Inhalation and dermal exposure of workers during timber impregnation with creosote and subsequent processing of impregnated wood.

OBJECTIVES: Coal tar creosote oils are used as highly effective wood protectants for, e.g., railway sleepers, utility poles and marine pilings. For impregnation of wood, the hot creosote oil is mostly applied in vacuum processes and by hot-and-cold dipping. From the perspective of an occupational hygienist, creosote tar oils are problematic because they have a number of hazardous properties, including carcinogenicity. We have studied inhalation and dermal exposure in six and four impregnation plants, respectively, in Germany. Some plants were visited repeatedly, for up to five measurement campaigns conducted over several years. Inhalation and dermal exposure resulting from vacuum impregnation and from hot-and-cold dipping, as well as secondary exposure resulting from assembly of impregnated railway sleepers have been measured. Accompanying, human biomonitoring of the employees has been performed. METHODS: Inhalation exposure was measured using personal air samplers, collecting particles and vapours simultaneously. Dermal exposure was investigated by whole body dosimetry using disposable chemical protective coveralls and split leather gloves. 18 polycyclic aromatic hydrocarbons (PAHs) have been determined separately by high performance liquid chromatography (HPLC) or gas chromatography-mass spectrometry (GC-MS), respectively. For human biomonitoring 1-hydroxypyrene (1-OHP) in urine related to creatinine has been measured using HPLC. Both, pre- and post-shift values have been determined for this metabolite. RESULTS: Dermal exposure towards pyrene and the sum of the determined 18 PAHs as well as inhalation exposure to naphthalene, pyrene and the sum of the determined 18 PAHs are presented in this paper. The plants performing vacuum impregnation have employed different constructive, technical and organisational measures, and some measures have also changed between the different measurement campaigns. We have found that cooling the vacuum impregnation vessel before unloading can reduce inhalation exposure to about one-third. However, our data shows that installation of structural or technical risk management measures (RMM) did not always reduce the exposure as intended, and can even lead to increased exposure in adverse constellations. Dermal exposure was strongly affected by differences in the working procedures. Measurements performed during assembly of impregnated railway sleepers indicate that secondary exposure leads to lower inhalation, but similar dermal exposure compared to the impregnation processes. Also 1-OHP excretion rates are similar after impregnation process and after assembly of impregnated railway sleepers. CONCLUSION: Our recent data underlines that efficient reduction of the exposure resulting from impregnation with creosote requires sophisticated risk reduction strategies. Structural measures such as the enclosure of the loading area and technical measures like local exhaust ventilation shall be coordinated carefully with organisational measures and provision of personal protective equipment. The data presented here represents a broad bandwidth of current workplace situations in the creosote oil processing industry and is therefore suitable for risk assessment in related plants as well as under regulatory frameworks like the European Biocides Regulation. Each plant in this investigation was unique. Together they represent the whole width of this branch in Germany. Additionally, the number of plants and exposed workers is limited and relative low. Therefore, a comprehensive consideration and statistical analysis were not feasible.

The 2'-OH group at the group II intron terminus acts as a proton shuttle.

Group II introns are self-splicing ribozymes that excise themselves from precursor RNAs and catalyze the joining of flanking exons. Excised introns can behave as parasitic RNA molecules: they can catalyze their own insertion into DNA and RNA via a reverse splicing reaction. Previous studies have identified mechanistic roles for various functional groups located in the catalytic core of the intron and within target molecules. Here we introduce a new method for synthesizing long RNA molecules with a modified nucleotide at the 3' terminus. This modification allows us to examine the mechanistic role of functional groups adjacent to the reaction nucleophile. During reverse splicing, the 3'-OH group of the intron terminus attacks the phosphodiester linkage of spliced exon sequences. Here we show that the adjacent 2'-OH group on the intron terminus plays an essential role in activating the nucleophile by stripping away a proton from the 3'-OH and then shuttling it from the active site.

Estimating Inhalation Exposure Resulting from Evaporation of Volatile Multicomponent Mixtures Using Different Modelling Approaches.

In many professional and industrial settings, liquid multicomponent mixtures are used as solvents, additives, coatings, biocidal products, etc. Since, in all of these examples, hazardous liquids can evaporate in the form of vapours, for risk assessments it is important to know the amount of chemicals in the surrounding air. Although several models are available in legal contexts, the current implementations seem to be unable to correctly simulate concentration changes that actually occur in volatile mixtures and in particular in thin films. In this research, the estimation of evaporation rates is based on models that take into account non-ideal behaviour of components in liquids and backpressure effects as well. The corresponding system of differential equations is solved numerically using an extended Euler algorithm that is based on a discretisation of time and space. Regarding air dispersion of volatile components, the model builds upon one-box and two-box mass balance models, because there is some evidence that these models, when selected and applied appropriately, can predict occupational exposures with sufficient precision. That way, numerical solutions for a wide variety of exposure scenarios with instantaneous and continuous/intermittent application, even considering "moving worker situations", can be obtained. A number of example calculations have been carried out on scenarios where binary aqueous solutions of hydrogen peroxide or glutaraldehyde are applied as a biocidal product to surfaces by wiping. The results reveal that backpressure effects caused by large emission sources as well as deviations from liquid-phase ideality can influence the shape of the concentration time curves significantly. The results also provide some evidence that near-/far-field models should be used to avoid underestimation of exposure in large rooms when small/medium areas are applied. However, the near-field/far-field model should not be used to estimate peak exposure assuming instantaneous application, because then the models tend to overestimate peak exposure significantly. Although the example calculations are restricted to aqueous binary mixtures, the proposed approach is general and can be used for arbitrary liquid multicomponent mixtures, as long as backpressure effects and liquid-phase non-idealities are addressed adequately.

Correction: Tischer, M.; Roitzsch, M. Estimating Inhalation Exposure Resulting from Evaporation of Volatile Multicomponent Mixtures Using Different Modelling Approaches. Int. J. Environ. Res. Public Health 2022, 19, 1957.

There was an error in the original publication [...].

The linear form of a group II intron catalyzes efficient autocatalytic reverse splicing, establishing a potential for mobility.

Self-splicing group II introns catalyze their own excision from pre-RNAs, thereby joining the flanking exons. The introns can be released in a lariat or linear form. Lariat introns have been shown to reverse the splicing reaction; in contrast, linear introns are generally believed to perform no or only poor reverse splicing. Here, we show that a linear group II intron derived from ai5gamma can reverse the second step of splicing with unexpectedly high efficiency and precision. Moreover, the linear intron generates dramatically more reverse-splicing product than its lariat equivalent. The finding that linear group II introns can readily undergo the critical first step of mobility by catalyzing efficient reverse splicing into complementary target molecules demonstrates their innate potential for mobility and transposition and raises the possibility that reverse splicing by linear group II introns may have played a significant role in certain forms of intron mobility and lateral gene transfer during evolution.

Modelling Exposure by Spraying Activities-Status and Future Needs.

Spray applications enable a uniform distribution of substances on surfaces in a highly efficient manner, and thus can be found at workplaces as well as in consumer environments. A systematic literature review on modelling exposure by spraying activities has been conducted and status and further needs have been discussed with experts at a symposium. This review summarizes the current knowledge about models and their level of conservatism and accuracy. We found that extraction of relevant information on model performance for spraying from published studies and interpretation of model accuracy proved to be challenging, as the studies often accounted for only a small part of potential spray applications. To achieve a better quality of exposure estimates in the future, more systematic evaluation of models is beneficial, taking into account a representative variety of spray equipment and application patterns. Model predictions could be improved by more accurate consideration of variation in spray equipment. Inter-model harmonization with regard to spray input parameters and appropriate grouping of spray exposure situations is recommended. From a user perspective, a platform or database with information on different spraying equipment and techniques and agreed standard parameters for specific spraying scenarios from different regulations may be useful.

Prediction of Dermal Exposure to Chemical Substances Using a Fluorescence Method within the SysDEA Project.

Dermal exposure is an important exposure route for occupational exposure and risk assessment. A fluorescence method has been developed to quantify occupational dermal exposure based on a visualization technique, using Tinopal SWN as a fluorescent tracer. The method was developed within the framework of a large experimental study, the SysDEA project. In SysDEA, dermal exposure was measured with different methods for 10 simulated exposure situations by sampling powder and liquid formulations containing Tinopal SWN on coveralls and patches and subsequently chemically analysing them. For the fluorescence method, photographs of exposed volunteers who performed the experiments were taken inside a room which consisted of an optimized arrangement of several UV irradiating tube light brackets, reflective and non-reflective backgrounds for maximum light diffusion and a camera. Image processing analysis software processed these photographs to obtain corresponding light intensity in terms of summed pixel values. To be able to estimate the amount of Tinopal SWN, 25% of the measured data from the SysDEA experiments were used to calibrate by correlating the summed pixel values from the photographs to actual measured exposure values using a second order regression model. For spraying both high and low viscosity liquids, showing uniformly distributed exposure patterns, strong Pearson correlation coefficients (R > 0.77) were observed. In contrast, the correlations were either inconsistently poor (R = -0.17 to 0.28 for pouring, rolling high viscosity liquid, manually handling objects immersed in low viscosity liquid and handling objects contaminated with powder), moderate (R = 0.73 for dumping of powder), or strong (R = 0.83 and 0.77 for rolling low viscosity liquid and manually handling objects immersed in high viscosity liquid). A model for spraying was developed and calibrated using 25% of the available experimental data for spraying and validated using the remaining 75%. Under given experimental conditions, the fluorescence method shows promising results and can be used for the quantification of dermal exposure for different body parts (excluding hands) for spraying-like scenarios that have a more uniform exposure pattern, but more research is needed for exposure scenarios with less uniform exposure patterns. For the estimation of exposure levels, the surface loading limit should be lower than 1.5░µg/cm2 (a lower limit could not be quantified based on experiments conducted in this study) on a large surface, like a coverall, which should be ideally perpendicular to the camera.

Comparison of Measurement Methods for Dermal Exposure to Hazardous Chemicals at the Workplace: The SysDEA Project.

There is a principal need for more precise methodology with regard to the determination of occupational dermal exposure. The goal of the Systematic analysis of Dermal Exposure to hazardous chemical Agents at the workplace project was therefore to generate scientific knowledge to improve and standardize measurement methods for dermal exposure to chemicals at the workplace. In addition, the comparability of different measurement methods was investigated. Different methods (body sampling by means of coveralls and patches, hand sampling by means of gloves and washing, and head sampling by means of headbands and wiping) were compared. Volunteers repeatedly performed a selection of tasks under standardized conditions in test chambers to increase the reproducibility and decrease variability. The selected tasks were pouring, rolling, spraying, and handling of objects immersed in liquid formulations, as well as dumping and handling objects contaminated with powder. For the chemical analysis, the surrogate test substance Tinopal SWN was analyzed by means of a high-performance liquid chromatographic method using a fluorescence detector. Tinopal SWN was either applied as a solid product in its pure form, or as a low and high viscosity liquid containing Tinopal SWN in dissolved form. To compare the sampling methods with patches and coveralls, the exposure values as measured on the patches were extrapolated to the surface areas of the respective parts of the coverall. Based on this extrapolation approach, using the patch method resulted in somewhat higher exposure values compared to using a coverall for all exposure situations, but the differences were only statistically significant in case of the liquid exposure situations. Using gloves resulted in significantly higher exposure values compared to hand wash for handling immersed objects, rolling, and handling contaminated objects, and slightly higher (not significant) exposure values during pouring and spraying. In the same context, applying wipe sampling resulted in higher exposure values than using a headband, which was at least partly due to extrapolation of the wipe results to the surface area of the headband. No 'golden standard' with regard to a preferred measurement method for dermal exposure could be identified from the methods as investigated in the current study.

Dermal and Inhalation Exposure of Workers during Control of Oak Processionary Moth (OPM) by Spray Applications.

BACKGROUND: The caterpillars of the oak processionary moth (OPM) form stinging hairs, which release an irritant poison. They cause skin and eye irritation and sometimes even breathing difficulties and allergic reactions. OPM is mainly controlled by spraying insecticides. Insecticides applied for protection of human health must be authorized under the Biocidal Products Regulation (BPR) (EU) No 528/2012. In order to assess safety of professional use, which is a key requirement for the authorization, a risk assessment based on exposure estimation has to be performed. However, no exposure data specific for OPM control was available until now. Existing models for agricultural spray applications such as Agricultural Operator Exposure Model cover different spray patterns and equipment and were therefore considered too unreliable for assessment of OPM control. METHODS: We have studied dermal and inhalation exposure of certified pest control operators resulting from spraying DimilinTM 80 WG suspensions with vehicle-mounted spraying (VMS) and with handheld spraying (HHS) devices for control of OPM. Exposure resulting from these applications, from weighing and portioning of the granular product and from cleaning of contaminated spraying devices was studied. Dermal exposure was investigated by whole body dosimetry using disposable chemical protective coveralls and cotton gloves as samplers. Inhalation exposure was measured using personal air samplers. The active substance diflubenzuron was quantified by gas chromatography-mass spectrometry with positive chemical ionization and by high-performance liquid chromatography for dermal and inhalation measurements, respectively. RESULTS: The exposure was dominated by the dermal pathway. HHS results in considerably higher operator exposure than VMS. Comparison with data from typical agricultural spraying applications revealed that OPM control results in much higher exposure of operators for both, vehicle-mounted and handheld equipment. CONCLUSIONS: Comprehensive data on potential dermal and inhalation exposure is presented in this article, along with typical figures for handled and applied amounts of product and respective task durations. This data is suitable for risk assessments in regulatory frameworks such as the European BPR.

Structural precursor of the hemideprotonated guanine pair.

A pairing scheme (GG7) between two neutral guanine nucleobases taking place via the Watson-Crick faces and involving two bridging water molecules is presented, which upon removal of a H5O2+ entity could convert into the hemideprotonated guanine pair (GG5).

On the many roles of NH3 ligands in mono- and multinuclear complexes of platinum.

The role of the NH(3) ligands in the highly successful antitumour agents cisplatin and carboplatin is not fully understood. Suggestions that the ammonia ligands are involved in target recognition through hydrogen bond formation, e.g. with guanine-O6, have been questioned. Here, we review the roles and functions of NH(3) ligands of cis-PtCl(2)(NH(3))(2) and likewise of its trans-isomer in complexes with model nucleobases as well as other N-heterocyclic ligands. Specifically, their roles in hydrogen bonding interactions with nucleobases as well as anions, the influence on acid-base properties of co-ligands, their involvement in condensation reactions, as well as a variety of displacement reactions will be examined. As a result, it can be stated that the ammonia ligands in cis- and trans-Pt(II)(NH(3))(2) entities display additional features to those generally discussed in the last four decades since the discovery of the antitumour activity of cisplatin.

Pyrazine as a building block for molecular architectures with PtII.

A series of pyrazine (pz) complexes containing cis-(NH(3))(2)Pt(II), (tmeda)Pt(II) (tmeda = N,N,N',N'-tetramethylethylenediamine), and trans-(NH(3))(2)Pt(II) entities have been prepared and characterized by X-ray crystallography and/or 1H NMR spectroscopy. In these compounds, the pz ligands act as monodentate (1-3) or bidentate bridging ligands (4-7). Three variants of the latter case are described: a dinuclear complex [Pt(II)]2 (4b), a cyclic tetranuclear [Pt(II)](4) complex (5), and a trinuclear mixed-metal complex [Pt2Ag] (7). Mono- and bidentate binding modes are readily differentiated by 1H NMR spectroscopy, and the assignment of pz protons in the case of monodentate coordination is aided by the observation of (195)Pt satellites. Formation of the open molecular box cis-[{(NH3)2Pt(pz)}4](NO3)8.3.67H2O (5) from cis-(NH3)2Pt(II) and pz follows expectations of the "molecular library approach" for the generation of a cyclic tetramer.

Isocytosine as a hydrogen-bonding partner and as a ligand in metal complexes.

Isocytosine (ICH; 1) exists in solution in an equilibrium of tautomers 1a and 1b with the N1 and N3 positions carrying the acidic proton, respectively. In the solid state, both tautomers coexist in a 1:1 ratio. As we show, the N3H tautomer 1b can selectively be crystallized in the presence of the model nucleobase 1-methylcytosine (1-MeC). The complex 1b x (1-MeC)2 x H2O (2) forms pairs through three hydrogen bonds between the components; hydrogen bonds between identical molecules are also formed, leading to an infinite tape structure. On the other hand, the N1H tautomer 1a co-crystallizes with protonated ICH to give [1a x ICH2]NO3 (3), again with three hydrogen bonds between the partners, yet the acidic proton is disordered over the two entities. With M(II)(dien) (M=Pt, Pd; dien=diethylenetriamine) preferential coordination of tautomer 1a through the N3 position is observed. DFT calculations, which were also extended to Pt(II)(tmeda) linkage isomers (tmeda=N,N,N',N'-tetramethylethylenediamine), suggest that intramolecular hydrogen bonding between the ICH tautomers and the co-ligands at M, while adding to the preference for N3 coordination, is not the major determining factor. Rather it is the inherently stronger Pt-N3 bond which favors complexation of 1a. With an excess of M(II)(dien), dinuclear species [M2(dien)2(IC-N1,N3)]3+ (M=Pd(II), 4 and Pt(II), 5) also form and were isolated as their ClO4(-) salts and structurally characterized. In strongly acidic medium 5 is converted to [Pt(dien)(ICH-N1)]2+ (6), that is, to the Pt(II) complex of tautomer 1b.

Metal ion coordination to azole nucleosides.

To evaluate the possibility of introducing azole nucleosides as building blocks for metal-mediated base pairs in artificial oligonucleotides, imidazole nucleoside, 1,2,4-triazole nucleoside and tetrazole nucleoside have been synthesized and characterized. The X-ray crystal structures of p-toluoyl-protected 1,2,4-triazole and tetrazole nucleosides are reported. Contrary to the situation primarily found for deoxyribonucleosides, the sugar moieties adopt C3'-endo conformations. The acidity of the beta nucleosides increases with increasing number of nitrogen ring atoms, giving pKa values of 6.01 +/- 0.05, 1.32+/-0.05 and <-3, respectively. This decrease in basicity results in a decreasing ability to form 2:1 complexes with linearly coordinating metal ions such as Ag+ and Hg2+. In all cases, the Ag+ complexes are of higher stability than the corresponding Hg2+ complexes. Whereas imidazole nucleoside forms highly stable 2:1 complexes with both metal ions (estimated log beta2 values of >10), only Ag+ is able to reach this coordination pattern in the case of triazole nucleoside (log beta2 = 4.3 +/- 0.1). Tetrazole nucleoside does not form 2:1 complexes at all under the experimental conditions used. These data suggest that imidazole nucleoside, and to a lesser extent 1,2,4-triazole nucleoside, are likely candidates for successful incorporation as ligands in oligonucleotides based on metal-mediated base pairs. DFT calculations further corroborate this idea, providing model complexes for such base pairs with glycosidic bond distances (10.8-11.0 Angstroms) resembling those in idealized B-DNA (10.85 Angstroms).

The role of intramolecular hydrogen bonding on nucleobase acidification following metal coordination: possible implications of an "indirect" role of metals in acid-base catalysis of nucleic acids.

The acidifying effect of Pt(II) on nucleobase -NH and -NH2 groups depends both on the site of metal coordination and on the efficiency of stabilization of the deprotonated nucleobase via intracomplex hydrogen bonding. Weakly acidic nucleobase protons with pK (a) values between 9 and 17 can be acidified by a single Pt(II) to have pK (a) values which are well within the physiological pH range. This could open the possibility of an acid-base catalysis occurring at pH 7, with the metal-nucleobase entity functioning either as an acid or a base. Examples of Pt(II) complexes studied here include, among others, mixed nucleobase systems of 1-methylcytosine and 1,9-dimethyladenine as well as a complex of the rare iminooxo tautomer of 1-methylcytosine having the metal bonded at N4.

Metal coordination and imine-amine hydrogen bonding as the source of strongly shifted adenine pKa values.

The X-ray crystal structure of a Pt(II) complex of composition trans-[(NH(3))(2)Pt(1,9-DimeA) (1,9-DimeAH)](ClO(4))(3) (2) with 1,9-DimeA = 1,9-dimethyladenine and 1,9-DimeAH(+) = 1,9-dimethyladeninium) is presented. Complex 2 forms upon deprotonation of one of the exocyclic amino groups of the adeninium ligands in trans-[(NH(3))(2)Pt(1,9-DimeAH)(2)](ClO(4))(4) (1), where the two nucleobases are in a head-tail arrangement. The low pK(a1) of 1 (4.1 +/- 0.2) is a consequence of a combination of the effects of metal coordination to N7 of the purine base and efficient stabilization of the deprotonated species. This feature is supported by the results of the structure determination of 2, which displays a head-head orientation of the two bases and intramolecular H-bonding between the imine group of 1,9-DimeA and the amino group of 1,9-DimeAH. In the fully deprotonated species trans-[(NH(3))(2)Pt(1,9-DimeA)(2)](ClO(4))(2) (3), the two nucleobases are again in a head-tail arrangement. The findings are of relevance with regard to the concept of "shifted pK(a) values" of nucleobases. This concept is applied to rationalize acid-base catalysis reactions involving nucleobases of DNA and RNA which occur in the near-physiological pH range.

Feasibility of a two-metal, four-purine nucleobase quartet motif.

A mixed-purine nucleobase complex of composition trans-[(NH(3))(2)Pt(9-EtA-N1)(9-MeHx-N7)](NO(3))(2).2H(2)O (1) (9-EtA = 9-ethyladenine; 9-MeHx = 9-methylhypoxanthine) has been prepared and characterized by X-ray crystallography. Cations of 1 are self-complementary as far as hydrogen bonding properties are concerned and form H bonded dimers, containing four intermolecular hydrogen bonds in addition to two intramolecular ones. The resulting mixed-purine square is considered a model compound for a putative mixed-purine tetrad consisting of two adenines and two guanines. In this model, the one-metal, four-nucleobase quartet motif, as seen in guanine or uracil quartets of nucleic acids, with the metal located in the center of the base tetrad, has been altered to a two-metal, four-nucleobase motif, with the two metal ions localized at the periphery.

Association patterns of platinated purine nucleobases in metal-modified pairs and triples.

Blocking of Watson-Crick or Hoogsteen edges in purine nucleobases by a metal entity precludes involvement of these sites in interbase hydrogen bonding, thereby leaving the respective other edge or the sugar edge as potential H bonding sites. In mixed guanine, adenine complexes of trans-a2PtII (a = NH3 or CH3NH2) of composition trans-[(NH3)2Pt(9-EtA-N1)(9-MeGH-N7)](NO3)2 (1a), trans-[(NH3)2Pt(9-EtA-N1)(9-MeGH-N7)](ClO4)2 (1b), and trans,trans-[(CH3NH2)2(9-MeGH-N7)Pt(N1-9-MeA-N7)Pt(9-MeGH-N7)(CH3NH2)2](ClO4)4*2H2O (2) (with 9-EtA = 9-ethyladenine, 9-MeA= 9-methyladenine, 9-MeGH = 9-methylguanine), this aspect is studied. Thus, in 1b pairing of two adenine ligands via Hoogsteen edges and in 2 pairing of two guanine bases via sugar edges is realized. These situations are compared with those found in a series of related complexes.