中水、乙酸乙酯和正丁醇部位提取物表现出较好的抗氧化活性,石油醚部位的抗氧化活性最弱;各部位提取物的抗氧化活性与总多酚含量呈现较好的相关关系。其中,水部位提取物对DPPH和ABTS+自由基清除率最高,IC50值分别为（0.76±0.03）mg/m L和（1.71±0.10）mg/m L;乙酸乙酯部位FRAP值最大,为（382.20±4.72）μmol Fe2+/g干样;正丁醇部位总酚含量最高,为（2763±3.91）mg GAE/100g干样。      

火棘果不同极性部位提取物体外抗氧化研究

目的:系统地评价火棘果粗分体系抗氧化活性,同时探究抗氧化能力与总多酚含量之间的关系。方法:用75%乙醇冷浸提取火棘果,分别用石油醚、乙酸乙酯、正丁醇和水分为四个不同极性部位,然后测定了各部位萃取物对DPPH自由基、ABTS+自由基的清除能力,并且测定了总还原力、FRAP值和总多酚含量,同时考察总酚含量与抗氧化活性的关系。结果:火棘果提取物的不同极性部位均有抗氧化活性,其中水、乙酸乙酯和正丁醇部位提取物表现出较好的抗氧化活性,石油醚部位的抗氧化活性最弱;各部位提取物的抗氧化活性与总多酚含量呈现较好的相关关系。其中,水部位提取物对DPPH和ABTS+自由基清除率最高,IC50值分别为(0.76±0.03)mg/m L和(1.71±0.10)mg/m L;乙酸乙酯部位FRAP值最大,为(382.20±4.72)μmol Fe2+/g干样;正丁醇部位总酚含量最高,为(2763±3.91)mg GAE/100g干样。     

定心藤醇提物不同极性部分的体外抗氧化活性研究

研究定心藤75%乙醇提取物不同极性部位的体外抗氧化活性,采用5种不同极性溶剂萃取（石油醚、氯仿、乙酸乙酯、正丁醇、水）得到5种萃取物,分别测定黄酮含量,并通过还原能力测定、DPPH自由基清除能力、羟自由基清除能力和超氧阴离子自由基清除能力4种测定方法,对各萃取物抗氧化能力进行研究。结果显示,各提取物对Fe3+均有一定的还原能力,乙酸乙酯萃取物还原效果最为明显;定心藤不同极性部位均具有一定的抗氧化活性,乙酸乙酯萃取物抗氧化能力最强,DPPH·的半数清除浓度IC50为0.28mg/m L,羟自由基半数清除浓度IC50为0.41mg/m L,在0.2mg/m L浓度下,对超氧阴离子自由基的清除率达到42.88%,而其黄酮含量最高,达到609.96mg/g,这也许与它具有较高的抗氧化活性有关。说明乙酸乙酯萃取物具有较好的开发天然抗氧化剂的前景。      

不同溶剂提取乳苣的抗氧化作用研究

以乳苣全草为原料,75%乙醇为溶剂提取乳苣,提取液用不同极性溶剂依次萃取,得石油醚萃取物、乙酸乙酯萃取物、正丁醇萃取物和水萃取物,同时测定了各相提取物对羟自由基、超氧阴离子自由基、DPPH自由基的清除能力,并与VC进行比较。结果表明:各萃取物均具有一定的抗氧化活性,且随着浓度的增加而增强;对羟自由基的清除能力大小依次为乙酸乙酯萃取物>正丁醇萃取物>VC>水萃取物>石油醚萃取物;对超氧阴离子自由基清除能力大小依次为VC>正丁醇萃取物>乙酸乙酯萃取物>石油醚萃取物>水萃取物;对DPPH自由基清除能力大小依次为VC>乙酸乙酯萃取物>正丁醇萃取物>水萃取物>石油醚萃取物;各萃取物还原能力大小依次为VC>正丁醇萃取物>乙酸乙酯萃取物>水萃取物>石油醚萃取物。      

不同溶剂提取乳苣的抗氧化作用研究

以乳苣全草为原料,75%乙醇为溶剂提取乳苣,提取液用不同极性溶剂依次萃取,得石油醚萃取物、乙酸乙酯萃取物、正丁醇萃取物和水萃取物,同时测定了各相提取物对羟自由基、超氧阴离子自由基、DPPH自由基的清除能力,并与VC进行比较。结果表明:各萃取物均具有一定的抗氧化活性,且随着浓度的增加而增强;对羟自由基的清除能力大小依次为乙酸乙酯萃取物>正丁醇萃取物>VC>水萃取物>石油醚萃取物;对超氧阴离子自由基清除能力大小依次为VC>正丁醇萃取物>乙酸乙酯萃取物>石油醚萃取物>水萃取物;对DPPH自由基清除能力大小依次为VC>乙酸乙酯萃取物>正丁醇萃取物>水萃取物>石油醚萃取物;各萃取物还原能力大小依次为VC>正丁醇萃取物>乙酸乙酯萃取物>水萃取物>石油醚萃取物。     

乌饭树果乙醇提取物不同极性分部的体外抗氧化活性研究

目的筛选乌饭树果乙醇提取物中抗氧化活性最强的极性分部。方法采用石油醚、乙酸乙酯、氯仿、正丁醇和水等5种不同极性溶剂对乌饭树果乙醇提取物进行进一步梯度萃取,并分析比较其总抗氧化能力(total antioxidant capacity,T_(AC))、抗脂质过氧化能力及对羟基自由基OH·、超氧阴离子自由基O_2~-·的清除效果。结果乌饭树果乙醇提取物的5个不同极性分部均具有一定的抗氧化活性,但其活性大小差异极显著(P0.01),T_(AC)大小依次为:乙酸乙酯部氯仿部正丁醇部石油醚部水部。同时,在OH·、O_2~-·自由基清除能力和抗脂质过氧化能力上,乙酸乙酯部均优于氯仿部和正丁醇部,且呈明显的量效关系。结论乌饭树果乙醇提取物的乙酸乙酯部具有最强的抗氧化活性,且对OH·、O_2~-·的清除能力及抗脂质过氧化能力均强于L-抗坏血酸及其它部位,可作为天然抗氧化剂的潜在有效来源。     

芒果叶不同极性部位提取物的抗氧化活性

对芒果叶不同极性部位提取物的抗氧化活性进行研究。用DPPH法考察最优反应条件,综合评价其抗氧化活性,测定其黄酮含量,以IC50值作为评价清除DPPH自由基能力的指标,用芒果苷和抗坏血酸作为对照品进行自由基清除率的比较。试验结果表明:芒果叶石油醚、乙酸乙酯、正丁醇萃取物及水部位提取物的黄酮含量依次为:(33.616±3.208)、(292.063±1.100)、(180.469±2.067)、(21.717±1.157)mg/g,IC50值分别为:102.877、9.014、19.494、221.784μg/mL。由此可以看出,芒果叶各类提取物均具有一定的抗氧化活性,其中乙酸乙酯萃取物抗氧化活性最强,其次为正丁醇、石油醚,最后为水部位提取物。相关性分析结果表明,芒果叶各极性部位提取物的黄酮含量与清除DPPH自由基的能力呈负相关,芒果叶各部位提取物的黄酮含量是影响其抗氧化活性的主要因素。     

玫瑰茄提取物多酚含量与抗氧化作用研究

研究玫瑰茄的体外抗氧化活性。采用不同极性的有机溶剂萃取玫瑰茄40%乙醇提取物(粗提物),得到石油醚萃取物、氯仿萃取物、乙酸乙酯萃取物、正丁醇萃取物,然后采用Folin-Ciocalteu比色法测定粗提物以及各萃取物的多酚含量,同时应用DPPH法、试剂盒法、ABTS法分别测定粗提物和各萃取物的DPPH自由基清除能力、还原Fe3+能力以及ABTS自由基抑制能力。DPPH法、试剂盒法、ABTS法测定各提取物抗氧化能力的结果为粗提物>正丁醇萃取物>乙酸乙酯萃取物>氯仿萃取物>石油醚萃取物。玫瑰茄提取物具有较高的多酚含量和较强的抗氧化能力;玫瑰茄提取物的多酚含量与抗氧化能力之间存在较好的相关性。     

Reliable identification of grapevine rootstock varieties using RAPD PCR on woody samples

Since grapevine ( Vitis spp .) rootstock material is being traded increasingly as disbudded woody material a lack of distinctive morphological features on such material necessitates an alternative and reliable means of identification. Methods described here were developed for rapid and efficient extraction of DNA from woody samples rich in phenolic compounds and polysaccharides, and for subsequent identification of varieties by RAPD PCR. Using these methods, and with the application of only one selected RAPD primer, we were able to differentiate sixteen rootstock varieties, including the seven varieties most commonly used in Germany. Problems commonly encountered with reproducibility of RAPD patterns were avoided by choosing primers with a dinucleotide sequence and a high G/C content that allowed a rather high annealing temperature of 45°C. Methods described here should also be useful for other horticultural crops, especially those with woody tissues rich in phenolic compounds and polysaccharides.     

An internet compendium of analytical methods and spectroscopic information for monomers and additives used in food packaging plastics

An internet website (http://cpf.jrc.it/smt/) has been produced as a means of dissemination of methods of analysis and supporting spectroscopic information on monomers and additives used for food contact materials (principally packaging). The site which is aimed primarily at assisting food control laboratories in the European Union contains analytical information on monomers, starting substances and additives used in the manufacture of plastics materials. A searchable index is provided giving PM and CAS numbers for each of 255 substances. For each substance a data sheet gives regulatory information, chemical structures, physico-chemical information and background information on the use of the substance in particular plastics, and the food packaging applications. For monomers and starting substances (155 compounds) the infra-red and mass spectra are provided, and for additives (100 compounds); additionally proton NMR are available for about 50% of the entries. Where analytical methods have been developed for determining these substances as residual amounts in plastics or as trace amounts in food simulants these methods are also on the website. All information is provided in portable document file (PDF) format which means that high quality copies can be readily printed, using freely available Adobe Acrobat Reader software. The website will in future be maintained and up-dated by the European Commission's Joint Research Centre (JRC) as new substances are authorized for use by the European Commission (DG-ENTR formerly DGIII). Where analytical laboratories (food control or other) require reference substances these can be obtained free-ofcharge from a reference collection housed at the JRC and maintained in conjunction with this website compendium.     

Aroma characterization of various apricot varieties using headspace–solid phase microextraction combined with gas chromatography–mass spectrometry and gas chromatography–olfactometry

The characterization of the aromatic profile of several apricot cultivars with molecular tracers in order to obtain objective data concerning the aromatic quality of this fruit was undertaken using headspace–solid phase microextraction (HS–SPME). Six apricot cultivars were selected according to their organoleptic characteristics: Iranien, Orangered, Goldrich, Hargrand, Rouge du Roussillon and A4025. The aromatic intensity of these varieties measured by HS–SPME–Olfactometry were defined and classified according to the presence and the intensity of grassy, fruity and apricot like notes. In the six varieties, 23 common volatile compounds were identified by HS–SPME–GC–MS. Finally, 10 compounds, ethyl acetate, hexyl acetate, limonene, β-cyclocitral, γ-decalactone, 6-methyl-5-hepten-2-one, linalool, β-ionone, menthone and (E)-hexen-2-al were recognized by HS–SPME–GC–O as responsible of the aromatic notes involved in apricot aroma and considered as molecular tracers of apricot aromatic quality which could be utilized to discriminate apricot varieties.     

Tests of potential functional barriers for laminated multilayer food packages. Part I: Low molecular weight permeants

The advent of the functional barrier concept in food packaging has brought with it a requirement for fast tests of permeation through potential barrier materials. In such tests it would be convenient for both foodstuffs and materials below the functional barrier (sub-barrier materials) to be represented by standard simulants. By means of inverse gas chromatography, liquid paraffin spiked with appropriate permeants was considered as a potential simulant of sub-barrier materials based on polypropylene (PP) or similar polyolefins. Experiments were performed to characterize the kinetics of the permeation of low molecular weight model permeants (octene, toluene and isopropanol) from liquid paraffin, through a surrogate potential functional barrier (25 μm-thick oriented PP) into the food simulants olive oil and 3% (w/v) acetic acid. These permeation results were interpreted in terms of three permeation kinetic models regarding the solubility of a particular model permeant in the post-barrier medium (i.e. the food simulant). The results obtained justify the development and evaluation of liquid sub-barrier simulants that would allow flexible yet rigorous testing of new laminated multilayer packaging materials.     

Analysis of benzo[a]pyrene in spiked fatty foods by second derivative synchronous spectrofluorimetry after microwave-assisted treatment of samples

A simple, rapid and inexpensive method has been developed for the determination of benzo[a     

The development of reference materials for paralytic shellfish poisoning toxins in lyophilized mussel. II: Certification study

This paper describes the second part of a project undertaken to develop certified mussel reference materials for paralytic shellfish poisoning toxins. In the first part two interlaboratory studies were undertaken to investigate the performance of the analytical methodology for several PSP toxins, in particular saxitoxin and decarbamoyl-saxitoxin in lyophilized mussels, and to set criteria for the acceptance of results to be applied during the certification exercise. Fifteen laboratories participated in this certification study and were asked to measure saxitoxin and decarbamoyl-saxitoxin in rehydrated lyophilized mussel material and in a saxitoxin-enriched mussel material. The participants were allowed to use a method of their choice but with an extraction procedure to be strictly followed. The study included extra experiments to verify the detection limits for both saxitoxin and decarbamoyl-saxitoxin. Most participants (13 of 15) were able to meet all the criteria set for the certification study. Results for saxitoxin.2HCl yielded a certified mass fraction of <0.07 mg/kg in the rehydrated lyophilized mussels. Results obtained for decarbamoyl-saxitoxin.2HCl yielded a certified mass fraction of 1.59+/-0.20 mg/kg. The results for saxitoxin.2HCl in enriched blank mussel yielded a certified mass fraction of 0.48 +/- 0.06 mg/kg. These certified reference materials for paralytic shellfish poisoning toxins in lyophilized mussel material are the first available for laboratories to test their method for accuracy and performance.     

Announcing a new international peer-reviewed journal:Food Science and Human Wellness now accepting manuscript submission in English

<正>We are pleased to announce the launch of a new international peer-reviewed journal-Food Science and Human Wellness,ISSN 2213-4530,which is an open access journal,produced and hosted by Elsevier B.V.on behalf of Beijing Academy of Food Sciences.Food Science and Human Wellness is an international peer-reviewed English journal that provides a forum for the dissemination of the     

Chinese CTP Market

According to Printing and Printing Equipment Industries Association of China（PEIAC）＇s statistics to the plate manufucturer in China, in 2013, the actual offset plate production has reached 346 million square meters in China. Among them, the CTP production volume was 245 million square meters, up by 11% than that of last year; the total sales of the CTP plate was 239 million square meters, up by 13%.     

Preparatory Work of Print China 2015 is Going Smoothly

正Held at Guangdong Modern International Exhibition Center,Print China 2015 will cover 7exhibition halls,besides the original Hall No.3,4,5,6,7,the newly built F zone of Hall 3 will be used too.The total area will be140,000 square meters.Hall 3:Offset and large printing equipment,package printing equipment,post press