Toxicological assessment of TiO2 nanoparticles by recombinant Escherichia coli bacteria

Rapid and efficient methods to assess nanoparticle toxicity are desired in current research. Here we showed that Escherichia coli labeled by green fluorescent protein can be a good model bacterium for assessing acute toxicity of TiO(2) (about 50% inhibition ratios after 135 min exposure). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed that TiO(2) nanoparticles (NPs) can influence certain protein expression in the recombinant bacterium, and the obvious effects in repressed expression and elevated expression were observed in 30/40, 10/20 μg mL(-1) treated cells, respectively. However, the GFP expression (27 kD) was not influenced by introduced TiO(2) NPs. The change of the fluorescence intensity may be caused by the damage in folding and chromophore formation of the GFP post-translational modification due to generated reactive oxygen species. Furthermore, TiO(2) NPs at higher concentrations decreased their toxicity because of aggregation. 20 μg mL(-1) humic acid (HA) introduced to the medium can decrease the fluorescent inhibition owing to the barrier of steric hindrance it provides between NPs and cells.     

Characterization and environmental implications of nano- and larger TiO(2) particles in sewage sludge, and soils amended with sewage sludge

Titanium dioxide (TiO(2)) is the most extensively used engineered nanoparticle to date, yet its fate in the soil environment has been investigated only rarely and is poorly understood. In the present study, we conducted two field-scale investigations to better describe TiO(2) nano- and larger particles in their most likely route of entry into the environment, i.e., the application of biosolids to soils. We particularly concentrated on the particles in the nano-size regime due to their novel and commercially useful properties. First, we analyzed three sewage sludge products from the US EPA TNSSS sampling inventory for the occurrence, qualitative abundance, and nature of TiO(2) nano- and larger particles by using analytical scanning electron microscopy and analytical (scanning) transmission electron microscopy. Nano- and larger particles of TiO(2) were repeatedly identified across the sewage sludge types tested, providing strong evidence of their likely concentration in sewage sludge products. The TiO(2) particles identified were as small as 40 nm, and as large as 300 nm, having faceted shapes with the rutile crystal structure, and they typically formed small, loosely packed aggregates. Second, we examined surface soils in mesocosms that had been amended with Ag nanoparticle-spiked biosolids for the occurrence of TiO(2) particles. An aggregate of TiO(2) nanoparticles with the rutile structure was again identified, but this time TiO(2) nanoparticles were found to contain Ag on their surfaces. This suggests that TiO(2) nanoparticles from biosolids can interact with toxic trace metals that would then enter the environment as a soil amendment. Therefore, the long-term behavior of TiO(2) nano- and larger particles in sewage sludge materials as well as their impacts in the soil environment need to be carefully considered.     

Impact of agglomeration and different dispersions of titanium dioxide nanoparticles on the human related in vitro cytotoxicity and genotoxicity

The published results on nanoparticles cytotoxicity and genotoxicity such as titanium dioxide nanoparticles (TiO(2) NPs) are inconsistent, and often conflicting and insufficient. Since different parameters may have impact on the toxicity results, there is need to lay stress on detailed characterization of NPs and the use of different testing conditions for assessment of NPs toxicity. In order to investigate whether dispersion procedures influence NP cytotoxicity and genotoxicity, we compared two protocols giving TiO(2) NP dispersions with different stability and agglomeration states. Detailed primary and secondary characteristics of both TiO(2) NP dispersions in culture media were carried out before toxicological testing; TK6 human lymphoblast cells, EUE human embryonic epithelial cells and Cos-1 monkey kidney fibroblasts were used to assess cytotoxicity (by trypan blue exclusion, proliferation activity and plating efficiency assays) and genotoxicity (by the comet assay). DNA strand breaks were detected by the alkaline comet assay. DNA oxidation lesions (especially 8-oxo-7,8-dihydroguanine, 8-oxoG) were measured with a modified comet assay including incubation with specific repair enzyme formamidopyrimidine DNA glycosylase (FPG). The TiO(2) NPs dispersion with large agglomerates (3 min sonication and no serum in stock solution) induced DNA damage in all three cell lines, while the TiO(2) NPs dispersed with agglomerates less than 200 nm (foetal serum in stock solution and sonication 15 min) had no effect on genotoxicity. An increased level of DNA oxidation lesions detected in Cos-1 and TK6 cells indicates that the leading mechanism by which TiO(2) NPs trigger genotoxicity is most likely oxidative stress. Our results show that the dispersion method used can influence the results of toxicity studies. Therefore at least two different dispersion procedures should be incorporated into assessment of cyto- and genotoxic effects of NPs. It is important, when assessing the hazard associated with NPs, to establish standard testing procedures and thorough strategies to consider the diverse conditions relevant to possible exposures.     

Preparation and measurement methods for studying nanoparticle aggregate surface chemistry

Despite best efforts at controlling nanoparticle (NP) surface chemistries, the environment surrounding nanomaterials is always changing and can impart a permanent chemical memory. We present a set of preparation and measurement methods to be used as the foundation for studying the surface chemical memory of engineered NP aggregates. We attempt to bridge the gap between controlled lab studies and real-world NP samples, specifically TiO(2), by using well-characterized and consistently synthesized NPs, controllably producing NP aggregates with precision drop-on-demand inkjet printing for subsequent chemical measurements, monitoring the physical morphology of the NP aggregate depositions with scanning electron microscopy (SEM), acquiring "surface-to-bulk" mass spectra of the NP aggregate surfaces with time-of-flight secondary ion mass spectrometry (ToF-SIMS), and developing a data analysis scheme to interpret chemical signatures more accurately from thousands of data files. We present differences in mass spectral peak ratios for bare TiO(2) NPs compared to NPs mixed separately with natural organic matter (NOM) or pond water. The results suggest that subtle changes in the local environment can alter the surface chemistry of TiO(2) NPs, as monitored by Ti(+)/TiO(+) and Ti(+)/C(3)H(5)(+) peak ratios. The subtle changes in the absolute surface chemistry of NP aggregates vs. that of the subsurface are explored. It is envisioned that the methods developed herein can be adapted for monitoring the surface chemistries of a variety of engineered NPs obtained from diverse natural environments.     

Acute and reproductive toxicity of nano-sized metal oxides (ZnO and TiO₂) to earthworms (Eisenia fetida)

An increase in nanomaterial applications will likely lead to an increased probability of environmental exposures, raising concerns regarding the safety of these materials. Recent studies have indicated that manufactured nanomaterials, such as metal oxides, have the potential to be harmful to aquatic and terrestrial organisms. The majority of nano-metal oxide research addressing potential toxicological issues has been focused in aquatic environments with very little terrestrial data. This study characterized the acute and reproductive toxicity of zinc oxide (ZnO) and titanium dioxide (TiO(2)) to earthworms (Eisenia fetida) in a terrestrial system. Following a 14 d exposure, nano-sized ZnO on filter paper was acutely toxic to E. fetida, while nano-sized TiO(2) did not exhibit acute toxicity. In contrast, neither nano-sized ZnO nor TiO(2) exhibited acute toxicity to earthworms in sand. Both nano-sized ZnO and TiO(2), following a 4 week exposure, caused reproductive effects in earthworms in artificial soil. Overall, nano-sized ZnO exhibited greater toxicity than nano-sized TiO(2) in Eisenia fetida.     

Preparation of 2-mercaptobenzothiazole-derivatized mesoporous silica and removal of Hg(ii) from aqueous solution

Mesoporous silicas (SBA-15 and MCM-41) have been functionalized by two different methods. Using the heterogeneous route the silylating agent, 3-chloropropyltriethoxysilane, was initially immobilized onto the mesoporous silica surface to give the chlorinated mesoporous silica Cl-SBA-15 or Cl-MCM-41. In a second reaction a multifunctionalized N,S donor compound (2-mercaptobenzothiazol) was incorporated to obtain the functionalized silicas denoted as MBT-SBA-15-Het and MBT-MCM-41-Het. Using the homogeneous route, the functionalization was achieved via the one step reaction of the mesoporous silica with an organic ligand containing the chelating functions, to give the modified mesoporous silicas denoted as MBT-SBA-15-Hom or MBT-MCM-41-Hom. The functionalized mesoporous silicas were employed as adsorbents for the regeneration of aqueous solutions at pH 6 contaminated with Hg(ii) at room temperature. Results obtained indicate that mercury adsorption was higher in the mesoporus silicas prepared by the homogeneous method, and the maximum adsorption value (0.24 +/- 0.02 mmol Hg(ii) g(-1)) was obtained for MBT-SBA-15-Hom. The chemically stability in acid medium of the functionalized silicas, possibility its regeneration washing with concentrate HCl, resulting in the reuse of the adsorbent material for several cycles.     

TiO2 and ZnO nanoparticles negatively affect wheat growth and soil enzyme activities in agricultural soil

The properties of nanoparticles and their increased use have raised concerns about their possible harmful effects within the environment. Most studies on their effects have been in aqueous systems. Here we investigated the effect of TiO(2) and ZnO nanoparticles on wheat growth and soil enzyme activities under field conditions. Both of the nanoparticles reduced the biomass of wheat. The TiO(2) nanoparticles were retained in the soil for long periods and primarily adhered to cell walls of wheat. The ZnO nanoparticles dissolved in the soil, thereby enhancing the uptake of toxic Zn by wheat. The nanoparticles also induced significant changes in soil enzyme activities, which are bioindicators of soil quality and health. Soil protease, catalase, and peroxidase activities were inhibited in the presence of the nanoparticles; urease activity was unaffected. The nanoparticles themselves or their dissolved ions were clearly toxic for the soil ecosystem.     

磁性硅基介孔材料对水中微囊藻毒素的吸附研究

采用水热合成法可控合成了磁性Fe 3O 4@SiO 2和Fe 3O 4@SiO 2@Cu^2+球状核壳介孔材料,研究了模板剂的种类及去除方式对形貌的影响,并将材料用作固相萃取剂选择性吸附水中微囊藻毒素,结合高效液相色谱定量分析来研究其对MC-LR的吸附性能。实验表明,十六烷基三甲基溴化铵(CTAB)模板剂更有利于壳层的形成,3次乙醇振荡萃取的方式对于两种材料均可达到很好的模板剂去除效果,对MC-LR的吸附率分别达到85%和95%以上,而马弗炉煅烧方式则适用于Fe 3O 4@SiO 2@Cu^2+介孔材料的制备。太湖水样中MC-LR的去除实验表明,两种材料能够很好地应用于实际水样处理。     

Trace metal concentrations in tidal flat coastal sediments, Yamaguchi Prefecture, southwest Japan

Geochemical investigations of tidal flat coastal sediments at Ogori, Ozuki, and Kasado in Yamaguchi Bay of southwest Japan were conducted to determine their metal concentrations and to assess contamination levels, compared with sediment quality guidelines (SQG) and several pollutant indicators. Selected major oxides, trace elements, and total sulfur (TS) were determined by X-ray fluorescence. pH values of most samples were alkaline, indicating anoxic conditions. Average abundances of As, Pb, Zn, Cu, Ni, and Cr in Ozuki sediments were 11, 27, 109, 21, 19, and 52 mg/kg, respectively, compared to 9, 29, 80, 16, 18, and 42 mg/kg at Ogori and 12, 27, 151, 34, 30 and 80 mg/kg at Kasado, respectively. Average concentrations of As, Zn, and Cu in all samples and TiO(2), Fe(2)O(3), and P(2)O(5) at Kasado were greater than those of the upper continental crust. Contamination levels were assessed based on SQG, contamination factors (CF), pollution load index (PLI), enrichment factor (EF), and index of geoaccumulation (Igeo). According to the SQG of the US EPA, the sediments were heavily polluted with respect to As, whereas Zn, Cu, Ni, and Cr were classed as moderately polluted. The elevated CF values of As, Pb, and Zn identify moderate to considerable contamination, indicating that these metals are potentially toxic in the study area. Based on PLI and EF, the study sites are moderate to moderately severe polluted with As and Pb, moderately polluted with Zn, and weakly contaminated to noncontaminated with Cu, Ni, and Cr. The highest Igeo values for As, Pb, and Zn in the surface and core sediments reflected the tendency of metal contamination that seems to be related to their fine-grained nature, organic matter-rich sediments, and anthropogenic point sources. Trace metal contents were strongly correlated with Fe(2)O(3) and TiO(2), suggesting that Fe oxyhydroxides and detrital clastic load play a role in controlling abundances in the study area.     

Ozone Destruction on Solid Particles

Ozone (O3) is an important constituent of the Earth atmosphere, either stratosphere, where it has a beneficial role to protect Earth's surface from harmful UV-B radiation, or troposphere where it is considered an air pollutant. We investigated the ozone destruction on solid particles of natural or anthropogenic origin as: silica-gel, pollen, coal fly ash, titanium dioxide with different specific surface (s) and sodium halides (NaCl, NaBr and NaI). The experiments were conducted in a fluidized bed reactor with elevated ambient concentrations of O3 (100 ppb) employed. The results indicate that the destruction of O3 depends upon: sample quantity (silica-gel with equal s), sample surface (TiO2 with different s) and chemical composition (coal fly ash comparative to wood ash). Interesting results were obtained with sodium halides: no effect on O3 concentrations was detected with NaCl, NaBr shows a certain destruction, while NaI removes completely O3 from the air stream. In the experiments with NaI doped NaCl, the destruction of O3 was dependent on NaI quantity.     

Spatial distribution, electron microscopy analysis of titanium and its correlation to heavy metals: occurrence and sources of titanium nanomaterials in surface sediments from Xiamen Bay, China

Titanium nanomaterials are likely to sink into sediments in substantial quantities due to their wide use in a number of applications for decades. To assess the potential environmental consequences, a better understanding is required of the occurrence and sources of titanium (Ti) nanomaterials in sediments. In this research, we provide the first report of the Ti concentrations and the morphology and composition of Ti-based solids in surface sediments from Xiamen Bay, China. Results indicated that the anthropogenic Ti concentrations in the surface sediments from Xiamen Bay reached approximately 2.74 g kg(-1). Ti nanomaterials could be found in sediments with elevated Ti concentrations, which were often aggregated to a few hundred nanometers (<300 nm) and were composed of several spherical particles, less than 50 nm in size, that were made solely of TiO(x). However, Ti particles (approx. 300-700 nm) could be also found in sediments with lower Ti concentrations, which were presumably components of the natural clay mineral kaolinite. Ti nanomaterials could be easily distributed in sediments associated with elevated levels of organic matter and preferentially attach to those sediments with elevated fine fractions. As a sentinel, or tracer, for other nanomaterials, the field-scale investigation of Ti nanomaterials would contribute to increasing our knowledge on the behavior of engineered nanomaterials in an aquatic environment.     

Translocation of Sb and Ti in an undisturbed floodplain soil after application of Sb2O3 and TiO2 nanoparticles to the surface

The pore water transport of antimony and titanium, applied as nanoparticles (NPs), was studied by spiking stable suspensions of two different nanomaterials on the surface of an undisturbed floodplain soil. For preparation of stable dispersions, two different strategies were followed. (i) Comparable to those used in industrial applications: titanium dioxide nanoparticles, with an average diameter of 99 nm, were prepared by high-energy ball milling in water, whereas for (ii) antimony trioxide (Sb(2)O(3); average diameter 121 nm) a dispersing agent (sodium salt of poly[(naphthaleneformaldehyde)sulfonate] (pNFS) in water) was used. The upper 17 cm of a floodplain soil (river Rhine, Germany) was sampled using the minimally invasive sediment or fauna incubation experiment (SOFIE? two compartment cell; 3 l volume each), which preserved the pore system of the soil. The cells were equipped with 450 and 100 nm filter probes at different depths providing a non-invasive sampling of the pore water. The pore water was sampled at different times (T = 0, 24, 48, 96 and 196 h) and analysed by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS). Sb and Ti were transported via the pore water of the floodplain soil to a depth of 14 cm, corresponding to the maximum cell depth. The highest Sb concentration in the pore water was detected after 24 h at a depth of 5.5-8 cm. Although the spiked concentration was higher for Ti than for Sb, the total Ti concentration in the pore water of the spiked cell was lower. This indicates a stronger agglomeration of TiO(2) NPs or a more intensive interaction of Ti with the solid matrix and a faster transport of Sb towards deeper soil layers. The results show that metal(loid)s from metal oxide NPs are transported in the soil pore water and, hence, have the potential to act as the source of contamination of deeper soil layers after soil surface contamination.     

牛骨炭对水溶液中Hg（Ⅱ）吸附性的研究

以牛骨为原料,氯化锌为活化剂制备牛骨基炭,通过静态吸附试验研究了牛骨炭对水中Hg（Ⅱ）的吸附效果并确定了影响吸附性能的因素。研究结果表明：牛骨炭对Hg（Ⅱ）的最佳吸附时间约为2h、吸附温度为25℃、pH值为1、投加量为0．1g、吸附溶液的最大初始浓度为600mg／L,其最大吸附容量Q^0为43．1mg／g,吸附行为符合Freundl—ich吸附等温模型;通过BET分析和扫描电镜（SEM）等手段表征了牛骨炭的孔结构参数及形貌特征,经分析,所制备牛骨炭的孔径分布为中孔。     

硝酸镧改性聚丙烯酸对水中氟离子的吸附试验探讨

以丙烯酸为原料,乙二醇二甲基丙烯酸酯为交联剂制得聚丙烯酸树脂(PAA),用于制备表面粗糙、介孔丰富的镧(Ⅲ)改性聚丙烯酸复合树脂(La-PAA)。试验表明,当500 mg/L氟离子溶液pH值为5、吸附时间为300 min时,La-PAA对氟离子的去除率在90%以上。Langmuir方程能较好地拟合氟离子在La-PAA上的吸附等温线,最大吸附量为159.24 mg/g,吸附动力学过程符合准二级动力学方程。     

凯氏法测定土壤全氮的方法改进

采用凯氏法测定土壤全氮对9种不同类型的土壤进行测定,通过实验比较不同的还原剂、氧化剂和催化剂,发现以五水合硫代硫酸钠做还原剂,以硫酸为主要氧化剂,以K2SO4＋CuSO4＋TiO2做催化剂,具有操作简便、省时、无污染的优点。该方法加标回收率82.5%～96.0%,标样测试相对误差1.4%,精密度1.9%～10.8%,检出限14mg/kg。     

Development of an integrated sensor to measure odors

Odorous air samples collected from several sources were presented to an olfactometer, an electronic nose, a hydrogen sulfide (H(2)S) detector and an ammonia (NH(3)) detector. The olfactometry measurements were used as the expected values while measurements from the other instrumentation values became input variables. Five hypotheses were established to relate the input variables and the expected values. Both linear regression and artificial neural network analyses were used to test the hypotheses. Principal component analysis was utilized to reduce the dimensionality of the electronic nose measurements from 33 to 3 without significant loss of information. The electronic nose or the H(2)S detector can individually predict odor concentration measurements with similar accuracy (R (2) = 0.46 and 0.50, respectively). Although the NH(3) detector alone has a very poor relationship with odor concentration measurements, combining the H(2)S and NH(3) detectors can predict odor concentrations more accurately (R (2) = 0.58) than either individual instrument. Data from the integration of the electronic nose, H(2)S, and NH(3) detectors produce the best prediction of odor concentrations (R (2) = 0.75). With this accuracy, odor concentration measurements can be confidently represented by integrating an electronic nose, and H(2)S and NH(3) detectors.     

Hygienic guidance values for wipe sampling of antineoplastic drugs in Swedish hospitals

The use of antineoplastic drugs in health care steadily increases. Health care workers can be occupationally exposed to antineoplastic drugs classified as carcinogenic or teratogenic. Monitoring of surface contamination is a common way to assess occupational exposure to antineoplastic drugs, since wipe sampling is used as a surrogate measure of dermal exposure. Since no occupational limits for antineoplastic drugs in work environments exist, 'hygienic guidance values' (HGVs) should be used instead. HGVs are practicable, achievable levels, not health based, and can be calculated from exposure data from representative workplaces with good occupational hygiene practices. So far, guidance values for surface monitoring of antineoplastic drugs only exist for pharmacies where antineoplastic drugs are prepared. The objective was to propose HGVs for surface monitoring of cyclophosphamide (CP) and ifosfamide (IF) in Swedish hospitals where antineoplastic drugs are administered to patients. In total, 17 workplaces located at six hospitals in Sweden were surveyed by wipe sampling. Wipe samples were collected, worked up and then analyzed with liquid chromatography tandem mass spectrometry. Surface contamination of CP and IF was found on 80% and 73% of the sampled surfaces, thus indicating that there is potential for health care workers to be exposed to CP and IF via the skin. The median surface load of CP was 3.3 pg cm(-2) (range <0.05-10,800 pg cm(-2)). The corresponding value for IF was 4.2 pg cm(-2) (range <0.13-95,000 pg cm(-2)). The highest surface loads were found on the floors. The proposed HGVs were set at 90th percentile values, and can be applicable to hospital workplaces where patients are treated with CP or IF. Surface monitoring combined with HGVs is a useful tool for health care workers to regularly benchmark their own surface loads which could control and reduce the occupational exposure to CP and IF in hospital workplaces. Thus, the occupational safety of the health care workers will be increased.     

Simultaneous determination of atmospheric sulfur and nitrogen oxides using a battery-operated portable filter pack sampler

We developed a method to analyze atmospheric SO(x) (particulate SO(4)(2-)+ gaseous SO(2)) and NO(x) (NO + NO(2)) simultaneously using a battery-operated portable filter pack sampler. NO(x) determination using a filter pack method is new. SO(x) and NO(x) were collected on a Na(2)CO(3) filter and PTIO (2-phenyl-4,4,5,5-tetramethylimidazoline-3-oxide-1-oxyl) + TEA (triethanolamine) filters (6 piled sheets), respectively. Aqueous solutions were then used to extract pollutants trapped by the filters and the resulting extracts were pre-cleaned (e.g. elimination of PTIO) and analyzed for sulfate and nitrite by ion chromatography. Recoveries of SO(2) and NO(x) from standard pollutant gases and consistency of the field data with those from other instrumental methods were examined to evaluate our method. SO(x) and NO(x) could be analyzed accurately with determination limits of 0.2 ppbv and 1.0 ppbv (as daily average concentrations), respectively. The sampler can determine SO(x) and NO(x) concentrations at mountainous or remote sites without needing an electric power supply.     

Natural mercury enrichment in a minerogenic fen--evaluation of sources and processes

Mercury (Hg) records in natural archives such as peat bogs are often used to evaluate anthropogenic or climatic influences on atmospheric Hg deposition. In this context, there is an ongoing discussion about natural sources or processes of Hg enrichment in natural archives. In the present study we estimated Hg fluxes from rock weathering, direct atmospheric deposition and from indirect atmospheric deposition in the catchment of a pristine minerogenic fen (GC2) located in the Magellanic Moorlands, southernmost Chile. The Hg record in the bog covers 11 174 cal. (14)C years and shows Hg concentrations of up to 570 [micro sign]g kg(-1) with an average of 268 [micro sign]g kg(-1). Hg was found to be enriched in the peat by a factor of 81 if compared to the mean Hg concentrations in the rocks of the catchment (3.2 [micro sign]g kg(-1)). Hg and also Pb, Fe, and As were found to be enriched predominately in goethite layers indicating high retention of these elements in the bog by iron oxyhydrates. It could also be demonstrated that the high peat decomposition rates in minerogenic bogs can increase the Hg concentrations in the minerogenic peat by a factor of approximately 2 at the same atmospheric Hg deposition rate if compared to ombrotrophic sites. This study has shown that Hg in minerogenic peat can be naturally enriched especially through the retention by autochthonous formed goethite and can be a solely internal process which does not require increased external Hg fluxes.     

Effects of humidity and filter material on diffusive sampling of isocyanates using reagent-coated filters

Diffusive sampling of methyl isocyanate (MIC) on 4-nitro-7-piperazinobenzo-2-oxa-1,3-diazole (NBDPZ)-coated glass fibre (GF) filters is strongly affected by high relative humidity (RH) conditions. It is shown that the humidity interference is a physical phenomenon, based on displacement of reagent from the filter surface. In this paper, this drawback has been overcome by changing the filter material to the less polar polystyrene divinyl benzene (SDB). A series of experiments was performed to compare the analyte uptake on the two filter materials for different sampling periods and analyte concentrations at both low and high RH conditions. Additionally, the materials were investigated as well for passive sampling of ethyl (EIC) and phenyl isocyanate (PhIC) with NBDPZ and 1-(2-methoxyphenyl) piperazine (2-MP) as an alternative derivatising agent. Using 2-MP, the mean GF/SDB response ratios were determined to be 1.02 for MIC (RSD: 6.1%) and 1.03 for EIC (RSD: 6.8%), whereas PhIC could only be determined on SDB filters. Using NBDPZ as reagent, the negative influence of high humidity disappeared when SDB filters were used instead of GF filters. Even at low RH conditions, sampling with SDB material generally resulted in a higher analyte uptake than with GF filters. The GF/SDB response ratios were independent of sampling time or analyte concentration and were determined to be 0.70 (RSD: 4.7%) for MIC, 0.84 (RSD: 4.5%) for EIC and 0.95 (RSD 5.4%) for PhIC, meaning that the NBDPZ diffusive sampler based on SDB can be used at all humidity conditions without any restrictions.