thiourea and diphenylthiourea

The gasotransmitter hydrogen sulfide (H

Topics: Animals; Aorta; Blood Pressure; Cells, Cultured; Coronary Vessels; Humans; Hydrogen Sulfide; Isolated Heart Preparation; KATP Channels; KCNQ Potassium Channels; Male; Membrane Potentials; Muscle, Smooth, Vascular; Myocytes, Smooth Muscle; Phenylthiourea; Rats, Wistar; Thiourea; Vasodilation; Vasodilator Agents

This study was conducted to design an electrochemical sensor for detection of l-glutamate (L-Glu) and Aspartate (Asp), which contribute largely to the umami taste of beef. Using N, N'-diphenylthiourea (DPTU), polypyrrole (PPy), and polyvinyl chloride (PVC), a composite electrode (DPTU/PVC/PPy/Pt) was prepared for rapidly electrochemical detection of l-Glu and Asp. The surface morphology of the synthesized functionalized electrode was characterized by Field Emission Scanning Electron Microscopy (FESEM). Potentials of umami amino acids accounted for 97.8%, while six interferential amino acids existed. The linear correlation between the content of l-Glu and Asp in beef broth was studied under different treatment conditions. The sensor compared with an amino acid analyzer well detected the contents of l-Glu and Asp in beef broths, with a coefficient of 0.991 in Pearson correlation analysis and an accuracy of 88.9%. The proposed electrochemical sensor showed good concurrence with previously reported methods and was effectively employed for the quantification of l- Glu and Asp in beef. PRACTICAL APPLICATION: The sensor exhibits the good performance with high stability and high accuracy. And it is a potential sensing platform with good reproducibility, making the proposed method suitable and reliable for routine analysis of L-Glu and Asp in beef. This method was proved promising for quantitative detecting amino acids in beef.

Topics: Animals; Aspartic Acid; Cattle; Electrochemical Techniques; Glutamic Acid; Red Meat; Reproducibility of Results; Thiourea

Contact allergy to chloroprene rubber products is well known. Thiourea compounds are considered the cause of allergy. Diethylthiourea commonly occurs in this type of product and can decompose to the sensitizer ethyl isothiocyanate.. To investigate the clinical importance of degradation products and metabolites from organic thioureas in contact allergy to chloroprene rubber with a focus on isothiocyanates and isocyanates.. Patients with contact allergy to diphenylthiourea were patch tested with phenyl isothiocyanate and phenyl isocyanate. Patients with known contact allergy to diethylthiourea were retested with diethylthiourea, while chemical analyses of their chloroprene rubber products were performed. The stability of diethylthiourea, diphenylthiourea and dibutylthiourea in patch-test preparations was investigated. Liquid chromatography/mass spectrometry and solid-phase microextraction/gas chromatography were used for determination of organic thioureas and isothiocyanates.. All patients allergic to diphenylthiourea reacted to phenyl isothiocyanate, two of eight reacted to phenyl isocyanate and six of eight reacted to diphenylthiourea. Four patients allergic to diethylthiourea reacted at retest; diethylthiourea was detected in all chloroprene rubber samples, with levels of 2-1200 nmol cm. Thiourea compounds are degraded to isothiocyanates, which are generally strong or extreme sensitizers, thus acting as prehaptens. This process occurs in both chloroprene rubber products and patch-test preparations. Positive reactions to phenyl isocyanate indicate cutaneous metabolism, as the only known source of exposure to phenyl isocyanate is through bioactivation of diphenylthiourea.

Topics: Adult; Chloroprene; Dermatitis, Allergic Contact; Female; Haptens; Humans; Isocyanates; Isothiocyanates; Male; Middle Aged; Patch Tests; Rubber; Thiourea

Exposure to chloroprene rubber has resulted in numerous cases of allergic contact dermatitis, attributed to organic thiourea compounds used as vulcanization accelerators. However, thiourea compounds are not considered to be strong haptens.. To analyse common commercial chloroprene materials for their contents of diethylthiourea (DETU), dibutylthiourea (DBTU), diphenylthiourea (DPTU), and their degradation products, isothiocyanates; and to investigate the sensitization potencies of possible degradation products of the mentioned thiourea compounds.. Liquid chromatography/mass spectrometry (MS) was used for quantification of organic thiourea compounds in chloroprene products, such as medical, sports and diving gear; isothiocyanates were measured by solid-phase microextraction/gas chromatography/MS. Sensitization potencies were determined with the murine local lymph node assay (LLNA).. DETU was identified at concentrations of 2.7-9.4 µg/cm(2) in all samples, whereas neither DBTU nor DPTU was detected. At 37°C, degradation of DETU in the materials to ethyl isothiocyanate (EITC) was detected. EITC and ethyl isocyanate showed extreme and strong sensitization potencies, respectively, in the LLNA.. DETU can act as a prehapten, being degraded to EITC when subjected to body temperature upon skin contact. EITC could thus be the culprit behind allergic contact dermatitis caused by chloroprene rubber.

Topics: Allergens; Dermatitis, Allergic Contact; Humans; Isothiocyanates; Local Lymph Node Assay; Neoprene; Thiourea

Diphenylthiourea (DPTU) is a known skin sensitizer commonly used as a vulcanization accelerator in the production of synthetic rubber, for example, neoprene. The versatile usage of neoprene is due to the multifaceted properties of the material; for example, it is stretchable, waterproof, and chemical- and abrasion-resistant. The wide application of neoprene has resulted in numerous case reports of dermatitis patients allergic to DPTU. The mechanism by which DPTU works as a contact allergen has not been described; thus, the aim of the present study was to investigate if DPTU is a prohapten that can be activated by skin metabolism. The metabolic activation and covalent binding of (14)C-labeled DPTU to proteins were tested using a skinlike cytochrome P450 (P450) cocktail containing the five most abundant P450s found in human skin (CYP1A1, 1B1, 2B6, 2E1, and 3A5) and human liver microsomes. The incubations were carried out in the presence or absence of the metabolite trapping agents glutathione, methoxylamine, and benzylamine. The metabolism mixtures were analyzed by LC-radiochromatography, LC-MS, and LC-MS/MS. DPTU was mainly metabolically activated to reactive sulfoxides resulting in desulfurated adducts in both enzymatic systems used. Also, phenylisothiocyanate and phenylisocyanate were found to be metabolites of DPTU. The sensitizing capacity of the substrate (DPTU) and three metabolites was tested in the murine local lymph node assay. Two out of three metabolites tested were strong skin sensitizers, whereas DPTU itself, as previously known, was negative using this mouse model. In conclusion, DPTU forms highly reactive metabolites upon bioactivation by enzymes present in the skin. These metabolites are able to induce skin sensitization and are probable causes for DPTU allergy. To increase the possibilities of diagnosing contact allergy to DPTU-containing items, we suggest that suitable metabolites of DPTU should be used for screening testing.

Topics: Animals; Benzylamines; Cytochrome P-450 Enzyme System; Dermatitis, Allergic Contact; Disease Models, Animal; Glutathione; Humans; Hydroxylamines; Isothiocyanates; Mice; Microsomes, Liver; Protein Binding; Rubber; Skin; Thiourea

Thiourea derivatives in rubber products may induce contact sensitization and allergic contact dermatitis. Sensitization is most often from neoprene rubber, but the multitude of possible sensitizing products has remained poorly characterized.. The aim of this study was to collect information on the occurrence of thiourea-related contact allergy and to show novel sources of sensitization.. A mixture of dibutyl-, diethyl-, and diphenylthiourea was included in patch test baseline series in five Finnish dermatology clinics during 2002-2007. In addition, an extended series of rubber chemicals was tested in patients with suspected rubber allergy. Sources of sensitization to thioureas were analysed in sensitized patients.. Thiourea mix yielded positive patch test reactions in 59 of 15,100 patients (0.39%); 33/59 patients were also tested with individual rubber chemicals. Diethylthiourea was positive in 24/33, diphenylthiourea in 5, and dibutylthiourea in 1 patient. The most common sources of sensitization included various neoprene-containing orthopaedic braces, sports equipment, and foot wear.. The sources of sensitization to thiourea chemicals were detected in most cases. These sources comprise a heterogenous group of products extending from orthopaedic materials to sports equipment.

Topics: Adolescent; Adult; Aged; Braces; Dermatitis, Allergic Contact; Female; Finland; Humans; Latex Hypersensitivity; Male; Middle Aged; Patch Tests; Rubber; Shoes; Sports Equipment; Thiourea; Young Adult

Crystallization of the copper(i) halides (CuX; X = Cl, Br, I) with N,N'-diphenylthiourea ('dptu' = (PhNH)(2)CS) in 1 : 2 ratio from acetonitrile solution in ambient conditions yields a mononuclear isomorphous series of complexes of the form [XCu(dptu)(2)].H(2)O, an unusually complete array, with the central copper atoms in quasi-trigonal planar environments, as shown by single crystal X-ray studies, in turn providing a platform for comparative spectroscopic studies. Under anhydrous conditions, anhydrous compounds may be obtained, a full series again being accessible, but now of the binuclear form [(dptu)XCu(mu-S-dptu)(2)CuX(dptu)], the chloride being a bis(acetonitrile) solvate, the isomorphous bromide and iodide pair being unsolvated. A (solvated) sulfate salt is found to be of the form [Cu(dptu)(2)](2)(SO(4)), providing a novel example of a copper(i) atom being (quasi-)linearly coordinated by the pair of unidentate (dptu) sulfur ligands, Cu-S 2.1770(5), 2.1811(5) A, S-Cu-S 162.18(2) degrees . The nu(CuX) vibrational frequencies are assigned in the far-IR spectra of [XCu(dptu)(2)].H(2)O (X = Cl, Br, I) at 274, 207, and 190 cm(-1) respectively. The broadline static (65)Cu NMR spectra of [Cl(2)Cu(2)(dptu)(4)].2CH(3)CN and [X(2)Cu(2)(dptu)(4)] (X = Br, I) have been recorded at 9.4 and 7.05 T, and the spectra have been analysed to yield the (65)Cu nuclear quadrupole coupling and chemical shift parameters. The (63,65)Cu nuclear quadrupole resonance frequencies of [XCu(dptu)(2)].H(2)O (X = Cl, Br, I) have also been measured, and the resulting (65)Cu quadrupole coupling constants are ca. 4x those of the dimeric [X(2)Cu(2)(dptu)(4)] compounds.

Topics: Bromides; Chlorides; Copper; Crystallography, X-Ray; Iodides; Magnetic Resonance Spectroscopy; Molecular Conformation; Spectrophotometry, Infrared; Thiourea

Very little is known about the molecular control of skin patterning and scale morphogenesis in teleost fish. We have found radially symmetrical epidermal placodes with down-regulation of retinol-binding protein 4 (rbp4) expression during the initial paired fin and scale morphogenesis in zebrafish (Danio rerio). This finding may be related to changes in keratinocyte cytodifferentiation and/or the integument retinoid metabolism. rbp4 transcripts are expressed afterward in the central epidermis of the scale papilla and gradually extend to the epidermis, covering the growing scale, whereas no transcripts were detected in posterior margin epidermis. In contrast, induction of apolipoprotein Eb (apoeb) and up-regulation of estrogen receptor 2a (esr2a) transcripts were observed in the epidermis at initiator sites of zebrafish ectodermal/dermal appendage morphogenesis. This expression was maintained in the posterior margin epidermis of the formed scales. esr2a was also strongly expressed in neuromasts, whereas no rbp4 and apoeb transcripts were detected in these mechanosensory structures. The observed epidermal molecular events suggest that epidermis patterning is due to an activator-inhibitor mechanism operational at epidermal-dermal interaction sites. rbp4 transcript expression was also strongly down-regulated by 1-phenyl-2-thio-urea (PTU). As this inhibitor is commonly used to block obscuring pigmentation during in situ hybridization studies, this finding suggests that PTU should be used with caution, particularly in studying skin development.

Topics: Animals; Apolipoproteins E; Carrier Proteins; Down-Regulation; Epidermis; Estrogen Receptor beta; Gene Expression Regulation, Developmental; Larva; Morphogenesis; Receptors, Estrogen; Retinol-Binding Proteins, Plasma; RNA, Messenger; Thiourea; Transcription, Genetic; Up-Regulation; Zebrafish; Zebrafish Proteins

The inclusion interaction of beta-cyclodextrin and sym-diphenyl-thiourea and sym-diphenyl-urea was studied by UV spectra. The stoichiometry ratio for the formation of the inclusion complexes was determined by Hildebrand-Benesi equation linear analysis and molar ratio method. The standard molar Gibbs energies, enthalpies, and entropies were derived for the inclusion process by Ks at different temperatrues. The result showed that the host:guest ratio of inclusion complex between the two diphenyl compounds and beta-CD is 2 : 1, the stability constant (Ks) of 2 : 1 inclusion complexes was higher than that of 1 : 1 inclusion complexes due to cooperative binding in the close two hydrophobic cyclodextrin cavities, and the association of the guest molecule with beta-CD was favored by enthalpy changes, proving that the Van der Waals interaction and the dipole-dipole interaction were main binding forces of cyclodextrin inclusion complex.

Topics: Algorithms; beta-Cyclodextrins; Hydrophobic and Hydrophilic Interactions; Kinetics; Models, Chemical; Spectrophotometry, Ultraviolet; Thiourea; Urea

The reaction between 2,3-dichloro-1,4-naphthoquinone and N,N'-diphenyl thiourea in acetonitrile medium, which yields the product, 2,3-(N,N'-diphenylthioureylene)-naphtho-1,4-quinone has been found to take place in two ways--thermal and photochemical. The thermal (dark) reaction occurs through an electron donor-acceptor (EDA) adduct as intermediate with evolution of HCl and kinetic data fit into the scheme A + B<==>AB(fast)-->product(slow) Formation constant of the EDA adduct and the rate constant of the slow process have been determined at four different temperatures from which the enthalpy of formation of AB has been determined. The photochemical reaction has been studied with 360 nm ordinary light and also with 365 and 370 nm laser beams. Use of laser causes about 10(3)-fold increase in the rate of the reaction but does not affect the quantum yield. The final product has been isolated and characterised by elemental analysis, 1H and 13C NMR, IR spectroscopy and mass spectrometry.

Topics: Electron Transport; Kinetics; Magnetic Resonance Spectroscopy; Naphthoquinones; Photochemistry; Spectrophotometry; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; Thiourea

About 21% of the patients with occupational contact dermatitis registered in the Information Network of Departments of Dermatology (IVDK) in the years 1995-2001 were patch tested due to suspected rubber glove allergy. We analysed reaction frequencies to thiurams, dithiocarbamates, mercaptobenzothiazole (MBT) and its derivatives, thioureas, and 1,3-diphenylguanidine (1,3-DPG). Thiurams were by far the most frequent rubber allergens in these patients (16.2% positive reactions, age- and sex-standardized), and the reaction frequency showed a decline from 20.9% in 1997 to 12.8% in 2000. However, this trend was not statistically significant, and was followed by an increase to 16.5% in 2001. All other rubber allergens showed no time trend at all. Although, according to manufacturers' information, the use of dithiocarbamates and MBT derivatives in rubber glove production increased in recent years, these allergens elicited positive reactions in only about 3% of the patients tested, and showed no increasing trend. Thioureas and 1,3-DPG are not widely used in rubber glove production, and play only a minor role in rubber glove contact allergy. Most of the positive reactions to 1,3-DPG are probably false-positive, irritant reactions.

Topics: Adult; Allergens; Benzothiazoles; Dermatitis, Allergic Contact; Dermatitis, Occupational; Female; Germany; Gloves, Protective; Hand Dermatoses; Humans; Latex Hypersensitivity; Male; Thiazoles; Thiocarbamates; Thiourea; Thiram

A method for the determination of Au, Pt, Pd and Rh by ICP-AES after preconcentration on a column containing diphenylthiourea immobilized on aluminum oxide was developed. The optimum acidity of solution, amount of adsorbent, elution solution, flow rate and volume of the samples were obtained for the elements studied. The effect of interfering ions on the recovery of the analytes was also investigated. Under the optimum measuring conditions, the recoveries were found to be between 95%-105%. The detection limits of Au, Pd, Pt and Rh was 0.0085, 0.022, 0.015 and 0.022 microgram.g-1, respectively, and the relative standard deviation was lower than 5%. This procedure was applied to the determination of Au, Pd, Pt and Rh in geological samples.

Topics: Aluminum Oxide; Geological Phenomena; Geology; Gold; Palladium; Platinum; Rhodium; Spectrophotometry, Atomic; Thiourea

Topics: Allergens; Butylated Hydroxytoluene; Dermatitis, Allergic Contact; Dermatitis, Occupational; Diagnosis, Differential; Humans; Male; Microcomputers; Middle Aged; Patch Tests; Thiourea; Thumb

Topics: Arthroplasty, Replacement, Hip; Dermatitis, Allergic Contact; Female; Humans; Middle Aged; Neoprene; Orthopedic Fixation Devices; Patch Tests; Phenylenediamines; Thiourea

Fluorescein-labeled oligodeoxynucleotides (ODNs) from automated synthesis commonly produce multiple peaks in high performance liquid chromatography (HPLC) chromatograms. We found that these peaks are due to chemical modifications of the ODNs instead of the common perception of isomers. To identify the modifications, a model ODN, fluorescein-T(25), was synthesized and five compounds were isolated. Nuclease P1 (NP1) digestion was employed to cleave these compounds into nucleotides and fluorescein-nucleotides in order that the modifications be determined by mass spectrometry (MS). Analyses of NP1 digestion products containing fluorescein by MS revealed the expected product F1-T (M) and four unexpected compounds with MWs at M-1, M-17, M-16 and M + 16, respectively. Collision-induced dissociation (CID) spectra of these digestion products indicate that all modifications occur on the thiourea linkage [-NH-C( = S)-NH-] to the fluorescein moiety and the adjacent phosphate group, and the modifications were determined. The modifications were also confirmed by accurate mass measurement with Fourier transform mass spectrometry (FT-MS), by the synthesis of a reference compound, and by a mechanistic study using model compounds. These results demonstrate the power of the mass spectrometric techniques by determining the structures of two pairs of ODNs with MW difference of 1 Da. The results also suggest that fluorescein phosphoramidite with a thiourea linkage is not appropriate for the automated synthesis of fluorescein-labeled ODNs of high purity.

Topics: Chromatography, High Pressure Liquid; Contrast Media; Fluorescein; Guanidines; Molecular Weight; Oligodeoxyribonucleotides; Reference Standards; Reproducibility of Results; Single-Strand Specific DNA and RNA Endonucleases; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Thiourea

Topics: Buttocks; Clothing; Dermatitis, Allergic Contact; Female; Humans; Middle Aged; Neoprene; Textiles; Thigh; Thiourea

In predicting human skin sensitization due to possible risky chemicals, it is not sufficient to evaluate solely the minimum induction dose (MID) or the standard challenge dose (SCD) in the Guinea Pig Maximization Test (GPMT). Nakamura et al. (1994) (Nakamura, A., Momma, J., Sekiguchi, H., Noda, T., Yamano, T., Kaniwa, M., Kojima, S., Tsuda, M., Kurokawa, Y., 1994. A new protocol and criteria for quantitative determination of sensitization potencies of chemicals by guinea pig maximization test. Contact Dermatitis 31, 72-85) previously measured the residual dose of chemicals in the products implicated in human allergic accidents, and stated that '... the level of chemical in the products (direct exposure-dose = DED) was similar to or higher than value of sensitization potency.' However, several of the chemicals listed in their article, show an even lower value of sensitization potency than the DED, although a potential correlation between results of the GPMT and the DED was seemed to be evident; a key question about the essential rule of those parameters therefore remains open. Using the data of Nakamura et al. (1994), we analyzed the functional rules of the three independent parameters, the MID, the SCD, and the DED on which the GPMT is based. Calculations of the degree of allergic reactions elicited in humans provided a range of discrimination constants (D) using the formula; D = DED/(MID*SCD). Possible human allergic accidents may be predicted when the dose of a candidate chemical in a chemical product (equal to DED) exceeds the value; D*(MID*SCD), following the correct evaluation of the MID as well as the SCD.

Topics: Allergens; Animals; Dermatitis, Contact; Dose-Response Relationship, Drug; Drug Hypersensitivity; Guinea Pigs; Household Products; No-Observed-Adverse-Effect Level; Phenylenediamines; Skin; Thiourea; Toxicity Tests

Topics: Braces; Dermatitis, Allergic Contact; Humans; Male; Middle Aged; Neoprene; Thiourea

Electron impact mass spectronomy analysis of the amino-terminal amino acid of the small subunit (SSU) of ribulose-1,5-bisphosphate carboxylase (Rubisco) showed that the amino-terminal methionine residue is post-translationally modified to N-methyl-methionine. Modification of the amino-terminal methionine residue was found in mature SSU proteins from the dicotyledonous plants pea and spinach as well as the monocotyledonous plants barley and corn. SSU methyltransferase is a soluble protein in the chloroplast stroma and accepts heterologously expressed non-methylated SSU as a substrate using S-adenosylmethionine as methyl-group donor. We show that this modification occurs after post-translational uptake of the precursor form of SSU into chloroplasts and processing to its mature size. This reaction represents a new step in the import and assembly pathway of Rubisco holoenzyme.

Topics: Chloroplasts; Chromatography, High Pressure Liquid; Hordeum; Kinetics; Macromolecular Substances; Mass Spectrometry; Methylation; Methyltransferases; Peptide Fragments; Pisum sativum; Ribulose-Bisphosphate Carboxylase; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Spinacia oleracea; Thiourea; Zea mays

Topics: Adult; Dermatitis, Allergic Contact; Diving; Humans; Male; Neoprene; Thiourea

Micellar capillary electrophoresis is optimized for separation of phenylthiohydantoin (PTH) amino acids produced in manual Edman degradation reaction for protein sequencing. There are also two major side-products produced by the Edman degradation reaction: diphenylthiourea and dimethylphenylthiourea. We report the complete separation of 19 PTH amino acids plus the two major side-reaction products in 10 min. Capillary electrophoresis is used to identify the five residues generated by manual Edman degradation sequencing of a pentapeptide.

Topics: Amino Acid Sequence; Amino Acids; Electrophoresis; Hydrogen-Ion Concentration; Micelles; Molecular Sequence Data; Peptide Fragments; Peptides; Phenylthiohydantoin; Phenylthiourea; Reference Standards; Thiourea; Thymopoietins

The oxidation of thiourea, phenylthiourea, 1,3-diphenylthiourea, 1,3-bis-(3,4-dichlorophenyl)-2-thiourea and 1,1-dibenzyl-3-phenyl-2-thiourea was measured in reactions catalyzed by purified pig liver flavin-containing monooxygenase (FMO-1) and by microsomal fractions isolated from pig, guinea pig, chicken, rat and rabbit tissues. The reactions, followed by measuring substrate-dependent thiocholine oxidation [Guo and Ziegler, Anal Biochem 198: 143-148, 1991], were carried out in the presence of 2 mM 1-benzylimidazole to minimize potential interference from reactions other than those catalyzed by isoforms of the flavin-containing monooxygenase (FMO). While at saturating substrate concentrations the Vmax for purified FMO-1 catalyzed oxidation of all five thiocarbamides was essentially constant, velocities for the microsomal catalyzed reactions varied not only with tissue and species but also with the van der Waals' surface area of the thiocarbamide. Rat liver, rat kidney and rabbit liver microsomes failed to catalyze detectable oxidation of thiocarbamides larger than 1,3-diphenylthiourea and lung microsomes from a female rabbit only accepted substrates smaller than 1,3-diphenylthiourea. On the other hand, liver microsomes from chickens, pigs and guinea pigs catalyzed the oxidation of larger thiocarbamides, but the rates decreased with increasing substrate size and chicken liver microsomes showed no detectable activity with the largest thiocarbamide tested. To define more precisely the parameters affecting thiocarbamide substrate specificity of microsomal preparations, activities present in detergent extracts of guinea pig liver microsomes were separated into three distinct fractions. The substrate specificities of these partially purified fractions were different and consistent with the difference observed with microsomal catalyzed reactions. This strongly suggests that thiocarbamides that differ in size may be useful probes for measuring the number of activities of FMO isoforms in crude tissue preparations.

Topics: Animals; Chickens; Female; Flavins; Guinea Pigs; Isoenzymes; Kidney; Male; Methimazole; Microsomes; Microsomes, Liver; Oxygenases; Rabbits; Rats; Substrate Specificity; Swine; Thiourea

Sprague-Dawley rats were administered ethylenethiourea (ETU), 1,3-dimethyl-2-thiourea (DMT), 1,3-dibutyl-2-thiourea (DBT), or 1,3-diphenyl-2-thiourea (DPT) by gavage from Days 6 to 20 of gestation. Daily dosage levels (mg/kg/day) were ETU at 0, 15, 25 and 35; DMT at 0, 15, 25, 50, 100, and 200; DBT at 0, 15, 25, 50, 100, and 200; and DPT at 0, 25, 50, 100, and 200. There was evidence of maternal toxicity at all doses of DMT and at doses greater than or equal to 50 mg DBT/kg/day. DPT was embryolethal at 200 mg/kg/day. Fetotoxicity was observed at doses greater than or equal to 15 mg DMT/kg/day, greater than or equal to 15 mg DBT/kg/day, and greater than or equal to 100 mg DPT/kg/day. ETU was the only chemical tested that proved to be teratogenic.

Topics: Animals; Behavior, Animal; Body Weight; Embryo, Mammalian; Ethylenethiourea; Female; Gestational Age; Intubation, Gastrointestinal; Pregnancy; Rats; Rats, Inbred Strains; Reproduction; Teratogens; Thiourea

11 cases of contact dermatitis from Vulkan heat retainers are reported. The skin eruptions started on days 1-11 after the 1st day of exposure. The clinical picture varied from eczema through urticaria to purpura. In some cases, the symptoms were severe. Patch testing was performed in 10 individuals and all reacted positively to the heat retainer and/or the rubber glue used in the heat retainer. A series of rubber chemicals was patch tested in 7 patients and all showed positive reactions to diphenylthiourea (DPTU), and all but one to ethylene thiourea (ETU). TLC examination revealed a spot with the same RF-value as DPTU in extracts of the adhesive, but no spot corresponding to ETU. There were no indications of impurities in the test preparations of DPTU and ETU. By HPLC, the content of DPTU in the adhesive was determined as 0.6% w/w.

Topics: Adhesives; Adult; Aged; Dermatitis, Occupational; Female; Hot Temperature; Humans; Hypersensitivity, Delayed; Male; Middle Aged; Patch Tests; Rubber; Thiourea

Topics: Adult; Dermatitis, Contact; Female; Humans; Male; Patch Tests; Thiourea

Topics: Adult; Biphenyl Compounds; Dermatitis, Occupational; Humans; Male; Neoprene; Protective Clothing; Thiourea

Topics: Animals; Dermatitis, Contact; Guinea Pigs; Isothiocyanates; Skin Tests; Thiocyanates; Thiourea

28 patients reacting to a PVC adhesive tape used in routine patch testing gave positive reactions to diphenylthiourea (DPTU) and to phenylisothiocyanate (PITC) in low concentrations. DPTU is a heat stabilizer in the PVC and is partly decomposed to PITC. The two substances were found in another type of PVC. Thioureas giving isothiocyanates are also used in certain types of rubber. Isothiocyanates are present in plants, mainly of the Cruciferae family, and are also formed from thiuram sulfides and thiocarbamates. The connection between isothiocyanates derived from different sources should be investigated.

Topics: Adhesives; Dermatitis, Contact; Female; Humans; Isothiocyanates; Male; Patch Tests; Polyvinyl Chloride; Thiocyanates; Thiourea

Topics: Dermatitis; Dermatitis Herpetiformis; Humans; Thiourea

Topics: Drug Tolerance; Immune Tolerance; Leprosy; Thiourea

Topics: Biphenyl Compounds; Diphenhydramine; Thiourea

Topics: Leprosy; Phenylthiourea; Thiouracil; Thiourea

Topics: Leprosy; Thiourea

Topics: Humans; Leprosy; Phenylthiourea; Thiourea