Biomedical subjects

Jacek Namieśnik

Publications and source records attributed to Jacek Namieśnik.

At least 19 recordsLinked to original sources

PubMed2006

Trends in solventless sample preparation techniques for environmental analysis.

The paper presents recent trends in solventless sample preparation techniques for environmental analysis. First, a general classification of solventless methods is given. Next, three of them, treated as preferable techniques, i.e. SPME, SDME and HS, are presented in detail, with respect to their usability and effectiveness for environmental samples. Examples of all discussed techniques are given in the tables.

Chromatography↗

PubMed2006

Study of the selection mechanism of heavy metal (Pb2+, Cu2+, Ni2+, and Cd2+) adsorption on clinoptilolite.

The study was carried out on the sorption of heavy metals (Ni2+, Cu2+, Pb2+, and Cd2+) under static conditions from single- and multicomponent aqueous solutions by raw and pretreated clinoptilolite. The sorption has an ion-exchange nature and consists of three stages, i.e., the adsorption on the surface of microcrystals, the inversion stage, and the moderate adsorption in the interior of the microcrystal. The finer clinoptilolite fractions sorb higher amounts of the metals due to relative enriching by the zeolite proper and higher cleavage. The slight difference between adsorption capacity of the clinoptilolite toward lead, copper, and cadmium from single- and multicomponent solutions may testify to individual sorption centers of the zeolite for each metal. The decrease of nickel adsorption from multicomponent solutions is probably caused by the propinquity of its sorption forms to the other metals and by competition. The maximum sorption capacity toward Cd2+ is determined as 4.22 mg/g at an initial concentration of 80 mg/L and toward Pb2+, Cu2+, and Ni2+ as 27.7, 25.76, and 13.03 mg/g at 800 mg/L. The sorption results fit well to the Langmuir and the Freundlich models. The second one is better for adsorption modeling at high metal concentrations.

Adsorption↗

PubMed2006

Application of the chromatographic retention index system for the estimation of the calibration constants of permeation passive samplers with polydimethylsiloxane membranes.

The paper presents the results of research on the calibration of permeation passive samplers equipped with polydimethylsiloxane (PDMS) membranes using the physico-chemical properties of the analytes. Strong correlations were found between the calibration constants of the samplers and the linear temperature-programmed retention indices of the analytes determined on columns coated with pure PDMS (r2 = 0.914). These correlations make it possible to estimate the calibration constants for unidentified analytes, which is impossible when using conventional procedures. This, in turn, enables the deployment of permeation passive samplers in the same way in which active samplers are deployed. The reproducibility of the calibration constants determined in different laboratories and retention indices determined using different chromatographic systems was very good, indicating that the calibration constants estimated using this approach should be reproducible as well. The approach proposed should lead to more widespread use of permeation passive samplers.

Calibration↗

PubMed2005

Porous structure of natural and modified clinoptilolites.

The evaluation of the pore-size distribution (PSD) of natural and modified mesoporous zeolites, i.e., clinoptilolites is presented. We demonstrate the SEM results showing that the pores of fracture-type from 25-50 nm to 100 nm in size between clinoptilolite grains, as well as pores between crystal aggregates up to 500 nm in size are present in the studied material. The detailed distribution of pore sizes and tortuosity factor of the above-mentioned materials are determined from the adsorption-desorption isotherms of nitrogen measured volumetrically at 77 K. To obtain the reliable pore size distribution (PSD) of the above-mentioned materials both adsorption and desorption branches of the experimental hysteresis loop are described simultaneously by recently developed corrugated pore structure model (CPSM) of Androutsopoulos and Salmas. Evaluated pore size distributions are characterized by well-defined smooth peaks placed in the region of the mesoporosity. Moreover, the mean pore diameter calculated from the classical static measurement of nitrogen adsorption at 77 K correspond very well to the pore diameters from SEM, showing the applicability of the CPSM for characterization of the porosity of natural zeolites. We conclude that classical static adsorption measurements combined with the proper modeling of the capillary condensation/evaporation phenomena are a powerful method which can be applied for pore structure characterization of natural and modified clinoptilolites.

Microscopy, Electron↗

PubMed2005

Relationships and bioaccumulation of chemical elements in the Baikal seal (Phoca sibirica).

Concentrations of Al, Ba, Cd, Cu, Fe, Mn, Mo, Si, Sr, Zn, Ca, K, Mg, Na and P in the livers of Baikal seal, plankton, zoobenthos, and fish, constituting the food sources for the seals, were determined by ICP-MS and ICP-AES. The accumulation of elements in the liver of seals, affected by internal and external (environmental) factors, was assessed by multidimensional (ANOVA, FA) and correlation analyses. FA has enabled identification of abiotic and biotic factors responsible for the accumulation of elements in the livers of Baikal seals. Significant influence of sex and development stage of the seals analysed on hepatic concentrations of some elements was found. The observed differences in element concentrations between pups, males and females could be attributable to the reproductive cycle of this species. ANOVA showed differences in concentrations of Fe, Zn, Cu and Cd in seals from the three separate basins of the lake. BMFs suggest biomagnification of Fe and Zn in the fish-seal trophic link.

Animals↗

PubMed2005

Volatile organohalogen compounds in human urine: the effect of environmental exposure.

The paper presents the results of determination of volatile organohalogen compounds (VOX) in urine samples from subjects exposed to these compounds in their workplaces and through consumption of chlorinated tap water. The analytes were isolated and preconcentrated from the complex urine samples using the thin layer headspace (TLHS) technique with autogenous generation of the liquid sorbent. Final gas chromatographic determination was carried out by direct aqueous injection with electron capture detection (DAI-ECD). The results indicate that only a small fraction (<4%) of the VOX input is excreted with urine in the non-metabolized form. A positive correlation was found between the occupational levels of VOX in the workplace and their levels in urine. VOX levels in the urine of subjects not exposed to them in the workplace were significantly lower. Their presence in the organisms was most probably related to consumption of tap water produced by chlorination of surface waters.

Drinking↗

PubMed2005

Determining PAHs and PCBs in aqueous samples: finding and evaluating sources of error.

This work describes the problems that occur during routine multi-step determinations of polyaromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), which can be present at trace levels in water, and identifies sources of analyte losses at particular steps during the analytical procedure. PAH and PCB adsorption onto the walls of the container ranged from 0 to 70%. PAH and PCB recoveries of >70% were achieved during the LLE and SPE extraction steps. During the process of enriching the dichloromethane extract with PAHs and PCBs, based on the gentle evaporation of solvent, losses were <24% and <19%, respectively. Model experiments show that neither isolation of PAHs and PCBs (performed using either LLE or SPE) nor extract enrichment reduce the reliability of PAH and PCB determination. The steps that lead to the greatest loss of analyte are the ones that involve sampling, transport and storage of the water samples.

Journal Article↗

PubMed2005

Chemically modified glass fiber as a matrix-free reference material for volatile compounds.

Difficulties with obtaining suitable reference materials, which are applied for validation of analytical procedures and calibration of measured devices used in gaseous examinations (atmospheric air, indoor air, workplace atmosphere), are one of the most important challenges that stand in front of analytics. Known gaseous standard mixtures preparation techniques, both static and dynamic, are burdened with lots of inconveniences and disadvantages, which can be responsible for false analytical results. It appears that a very important step in the way of obtaining suitable reference materials useful in gaseous analysis is the technique of thermal decomposition of surface compounds. The paper describes a new type of matrix-free reference material-chemically modified glass fiber, which significantly makes it easier and simplifies the usage of reference materials produced using this technique.

Letter↗

PubMed2005

Ammonium sorption from aqueous solutions by the natural zeolite Transcarpathian clinoptilolite studied under dynamic conditions.

The scope of this study is ammonium-ion uptake from synthetic aqueous solutions onto raw and pretreated forms of the natural zeolite Transcarpathian clinoptilolite under dynamic conditions. Hydrogen ions displaced exchangeable cations on the clinoptilolite in distilled water (sodium ions) and hydrochloric acid (sodium, potassium, and calcium ions) and destroyed the zeolite framework structure in the last case. Ammonium uptake onto the zeolite occurs by exchange with Na(+), Ca(2+), and K(+) ions. Although Na(+) ions were observed to be more easily exchanged for both hydrogen and ammonium ions, the role of Ca(2+) ions increased with zeolite saturation by NH(+)(4) ions. The maximum sorption capacity of the clinoptilolite toward NH(+)(4) ions, estimated under dynamic conditions, is significantly higher than that measured under static conditions; proximity of the values of a distribution coefficient and a retardation factor for different conditions (215-265 dm(3)/kg and 979-1107, respectively) allows us to use these parameters to model ammonium uptake onto the clinoptilolite. Slowing down or interruption in filtration resulted in the improvement of ammonium sorption properties of the zeolite. The ammonium removal improves with use of the finer fractions of the clinoptilolite up to 0.35 mm. A recycling study results confirmed the importance of external diffusion for ammonium sorption by the clinoptilolite. Preliminary treatment of the sorbent confirmed the predominant importance of the ion-exchange mechanism. The advantage of prior NaCl treatment of the clinoptilolite in improvement of ammonium removal over the other techniques was shown.

Journal Article↗

PubMed2004

Passive sampling and/or extraction techniques in environmental analysis: a review.

The current state-of-the-art of passive sampling and/or extraction methods for long-term monitoring of pollutants in different environmental compartments is discussed in this review. Passive dosimeters that have been successfully used to monitor organic and inorganic contaminants in air, water, sediments, and soil are presented. The application of new approaches to the determination of pollutants at the sampling stage is discussed. The main milestones in the development of passive techniques for sampling and/or extraction of analytes, and in biomonitors used in environmental analysis, are summarized in this review. Passive samplers and biomonitors are compared.

Journal Article↗

PubMed2004

Organotin compounds in the liver tissue of marine mammals from the Polish coast of the Baltic Sea.

Butyltins (BTs) and phenyltins (PhTs) were determined in the livers of marine mammals found by-caught or stranded along the Polish coast of the Baltic Sea. During the investigation an original analytical method was developed. Butyltin compounds were detected in all the liver samples, whereas phenyltins were not detected in any of the samples. The total concentrations of BTs ranged from 43.9 to 7698 ng(Sn) x g(-1) dry weight. Age-related trends to accumulate BTs in immature porpoises were found. At the same time there were no male-female differences in BTs concentrations observed. No statistically significant spatial distribution differences were found between the locations corresponding to the open Baltic Sea waters and inside the Gulf of Gdańsk, which is characterized by high maritime activity. In comparison to butyltin levels in marine mammals from other geographic regions, the samples analyzed indicate a significant degree of tributyltin pollution along the Polish coast of the Baltic Sea. On the basis of a literature review, higher BT levels are usually found in waters close to highly industrialized areas, such as Japan, Hong Kong, and the United States.

Age Factors↗

PubMed2004

Monitoring of organic pollutants in coastal waters of the Gulf of Gdańsk, Southern Baltic.

This paper presents an overview of changes in organic pollution of coastal waters of the Gulf of Gdańsk (Baltic Sea). Toxic pollutants including volatile organic compounds (VOC), volatile organohalogen compounds (VOX), chlorophenols, phenoxyacids, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) were determined in seawater from the Gulf of Gdańsk coastal waters in the period 1996-2001. In the case of the Gulf of Gdańsk, non-conservative behaviour of VOC was observed due to random temporal and spatial of inputs along the Vistula estuary and to the dilution of VOC-enriched river water with seawater. The concentrations of VOX in seawater decreased throughout the period and the concentrations of VOX were in the range of few ng dm(-3) up to 250 ng dm(-3), similar to estuaries elsewhere. The average concentrations of chlorophenols and phenoxyacids were between 0.1 and 6.0 and 0.05 and 2.2 microg dm(-3), respectively. However, remarkably high concentrations of 2,4-dichlorophenol (6 microg dm(-3)) were obtained in samples collected from the Vistula River. Generally concentrations of PCBs did not exceed few ng dm(-3) with the exception of 1999, when all samples exhibited elevated concentrations of PCBs. In addition, higher concentrations of PCBs in the open sea compared to river waters suggested localised inputs. Due to the ability of most organic pollutants to bioaccumulate and biomagnify, especially the persistent organic pollutants, continued monitoring is of crucial importance for the health of marine life in the Gulf of Gdańsk.

Animals↗

PubMed2004

Abnormal features of Macoma balthica (Bivalvia) in the Baltic Sea: alerting symptoms of environmental adversity?

Recent studies of the Baltic clam Macoma balthica (L.) from the southern Baltic (the Gulf of Gdansk) have revealed striking morphological, histological and cytogenetic features. Strong deformation of the shell, including elongation of the posterior end and the appearance of an easily visible flexure in this part, has been recorded. The population contribution of the deformed blunt shelled ("irregular") clams ranged from 0% to 65% and tended to increase with depth. The morphologically "irregular" clams had higher accumulated tissue concentrations of trace metals (As, Ag, Cd, Pb, Cu and Zn), indicating a different metal handling ability. Adverse conditions in deeper water regions of the Gulf (e.g. hypoxia, hydrogen sulphide, elevated bioavailability of contaminants) have been suggested as inducers of the phenotypical changes (morphological deformation) in part of the population and, in parallel, of the specific physiological adaptations that result in higher metal accumulation in the "irregular" clams. Cytogenetic and histological analyses showed the presence of tumours in gill cells and digestive system of the affected clams, the prevalence of disseminated neoplasia ranging from 0% to 94% depending on the site. The disease was manifested by a modified karyotype (i.e. an abnormal number and morphology of chromosomes), a higher activity of nucleolar organizer regions (AgNORs), and tissue lesions (enlarged cells, actively proliferative with pleomorphic nuclei). Bottom sediments showed acute toxicity and have been proposed as a source of an initialising carcinogenic factor. However, none of the ecotoxicological studies provided was successful in the clear demonstration of a single (or multifactorial) agent that can account for the disseminated neoplasia.

Animals↗

PubMed2003

Determination of volatile aliphatic amines in air by solid-phase microextraction coupled with gas chromatography with flame ionization detection.

Practical aspects of the application of solid-phase microextraction (SPME) to the determination of volatile aliphatic amines in air are described. Analytes included methylamine (MA), ethylamine (EA), dimethylamine (DMA), diethylamine (DEA), trimethylamine (TMA) and triethylamine (TEA). New SPME stationary phases were examined. The effects of relative humidity and temperature on analytes uptake were taken into account in analysis. Gas chromatography (GC) with flame ionization detector (FID) was used for the final analysis.

Air↗

PubMed2003

Calibration of permeation passive samplers with silicone membranes based on physicochemical properties of the analytes.

Passive sampling is a very attractive alternative to active sampling due to its simplicity and low cost. Among the passive samplers used in air analysis, permeation passive samplers are the least affected by ambient conditions, including humidity, air currents, and temperature changes. The biggest drawback of permeation passive samplers is the need to calibrate them experimentally for each individual target analyte. The paper presents the results of research on the calibration of permeation passive samplers based on physicochemical properties of the analytes. Strong correlations were found between the calibration constants of the samplers and the number of carbon atoms among families of compounds (R2 ranging from 0.8507 for alcohols to 0.9995 for aromatic hydrocarbons), the molecular weights of the compounds (R2 = 0.8742), their boiling points (R2 = 0.8911), and linear temperature-programmed retention indexes (R2 = 0.9225). The last correlation makes it possible to estimate the calibration constants for unidentified analytes, which is impossible when the conventional procedure is used. This makes it possible to deploy permeation passive samplers in the same way in which active sampling is deployed.

Journal Article↗

PubMed2003

Physical, chemical, and biological changes in the Gulf of Gdańsk ecosystem (southern Baltic sea).

This review presents the present state of knowledge of the physical, chemical, and biological changes in waters of the Gulf of Gdańsk (Baltic Sea). The general characteristics of the Baltic Sea and the Gulf of Gdańsk with brief description of changes in the ecosystem are included. Among meteorological parameters describing climate in the coastal zone, water temperature changes together with considerations of precipitation and sea level are presented. It has been confirmed that the sea level rise over the past 40 yr was very distinct. Throughout the past 30 yr an evident increase in eutrophication has been observed. Therefore, changes in salinity, oxygen content, and nutrient fluctuations with special attention paid to variability in silicate, nitrate, and phosphate concentrations in the water layer are presented. Also, discussion on the presence of toxic pollutants, such as heavy metals, PCBs, PAHs, and some pesticides, in the water body of the Gulf of Gdańsk has been included. Because of their ability to bioaccumulate and biomagnify in living organisms, these substances are of crucial importance for future marine life in the Gulf of Gdańsk. Finally, biological conditions of the coastal waters of the Gulf of Gdańsk were discussed. Data show that the ecosystem structure of the Gulf of Gdańsk has undergone tremendous changes. The species pattern has changed significantly--many species have disappeared and others have become dominant.

Animals↗

PubMed2003

Organic pollutants in the Odra river ecosystem.

The paper presents the results of the analysis of water and bottom sediment samples from different locations along the Odra river, collected during eight campaigns in the years 1997-2000. All the basic organic pollutants were determined. Pollution of water with PCBs was negligible while with PAHs was not critical. Concentrations of volatile organochlorine compounds in water were the highest in Brzeg Dolny and its surroundings. Concentrations of tetrachloroethene were exceptionally high in the Szczecin Lagoon. The Odra sediments were non-polluted or only slightly polluted with PCBs, pesticides and different classes of volatile organic pollutants. However, PAHs were present in rather large concentrations, especially in the upper course of the Odra river. The data obtained contributed to the evaluation of pollutants discharges to the Baltic sea via Szczecin Lagoon as well as to the characterization of pollution sources (point sources and area sources) in the Odra catchment area.

Environment↗

PubMed2003

Relationship between volatile organohalogen compounds in drinking water and human urine in Poland.

Selected volatile organohalogen compounds (VOX) were investigated in urine samples from people living in different areas of the Gdańsk-Sopot-Gdynia TriCity (Poland). The analytes were isolated and preconcentrated using the so-called thin layer headspace technique with autogenous generation of the liquid sorbent. Final gas chromatographic determination was carried out by direct aqueous injection with electron capture detection. Analyte concentrations in drinking water ranged from not detected to approximately 8 microg/l (chloroform), depending on the source of drinking water in a given part of the TriCity (underground, surface or mixed). The corresponding urine levels were typically lower by about an order of magnitude. VOX levels in urine of people living in the parts of the TriCity supplied with drinking water containing elevated levels of the analytes were higher than the levels in urine of people whose drinking water originated from deep underground wells. The linear correlation coefficients for the relationships between total VOX and chloroform levels in drinking water and in urine were r2=0.65 and 0.88, respectively. The fraction of VOX excreted with urine in unchanged form did not exceed 20%.

Chloroform↗