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Magnetic solid phase extraction and gas chromatography-mass spectrometrical analysis of sixteen polycyclic aromatic hydrocarbons 2015 State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China.; Key Laboratory of Modern Preparation of TCM, Ministry of Education, Jiangxi University of Traditional Chinese
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
7-Aug
Volume
1406
Issue
Start Page
40
Other Pages
47
Notes
CI: Copyright (c) 2015; JID: 9318488; 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Water Pollutants, Chemical); 059QF0KO0R (Water); 7631-86-9 (Silicon Dioxide); OTO: NOTNLM; 2015/04/01 [received]; 2015/06/08 [revised]; 2015/06/10 [accepted]; 2015/06/20 [ahea
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 26122856
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.chroma.2015.06.024 [doi]
Output Language
Unknown(0)
PMID
26122856
Abstract
Fluorenyl functionalized superparamagnetic core/shell magnetic nanoparticles (MNPs, Fe3O4@SiO2@Flu) were prepared and characterized by transmission electron microscope, X-ray diffraction and infrared spectroscopy. The MNPs having an average diameter of 200nm were then used as solid-phase extraction sorbent for the determination of 16 priority pollutants polycyclic aromatic hydrocarbons (PAHs) in water samples designated by United States Environmental Protection Agency (U.S. EPA). The main influencing parameters, including sorbent amount, desorption solvent, sample volume and extraction time were optimized. Analyses were performed on gas chromatography-mass spectrometry (GC-MS) using selected ion monitoring (SIM) mode. Method validation proved the feasibility of the developed sorbents for the quantitation of the investigated analytes at trace levels. Limit of detection ranging from 0.5 to 4.0ng/L were obtained. The repeatability was investigated by evaluating the intra- and inter-day precisions with relative standard deviations (RSDs) lower than 13.1%. Finally, the proposed method was successfully applied for the determination of PAHs in water samples with the recoveries in the range of 96.0-106.7%.
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Cai,Y., Yan,Z., NguyenVan,M., Wang,L., Cai,Q.
Original/Translated Title
URL
Date of Electronic
20150620
PMCID
Editors
Magnetic solid phase extraction and static headspace gas chromatography-mass spectrometry method for the analysis of polycyclic aromatic hydrocarbons 2016 State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China.; Key Laboratory of Modern Preparation of TCM, Ministry of Education, Jiangxi University of Traditional Chinese
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
15-Jan
Volume
1429
Issue
Start Page
97
Other Pages
106
Notes
CI: Copyright (c) 2015; JID: 9318488; 0 (Drinking Water); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Solvents); 0 (Water Pollutants, Chemical); OTO: NOTNLM; 2015/07/01 [received]; 2015/12/01 [revised]; 2015/12/10 [accepted]; 2015/12/14 [aheadofprint]; ppub
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 26724892
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.chroma.2015.12.032 [doi]
Output Language
Unknown(0)
PMID
26724892
Abstract
A magnetic solid phase extraction (MSPE) protocol combining a static headspace gas chromatography coupled to mass spectrometry (HS-GC-MS) method has been developed for extraction, and determination of 16 polycyclic aromatic hydrocarbons (PAHs) in drinking water samples. Magnetic nanoparticles (MNPs) were coated with 3-aminopropyltriethoxysilane and modified by cholesterol chloroformate. Transmission electron microscope, vibrating sample magnetometer, Fourier transform infrared spectrometry and X-ray photoelectron spectroscopy were used to characterize the cholesterol-functionalized sorbents, and the main parameters affecting the extraction as well as HS sampling, such as sorbent amount, extraction time, oven temperature and equilibration time have been investigated and established. Combination with HS sampling, the MSPE procedure was simple, fast and environmentally friendly, without need of any organic solvent. Method validation proved the feasibility of the developed sorbents for the quantitation of the investigated analytes at trace levels obtaining the limit of detection (S/N=3) ranging from 0.20 to 7.8 ng/L. Good values for intra and inter-day precision were obtained (RSDs = 9.9%). The proposed method was successfully applied to drinking water samples.
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Cai,Y., Yan,Z., Wang,L., NguyenVan,M., Cai,Q.
Original/Translated Title
URL
Date of Electronic
20151214
PMCID
Editors
Development of a solid-phase microextraction fiber by chemical binding of polymeric ionic liquid on a silica coated stainless steel wire 2012 State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
23-Mar
Volume
1230
Issue
Start Page
8
Other Pages
14
Notes
LR: 20131121; CI: Copyright (c) 2012; JID: 9318488; 0 (Ionic Liquids); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Water Pollutants, Chemical); 059QF0KO0R (Water); 12597-68-1 (Stainless Steel); 7631-86-9 (Silicon Dioxide); 2011/11/28 [received]; 2012/01/17
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 22340892
Language
eng
SubFile
Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.chroma.2012.01.052 [doi]
Output Language
Unknown(0)
PMID
22340892
Abstract
A novel approach was developed for the fabrication of solid-phase microextraction (SPME) fiber by coating stainless steel fiber with a polymeric ionic liquid (PIL) through covalent bond. The stainless steel fiber was sequentially coated with a gold film by replacement reaction between Fe and Au when immerged in chloroauric acid, assembled with a monolayer of 3-(mercaptopropyl) triethoxysilane on the gold layer through the Au-S bond, and coated with a silica layer by the hydrolysis and polycondensation reaction of the surface-bonded siloxane moieties and the active silicate solution. Then, 1-vinyl-3-(3-triethoxysilylpropyl)-4,5-dihydroimidazolium chloride ionic liquid was anchored on the silica layer by covalent bond, and the PIL film was further formed by free radical copolymerization between 1-vinyl-3-(3-triethoxysilylpropyl)-4,5-dihydroimidazdium and vinyl-substituted imidazolium with azobisisobutyronitrile (AIBN) as initiator. Parameters influencing the preparation of PIL fiber were optimized, and the developed SPME fiber has a coating thickness of ~20 mum with good thermal stability and long lifetime. The performance of the PIL fiber was evaluated by analysis of polycyclic aromatic hydrocarbons (PAHs) in water samples. The developed PIL fiber showed good linearity between 0.5 and 20 mug l(-1) with regression coefficient in the range of 0.963-0.999, detection limit ranging from 0.05 to 0.25 mug l(-1), and relative standard deviation of 9.2-29% (n=7). This developed PIL fiber exhibited comparable analytical performance to commercial 7 mum thickness PDMS fiber in the extraction of PAHs. The spiked recoveries for three real water samples at 0.5-5 mug l(-1) levels were 49.6-111% for the PIL fiber and 40.8-103% for the commercial PDMS fiber.
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Pang,L., Liu,J.F.
Original/Translated Title
URL
Date of Electronic
20120125
PMCID
Editors
Continuous-flow microextraction and gas chromatographic-mass spectrometric determination of polycyclic aromatic hydrocarbon compounds in water 2007 State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Analytica Chimica Acta
Periodical, Abbrev.
Anal.Chim.Acta
Pub Date Free Form
7-Mar
Volume
585
Issue
2
Start Page
294
Other Pages
299
Notes
LR: 20131121; JID: 0370534; 0 (Ions); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Salts); 0 (Solvents); 0 (Water Pollutants, Chemical); 059QF0KO0R (Water); 2006/09/21 [received]; 2006/12/30 [revised]; 2007/01/08 [accepted]; 2007/01/13 [aheadofprint]; ppubli
Place of Publication
Netherlands
ISSN/ISBN
1873-4324; 0003-2670
Accession Number
PMID: 17386677
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
S0003-2670(07)00059-1 [pii]
Output Language
Unknown(0)
PMID
17386677
Abstract
A new method of the determination polycyclic aromatic hydrocarbons (PAHs) in water samples was developed by continuous-flow microextraction (CFME) coupled with gas chromatography-mass spectrometry (GC-MS). In this experiment, 15 mL sample solution with no salt-added was flowed at the rate of 1.0 mL min(-1) through 3 microL benzene as extraction solvent. Under the optimal extraction conditions, the developed method was found to yield a linear calibration curve in the concentration range from 0.05 to 15 ng mL(-1). Furthermore, the accuracy and repeatability of the method were good by calculating from water samples spiked at known concentrations of PAHs, and the recovery of optimal method was satisfactory. The results showed that CFME was an efficient preconcentration method for extraction of PAHs from spiked water samples.
Descriptors
Calibration, Chemistry Techniques, Analytical/methods, Gas Chromatography-Mass Spectrometry/methods, Ions, Polycyclic Hydrocarbons, Aromatic/chemistry, Reproducibility of Results, Salts/pharmacology, Sensitivity and Specificity, Solvents/chemistry, Time Factors, Water/chemistry, Water Pollutants, Chemical/analysis
Links
Book Title
Database
Publisher
Data Source
Authors
Liu,Y., Hashi,Y., Lin,J. M.
Original/Translated Title
URL
Date of Electronic
20070113
PMCID
Editors
The pollution levels of BTEX and carbonyls under haze and non-haze days in Beijing, China 2014 State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, China; Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China. Electronic a
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
The Science of the total environment
Periodical, Abbrev.
Sci.Total Environ.
Pub Date Free Form
15-Aug
Volume
490
Issue
Start Page
391
Other Pages
396
Notes
CI: Copyright (c) 2014; JID: 0330500; 0 (Air Pollutants); 0 (Benzene Derivatives); 0 (Xylenes); 3FPU23BG52 (Toluene); J64922108F (Benzene); L5I45M5G0O (ethylbenzene); OTO: NOTNLM; 2013/10/24 [received]; 2014/04/27 [revised]; 2014/05/06 [accepted]; 2014/05
Place of Publication
Netherlands
ISSN/ISBN
1879-1026; 0048-9697
Accession Number
PMID: 24867703
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.scitotenv.2014.05.025 [doi]
Output Language
Unknown(0)
PMID
24867703
Abstract
The North China Plain including Beijing is frequently suffering from serious haze days in recent years. To best recognize the influence of haze days on regional air quality, the pollution levels of deleterious gases of BTEX (benzene, toluene, ethylbenzene, m,p-xylene and o-xylene) and carbonyls (formaldehyde, acetaldehyde and acetone) under haze and non-haze days were contrastively investigated during the period of September 2008-August 2010 in Beijing. In comparison with non-haze days, remarkable enhancement of BTEX and the carbonyls under haze days in winter was found, with enhancement factors of 1.9-5.7 for BTEX and of 1.5-4.2 for the carbonyls. Whereas the enhancement factors for both BTEX (1.0-3.0) and the carbonyls (1.2-1.9) under haze days in summer were relatively small. The ratios of each BTEX to CO under both haze days and non-haze days exhibited a minimal value in the afternoon, whereas maximal values for the ratios of the carbonyls to CO were usually found in the afternoon. The ratios of each BTEX to CO were extremely greater under haze days than those under non-haze days in winter, but no evident difference was found in summer. The ratios of each carbonyl under both haze days and non-haze days in summer were at least a factor of 2 greater than those in winter and only enhancement of the ratios under haze days was found in winter. The remarkably higher ratios of ethylbenzene to m,p-xylene under haze days than non-haze days in both winter and summer revealed high reactivity of photochemical reactions initiated by OH radicals under haze days.
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Zhang,Y., Mu,Y., Meng,F., Li,H., Wang,X., Zhang,W., Mellouki,A., Gao,J., Zhang,X., Wang,S., Chai,F.
Original/Translated Title
URL
Date of Electronic
20140524
PMCID
Editors
Release of bisphenols from can coatings into canned beer in China market 2015 State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, Jiangsu, 214122, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of the science of food and agriculture
Periodical, Abbrev.
J.Sci.Food Agric.
Pub Date Free Form
15-Mar
Volume
95
Issue
4
Start Page
764
Other Pages
770
Notes
CI: (c) 2014; JID: 0376334; 0 (Benzhydryl Compounds); 0 (Carcinogens); 0 (Epoxy Compounds); 0 (Phenols); F3XRM1NX4H (2,2-bis(4-glycidyloxyphenyl)propane); MLT3645I99 (bisphenol A); OTO: NOTNLM; 2013/09/12 [received]; 2014/06/14 [revised]; 2014/07/20 [acce
Place of Publication
England
ISSN/ISBN
1097-0010; 0022-5142
Accession Number
PMID: 25092470
Language
eng
SubFile
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1002/jsfa.6862 [doi]
Output Language
Unknown(0)
PMID
25092470
Abstract
BACKGROUND: The aim of this research was to understand the migration of bisphenols from can coatings into foods in the Chinese market. RESULTS: The migration of bisphenols was studied in commercial cans from the Chinese market filled with four types of food simulant (FS), which were heated at 121 degrees C for 30 min and stored at 40 degrees C for 30 days. Only bisphenol A (BPA) and bisphenol A diglycidyl ether (BADGE) were found in the can coatings, and SimC (10% (v/v) ethanol/water) was the most suitable FS for their release. The levels of these bisphenols in 24 kinds of canned beer from Chinese markets were also investigated. The average concentrations of BPA and BADGE were 2.85 +/- 0.79 and 0.38 +/- 0.19 microg . L(-)(1) respectively, which were both lower than the EU limits, and their respective daily intakes were estimated at 0.015 and 0.0020 microg . kg(-)(1) body weight . day(-)(1). Besides, increasing storage temperature and time accelerated the release of bisphenols into FSs. CONCLUSION: The present results provide some guidance to reduce the migration of bisphenols during the transport and storage of canned foods.
Descriptors
Links
Book Title
Database
Publisher
Society of Chemical Industry
Data Source
Authors
Xie,Y., Bao,Y., Wang,H., Cheng,Y., Qian,H., Yao,W.
Original/Translated Title
URL
Date of Electronic
20140911
PMCID
Editors
Metal-organic frameworks for analytical chemistry: from sample collection to chromatographic separation 2012 State Key Laboratory of Medicinal Chemical Biology and Research Center for Analytical Sciences, College of Chemistry, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Accounts of Chemical Research
Periodical, Abbrev.
Acc.Chem.Res.
Pub Date Free Form
15-May
Volume
45
Issue
5
Start Page
734
Other Pages
745
Notes
LR: 20131121; JID: 0157313; 0 (Metals); 0 (Organometallic Compounds); 0 (Polycyclic Hydrocarbons, Aromatic); 059QF0KO0R (Water); J64922108F (Benzene); 2012/03/12 [aheadofprint]; ppublish
Place of Publication
United States
ISSN/ISBN
1520-4898; 0001-4842
Accession Number
PMID: 22404189
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1021/ar2002599 [doi]
Output Language
Unknown(0)
PMID
22404189
Abstract
In modern analytical chemistry researchers pursue novel materials to meet analytical challenges such as improvements in sensitivity, selectivity, and detection limit. Metal-organic frameworks (MOFs) are an emerging class of microporous materials, and their unusual properties such as high surface area, good thermal stability, uniform structured nanoscale cavities, and the availability of in-pore functionality and outer-surface modification are attractive for diverse analytical applications. This Account summarizes our research on the analytical applications of MOFs ranging from sampling to chromatographic separation. MOFs have been either directly used or engineered to meet the demands of various analytical applications. Bulk MOFs with microsized crystals are convenient sorbents for direct application to in-field sampling and solid-phase extraction. Quartz tubes packed with MOF-5 have shown excellent stability, adsorption efficiency, and reproducibility for in-field sampling and trapping of atmospheric formaldehyde. The 2D copper(II) isonicotinate packed microcolumn has demonstrated large enhancement factors and good shape- and size-selectivity when applied to on-line solid-phase extraction of polycyclic aromatic hydrocarbons in water samples. We have explored the molecular sieving effect of MOFs for the efficient enrichment of peptides with simultaneous exclusion of proteins from biological fluids. These results show promise for the future of MOFs in peptidomics research. Moreover, nanosized MOFs and engineered thin films of MOFs are promising materials as novel coatings for solid-phase microextraction. We have developed an in situ hydrothermal growth approach to fabricate thin films of MOF-199 on etched stainless steel wire for solid-phase microextraction of volatile benzene homologues with large enhancement factors and wide linearity. Their high thermal stability and easy-to-engineer nanocrystals make MOFs attractive as new stationary phases to fabricate MOF-coated capillaries for high-resolution gas chromatography (GC). We have explored a dynamic coating approach to fabricate a MOF-coated capillary for the GC separation of important raw chemicals and persistent organic pollutants with high resolution and excellent selectivity. We have combined a MOF-coated fiber for solid-phase microextraction with a MOF-coated capillary for GC separation, which provides an effective MOF-based tandem molecular sieve platform for selective microextraction and high-resolution GC separation of target analytes in complex samples. Microsized MOFs with good solvent stability are attractive stationary phases for high-performance liquid chromatography (HPLC). These materials have shown high resolution and good selectivity and reproducibility in both the normal-phase HPLC separation of fullerenes and substituted aromatics on MIL-101 packed columns and position isomers on a MIL-53(Al) packed column and the reversed-phase HPLC separation of a wide range of analytes from nonpolar to polar and acidic to basic solutes. Despite the above achievements, further exploration of MOFs in analytical chemistry is needed. Especially, analytical application-oriented engineering of MOFs is imperative for specific applications.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Gu,Z.Y., Yang,C.X., Chang,N., Yan,X.P.
Original/Translated Title
URL
Date of Electronic
20120312
PMCID
Editors
Indoor and outdoor carbonyl compounds and BTEX in the hospitals of Guangzhou, China 2006 State Key Laboratory of Organic Geochemistry, Key Laboratory of GD for Utilization and Protection of Environmental Resources, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, P.R. China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
The Science of the total environment
Periodical, Abbrev.
Sci.Total Environ.
Pub Date Free Form
15-Sep
Volume
368
Issue
3-Feb
Start Page
574
Other Pages
584
Notes
LR: 20131121; JID: 0330500; 0 (Air Pollutants); 0 (Aldehydes); 0 (Xylenes); 3FPU23BG52 (Toluene); J64922108F (Benzene); 2005/11/15 [received]; 2006/03/23 [revised]; 2006/03/29 [accepted]; 2006/06/05 [aheadofprint]; ppublish
Place of Publication
Netherlands
ISSN/ISBN
0048-9697; 0048-9697
Accession Number
PMID: 16740294
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
S0048-9697(06)00298-1 [pii]
Output Language
Unknown(0)
PMID
16740294
Abstract
Indoor and outdoor concentration levels of 21 carbonyl compounds and five BTEX (benzene, toluene, ethylbenzene and xylenes) were measured in four hospitals of Guangzhou from 2nd January to 20th March 2004. Samples were collected in five consecutive daytimes for each hospital. Among most of the samples, acetone was the most abundant carbonyl, followed by acetaldehyde, 2-butanone or formaldehyde. Toluene was the most abundant BTEX and the others were at similar levels. The relatively higher acetone concentrations might have resulted from the high level of background in Guangzhou area due to emission of the factories and LPG-fuel vehicles, and also for the special weather conditions during sampling time. The high concentration of acetaldehyde, which was even higher than that of formaldehyde, might be resulted from the wide use of ethanol in hospital. The partial oxidation of ethanol may form acetaldehyde. The indoor concentrations of carbonyls and BTEX were found a little higher than their outdoor counterparts with only a few exceptions, which showed the anthropogenic sources for these compounds. The low correlations between most carbonyls and BTEX concentrations might be caused by their complex sources. Finally, the human exposure levels of formaldehyde and acetaldehyde in hospitals are discussed.
Descriptors
Air Pollutants/analysis, Air Pollution, Indoor/analysis, Aldehydes/analysis, Benzene/analysis, China, Environmental Monitoring, Hospitals, Inhalation Exposure/analysis, Risk Assessment, Toluene/analysis, Xylenes/analysis
Links
Book Title
Database
Publisher
Data Source
Authors
Lu,H., Wen,S., Feng,Y., Wang,X., Bi,X., Sheng,G., Fu,J.
Original/Translated Title
URL
Date of Electronic
20060605
PMCID
Editors
7-O-methylkaempferol and -quercetin glycosides from the whole plant of Nervilia fordii 2009 State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, People's Republic of China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of natural products
Periodical, Abbrev.
J.Nat.Prod.
Pub Date Free Form
Jun
Volume
72
Issue
6
Start Page
1057
Other Pages
1060
Notes
LR: 20131121; JID: 7906882; 0 (Antiviral Agents); 0 (Drugs, Chinese Herbal); 0 (Glycosides); 0 (Umbelliferones); 9IKM0I5T1E (Quercetin); SM2XD6V944 (esculetin); ppublish
Place of Publication
United States
ISSN/ISBN
1520-6025; 0163-3864
Accession Number
PMID: 19422205
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1021/np800760p [doi]
Output Language
Unknown(0)
PMID
19422205
Abstract
Five new 7-O-methylkaempferol and -quercetin glycosides, namely, nervilifordins A-E (1-5), were isolated from the whole plant of Nervilia fordii, together with seven known flavonoids (6, 7, and 9-13) and one known coumarin (8). Their structures were elucidated on the basis of extensive spectroscopic analyses, including HSQC, HMBC, ROESY, and chemical methods. Compounds 1-3 and 6-13 were evaluated for their anti-herpes simplex virus 1 (HSV-1) activity and cytotoxicity on African green monkey kidney cells (Vero cells) in vitro. Of the tested compounds, only esculetin (8) exhibited antiviral activity against HSV-1, while the aglycones (11-13) showed stronger cytotoxicity on Vero cells than their glycosides (1-3, 6, and 7).
Descriptors
Animals, Antiviral Agents/chemistry/isolation & purification/pharmacology, Cercopithecus aethiops, Drugs, Chinese Herbal/chemistry/isolation & purification/pharmacology, Glycosides/chemistry/isolation & purification/pharmacology, Herpesvirus 1, Human/drug effects, Orchidaceae/chemistry, Plants, Medicinal/chemistry, Quercetin/chemistry/isolation & purification/pharmacology, Umbelliferones/chemistry/isolation & purification/pharmacology, Vero Cells
Links
Book Title
Database
Publisher
Data Source
Authors
Tian,L. W., Pei,Y., Zhang,Y. J., Wang,Y. F., Yang,C. R.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Determination of 16 polycyclic aromatic hydrocarbons in water using fluorinated polyaniline-based solid-phase microextraction coupled with gas chromatography 2012 State key Laboratory of Pollutant Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, 210046, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Environmental monitoring and assessment
Periodical, Abbrev.
Environ.Monit.Assess.
Pub Date Free Form
Jul
Volume
184
Issue
7
Start Page
4345
Other Pages
4353
Notes
JID: 8508350; 0 (Aniline Compounds); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Water Pollutants, Chemical); 0 (polyaniline); 2011/01/24 [received]; 2011/07/15 [accepted]; 2011/08/06 [aheadofprint]; ppublish
Place of Publication
Netherlands
ISSN/ISBN
1573-2959; 0167-6369
Accession Number
PMID: 21822575
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1007/s10661-011-2268-3 [doi]
Output Language
Unknown(0)
PMID
21822575
Abstract
The study on the performance of a fluorinated polyaniline (PANI) as a fiber coating for solid-phase microextraction (SPME) had been reported and 16 polycyclic aromatic hydrocarbons (PAHs) were selected to evaluate the performance of this fiber. Various parameters including sample volume, extraction temperature, time of desorption and extraction, pH and ionic strength were investigated intensively. A direct comparison between PANI-SPME fiber and commercial fiber was conducted. The results showed that the PANI-SPME coating had high affinity towards target compounds and the proposed method was successfully applied for the detection of real samples: rainfall and Taihu Lake water collected from Southern China. The whole PANI-SPME-GC method offers acceptable accuracy, precision and sensitivity and low detection limits, which is applicable to monitor trace levels of PAHs in real water bodies.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Li,Y., Wang,Y., Zhang,J., Sun,C.
Original/Translated Title
URL
Date of Electronic
20110806
PMCID
Editors