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1.
Talanta ; 234: 122641, 2021 Nov 01.
Article in English | MEDLINE | ID: mdl-34364450

ABSTRACT

In the present study, 12 volatile benzene and naphthalene derived co-formulants were identified by suspect screening and unknown analysis in 14 plant protection products (PPPs) corresponding to several types of formulations, as emulsifiable concentrates (EC), suspension concentrates (SC), dispersible concentrates (DC) and ZC, which is a mixture of a capsule suspension (CS) in an SC, containing either difenoconazole or chlorantraniliprole as main active ingredients. The selected technique was gas chromatography coupled to Q-Orbitrap high resolution mass accuracy spectrometry (GC-Q-Orbitrap-MS), providing efficient separation and detection of all identified compounds. Finally, 42 compounds were tentatively identified, and 12 of them were confirmed and quantified using analytical standards. Results showed that the applied methodology was able to detect these co-formulants at concentrations as low as 0.03 g/L (tert-butylbenzene), encompassing a wide concentration range, up to 9.63 g/L (pentamethylbenzene). Pentamethylbenzene was the only compound detected in all studied samples.


Subject(s)
Benzene , Gas Chromatography-Mass Spectrometry , Mass Spectrometry , Spectrum Analysis
2.
Eur Cell Mater ; 35: 209-224, 2018 04 13.
Article in English | MEDLINE | ID: mdl-29652075

ABSTRACT

The success of cell-based approaches for the treatment of cartilage defects requires an optimal autologous cell source with chondrogenic differentiation ability that maintains its differentiated properties and stability following implantation. The objective of this study was to compare the chondrogenic capacity of mesenchymal stem cells (MSCs) isolated from lipoaspirates (ASCs) and the infrapatellar fat pad (IFPSCs) of osteoarthritic patients and treated with transforming growth factor (TGF)-ß family-related growth factors. Cells were cultured for 6 weeks in a 3D pellet culture system with the chimeric activin A/bone morphogenic protein (BMP)-2 ligand (AB235), the chimeric nodal/BMP-2 ligand (NB260) or BMP-2. To investigate the stability of the new cartilage, ASCs-treated pellets were transplanted subcutaneously into severe combined immunodeficiency (SCID) mice. Histological and immunohistochemical assessment confirmed that the growth factors induced cartilage differentiation in both isolated cell types. However, reverse transcription-quantitative PCR results showed that ASCs presented a higher chondrogenic potential than IFPSCs. In vivo results revealed that AB235-treated ASCs pellets were larger in size and could form stable cartilage-like tissue as compared to NB260-treated pellets, while BMP-2-treated pellets underwent calcification. The chondrogenic induction of ASCs by AB235 treatment was mediated by SMAD2/3 activation, as proved by immunofluorescence analysis. The results of this study indicated that the combination of ASCs and AB235 might lead to a cell-based cartilage regeneration treatment.


Subject(s)
Adipose Tissue/pathology , Cell Differentiation/drug effects , Cell Separation , Chondrogenesis/drug effects , Lipectomy , Osteoarthritis/pathology , Stem Cells/pathology , Transforming Growth Factor beta/pharmacology , Aged , Animals , Female , Humans , Male , Mice, SCID , Middle Aged , Phenotype , Smad Proteins/metabolism , Stem Cell Transplantation
3.
J Chromatogr A ; 1518: 15-24, 2017 Oct 06.
Article in English | MEDLINE | ID: mdl-28864112

ABSTRACT

With the aim of monitoring water quality according to the regulations established by the European Union it would be necessary to implement analytical methodologies capable of simultaneously determining a broad range of organic pollutants at ultra-trace levels, allowing for increased sample throughput. In addition, the high number of samples to be analyzed requires a particular focus on setting up fully automated analytical methodologies. In view of that, this study is aimed at the development of a complete automated procedure for the ultra-trace determination of certain pesticides, polycyclic aromatic hydrocarbons (PAHs), brominated diphenyl ethers (BDEs) and polychlorinated biphenyls (PCBs) in surface waters. The proposed method is based on an on-line combination of solid phase microextraction (SPME) and gas chromatography coupled to double-focusing magnetic sector high resolution mass spectrometry (GC-HRMS). SPME as well as GC-HRMS conditions were optimized to achieve maximum extraction efficiency and sensitivity, which was reinforced by using multiple ion detection (MID) as acquisition mode. Using only 19mL of water and with minimum sample manipulation, the method allowed for the determination of 53 compounds exhibiting good linearity (R2>0.99), recoveries between 84 and 118% and relative standard deviation (RSD) values <20% for intra-day and inter-day precision. In addition, the method provides quantification limits (LOQs) between 0.1-50ngL-1, lower than the Environmental Quality Standards (EQS) fixed by Directive 2013/39/EC. Finally, the method was successfully applied to determine target contaminants in Almería surface water compartments, detecting dioxin-like PCBs, BDEs and some pesticides.


Subject(s)
Environmental Monitoring/methods , Gas Chromatography-Mass Spectrometry , Solid Phase Microextraction , Dioxins/analysis , Halogenated Diphenyl Ethers/analysis , Pesticides/analysis , Polychlorinated Biphenyls/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Water Pollutants, Chemical/analysis
4.
Anim Reprod Sci ; 181: 175-185, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28461086

ABSTRACT

The aim of this study was to analyse the characteristics of ram spermatozoa subjected to varying concentrations of sucrose, and the influence of storage temperature (22°C or 5°C) prior to vitrification. Ejaculated semen was diluted in TCFEY (tris-citric acid-fructose 20% egg yolk), and two aliquots were prepared at a final concentration of 100×106spz/ml, one maintained at room temperature (22°C) and the other at 5°C. In the first experiment, the toxicity of sucrose diluents on the sperm was analysed; sperm samples at different temperatures were diluted (1:2) in TCF-BSA 2% (control) or in the same extender supplemented with various sucrose concentrations (0.4M, 0.6M and 0.8M). The effects of vitrification were studied in the second experiment, where sperm samples were mixed with different concentrations of cryoprotectants (sucrose) and vitrified by being plunged directly into liquid nitrogen. In both experiments, the sperm quality was assessed by measuring motility, morphology, membrane functionality (HOST), viability, acrosome integrity and DNA fragmentation. The toxicity test revealed significant differences (p≤0.05) when different sucrose concentrations were used; lower total and progressive motility, normal morphology and membrane functionality were noted when sucrose concentration was higher, compared to the control treatment. Samples maintained at room temperature showed significantly (p≤0.05) higher viability than samples stored at 5°C. In contrast, although the quality of vitrified sperm was drastically decreased in comparison with fresh sperm, sucrose was associated with greater total motility, viability and membrane functionality. This improvement was closely linked to the temperature at which the sperm had been previously maintained, showing higher values when sperm was stored at 5°C. The main conclusions to be drawn from the study are therefore that sucrose shows promising potential as a cryoprotectant, and storing samples at 5°C is linked to improved sperm quality following vitrification.


Subject(s)
Semen Analysis/veterinary , Semen Preservation/veterinary , Sheep/physiology , Sucrose/pharmacology , Animals , Cryopreservation , Cryoprotective Agents/pharmacology , DNA Fragmentation/drug effects , Male , Semen/drug effects , Sperm Count , Sperm Motility/drug effects , Temperature , Vitrification
5.
Int J Biometeorol ; 60(10): 1603-1609, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26951115

ABSTRACT

A total number of 1092 artificial inseminations (AIs) performed from March to May were documented over four consecutive years on 10 Payoya goat farms (36° N) and 19,392 AIs on 102 Rasa Aragonesa sheep farms (41° N) over 10 years. Mean, maximum, and minimum ambient temperatures, mean relative humidity, mean solar radiation, and total rainfall on each insemination day were recorded. Overall, fertility rates were 58 % in goats and 45 % in sheep. The fertility rates of the highest and lowest deciles of each of the meteorological variables indicated that temperature and rainfall had a significant effect on fertility in goats. Specifically, inseminations that were performed when mean (68 %), maximum (68 %), and minimum (66 %) temperatures were in the highest decile, and rainfall was in the lowest decile (59 %), had a significantly (P < 0.0001) higher proportion of does that became pregnant than did the ewes in the lowest decile (56, 54, 58, and 49 %, respectively). In sheep, the fertility rates of the highest decile of mean (62 %), maximum (62 %), and minimum (52 %) temperature, RH (52 %), THI (53 %), and rainfall (45 %) were significantly higher (P < 0.0001) than were the fertility rates among ewes in the lowest decile (46, 45, 45, 45, 46, and 43 %, respectively). In conclusion, weather was related to fertility in small ruminants after AI in spring. It remains to be determined whether scheduling the dates of insemination based on forecasted temperatures can improve the success of AI in goats and sheep.


Subject(s)
Fertility , Goats , Insemination, Artificial/veterinary , Sheep , Weather , Animals , Female , Pregnancy
6.
Sci Rep ; 5: 16400, 2015 Nov 13.
Article in English | MEDLINE | ID: mdl-26563344

ABSTRACT

Autologous chondrocyte implantation (ACI) depends on the quality and quantity of implanted cells and is hindered by the fact that chondrocytes cultured for long periods of time undergo dedifferentiation. Here we have developed a reproducible and efficient chondrogenic protocol to redifferentiate chondrocytes isolated from osteoarthritis (OA) patients. We used morphological, histological and immunological analysis together with a RT-PCR detection of collagen I and collagen II gene expression to show that chondrocytes isolated from articular cartilage biopsies of patients and subjected to long-term culture undergo dedifferentiation and that these cells can be redifferentiated following treatment with the chimeric Activin A/BMP2 ligand AB235. Examination of AB235-treated cell pellets in both in vitro and in vivo experiments revealed that redifferentiated chondrocytes synthesized a cartilage-specific extracellular matrix (ECM), primarily consisting of vertically-orientated collagen fibres and cartilage-specific proteoglycans. AB235-treated cell pellets also integrated into the surrounding subcutaneous tissue following transplantation in mice as demonstrated by their dramatic increase in size while non-treated control pellets disintegrated upon transplantation. Thus, our findings describe an effective protocol for the promotion of redifferentiation of autologous chondrocytes obtained from OA patients and the formation of a cartilage-like ECM that can integrate into the surrounding tissue in vivo.


Subject(s)
Activins/metabolism , Bone Morphogenetic Protein 2/metabolism , Cell Differentiation , Chondrocytes/pathology , Activins/genetics , Aged , Animals , Bone Morphogenetic Protein 2/genetics , Cartilage, Articular/metabolism , Cartilage, Articular/pathology , Chondrocytes/transplantation , Collagen/genetics , Collagen/metabolism , Extracellular Matrix/metabolism , Female , Gene Expression , Humans , Immunohistochemistry , Ligands , Male , Mice , Mice, Inbred NOD , Mice, SCID , Middle Aged , Osteoarthritis/pathology , Osteoarthritis/therapy , Proteoglycans/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Time Factors , Transplantation, Autologous , Transplantation, Heterologous
7.
Osteoarthritis Cartilage ; 21(1): 246-58, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23085560

ABSTRACT

OBJECTIVE: Infrapatellar fat pad of patients with osteoarthritis (OA) contains multipotent and highly clonogenic adipose-derived stem cells that can be isolated by low invasive methods. Moreover, nuclear and cytoplasmic cellular extracts have been showed to be effective in induction of cell differentiation and reprogramming. The aim of this study was to induce chondrogenic differentiation of autologous mesenchymal stem cells (MSCs) obtained from infrapatellar fat pad (IFPSCs) of patients with OA using cellular extracts-based transdifferentiation method. DESIGN: IFPSCs and chondrocytes were isolated and characterized by flow cytometry. IFPSCs were permeabilized with Streptolysin O and then exposed to a cell extract obtained from chondrocytes. Then, IFPSCs were cultured for 2 weeks and chondrogenesis was evaluated by morphologic and ultrastructural observations, immunologic detection, gene expression analysis and growth on 3-D poly (dl-lactic-co-glycolic acid) (PLGA) scaffolds. RESULTS: After isolation, both chondrocytes and IFPSCs displayed similar expression of MSCs surface makers. Collagen II was highly expressed in chondrocytes and showed a basal expression in IFPSCs. Cells exposed to chondrocyte extracts acquired a characteristic morphological and ultrastructural chondrocyte phenotype that was confirmed by the increased proteoglycan formation and enhanced collagen II immunostaining. Moreover, chondrocyte extracts induced an increase in mRNA expression of chondrogenic genes such as Sox9, L-Sox5, Sox6 and Col2a1. Interestingly, chondrocytes, IFPSCs and transdifferentiated IFPSCs were able to grow, expand and produce extracellular matrix (ECM) on 3D PLGA scaffolds. CONCLUSIONS: We demonstrate for the first time that extracts obtained from chondrocytes of osteoarthritic knees promote chondrogenic differentiation of autologous IFPSCs. Moreover, combination of transdifferentiated IFPSCs with biodegradable PLGA 3D scaffolds can serve as an efficient system for the maintenance and maturation of cartilage tissue. These findings suggest its usefulness to repair articular surface in OA.


Subject(s)
Chondrocytes/metabolism , Chondrogenesis/physiology , Mesenchymal Stem Cells/metabolism , Osteoarthritis, Knee/metabolism , Cell Transdifferentiation/genetics , Cell Transdifferentiation/physiology , Chondrogenesis/genetics , Collagen Type II/metabolism , Extracellular Matrix/metabolism , Flow Cytometry , Humans , Patella/metabolism , Proteoglycans/metabolism , Tissue Scaffolds
8.
Theriogenology ; 79(3): 436-42, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23174771

ABSTRACT

This study was designed to compare the sperm nuclear morphometry of four species of domestic artiodactyls (cattle, sheep, goats, and pigs), using the newly developed automatic computer-assisted sperm morphometry analysis-F. The study was divided into two experiments. In the first experiment, samples from 20 males from each species were collected, diluted, and divided into four sample aliquots. The first was labeled directly with Hoechst 33342, and the others were processed as smears. Between smears, one group was directly labeled with Hoechst after air drying, and the other was fixed either with glutaraldehyde (GLUT), or with methanol, and afterward labeled with Hoechst. Digital images of the fluorescence-labeled sperm were recorded with a digital camera, and at least 200 sperm cells per sample were processed using the Image J analysis open software. Air-drying significantly reduced nuclear sperm dimensions in ruminant species, whereas no effect was observed in pigs. For most of the primary morphometric parameters, the relationship between the four species for the sperm nuclear dimensions can be described as follows: bull > ram ≥ boar > goat. However, ram sperm nuclei had greater width than those of the other species studied. For the secondary morphometric parameters, ram sperm nuclei were clearly less elliptical and elongated and showed greater regularity than in the other studied species. In the second experiment, ejaculates from 10 males per species were used to compare the sperm head morphometric results obtained with the computer-assisted sperm morphometry analysis-F system (using the GLUT treatment as reference) to a more conventional CASMA method (semen smears stained with Harris's hematoxylin and processed with the Integrated Sperm Analysis System [ISAS] commercial software [Proiser R&D SL, Buñol, Spain]). Spermatozoa displayed a bigger size when processed with Harris's hematoxylin than with the GLUT method in all primary sperm head morphometric parameters for the four species studied. A significant correlation was observed between the two methods used in this experiment for all morphometric size parameters in the four species studied. It was concluded that drying and fixation has little effect on sperm nuclear morphometry, with differences between species, and that there are significant variations in size of the sperm nucleus and in the hydrodynamic properties between the four species studied.


Subject(s)
Cattle , Cell Nucleus/ultrastructure , Goats , Sheep , Spermatozoa/ultrastructure , Swine , Animals , Benzimidazoles , Fluorescent Dyes , Image Processing, Computer-Assisted/methods , Male , Microscopy, Fluorescence , Species Specificity
9.
J Anim Breed Genet ; 129(4): 306-15, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22775263

ABSTRACT

Monthly test-day records of milk yield and composition in Murciano-Granadina (MG) and Payoya (PYA) dairy goats were combined with weather data from meteorological stations, to analyse the effects of heat stress on dairy traits, measured with an index of temperature and relative humidity (THI). A 'repeatability animal model' and a 'reaction norm animal model' were used to estimate genetic (co)variance components. Estimates obtained with both models were very similar. The h(2) of daily yields in MG did not vary throughout the THI scale, but the pattern of variation of content traits showed negative trends for increasing THI values. In PYA, a slight positive tendency throughout the THI scale was observed for the same traits. The genetic correlations between subsequent points in the THI scale were lower than 0.80 when they were computed between low and high THI points. The same reaction norm was observed for all traits. Using the 'reaction norm animal model', it was possible to identify those animals that show the same performance throughout the THI trajectory (robust) and those with varying performances (tolerant and non-tolerant to heat stress). Results in this study also show that heat tolerance decreases, while the genetic level for milk traits increases. Losses because of heat stress were equivalent to 1.9 and 3.1% in the yearly yield of fat and protein for MG and PYA, respectively.


Subject(s)
Adaptation, Physiological/genetics , Dairying , Genetic Variation , Goats/genetics , Goats/physiology , Heat-Shock Response/genetics , Heat-Shock Response/physiology , Analysis of Variance , Animals , Breeding , Environment , Goats/classification , Models, Statistical , Regression Analysis , Spain
10.
J Dairy Sci ; 93(6): 2718-26, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20494181

ABSTRACT

Records from the milk recording scheme of Spanish Murciano-Granadina goats were studied to estimate genetic (co)variance components and breeding values throughout the first and second lactations. The data used consisted of 49,696 monthly test-day records of milk (MY), protein (PY), fat (FY), and dry matter (DMY) yields from 5,163 goats, distributed in 20 herds, offspring of 2,086 does and 206 bucks. These records were analyzed by 2-trait random regression models (RRM) and a repeatability test-day model (RTDM). At the middle of lactation, heritability estimates for MY, DMY, and FY obtained with RTDM were larger than those estimated with RRM, and the opposite was true for PY. The RRM estimates of heritability for MY, FY, and PY were very similar throughout the trajectories of both lactations. Heritability estimates for DMY decreased through the lactation period. The genetic correlations between the first and second lactation records estimated for all traits by RRM were positive and ranged from 0.43 to 0.80 throughout the lactation curves. The correlation between BV estimated with RTDM and RRM was 0.742 for MY and 0.664 for DMY. The RRM could be a useful alternative to RTDM for the prediction of BV in this breed.


Subject(s)
Goats/genetics , Lactation/genetics , Milk/metabolism , Animals , Breeding , Female , Goats/physiology , Lactation/physiology , Milk/chemistry , Milk Proteins/analysis , Models, Genetic , Quantitative Trait, Heritable , Regression Analysis
11.
N Z Vet J ; 57(3): 141-5, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19521462

ABSTRACT

AIM: To determine the effects of annual rainfall and farm on the efficacy of melatonin implants in improving lamb production in Merino sheep in Spain. METHODS: A study was conducted on 3,871 Merino sheep on six farms over a 4-year period (2004-2007). Melatonin implants were inserted during the second half of February or early March (winter) (Melatonin group) or not (Control group). Multinomial logistic regression was used to determine the effects of melatonin, farm and year, and their interactions, on reproductive outcomes. Regression analysis was used to examine the relationship between annual rainfall and the percentage of ewes lambing, percentage of lambs born to ewes lambing, and overall lambing percentage, for each year and treatment group within farm. RESULTS: Annual rainfall, farm and treatment with melatonin, and their interactions, had a significant effect on the reproductive performance of ewes (p<0.001). Treatment with melatonin increased the percentage of ewes lambing (Melatonin group = 77 (SEM 4)%, Control group = 44 (SEM 7)%; p<0.0001), and overall lambing percentage (Melatonin group = 109 (SEM 1)%, Control group = 59 (SEM 2)%; p<0.0001). Treatment differences were especially pronounced in 2005 and 2006, when annual rainfall was exceptionally low; ewes in the Control group had the lowest lambing rates those years. Lambing rates and overall lambing percentage were positively correlated (p<0.05) with the amount of annual rainfall but the correlation coefficients were higher in the Control than Melatonin group. CONCLUSIONS: Melatonin implants are an effective means of improving lamb production of Merino ewes, especially in harsh environments where low annual rainfall limits the availability of food. When melatonin treatment was used, however, the responses of flocks on individual farms were difficult to predict because within a year, responses did not occur on all farms.


Subject(s)
Animal Husbandry/methods , Estrus/drug effects , Melatonin/pharmacology , Reproduction/drug effects , Sheep/physiology , Animals , Case-Control Studies , Drug Implants , Female , Logistic Models , Male , Melatonin/administration & dosage , Pregnancy , Rain , Spain
12.
Am J Physiol Cell Physiol ; 290(2): C638-49, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16162654

ABSTRACT

Decreases in the intracellular concentrations of both K(+) and Cl(-) have been implicated in playing a major role in the progression of apoptosis, but little is known about the temporal relationship between decreases in electrolyte concentration and the key events in apoptosis, and there is no information about how such decreases affect different intracellular compartments. Electron probe X-ray microanalysis was used to determine changes in element concentrations (Na, P, Cl, and K) in nucleus, cytoplasm, and mitochondria in U937 cells undergoing UV-induced apoptosis. In all compartments, the initial stages of apoptosis were characterized by decreases in [K] and [Cl]. The largest decreases in these elements were in the mitochondria and occurred before the release of cytochrome c. Initial decreases in [K] and [Cl] also preceded apoptotic changes in the nucleus. In the later stages of apoptosis, the [K] continued to decrease, whereas that of Cl began to increase toward control levels and was accompanied by an increase in [Na]. In the nucleus, these increases coincided with poly(ADP-ribose) polymerase cleavage, chromatin condensation, and DNA laddering. The cytoplasm was the compartment least affected and the pattern of change of Cl was similar to those in other compartments, but the decrease in [K] was not significant until after active caspase-3 was detected. Our results support the concept that normotonic cell shrinkage occurs early in apoptosis, and demonstrate that changes in the intracellular concentrations of K and Cl precede apoptotic changes in the cell compartments studied.


Subject(s)
Apoptosis/radiation effects , Cell Nucleus/chemistry , Cytoplasm/chemistry , Electrolytes , Mitochondria/chemistry , Animals , Cell Line, Tumor , Cell Nucleus/radiation effects , Chlorine/metabolism , Electron Probe Microanalysis , Humans , Lymphoma , Mitochondria/radiation effects , Phosphorus/metabolism , Potassium/metabolism , Sodium/metabolism , Ultraviolet Rays
13.
Apoptosis ; 10(6): 1317-31, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16215671

ABSTRACT

Although the identification of events that occur during apoptosis is a fundamental goal of apoptotic cell death research, little is know about the precise sequence of changes in total elemental composition during apoptosis. We evaluated total elemental composition (Na, Mg, P, Cl, S, and K) in relation to molecular and morphological features in human U937 cells induced to undergo apoptosis with staurosporine, an intrinsic pathway activator. To evaluate total elemental content we used electron probe X-ray microanalysis to measure simultaneously all elements from single, individual cells. We observed two phases in the changes in elemental composition (mainly Na, Cl and K). The early phase was characterized by a decrease in intracellular K (P<0.001) and Cl (P<0.001) content concomitant with cell shrinkage, and preceded the increase in proteolytic activity associated with the activation of caspase-3. The later phase started with caspase-3 activation, and was characterized by a decrease in the K/Na ratio (P<0.001) as a consequence of a significant decrease in K and increase in Na content. The inversion of intracellular K and Na content was related with the inhibition of Na+/K+ ATPase. This later phase was also characterized by a significant increase (P<0.001) in intracellular Cl with respect to the early phase. In addition, we found a decrease in S content and an increase in the P/S ratio. These distinctive changes coincided with chromatin condensation and DNA fragmentation. Together, these findings support the concept that changes in total elemental composition take place in two phases related with molecular and morphological features during staurosporine-induced apoptosis.


Subject(s)
Apoptosis/drug effects , Elements , Staurosporine/pharmacology , Caspase 3/metabolism , Cell Nucleus/drug effects , Cell Nucleus/enzymology , Cell Shape/drug effects , Cell Size/drug effects , Electrolytes/metabolism , Electron Probe Microanalysis , Enzyme Activation/drug effects , Humans , Protein Processing, Post-Translational/drug effects , Sodium-Potassium-Exchanging ATPase/metabolism , Time Factors , U937 Cells
14.
Anal Bioanal Chem ; 377(6): 1038-46, 2003 Nov.
Article in English | MEDLINE | ID: mdl-12955396

ABSTRACT

A wide range of pesticides used to control pests in vegetables have been determined in agricultural plant waste from beans, watermelons, and melons grown in greenhouses located in a predominantly agricultural area in Southeast Spain (Almería). Analysis of the pesticides was carried out by low-pressure gas chromatography (LP-GC) with mass spectrometry in tandem (MS-MS) mode, after extraction of the lyophilized samples with dichloromethane. The influence of the sample matrix on the analysis was avoided by use of matrix-matched standards. Linearity, detection limit ( LOD), quantitation limit ( LOQ), recovery, and precision for each pesticide were calculated. The most frequently encountered pesticides were endosulfan (>73% of the analyzed samples) and buprofezin (>55% of the samples), followed by cypermethrin, pirimifos-methyl, bifentrin, and chlorpyrifos (>30% of the samples). The pesticide found at the highest concentration level was endosulfan (223.33 mg kg(-1)) in a watermelon sample.


Subject(s)
Animal Feed/analysis , Gas Chromatography-Mass Spectrometry/methods , Pesticides/analysis , Plants/chemistry , Calibration , Citrullus/chemistry , Cucumis/chemistry , Environmental Pollutants/analysis , Fabaceae/chemistry , Plant Leaves/chemistry , Plant Stems/chemistry , Pressure , Reproducibility of Results , Sensitivity and Specificity , Spain , Time Factors
15.
Rapid Commun Mass Spectrom ; 17(18): 2099-106, 2003.
Article in English | MEDLINE | ID: mdl-12955740

ABSTRACT

A fast method for the determination of eight organotin compounds (OTs), monobutyltin (MBT), dibutyltin (DBT), tributyltin (TBT), tetrabutyltin (TeBT), monophenyltin (MPhT), diphenyltin (DPhT), triphenyltin (TPhT) and tetraphenyltin (TePhT), in water, sediments and mussels, was developed using low-pressure gas chromatography/tandem mass spectrometry (LPGC/MS/MS). The method is based on sodium diethyldithiocarbamate (DDTC) complexation of the ionic organotins, followed by extraction of the target matrices and derivatization by a Grignard reagent, as described in a previously published method for water samples. Solid-phase extraction was selected as extraction method from water samples after comparison with liquid-liquid extraction, but extraction of the OTs from sediment and mussel samples was performed using toluene. Matrix-matched calibration standards were used to minimize matrix effects. The analytical process was validated by the analysis of spiked blank samples. Performance characteristics such as linearity, detection limit (LOD), quantitation limit (LOQ), precision, and recovery were determined. Recoveries of OTs in spiked matrices ranged from 86-108% in water and from 78-110% in sediments and mussels, with precision values lower than 18%. Detection limits ranged from 0.1-9.6 ng L(-1) in water, and 0.03-6.10 microg kg(-1) in the other matrices. The present implementation of LPGC rather than conventional capillary GC permitted use of large-volume injection and reduced analysis time by a factor of two. The proposed methodology was applied to the determination of OTs in real samples of water, marine sediments and mussels from the west coast of the Mediterranean Sea (Spain).


Subject(s)
Bivalvia/chemistry , Gas Chromatography-Mass Spectrometry/methods , Geologic Sediments/chemistry , Organic Chemicals/analysis , Seawater/chemistry , Tin Compounds/analysis , Animals , Calibration , Molecular Structure , Pressure , Reproducibility of Results
16.
J Chromatogr A ; 1005(1-2): 131-41, 2003 Jul 11.
Article in English | MEDLINE | ID: mdl-12924788

ABSTRACT

An alternative to conventional capillary gas chromatography (GC) is evaluated as a new approach to determine pesticide residues in vegetables. Low-pressure gas chromatography-tandem mass spectrometry (LP-GC-MS-MS) is proposed after a fast and simple extraction of the vegetable samples with dichloromethane and without clean up. The use of the above-mentioned GC technique reduced the total time required to determine 72 pesticides to less than half the present time (31 min), increasing the capability of a monitoring routine laboratory. The use of guard column and plug of carbofrit into the glass liner in combination with LP-GC was evaluated. The method was validated with limits of quantitation low enough to determine the pesticide residues at concentrations below the maximum residue levels stated by legislation. In order to assess its applicability to the analysis of real samples, 25 vegetable samples previously determined using conventional-capillary GC-MS-MS were analysed by LP-GC-MS-MS. The results obtained with the compared techniques showed differences lower than 0.01 mg kg(-1).


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Pesticide Residues/analysis , Vegetables/chemistry , Pressure , Reproducibility of Results
17.
Anal Sci ; 19(5): 701-4, 2003 May.
Article in English | MEDLINE | ID: mdl-12769368

ABSTRACT

A new analytical method has been validated for determining the insecticide acetamiprid in vegetables using gas chromatography (OC) and different mass spectrometric detection techniques, such as full-scan mass spectrometry (MS), and tandem mass spectrometry (MS/MS). For this purpose, a previous extraction of the vegetable sample was carried out with ethyl acetate. In GC-MS/MS, the lowest detectable concentration was 0.001 mg kg(-1), the average recovery rates at various fortification levels (0.015 and 0.030 mg kg(-1)) ranged between 82.4 and 85.7% and the relative standard deviations were lower than 12.2% in all cases.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Pyridines/analysis , Vegetables/chemistry , Neonicotinoids , Reproducibility of Results
18.
Rapid Commun Mass Spectrom ; 16(12): 1216-24, 2002.
Article in English | MEDLINE | ID: mdl-12112274

ABSTRACT

A rapid multiresidue method for the analysis of 72 pesticides has been developed using a single injection with low-pressure gas chromatography/tandem mass spectrometry (LP-GC/MS/MS). The LP-GC/MS/MS method used a short capillary column of 10 m x 0.53 mm i.d. x 0.25 microm film thickness coupled with a 0.6 m x 0.10 mm i.d. restriction at the inlet end. Optimal LP-GC conditions were determined which achieved the fastest separation in MS/MS detection mode. Also MS/MS conditions were optimized in order to increase sensitivity and selectivity. The analytical parameters of the LP-GC/MS/MS method were compared with those obtained by GC/MS/MS using a conventional capillary column (30 m x 0.25 mm i.d. x 0.25 microm film thickness). Better precision and sensitivity values were obtained with the LP-GC/MS/MS approach. The limits of detection (LOD) of the compounds ranged from 0.1 to 14.1 microg L(-1) for LP-GC/MS/MS, lower than those obtained for conventional GC/MS/MS that ranged from 0.1 to 17.5 microg L(-1). The peak widths obtained with the short column in LP-GC are similar to those obtained using conventional capillary GC columns, and the peaks can be successfully identified by MS/MS detection with the conventional scan speed of ion-trap instruments. In addition, the analysis time was significantly reduced with LP-GC/MS/MS (32 min) versus GC/MS/MS (72 min), allowing the number of samples analyzed per day in a routine laboratory to be doubled.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Pesticide Residues/analysis , Gas Chromatography-Mass Spectrometry/instrumentation , Pesticide Residues/classification , Sensitivity and Specificity , Time Factors , Workload
19.
J Chromatogr A ; 959(1-2): 203-13, 2002 Jun 14.
Article in English | MEDLINE | ID: mdl-12141546

ABSTRACT

A new analytical method was devised using gas chromatography with tandem mass spectrometry (GC-MS-MS) for the routine analysis of 31 multi-class pesticide residues and approximately 8000 fresh fruit and vegetable samples (green bean, cucumber, pepper, tomato, eggplant, watermelon, melon, and marrow). Extraction of the pesticides with dichloromethane was carried out. The optimal ionization mode, either electron impact or chemical ionization, was selected for each pesticide in the same run. Carbofrit was used in the liner and combined with the selectivity of the detector this avoided additional clean-up. Thus, not only was money and time saved, the uncertainty of the method was decreased in its application to routine analysis. The average recoveries in cucumber obtained for each pesticide ranged between 71 and 119% at two different fortification levels (n=10 each) that ranged between 7 and 300 ng g(-1) (depending on the pesticide). The relative standard deviation was lower than 19% for all compounds tested. The calculated limits of detection and quantification were typically <1 ng g(-1) which were much lower than the maximum residue levels established by European legislations.


Subject(s)
Fruit/chemistry , Gas Chromatography-Mass Spectrometry/methods , Pesticides/analysis , Vegetables/chemistry , Reproducibility of Results , Sensitivity and Specificity
20.
Rapid Commun Mass Spectrom ; 16(11): 1106-15, 2002.
Article in English | MEDLINE | ID: mdl-11992515

ABSTRACT

The use of gas chromatography/tandem mass spectrometry (GC/MS/MS) applied to determine multiple pesticide residues in fresh vegetables has been thoroughly studied. A single injection method to detect, confirm and quantify 54 multiclass pesticides has been developed and applied in a routine analysis laboratory. The proposed method consists of a rapid extraction of 15 g of vegetable sample with dichloromethane. An additional clean-up step is not necessary even when injecting 10 microL of extract. Instead the gas chromatograph was fitted with a carbofrit inserted into the glass liner and a guard column. In addition, the detection mode chosen (MS/MS) provides additional selectivity. The method has been validated and applied to 1300 samples in a routine laboratory following specified quality criteria. The recovery efficiencies obtained for all the pesticides ranged between 70.2 and 110.8% at two different fortification levels. The relative standard deviation for quantification (RSD) was lower than 16.7% for all the compounds. Important experimental parameters, such as the conditioning of carbofrit, overload of the analytical column, and cleanliness of the ion trap, were evaluated for their influence on the performance of the method.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Pesticide Residues/analysis , Vegetables/chemistry , Gas Chromatography-Mass Spectrometry/instrumentation , Spectrometry, Mass, Electrospray Ionization/instrumentation , Spectrometry, Mass, Electrospray Ionization/methods
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