ABSTRACT
BACKGROUND AND OBJECTIVE: Residues from shrimp farming have a great potential for sugar production and the production of derivatives for the low-carbon chemical industry. Obtainment of bioactives from chitosan has been extensively investigated using different methodologies. The purpose of this work was to study the chitosan depolymerization reaction aiming at the production of monomers without the use of additional enzymes or mineral acids. MATERIALS AND METHODS: In this work, we systematically study the effect of sodium nitrite concentration and reaction conditions (pH and temperature ranges) with acetic acid as the solvent on the chitosan depolymerization reaction aiming at the production of monomers, specifically 2,5- anhydromannose, without the use of additional enzymes or mineral acids. RESULTS: The results indicate that only a small range of reaction conditions and nitrite concentrations allow for obtaining the monomer, while in most combinations of these parameters, oligomers are obtained. We found that the temperature decisively affects the reaction yield, with the attainment of 2,5-anhydromannose favored at lower temperatures. CONCLUSION: The method proved to be simple and easy to perform allowing to obtain 2,5- anhydromannose with the use of low-cost reagents. This monomer can be converted into several derivatives for industrial application (5-Hydroxymethylfurfural, ethanol, etc.).
Subject(s)
Chitosan , Acids , Chitin/chemistry , Chitosan/chemistry , Hexoses , Nitrous Acid/chemistryABSTRACT
Nitrogen oxyanions and oxyacids are important agents in atmospheric chemistry and medical biology. Although their chemical behavior in solution is relatively well understood, they may behave very differently at the water/air interface of atmospheric aerosols or at the membrane/water interface of cells. Here, we developed a fully classical model for molecular dynamics simulations of NO3-, NO2-, HNO3, and HNO2 in the framework of the GROMOS 53A6 and 54A7 force field versions. The model successfully accounted for the poorly structured solvation shell and ion pairing tendency of NO3-. Accurate pure-liquid properties and hydration free energies were obtained for the oxyacids. Simulations at the water/air interface showed a local enrichment of HNO3 and depletion of NO3-. The effect was discussed in light of earlier spectroscopic data and ab initio calculations, suggesting that HNO3 behaves as a weaker acid at the surface of water. Our model will hopefully allow for efficient and accurate simulations of nitrogen oxyanions and oxyacids in solution and at microheterogeneous interface environments.
Subject(s)
Atmosphere/chemistry , Molecular Dynamics Simulation , Nitrates/chemistry , Nitric Acid/chemistry , Nitrites/chemistry , Nitrous Acid/chemistry , Particle Size , Surface PropertiesABSTRACT
The effect of free ammonia (NH3 or FA), free nitrous acid (HNO2 or FNA), and total alkalinity (TA) on the performance of a partial nitrification (PN) sequencing batch reactor (SBR) treating anaerobically pretreated pig slurry was studied. The SBR was operated under alternating oxic/anoxic (O/A) conditions and was fed during anoxic phases. This strategy allowed using organic matter to partially remove nitrite (NO2-) and nitrate (NO3-) generated during oxic phases. The desired NH4+ to NO2- ratio of 1.3 g N/g N was obtained when an Ammonium Loading Rate (ALR) of 0.09 g NH4+-N/L·d was applied. The system was operated at a solid retention time (SRT) of 15-20 d and dissolved oxygen (DO) levels higher than 3 mg O2/L during the whole operational period. PN mainly occurred caused by the inhibitory effect of FNA on nitrite oxidizing bacteria (NOB). Once HNO2 concentration was negligible, NH4+ was fully oxidized to NO3- in spite of the presence of FA. The use of biomass acclimated to ammonium as inoculum avoided a possible effect of FA on NOB activity.
Subject(s)
Ammonia/chemistry , Bioreactors/microbiology , Nitrification/drug effects , Nitrous Acid/chemistry , Ammonium Compounds/chemistry , Animals , Bacteria/growth & development , Biomass , Nitrites/chemistry , Oxidation-Reduction , Oxygen/chemistry , Swine , Waste Disposal, Fluid/methods , Water Purification/methodsABSTRACT
The primary S-nitrosothiol, S-nitroso-N-acetylcysteine (SNAC) is a nitric oxide donor with potential pharmaceutical applications for the oral treatment of hepatic steatosis and cirrhosis and for protection against gastric acid-peptic disorders. However, its low thermal stability precludes the preparation of stable dosage forms based on presynthesized SNAC. In this study, we describe an innovative strategy for the oral administration of SNAC based on its intratablet formation via the S-nitrosation reaction of its parent stable thiol, N-acetyl-L-cysteine by nitrous acid during the absorption of water by the tablet. The proposed strategy allows for the manufacturing of thermally stable oral dosage forms for the controlled release of SNAC in the enteric medium.
Subject(s)
Nitric Oxide Donors/administration & dosage , Nitric Oxide Donors/chemistry , Nitroso Compounds/chemistry , S-Nitrosothiols/administration & dosage , S-Nitrosothiols/chemistry , Acetylcysteine/chemistry , Acetylcysteine/pharmacology , Administration, Oral , Chemistry, Pharmaceutical , Delayed-Action Preparations , Nitrosation , Nitrous Acid/chemistry , Tablets/chemistry , Water/chemistryABSTRACT
In the present work we studied the reaction under gastric conditions of pyrogallol red (PGR), a polyphenolic dye, with nitrous acid (HONO). PGR has been used as a model polyphenol due to its strong UV-visible absorption and its high reactivity towards reactive species (radicals and non-radicals, RS). The reaction was followed by UV-visible spectroscopy and high performance liquid chromatography (HPLC). A clear decrease of the PGR absorbance at 465 nm was observed, evidencing an efficient bleaching of PGR by HONO. In the initial stages of the reaction, each HONO molecule nearly consumed 2.6 PGR molecules while, at long reaction times, ca. 7.0 dye molecules were consumed per each reacted HONO. This result is interpreted in terms of HONO recycling. During the PGR-HONO reaction, nitric oxide was generated in the micromolar range. In addition, the rate of PGR consumption induced by HONO was almost totally abated by argon bubbling, emphasising the role that critical volatile intermediates, such as NO and/or nitrogen dioxide (NO2), play in the bleaching of this phenolic compound.
Subject(s)
Nitrous Acid/chemistry , Pyrogallol/analogs & derivatives , Chromatography, High Pressure Liquid , Nitric Oxide/chemistry , Nitrogen Dioxide/chemistry , Pyrogallol/chemical synthesis , Pyrogallol/chemistryABSTRACT
A new clock reaction based on chlorate, iodine and nitrous acid is presented. The induction period of this new clock reaction decreases when the initial concentrations of chlorate, nitrous acid and perchloric acid increase, but it is independent on the initial iodine concentration. The proposed mechanism is based on the LLKE autocatalytic mechanism for the chlorite-iodide reaction and the initial reaction between chlorate and nitrous acid to produce nitrate and chlorite. This new clock reaction opens the possibility for a new family of oscillating reactions containing chlorate or nitrous acid, which in both cases has not been observed until now.
Subject(s)
Iodine/chemistry , Nitrous Acid/chemistry , Perchlorates/chemistry , CatalysisABSTRACT
Heparin-like glycans with diverse disaccharide composition and high anticoagulant activity have been described in several families of marine mollusks. The present work focused on the structural characterization of a new heparan sulfate (HS)-like polymer isolated from the mollusk Nodipecten nodosus (Linnaeus, 1758) and on its anticoagulant and antithrombotic properties. Total glycans were extracted from the mollusk and fractionated by ethanol precipitation. The main component (>90%) was identified as HS-like glycosaminoglycan, representing approximately 4.6 mg g(-1) of dry tissue. The mollusk HS resists degradation with heparinase I but is cleaved by nitrous acid. Analysis of the mollusk glycan by one-dimensional (1)H, two-dimensional correlated spectroscopy, and heteronuclear single quantum coherence nuclear magnetic resonance revealed characteristic signals of glucuronic acid and glucosamine residues. Signals corresponding to anomeric protons of nonsulfated, 3- or 2-sulfated glucuronic acid as well as N-sulfated and/or 6-sulfated glucosamine were also observed. The mollusk HS has an anticoagulant activity of 36 IU mg(-1), 5-fold lower than porcine heparin (180 IU mg(-1)), as measured by the activated partial thromboplastin time assay. It also inhibits factor Xa (IC(50) = 0.835 microg ml(-1)) and thrombin (IC(50) = 9.3 microg ml(-1)) in the presence of antithrombin. In vivo assays demonstrated that at the dose of 1 mg kg(-1), the mollusk HS inhibited thrombus growth in photochemically injured arteries. No bleeding effect, factor XIIa-mediated kallikrein activity, or toxic effect on fibroblast cells was induced by the invertebrate HS at the antithrombotic dose.
Subject(s)
Anticoagulants/chemistry , Anticoagulants/metabolism , Arteries , Carotid Artery Thrombosis/prevention & control , Endothelium, Vascular , Extracellular Matrix/chemistry , Heparan Sulfate Proteoglycans/metabolism , Heparan Sulfate Proteoglycans/therapeutic use , Animals , Anticoagulants/isolation & purification , Anticoagulants/therapeutic use , Antithrombins/metabolism , Arteries/drug effects , Arteries/pathology , Arteries/radiation effects , Bivalvia/metabolism , Carbohydrate Conformation , Cell Line , Endothelium, Vascular/drug effects , Endothelium, Vascular/pathology , Endothelium, Vascular/radiation effects , Extracellular Matrix/metabolism , Factor Xa/metabolism , Factor Xa Inhibitors , Female , Heparan Sulfate Proteoglycans/chemistry , Heparan Sulfate Proteoglycans/isolation & purification , Heparin/metabolism , Heparin/therapeutic use , Heparin Cofactor II/metabolism , Heparin Lyase/metabolism , Humans , Male , Nitrous Acid/metabolism , Rats , Spectrum Analysis/methods , Swine , Thrombin/antagonists & inhibitors , Thrombin/metabolismABSTRACT
The zebrafish Danio rerio (Chordata-Cyprinidae) is a model organism frequently used to study the functions of proteoglycans and their glycosaminoglycan (GAG) chains. Although several studies clearly demonstrate the participation of these polymers in different biological and cellular events that take place during embryonic development, little is known about the GAGs in adult zebrafish. In the present study, the total GAGs were extracted from the whole fish by proteolytic digestion, purified by anion-exchange chromatography and characterized by electrophoresis after degradation with specific enzymes and/or by high-performance liquid chromatography (HPLC) analysis of the disaccharides. Two GAGs were identified: a low-molecular-weight chondroitin sulfate (CS) and keratan sulfate (KS), corresponding to approximately 80% and 20% of the total GAGs, respectively. In the fish eye, KS represents approximately 80% of total GAGs. Surprisingly, no heparinoid was detected, but may be present in the fish at concentrations lower than the limit of the method used. HPLC of the disaccharides formed after chondroitin AC or ABC lyase degradation revealed that the zebrafish CS is composed by DeltaUA-1-->3-GalNAc(4SO4) (59.4%), DeltaUA-1-->3-GalNAc(6SO4) (23.1%), and DeltaUA-1-->3-GalNAc (17.5%) disaccharide units. No disulfated disaccharides were detected. Immunolocalization on sections from zebrafish retina using monoclonal antibodies against CS4- or 6-sulfate showed that in the retina these GAGs are restricted to the outer and inner plexiform layers. This is the first report showing the presence of KS in zebrafish eye, and the structural characterization of CS and its localization in the zebrafish retina. Detailed information about the structure and tissue localization of GAGs is important to understand the functions of these polymers in this model organism.
Subject(s)
Chondroitin Sulfates/chemistry , Glycosaminoglycans/metabolism , Keratan Sulfate/chemistry , Animals , Chondroitin Sulfates/physiology , Cornea/metabolism , Disaccharides/chemistry , Electrophoresis, Agar Gel , Electrophoresis, Polyacrylamide Gel , Gene Expression Regulation , Hexuronic Acids/chemistry , Keratan Sulfate/physiology , Models, Biological , Molecular Weight , Nitrous Acid/chemistry , Retina/metabolism , Uronic Acids/chemistry , ZebrafishABSTRACT
The interpolyelectrolyte reaction between chitosan (CHI) and alginate (ALG) was followed by conductimetry and potentiometry. Five chitosan samples, all with almost the same degree of N-acetylation (DA approximately 0.20) and molecular weights ranging from 5 x 10(3) to 2.5 x 10(5) Da were used. The polyelectrolyte complex was formed using alginate samples with three different M/G values (0.44, 1.31 and 1.96). The composition of the complex, Z (Z = [CHI]/[ALG]) resulted 0.70 +/- 0.02, independently of the molecular weight of chitosan and the composition of the alginate used. The degree of complexation was 0.51 with no dependence on the alginate composition.
Subject(s)
Alginates/chemistry , Chitosan/chemistry , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Electrolytes/chemistry , Molecular Weight , Nitrous Acid/chemistry , SolutionsABSTRACT
Heparan sulfate (HS) present on the surface of hemopoietic stromal cells has important roles in the control of adhesion and growth of hemopoietic stem and progenitor cells. Recent studies have characterized several different heparan sulfate proteoglycans (HSPGs) from both human and murine bone marrow stromal cells. In the present study, we have compared the molecular structure of HS, metabolically labeled with [(35)S]-sulfate produced by two distinct preparations of murine hemopoietic stromal cell lines. These comprised a bone marrow-derived cell line S17 and a fetal liver-derived cell line AFT024. [(35)S]-HS was examined in the cell layers and in the culture medium. We identified and measured the relative proportions of the various glycosaminoglycans (GAGs) in the two stromal cell lines. Chondroitin sulfate (CS) was preponderantly secreted by the stromal cell lines, while HS was relatively more abundant in the cell-associated fractions. The two types of stromal cells differ in their HS composition, mainly due to different patterns of N- and O-sulfation. The two stromal cell lines expressed mRNA for different HSPGs. Data from reverse transcription PCR revealed that the two stromal cell lines expressed mRNA for glypican and syndecan4. Only AFT024 cell line expressed mRNA for betaglycan. There was no evidence for expression of mRNA for both syndecan1 and syndecan2. [(35)S]-sulfated macromolecules could be released from the cell surface of both stromal cell lines by phosphatidylinositol phospholipase C (PI-PLC), which is consistent with the expression of glypican detected by PCR experiments.
Subject(s)
Bone Marrow Cells/metabolism , Hematopoietic Stem Cells/metabolism , Heparitin Sulfate/metabolism , Liver/metabolism , Animals , Cell Line, Transformed , Cell Membrane/metabolism , Chondroitin Lyases/chemistry , Chondroitin Lyases/metabolism , Chromatography, Ion Exchange/methods , Cytokines/biosynthesis , DNA Primers , Disaccharides/biosynthesis , Disaccharides/chemistry , Electrophoresis, Agar Gel , Fetal Blood/cytology , Fetal Blood/metabolism , Hematopoiesis , Hematopoietic Stem Cells/cytology , Heparin/chemistry , Heparin/metabolism , Heparitin Sulfate/analysis , Humans , Liver/cytology , Mice , Nitrous Acid/chemistry , Reverse Transcriptase Polymerase Chain Reaction , Stromal Cells/metabolism , Sulfur Radioisotopes , Time FactorsABSTRACT
Sedação com óxido nitroso auxilia controle de ansiedade e dor no consultório dentário. Propriedade analgésica foi descoberta por CD
Subject(s)
Analgesia , Dental Anxiety , Nitrous Acid , PainABSTRACT
El óxido nítrico pasó de ser una molécula tóxica, producto de la combustión a ser un mediador de múltiples procesos biológicos. Los principales investigadores que trabajaron sobre el mismo recibieron en el año 1998 el premio Nobel. Se lo encuentra presente en las células del endotelio de todos los mamíferos y juega un papel fundamental en el proceso de relajación. Posteriormente se ha demostrado que se sintetiza en las plaquetas, células del sistema inmune, neuronas y otras células del organismo donde ejerce, otras acciones más allá de la vasodilatación. Su exceso o defecto permitió la comprensión de distintos mecanismos fisiopatológicos (shock séptico, hipertensión arterial). Su modulación permite tratar distintas entidades. La administración por vía inhalatoria tiene utilidad en diversas patologías. El tratamiento de la hipertensión pulmonar del recién nacido es el ejemplo más relevante, porque permitió mejorar la sobrevida y disminuyó el número de pacientes sometidos a Membrana de Oxigenación Extracorpórea. En el tratamiento de las cardiopatías congénitas que cursan con hipertensión pulmonar ocupa un lugar destacado en el intra, pre y postoperatorio. El Síndrome de Distrés Respiratorio del Adulto es quizá la entidad más cuestionada; ya que, si bien mejora la hipoxemia, no hay estudios que demuestren que mejora la sobrevida.
Subject(s)
Humans , Adult , Infant, Newborn , Nitric Oxide/administration & dosage , Nitric Oxide/pharmacokinetics , Nitric Oxide/pharmacology , Nitric Oxide/physiology , Nitric Oxide/chemical synthesis , Nitric Oxide/toxicity , Nitric Oxide/therapeutic use , Nitrous Acid/adverse effects , Administration, Inhalation , Anesthetics, Inhalation , Heart Defects, Congenital/therapy , Nitrogen Dioxide/toxicity , Endothelium , Extracorporeal Membrane Oxygenation , Hypertension, Pulmonary/therapy , Methemoglobin , Neonatology , Respiratory Insufficiency , Shock, SepticABSTRACT
El óxido nítrico pasó de ser una molécula tóxica, producto de la combustión a ser un mediador de múltiples procesos biológicos. Los principales investigadores que trabajaron sobre el mismo recibieron en el año 1998 el premio Nobel. Se lo encuentra presente en las células del endotelio de todos los mamíferos y juega un papel fundamental en el proceso de relajación. Posteriormente se ha demostrado que se sintetiza en las plaquetas, células del sistema inmune, neuronas y otras células del organismo donde ejerce, otras acciones más allá de la vasodilatación. Su exceso o defecto permitió la comprensión de distintos mecanismos fisiopatológicos (shock séptico, hipertensión arterial). Su modulación permite tratar distintas entidades. La administración por vía inhalatoria tiene utilidad en diversas patologías. El tratamiento de la hipertensión pulmonar del recién nacido es el ejemplo más relevante, porque permitió mejorar la sobrevida y disminuyó el número de pacientes sometidos a Membrana de Oxigenación Extracorpórea. En el tratamiento de las cardiopatías congénitas que cursan con hipertensión pulmonar ocupa un lugar destacado en el intra, pre y postoperatorio. El Síndrome de Distrés Respiratorio del Adulto es quizá la entidad más cuestionada; ya que, si bien mejora la hipoxemia, no hay estudios que demuestren que mejora la sobrevida. (AU)
Subject(s)
Humans , Adult , Infant, Newborn , Nitric Oxide/physiology , Nitric Oxide/pharmacology , Nitric Oxide/administration & dosage , Nitric Oxide/pharmacokinetics , Nitric Oxide/therapeutic use , Nitric Oxide/toxicity , Nitric Oxide/chemical synthesis , Endothelium/physiology , Administration, Inhalation , Hypertension, Pulmonary/therapy , Heart Defects, Congenital/therapy , Respiratory Insufficiency/therapy , Neonatology , Anesthetics, Inhalation , Nitrogen Dioxide/toxicity , Nitrous Acid/adverse effects , Methemoglobin , Methemoglobin/toxicity , Shock, Septic , Extracorporeal Membrane OxygenationABSTRACT
Uric acid has been considered to be an efficient scavenger of peroxynitrite but the reaction between urate and peroxynitrite has been only partially characterized. Also, previous studies have indicated that urate may increase peroxynitrite-mediated oxidation of low density lipoprotein (LDL). Here, we examined the reaction between urate and peroxynitrite by combining kinetic, oxygen consumption, spin trapping, and product identification studies; in parallel, we tested the effect of urate upon peroxynitrite-mediated lipid oxidation. Our results demonstrated that urate reacts with peroxynitrite with an apparent second order rate constant of 4.8 x 10(2) M(-1). s(-1) in a complex process, which is accompanied by oxygen consumption and formation of allantoin, alloxan, and urate-derived radicals. The main radical was identified as the aminocarbonyl radical by the electrospray mass spectra of its 5, 5-dimethyl-l-pyrroline N-oxide adduct. Mechanistic studies suggested that urate reacts with peroxynitrous acid and with the radicals generated from its decomposition to form products that can further react with peroxynitrite anion. These many reactions may explain the reported efficiency of urate in inhibiting some peroxynitrite-mediated processes. Production of the aminocarbonyl radical, however, may propagate oxidative reactions. We demonstrated that this radical is likely to be the species responsible for the effects of urate in amplifying peroxynitrite-mediated oxidation of liposomes and LDL, which was monitored by the formation of lipid peroxides and thiobarbituric acid-reactive substances. The aminocarbonyl radical was not detectable during urate attack by other oxidants and consequently it is unlikely to be responsible for all previously described prooxidant effects of uric acid.
Subject(s)
Free Radicals/metabolism , Lipid Metabolism , Nitrates/metabolism , Oxidants/metabolism , Uric Acid/metabolism , Allantoin/metabolism , Alloxan/metabolism , Cyclic N-Oxides/metabolism , Electron Spin Resonance Spectroscopy , Free Radical Scavengers/metabolism , Horseradish Peroxidase/metabolism , Humans , Hydrogen Peroxide/metabolism , Hydrogen-Ion Concentration , Kinetics , Lipid Peroxides/metabolism , Lipoproteins, LDL/metabolism , Liposomes/metabolism , Nitrous Acid/metabolism , Oxidation-Reduction , Oxygen/metabolism , Peroxynitrous Acid , Thiobarbituric Acid Reactive Substances/metabolismABSTRACT
The isolation, some structural features, physicochemical properties and pharmacological activities of a heparin from Anomalocardia brasiliana are reported. It is shown that the mollusc heparin is very similar to those present in mammalian tissues with regard to chemical composition, physicochemical properties, pharmacological activities and susceptibility to heparinase and heparitinase II from Flavobacterium heparinum, as well as to the types of products formed by the action of these enzymes. Three significant quantitative differences were observed for the mollusc heparin when compared with the ones from mammalian origin, namely, a higher degree of binding with antithrombin III (45%), higher molecular weight (27-43 kDa) and higher anticoagulant activity (320 I.U./mg). The possible biological role of heparin is discussed in view of the present findings.
Subject(s)
Heparin/isolation & purification , Mollusca/analysis , Animals , Antithrombins/analysis , Barium , Blood Coagulation/drug effects , Cattle , Chemical Precipitation , Heparin/pharmacology , Hydrolysis , Isoelectric Focusing , Nitrous Acid , Protein BindingSubject(s)
DNA, Bacterial/radiation effects , Haemophilus influenzae/genetics , Nitrites/pharmacology , Nitrous Acid/pharmacology , Transformation, Genetic , Haemophilus influenzae/drug effects , Haemophilus influenzae/radiation effects , Nucleic Acid Denaturation , Transformation, Genetic/drug effects , Transformation, Genetic/radiation effects , Ultraviolet RaysABSTRACT
One hundred and eleven strains of beta-hemolytic streptococci of human origin were grouped by the new nitrous acid procedure described by El Kholy et al. The results were comparable to the grouping obtained by the classical Lancefield hot-hydrochloric acid method. The El Kholy technique is simple and economic and is shown to be as sensitive and specific as the Lancefield procedure. We recommend the new method for routine use in the clinical laboratory and in studies on the prevalence of Streptococcus pyogenes in a developing country such as Brazil.
Subject(s)
Serotyping/methods , Streptococcus/classification , Humans , Hydrochloric Acid , Nitrous AcidABSTRACT
Fifteen temperature-sensitive (ts) mutants were isolated from 4 Venezuelan equine encephalomyelitis virus clones by nitrous acid treatment or by growing the virus in the presence of 5-fluoruracil. Three of them were classified as RNA- mutants by their inability to synthesize RNA at nonpermissive temperature (1.5-3.3% in respect to the wild type). The remaining 11 mutants showed a slight decrease of RNA synthesis at the nonpermissive temperature (32-73+) and were referred to the RNA+ phenotype. One mutant possessed RNA +/- phenotype (18%). Five complementation groups were determined by complementation analysis of the mutants.
Subject(s)
Encephalitis Virus, Venezuelan Equine/genetics , Mutation , RNA, Viral/genetics , Encephalitis Virus, Venezuelan Equine/drug effects , Fluorouracil/pharmacology , Genetic Complementation Test , Mutagens , Nitrous Acid/pharmacology , Phenotype , TemperatureABSTRACT
Nitrohexane has been identified as a major product formed following treatment of corn (Zea mays) with nitrous acid. Preliminary evidence suggests that another compound isolated from the nitrosated corn is an unsaturated nitrolic acid. As an aid to the analysis of N-nitro compounds, we have characterized the response of a chemiluminescence detector (Thermal Energy Analyzer) as a function of pyrolysis chamber temperature for several nitrosamines and for an aliphatic C-nitroso compound, an aromatic C-nitro compound, a nitramine and an alkyl nitrite. The response-temperature profiles are valuable in distinguishing among the various compounds and in optimizing the sensitivity of the detector for use in chromatography. Other tests, including photolysis and stability toward nitrite-scavenging reagents, further aid in distinguishing among the various compounds.
Subject(s)
Nitrites , Nitroso Compounds/analysis , Nitrous Acid , Zea mays , Chromatography, Gas , Colombia , Hexanes/analysis , Massachusetts , Nitro Compounds/analysis , Nitrosamines/analysis , Stomach Neoplasms/chemically induced , Zea mays/analysisABSTRACT
Fifteen ts mutants of Venezuelan equine encephalomyelitis (VEE) virus have been produced and studied. Two of them were isolated from a virus population grown in the presence of 5-fluorouracyl and 13 from a virus suspension treated with nitrous acid. The efficiency of plating 40 degrees/35 degrees of various mutants varied from 2 X 10(-2) to 6 X 10(-6). Three ts mutants had RNA- phenotype (RNA synthesis at a nonpermissive temperature was 1.5-3.3% of that of the wild type), 11 ts mutants had RNA+ phenotype (RNA synthesis decreased insignificantly, 32-75%), and one ts mutant was intermediate (18%).