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Simultaneous determination of polycyclic aromatic hydrocarbons and benzene, toluene, ethylbenzene and xylene in water samples using a new sampling strategy combining different extraction modes and temperatures in a single extraction solid-phase microextra 2012 Departamento de Quimica, Universidade Federal de Santa Catarina, Florianopolis 88040900, SC, Brazil.
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Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
13-Apr
Volume
1233
Issue
Start Page
22
Other Pages
29
Notes
LR: 20131121; CI: Copyright (c) 2012; JID: 9318488; 0 (Benzene Derivatives); 0 (Polycyclic Compounds); 0 (Water Pollutants, Chemical); 0 (Xylenes); 3FPU23BG52 (Toluene); J64922108F (Benzene); L5I45M5G0O (ethylbenzene); 2011/12/13 [received]; 2012/02/08 [r
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 22386255
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; Validation Studies; IM
DOI
10.1016/j.chroma.2012.02.022 [doi]
Output Language
Unknown(0)
PMID
22386255
Abstract
This study proposes a new optimization approach for the simultaneous determination of polycyclic aromatic hydrocarbons (PAHs) and benzene, toluene, ethylbenzene and xylene isomers (BTEX) from water samples using the solid-phase microextraction technique followed by gas chromatography-mass spectrometry (GC-MS) separation and detection. The objective of the study was to achieve compromise extraction conditions, suitable for all semi-volatile and volatile compounds, under which the amount extracted is maximized for all analytes. This was achieved by careful optimization of the fiber coating, salting-out effect, extraction time and temperature and extraction mode (headspace or direct immersion). With the optimized fiber coating - PDMS/DVB 65 mum - the other selected factors were optimized using a response surface methodology through central composite designs. As expected, the optimized results for each class of analytes varied significantly, probably due to the differences in their volatility and the equilibrium constants for the analyte/fiber coating. In order to overcome this issue, a new optimization approach was proposed based on a combination of extraction modes and extraction temperatures in a single extraction procedure. The final optimized procedure was: 48 min of extraction in direct immersion mode with the sample maintained at 80 degrees C followed by a further 32 min of headspace extraction with the sample temperature kept at 10 degrees C. The proposed procedure was compared with conventional methods based on the use of a single extraction mode and temperature (80 min of headspace extraction at 60 degrees C or 80 min of direct immersion extraction at 50 degrees C). The newly proposed method was shown to be more attractive as it extracted higher amounts of both semi-volatile and volatile compounds in a single extraction procedure compared to the conventional approaches. The optimized method was validated and excellent results were obtained.
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Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Bianchin,J.N., Nardini,G., Merib,J., Dias,A.N., Martendal,E., Carasek,E.
Original/Translated Title
URL
Date of Electronic
20120217
PMCID
Editors
Clinical laboratory assessment of the abuse liability of an electronic cigarette 2012 Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Source Type
Print(0)
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Journal Article
Periodical, Full
Addiction (Abingdon, England)
Periodical, Abbrev.
Addiction
Pub Date Free Form
Aug
Volume
107
Issue
8
Start Page
1493
Other Pages
1500
Notes
LR: 20151119; CI: (c) 2012 The Authors, Addiction (c) 2012; GR: R01 CA120142/CA/NCI NIH HHS/United States; GR: R01 CA120142-04/CA/NCI NIH HHS/United States; GR: R01CA 120142/CA/NCI NIH HHS/United States; GR: T32 DA007027/DA/NIDA NIH HHS/United States; GR:
Place of Publication
England
ISSN/ISBN
1360-0443; 0965-2140
Accession Number
PMID: 22229871
Language
eng
SubFile
Journal Article; Research Support, N.I.H., Extramural; IM
DOI
10.1111/j.1360-0443.2012.03791.x [doi]
Output Language
Unknown(0)
PMID
22229871
Abstract
AIMS: To provide an initial abuse liability assessment of an electronic cigarette (EC) in current tobacco cigarette smokers. DESIGN: The first of four within-subject sessions was an EC sampling session that involved six, 10-puff bouts (30 seconds inter-puff interval), each bout separated by 30 minutes. In the remaining three sessions participants made choices between 10 EC puffs and varying amounts of money, 10 EC puffs and a varying number of own brand cigarette (OB) puffs, or 10 OB puffs and varying amounts of money using the multiple-choice procedure (MCP). The MCP was completed six times at 30-minute intervals, and one choice was reinforced randomly at each trial. SETTING: Clinical laboratory. PARTICIPANTS: Twenty current tobacco cigarette smokers. MEASUREMENTS: Sampling session outcome measures included plasma nicotine, cardiovascular response and subjective effects. Choice session outcome was the cross-over value on the MCP. FINDINGS: EC use resulted in significant nicotine delivery, tobacco abstinence symptom suppression and increased product acceptability ratings. On the MCP, participants chose to receive 10 EC puffs over an average of $1.06 or three OB puffs and chose 10 OB puffs over an average of $1.50 (P
Descriptors
Links
Book Title
Database
Publisher
Society for the Study of Addiction
Data Source
Authors
Vansickel,A.R., Weaver,M.F., Eissenberg,T.
Original/Translated Title
URL
Date of Electronic
20120508
PMCID
PMC3330136
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.
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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
A multiyear survey of waterpipe and cigarette smoking on a US university campus 2012 Department of Psychology and Institute for Drug and Alcohol Studies, Virginia Commonwealth University, Richmond, VA 23298, USA.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of American college health : J of ACH
Periodical, Abbrev.
J.Am.Coll.Health
Pub Date Free Form
Volume
60
Issue
7
Start Page
521
Other Pages
527
Notes
LR: 20160309; GR: F31 DA028102/DA/NIDA NIH HHS/United States; GR: F31DA028102/DA/NIDA NIH HHS/United States; GR: R01 CA120142/CA/NCI NIH HHS/United States; GR: R01 DA025659/DA/NIDA NIH HHS/United States; GR: R01CA120142/CA/NCI NIH HHS/United States; GR: R
Place of Publication
United States
ISSN/ISBN
1940-3208; 0744-8481
Accession Number
PMID: 23002800
Language
eng
SubFile
Journal Article; Research Support, N.I.H., Extramural; IM
DOI
10.1080/07448481.2012.692416 [doi]
Output Language
Unknown(0)
PMID
23002800
Abstract
OBJECTIVES: To examine the prevalence and characteristics of dual users of cigarettes and waterpipes by comparing them with individuals who use either product exclusively. PARTICIPANTS: Cross-sections of undergraduate students at a public university recruited each spring semester from 2006 to 2011 (total N = 2,998). METHODS: Participants completed an Internet survey that assessed demographics, tobacco use, perceptions, and norms concerning various tobacco products. Individuals who reported exclusive cigarette, exclusive waterpipe, and dual (waterpipe + cigarette) use were examined. RESULTS: Across years, 22% reported exclusive cigarette, 6.1% exclusive waterpipe, and 9.3% dual cigarette and waterpipe use. Dual users differed in demographics and social influences from their exclusive counterparts. CONCLUSIONS: Findings suggest that dual waterpipe and cigarette use was more prevalent than exclusive waterpipe use, and dual users may differ from individuals who use either product alone. These results warrant the inclusion of waterpipe-specific content in state and national surveys as well as tobacco prevention and intervention efforts.
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Book Title
Database
Publisher
Data Source
Authors
Cobb,C.O., Khader,Y., Nasim,A., Eissenberg,T.
Original/Translated Title
URL
Date of Electronic
PMCID
PMC4487802
Editors
Application of counter-current chromatography as a new pretreatment method for the determination of polycyclic aromatic hydrocarbons in environmental water 2012 Beijing Technology and Business University, School of Food and Chimerical Engineering, Beijing, PR China. caoxl@th.btbu.edu.cn
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of separation science
Periodical, Abbrev.
J.Sep.Sci.
Pub Date Free Form
Feb
Volume
35
Issue
4
Start Page
596
Other Pages
601
Notes
LR: 20150325; CI: Copyright (c) 2012; GR: Z99 HL999999/Intramural NIH HHS/United States; JID: 101088554; 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Water Pollutants, Chemical); NIHMS339391; OID: NLM: NIHMS339391; OID: NLM: PMC3270381; ppublish
Place of Publication
Germany
ISSN/ISBN
1615-9314; 1615-9306
Accession Number
PMID: 22282420
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1002/jssc.201100852 [doi]
Output Language
Unknown(0)
PMID
22282420
Abstract
Counter-current chromatography (CCC) was investigated as a new sample pretreatment method for the determination of trace polycyclic aromatic hydrocarbons (PAHs) in water environmental samples. The experiment was performed with a non-aqueous binary two-phase solvent system composed of n-heptane and acetonitrile. The CCC column was first filled with the upper stationary phase, and then a large volume of water sample was pumped into the column while the CCC column was rotated at 1600 rpm. Finally, the trace amounts of PAHs extracted and enriched in the stationary phase were eluted out by the lower mobile phase and determined by gas chromatography-flame ionization detector (GC-FID) or gas chromatography-mass spectrometry (GC-MS). The enrichment and cleanup of PAHs can be fulfilled online by this method with high recoveries (84.1-103.2%) and good reproducibility (RSDs: 4.9-12.2%) for 16 EPA PAHs under the optimized CCC pretreatment conditions. This method has been successfully applied to determine PAHs in lake water where 8 PAHs were detected in the concentration of 40.9-89.9 ng/L. The present method is extremely suitable for the preparation of large volume of environmental water sample for the determination of trace amounts of organic pollutants including PAHs as studied in this paper.
Descriptors
Links
Book Title
Database
Publisher
WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Data Source
Authors
Cao,X., Yang,C., Pei,H., Li,X., Xu,X., Ito,Y.
Original/Translated Title
URL
Date of Electronic
PMCID
PMC3270381
Editors
Aniline-silica nanocomposite as a novel solid phase microextraction fiber coating 2012 Environmental and Bio-Analytical Laboratories, Department of Chemistry, Sharif University of Technology, P.O. Box 11365-9516, Tehran, Iran. bagheri@sharif.edu
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
18-May
Volume
1238
Issue
Start Page
22
Other Pages
29
Notes
LR: 20121115; CI: Copyright (c) 2012; JID: 9318488; 0 (Aniline Compounds); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Water Pollutants, Chemical); 7631-86-9 (Silicon Dioxide); SIR7XX2F1K (aniline); 2011/12/19 [received]; 2012/03/05 [revised]; 2012/03/07 [a
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 22498354
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.chroma.2012.03.027 [doi]
Output Language
Unknown(0)
PMID
22498354
Abstract
A new unbreakable solid phase microextraction (SPME) fiber coating based on aniline-silica nanocomposite was electrodeposited on a stainless steel wire. The electropolymerization process was carried out at a constant deposition potential, applied to the corresponding aqueous electrolyte containing aniline and silica nanoparticles. The scanning electron microscopy (SEM) images showed the non-smooth and the porous surface structure of the prepared nanocomposite. The applicability of the new fiber coating was examined by headspace-solid phase microextraction (HS-SPME) of some environmentally important polycyclic aromatic hydrocarbons (PAHs), as model compounds, from aqueous samples. Subsequently, the extracted analytes were transferred into a gas chromatography (GC) by thermal desorption. Parameters affecting the synthesizing and extraction processes including the voltage of power supply, the weight ratio of components, the time of electrodeposition, extraction time and temperature, the ionic strength, and desorption temperature and time were optimized. Eventually, the developed method was validated by gas chromatography-mass spectrometry (GC-MS). At the optimum conditions, the relative standard deviation (%RSD) values for a double distilled water spiked with the selected PAHs at 40 ng L(-1) were 6-13% (n=3) while the limit of detection (LOD) results were between 1 and 3 ng L(-1). The calibration graphs were linear in the concentration range from 20 to 4000 ng L(-1) (R(2)>0.995). Finally the developed method was applied to the analysis of Kalan dam, rain and tap water samples and the relative recovery values were found to be in the range of 76-109%, under optimized conditions. In addition, the synthesis of the nanocomposite coating was carried out conveniently while it is rather inexpensive, easy, simple, rapid and highly durable and can be used frequently.
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Bagheri,H., Roostaie,A.
Original/Translated Title
URL
Date of Electronic
20120315
PMCID
Editors
Mobility, expansion and management of a multi-species scuba diving fishery in East Africa 2012 Department of Systems Ecology, Stockholm University, Stockholm, Sweden. hampus@ecology.su.se
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
PloS one
Periodical, Abbrev.
PLoS One
Pub Date Free Form
Volume
7
Issue
4
Start Page
e35504
Other Pages
Notes
LR: 20150225; JID: 101285081; OID: NLM: PMC3328463; 2012/01/11 [received]; 2012/03/16 [accepted]; 2012/04/17 [epublish]; ppublish
Place of Publication
United States
ISSN/ISBN
1932-6203; 1932-6203
Accession Number
PMID: 22530034
Language
eng
SubFile
Journal Article; IM
DOI
10.1371/journal.pone.0035504 [doi]
Output Language
Unknown(0)
PMID
22530034
Abstract
BACKGROUND: Scuba diving fishing, predominantly targeting sea cucumbers, has been documented to occur in an uncontrolled manner in the Western Indian Ocean and in other tropical regions. Although this type of fishing generally indicates a destructive activity, little attention has been directed towards this category of fishery, a major knowledge gap and barrier to management. METHODOLOGY AND PRINCIPAL FINDINGS: With the aim to capture geographic scales, fishing processes and social aspects the scuba diving fishery that operate out of Zanzibar was studied using interviews, discussions, participant observations and catch monitoring. The diving fishery was resilient to resource declines and had expanded to new species, new depths and new fishing grounds, sometimes operating approximately 250 km away from Zanzibar at depths down to 50 meters, as a result of depleted easy-access stock. The diving operations were embedded in a regional and global trade network, and its actors operated in a roving manner on multiple spatial levels, taking advantage of unfair patron-client relationships and of the insufficient management in Zanzibar. CONCLUSIONS AND SIGNIFICANCE: This study illustrates that roving dynamics in fisheries, which have been predominantly addressed on a global scale, also take place at a considerably smaller spatial scale. Importantly, while proposed management of the sea cucumber fishery is often generic to a simplified fishery situation, this study illustrates a multifaceted fishery with diverse management requirements. The documented spatial scales and processes in the scuba diving fishery emphasize the need for increased regional governance partnerships to implement management that fit the spatial scales and processes of the operation.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Eriksson,H., de la Torre-Castro,M., Olsson,P.
Original/Translated Title
URL
Date of Electronic
20120417
PMCID
PMC3328463
Editors
Solid-phase extraction combined with large volume injection-programmable temperature vaporization-gas chromatography-mass spectrometry for the multiresidue determination of priority and emerging organic pollutants in wastewater 2012 Department of Analytical Chemistry, Faculty of Science and Technology, University of the Basque Country-UPV/EHU, PK 644, 48080 Bilbao, Spain.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of chromatography.A
Periodical, Abbrev.
J.Chromatogr.A
Pub Date Free Form
20-Jul
Volume
1247
Issue
Start Page
104
Other Pages
117
Notes
CI: Copyright (c) 2012; JID: 9318488; 0 (Organic Chemicals); 0 (Water Pollutants, Chemical); 2012/02/27 [received]; 2012/04/16 [revised]; 2012/05/06 [accepted]; 2012/05/14 [aheadofprint]; ppublish
Place of Publication
Netherlands
ISSN/ISBN
1873-3778; 0021-9673
Accession Number
PMID: 22673809
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.chroma.2012.05.022 [doi]
Output Language
Unknown(0)
PMID
22673809
Abstract
In the present work the simultaneous extraction for the multiresidue determination in wastewater samples of organic compounds such as polychlorinated biphenyls (PCBs), polybrominated biphenyls (PBBs), pesticides, polycyclic aromatic hydrocarbons (PAHs), phthalate esters (PEs), alkylphenols (APs), bisphenol A (BPA) or hormones included in different lists of priority and emerging pollutants because of their action as endocrine disrupting compounds (EDCs) was developed. Different solid phase extraction (SPE) variables such as the nature of the solid phase (Oasis-HLC, C18 and Lichrolut), the sample volume, the addition of MeOH and NaCl, the pH of the water phase and the volume of the eluent solvent were optimized in order to analyze simultaneously the priority and emerging families of pollutants mentioned above. Good recoveries were obtained for Milli-Q water (80-120%), however, since the use of deuterated analogues and dilution of the sample did not correct the matrix effect, additional SPE clean-up step using Florisil(R) cartridges was necessary to obtain good results for wastewater samples (80-125%). In order to improve the limits of detection (LODs), large volume injection (LVI) using programmable temperature vaporizer (PTV) coupled to gas chromatography-mass spectrometry (GC-MS) was also optimized. Since analytes losses in the case of the most volatile congeners occurred during the derivatization step and no separation of the derivatized and the non-derivatized analytes was possible during SPE elution, two different injections were optimized for each analyte group. LODs were in good agreement with those found in the literature and relative standard deviations (RSDs) were in the 10-25% range for Milli-Q and 12-30% for wastewater samples. The method was finally applied to the determination of target analytes in three different wastewater treatment plants (WWTPs, Bakio, Gernika and Galindo (Spain)) and in one water purification plant (WPP) in Zornotza (Spain).
Descriptors
Links
Book Title
Database
Publisher
Elsevier B.V
Data Source
Authors
Bizkarguenaga,E., Ros,O., Iparraguirre,A., Navarro,P., Vallejo,A., Usobiaga,A., Zuloaga,O.
Original/Translated Title
URL
Date of Electronic
20120514
PMCID
Editors
Genetic characterisation of extended-spectrum beta-lactamases in Escherichia coli isolated from retail chicken products including CTX-M-9 containing isolates: a food safety risk factor 2012 Centre of Studies of Animal and Veterinary Sciences, Vila Real, Portugal.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
British poultry science
Periodical, Abbrev.
Br.Poult.Sci.
Pub Date Free Form
Volume
53
Issue
6
Start Page
747
Other Pages
755
Notes
JID: 15740290R; 0 (Escherichia coli Proteins); 0 (beta-Lactams); EC 3.5.2.- (CTX-M-9 protein, E coli); EC 3.5.2.6 (beta-Lactamases); ppublish
Place of Publication
England
ISSN/ISBN
1466-1799; 0007-1668
Accession Number
PMID: 23398418
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1080/00071668.2012.740554 [doi]
Output Language
Unknown(0)
PMID
23398418
Abstract
1. Bacterial resistance to beta-lactam antibiotics has risen dramatically in Escherichia coli from food animals. In a previous study, 29 randomly selected chicken products, collected in Portugal, were analysed for the presence of extended-spectrum beta-lactamases (ESBLs)-producing E. coli; and during this study the genetic characterisation of ESBLs genes was investigated. 2. The presence of genes encoding TEM, OXA, SHV, and CTX-M type beta-lactamases was studied by PCR followed by sequencing. Additionally, other mechanisms of antimicrobial resistance, phylogenetic groups and the presence of virulence determinants were evaluated among the isolates. 3. beta-lactamases genes were identified as follows: bla (CTX-M-14) (n = 4), bla (CTX-M-1) (n = 2), bla (CTX-M-9) (n = 4) and bla (TEM-52) (n = 13). Mutations at positions -42, -18, -1, and +58 of ampC promoter region were identified in 4 non-ESBL-producing isolates. The tet(A) or tet(B) genes were identified in all tetracycline-resistant isolates; the aadA gene detected in 8 of 10 streptomycin-resistant isolates; the aac(3)-II gene in all gentamicin-resistant isolates; the cmlA gene in the chloramphenicol-resistant isolate; and sul1 and/or sul2 and/or sul3 genes were found in all trimethoprim-sulfamethoxazole-resistant isolates. The intI1 gene was detected in 8 trimethoprim-sulfamethoxazole-resistant isolates and the intI2 gene in 4 isolates; one gene cassette arrangements were identified among class 1 integrons (dfrA1 + aadA1) and among the class 2 integrons (dfrA1 + sat2 + aadA1). Among cefotaxime-resistant isolates, 16 belonged to A or B1 phylogenetic groups, while 11 isolates were classified into the D or B2 phylogroups. At least one virulence-associated gene (aer, fimA, or papC) was detected in 74.1% of the cefotaxime-resistant isolates. 4. Because ESBLs-producing bacteria are resistant to a broad range of beta-lactams, infections caused by these organisms complicate therapy and limit treatment options.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Silva,N., Costa,L., Goncalves,A., Sousa,M., Radhouani,H., Brito,F., Igrejas,G., Poeta,P.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Determination of ten monohydroxylated polycyclic aromatic hydrocarbons by liquid-liquid extraction and liquid chromatography/tandem mass spectrometry 2012 Key Laboratory of Ecology and Environmental Science in Guangdong Higher Education, School of Life Science, South China Normal University, Guangzhou 510631, China.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Talanta
Periodical, Abbrev.
Talanta
Pub Date Free Form
15-May
Volume
93
Issue
Start Page
383
Other Pages
391
Notes
CI: Published by Elsevier B.V.; GR: 1U38DD000481-01/DD/NCBDD CDC HHS/United States; JID: 2984816R; 0 (Polycyclic Hydrocarbons, Aromatic); 2012/01/27 [received]; 2012/02/17 [revised]; 2012/02/22 [accepted]; 2012/03/01 [aheadofprint]; ppublish
Place of Publication
Netherlands
ISSN/ISBN
1873-3573; 0039-9140
Accession Number
PMID: 22483926
Language
eng
SubFile
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.talanta.2012.02.059 [doi]
Output Language
Unknown(0)
PMID
22483926
Abstract
The aim of this study is to develop and validate an analytical method for the quantitation of ten urinary monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) through high pressure liquid chromatography/tandem mass spectrometry (HPLC/MS/MS). After enzymatic deconjugation, urine samples were extracted by liquid-liquid extraction (LLE) and OH-PAHs were analyzed by HPLC/MS/MS operated in negative electrospray ionization (ESI) and multiple reaction monitoring (MRM) mode. LLE was conducted with the solvent mixture of pentane and toluene, which reduced the matrix interferences and enhanced the method sensitivity significantly. Deuterated and (13)C-labeled analogs are used as internal standards. Calibration curves of all target analytes shows favorable linearity within the concentration range of 5.9-15,000.0 ng/L for different OH-PAHs with the regression coefficients above 0.993. The limits of detection (LODs) in pooled urine ranged from 1.72 to 17.47 ng/L, which were much lower than those obtained by a gas chromatography/high resolution mass spectrometry (GC/HRMS) method. The method shows satisfactory accuracy and precision when analyzing three different levels of OH-PAHs spiked in pooled urine. Except for 1-hydroxynaphthalene, recoveries of other OH-PAHs were in the range of 100 +/- 20% with a variation coefficient of less than 13%. The measurement of OH-PAHs from a QC sample of the Centers for Disease Control and Prevention (CDC) generated results close to the values measured by CDC. This method has been successfully employed in the California Biomonitoring Program.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Fan,R., Ramage,R., Wang,D., Zhou,J., She,J.
Original/Translated Title
URL
Date of Electronic
20120301
PMCID
Editors