PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

N-Nitrozodimetyloamina : dokumentacja proponowanych dopuszczalnych wielkości narażenia zawodowego

Treść / Zawartość
Identyfikatory
Warianty tytułu
EN
N-Nitrosodimethylamine : documentation of proposed values of occupational exposure limits (OELs)
Języki publikacji
PL
Abstrakty
PL
N-Nitrozodimetyloamina to palna, lotna, oleista ciecz o żółtej barwie i charakterystycznym zapachu. Stosowana jest w: przemyśle gumowym, skórzanym, odlewniczym oraz w rolnictwie. W Polsce w latach 2005-2016 na N-nitrozodimetyloaminę było narażonych od kilkudziesięciu do kilkuset osób rocznie. Największe stężenia, na które byli narażani pracownicy przemysłu gumowego, wynosiły 4,5 ÷ 9,2 μg/m3. Zatrucia ostre N-nitrozodimetyloaminą u ludzi zdarzały się w wyniku wypadków lub działań o podłożu kryminalnym. Brak jest informacji na temat toksycznego działania N-nitrozodimetyloaminy w warunkach narażenia zawodowego ludzi. Po dożołądkowym podaniu N-nitrozodimetyloaminy szczurom wartość LD50 wynosiła poniżej 50 mg/kg mc. Przewlekłe narażenie (przez 45 ÷ 52 tygodnie) szczurów na N-nitrozodimetyloaminę drogą pokarmową, w dawkach 0,144 ÷ 3,6 mg/kg mc./dzień, powodowało zależne od dawki nasilenie występowania przypadków nowotworów: wątroby, nerek i płuc oraz skrócenie czasu życia. U szczurów, które narażano inhalacyjnie na N-nitrozodimetyloaminę o stężeniach: 120; 600 lub 3 000 μg/m3 przez 207 dni, obserwowano – zależne od stężenia – zwiększenie śmiertelności zwierząt oraz występowanie nowotworów nosa. Najwięcej informacji na temat zależności skutku działania toksycznego od poziomu narażenia pochodzi z doświadczenia wykonanego na szczurach, którym N-nitrozodimetyloaminę podawano przewlekle w wodzie do picia w dawkach 0,001 ÷ 0,697 mg/kg mc./dzień (samcom) lub 0,002 ÷ 1,244 mg/kg mc./dzień (samicom). Dla dawek do 0,2 mg/kg mc./ dzień ryzyko występowania nowotworów wątroby rosło (w zależności od podanej dawki). N-Nitrozodimetyloamina działa mutagennie i genotoksycznie po aktywacji metabolicznej. Ma to związek z mechanizmem działania genotoksycznego i rakotwórczego, za który są odpowiedzialne metabolity. Międzynarodowa Agencja Badań nad Rakiem (IARC) zaliczyła N-nitrozodimetyloaminę do grupy 2A (prawdopodobnie rakotwórczy dla ludzi), w ACGIH (w 2001 r.) zakwalifikowano N-nitrozodimetyloaminę do grupy A3 (udowodnione działanie rakotwórcze na zwierzęta i nieznane działanie rakotwórcze na ludzi). Unia Europejska zaliczyła związek do kategorii kancerogenności 1B z przypisem „H350 – może powodować raka”. Podstawą obliczenia wartości NDS dla N-nitrozodimetyloaminy było przewlekłe narażenie szczurów na związek w wodzie do picia i obserwowane zmiany w wątrobie. Na podstawie tych badań przeprowadzono ocenę ryzyka powstania dodatkowego nowotworu, które posłużyło do zaproponowania wartości NDS na poziomie 0,0025 mg/m3, w którym ryzyko nowotworowe wynosiłoby 6,15 10-4. Nie ma podstaw do wyznaczenia wartości najwyższego dopuszczalnego stężenia chwilowego (NDSCh) oraz dopuszczalnego stężenia w materiale biologicznym (DSB). Zaproponowano także oznaczenie związku „Carc. 1B” (substancja rakotwórcza kat. 1B) oraz „skóra” – wchłanianie substancji przez skórę może być tak samo istotne, jak przy narażeniu drogą oddechową. Zakres tematyczny artykułu obejmuje zagadnienia zdrowia oraz bezpieczeństwa i higieny środowiska pracy będące przedmiotem badań z zakresu nauk o zdrowiu oraz inżynierii środowiska.
EN
N-Nitrosodimethylamine is a flammable, volatile, oily liquid with a yellow color and a characteristic odor. It is used in the rubber and leather industry, foundry and agriculture. In Poland, in the years 2005-2016, several dozen to several hundred people per year were exposed on N-nitrosodimethylamine. The highest concentrations to which rubber industry workers in Poland were exposed were 4.5–9.2 µg/m³ . Acute poisoning with N-nitrosodimethylamine in humans occurred as a result of accidents or criminal activities. After intragastric administration of N-nitrosodimethylamine to rats, LD50 was below 50 mg/kg bw. Chronic oral exposure (45–52 weeks) of rats to N-nitrosodimethylamine at doses of 0.144–3.6 mg/kg/day resulted in a dose-dependent increase in the cancer incidence of the liver, kidneys and lungs, and shortening of lifespan. Most information about the relationship between the toxic effects and level of exposure comes from an experiment performed on rats, in which N-nitrosodimethylamine was administered chronically in drinking water at doses of 0.001–0.697 mg/kg body weight/day (males) or 0.002–1.244 mg/kg bw./day (females). For doses up to 0.2 mg/kg/day, the risk of liver cancer increased (depending on the dose). N-Nitrosodimethylamine was mutagenic and genotoxic after metabolic activation. This is related to the mechanism of genotoxic and carcinogenic action of the metabolites. The International Agency for Research on Cancer (IARC) has included N-nitrosodimethylamine to 2A group (probably carcinogenic to humans), ACGIH (in 2001) qualified N-nitrosodimethylamine to A3 group (proven carcinogenicity to animals and unknown human carcinogenicity). The European Union has classified the compound with the inscription “H350 - can cause cancer”. The basis for the calculation of a threshold limit value-time weighted average (TLV-TWA; maximum acceptable concentration – MAC) for N-nitrosodimethylamine was the chronic exposure of rats to the compound in drinking water and observed changes in the liver. On the basis of these studies, an assessment of the risk of an additional tumor was made, which has been used to propose MAC-TWA values at 0.0025 mg/m³ , for which the cancer risk would be 6.15 × 10-4. There is no basis for the short-term exposure limit (STEL) or biological limit value (BLV). The notations “Carc. 1B” (carcinogenic substance Cat. 1B) and “skin” (absorption through the skin may be as important as in the case of inhalation) were proposed. This article discusses the problems of occupational safety and health, which are covered by health sciences and environmental engineering.
Rocznik
Strony
65--119
Opis fizyczny
Bibliogr. 219 poz., rys., tab.
Twórcy
  • Uniwersytet Medyczny w Łodzi 90-151 Łódź, ul. J. Muszyńskiego 1 POLAND
  • Uniwersytet Medyczny w Łodzi 90-151 Łódź, ul. J. Muszyńskiego 1 POLAND
  • Uniwersytet Medyczny w Łodzi 90-151 Łódź, ul. J. Muszyńskiego 1 POLAND
Bibliografia
  • 1. ACGIH, American Conference of Governmental Industrial Hygienists (2001). N-Nitrosodimethylamine. TLV documentation. Cincinnati, OH,
  • 2. ACGIH. ACGIH, American Conference of Governmental Industrial Hygienists (2015). Threshold Limit Values for chemical substances and physical agents and Biological Exposure Indices. CD-ROM 2015-TLVs and BEI with 7th Edition Documentation. Cincinnati, OH, ACGIH.
  • 3. Alexandrov V.A. (1968). Blastomogenic effect of dimethylnitrosamine on pregnant rats and their offspring. Nature 281, 218–280 [cyt. za: Anderson i in. 1989; KZŚ 1986].
  • 4. Alexandrov V.A. (1974). Embryotoxic and transplacental oncogenic action of symmetrical dialkylnitrosamines on the progeny of rats. Byull. Eksp. Biol. Med. 11; 89–92 [cyt za: Anderson i in. 1989].
  • 5. Althoff J., Pour P., Grandjean C., Marsh S. (1977). Transplacental effects of nitrosamines in Syrian hamsters. III. Dimethyl and dipropylnitrosamine. Z. Krebsforsch. 90, 79–86 [cyt. za: Anderson i in. 1989; Toxicological Profile 1989].
  • 6. Althoff J., Grandjean C. (1979). In vivo studies with Syrian golden hamsters, a transplacental bioassay of ten nitrosamines. Natl. Cancer Inst. Monogr. 51, 251–255 (cyt. za: Anderson i in. 1989).
  • 7. Anderson L.M., Giner-Sorolla A., Ebeling D. (1978). Effects of imipramine, nitrite, and dimethylnitrosamine on reproduction in mice. Res. Commun. Chem. Pathol. Pharmacol. 19(2), 311–327 [cyt. za: Public Health Goal… 2006].
  • 8. Anderson L.M., Hagiwara A., Kovatch R.M., Rehm S., Rice J.M. (1989). Transplacental initiation of liver, lung neurogenic and connective tissue tumors by N-nitroso compounds in mice. Fundam. Appl. Toxicol. 12(3), 604–620.
  • 9. Anderson L.M., van Havere K., Budinger J.M. (1983). Effects of polychlorinated biphenyls on lung and liver tumors initiated in suckling mice by N-nitrosodimethylamine. J. Natl. Cancer Inst. 71(1), 157–163 [cyt. za: HSDB 2017].
  • 10. Anderson T.M., Harrington G.W. Pylypiw H.M., Hagiwara A., Magee P.N. (1986). Tissue levels and biological effects of N-nitrosodimethylamine in mice during chronic low or hiht dose exposure with or without ethanol. Drug Metab. Dispos. 14(6), 733-739 [cyt. za: Toxicological Profile 1989].
  • 11. Arai M., Aoki Y., Nakanishi K., Miyata Y., Mori T., Ito N. (1979). Long-term experiment of maximal non-carcinogenic dose of dimethylnitrosamine for carcimogenesis In rats. Gann 70(4), 749–758 [cyt. za: Public Health Goal… 2006; Toxicological Profile 1989].
  • 12. Asakura S., Daimon H., Sawada S., Sagami F. (1998). A short- -term assessment of tumor-promotion activity in the livers of rats treated with two genotoxic methylating agents: dimethylnitrosamine nad methylnitrosourea. Toxicol. Lett. 98, 155–167.
  • 13. Barnes J.M., Magee P.N. (1954). Some toxic properties of dimethylnitrosamine. Br. J. Ind. Med. 11, 167–174.
  • 14. Belinsky S.A., Devereux T.R., Anderson M.W. (1990). Role of DNA methylation in the activation of proto-oncogenes and the induction of pulmonary neoplasia by nitrosamines. Mutat. Res. 233, 105–116 (cyt. za: Jabłoński 2001).
  • 15. Benemanskii V.V., Katul’skiĭ I.N., Levina V. (1990). Modifying effects of ascorbic acid on nitrosodimethylamine-induced carcinogenesis. Vopr. Oncol. 36(3), 327–331 [cyt. za: HSDB 2017], [publication in Russian].
  • 16. Brams A., Buchet J.P., Crutzen-Fayt MC., de Meester C., Lauwerys R., Leonard A. (1987). A comparative study, with 40 chemicals, of the efficiency of the Salmonella assay and the SOS Chromotest (kit procedure). Toxicol. Lett. 38(1-2), 123– 133 [cyt. za: CCRIS 2010].
  • 17. Brendler S.Y., Tompa A., Hutter K.F., Preussmann R., Pool- -Zobel B.L. (1992). In vivo and in vitro genotoxicity of several N-nitrosamines in extrahepatic tissues of tha rat. Carcinogenesis 13, 2435–2441 [cyt. za: Jabłoński 2001].
  • 18. Brooks A.L., Cregger V. (1973). Production of chromosome type aberrations in the liver cells of the Chinese hamster by dimethylnitrosamine (DMN), (Abstract No. 8). Mutat. Res. 21, 214 [cyt. za: IARC 1978].
  • 19. Brunnemann K.D., Hoffmann D. (1978). Analysis of volatile nitrosoamines in tabacco smoke and polluted indoor environments. Chemical studies on tobacco smoke LIX. IARC Sci. Publ. 19, 343–356 [cyt. za: CICAD 2002; van Bruggen i in. 2007].
  • 20. Brusick D.J., Simmon V.F., Rosenkranz H.S., Ray V.A., Stafford R.S. (1980). An evaluation of the Escherichia coli WP2 and WP2uvra reverse mutation assay. Mutat. Res. 76, 169–190.
  • 21. Campbell J.W., Wiberg G.S., Grice H.C., Lou P. (1974). Stromal nephromas and renal cell tumors in suckling and weaned rats. Cancer Res. 34, 2399–2404 [cyt. za: IARC 1978; MAK 1987; DECOS 1999; Public Health Goal… 2006].
  • 22. Cardesa A., Pour P., Althoff J., Mohr U. (1973). Vascular tumors in female Swiss mice after intrape-ritoneal injection of dimethylnitrosamine. J. Nat. Cancer Inst. 51, 201–208 [cyt. za: IARC 1978; MAK 1987].
  • 23. Cardesa A., Pour P., Althoff J., Mohr U. (1974). Comparative studies of neoplastic response to a single dose of nitroso compounds. IV. The effect of dimethyl and diethyl nitrosamine in Swiss mice. Z. Krebsforsch. 81, 229–233 [cyt. za: ECETOC 1990; IARC 1978; KZŚ 1986].
  • 24. Carlton W.W., Price P.S. (1973). Dietary copper and the induction of neoplasms in the rat by acettlaminofluorene and dimethylnitrosamine. Food Cosmet. Toxicol. 11(5), 827–840 [cyt. za: Toxicological Profile 1989].
  • 25. Carter R.L., Percival W.H., Roe F.J.C. (1968). Exceptional sensitivity of mink to the hepatotoxic effects of dimethylnitrosamine. J. Path. 97, 79–88.
  • 26. CCRIS (2010). Chemical Carcinogenisis Research Information System. N-Nitrosodimethylamine. CASRN: 62-75-9 – komputerowa baza danych [dostęp: 20.05.2017].
  • 27. ChemIDplus (2017). A Toxnet database. Komputerowa baza danych toksykologicznych.
  • 28. Chhabra S.K., Souliotis V.L., Horbaught J.W., Krasnow S.W., Jones A.B., Anderson L.M., Kyrtopoulos S.A. (1995). O6 -Methylguanine DNA adduct formation and modulation by etanol in placenta and fetal tissue after exposure of pregnant patas monkey to N-nitrosodimethylamine. Cancer Res. 55, 6017–6020.
  • 29. CICAD (2002). Concise International Chemical Assessment Document 38. N-Nitrosodimethylamine. First draft prepared by Liteplo R.G. and Meek M.E. Health Canada, Ottawa, and Windle W., Environment Canada. Geneva, WHO.
  • 30. Ciemniak A. (2006). Porównanie zawartości N-nitrozodimetyloaminy w wybranych produktach mięsnych. Roczn. PZH 57(4), 341–346.
  • 31. Clapp N.K. (1973). Carcinogenicity of nitrosamines and methanesulphonate esters given introperitoneally in RF mice. Int. J. Cancer 12, 728–733 [cyt. za: IARC 1978; MAK 1987; Public Health Goal… 2006].
  • 32. Clapp N.K., Toya R.E. (1970). Effects of cumulated dose and dose rate on dimethylnitrosamine oncogenesis in RF mice. J. Nat. Cancer Inst. 45, 495–498 [cyt. za: ECETOC 1990; IARC 1978; KZŚ 1986].
  • 33. Clapp R., Jacobs M., Lijinsky W. (2012). N-Nitroso compounds. [eds.] E. Bingham, b. Cohrssen. Patty’s toxicology. 6th ed. Vol. 2, Chapter 33. Wiley & Sons, Inc., 401–432.
  • 34. Cooper M.T., Porter T.D. (2000). Mutagenicity of nitrosamines in methyltransferase-deficient strains of Salmonella typhimurium coexpressing human cytochrome P4502E1 and reductase. Mutat. Res. 454(1-2), 45–52 [cyt. za: CCRIS 2010].
  • 35. Cooper S.W., Kimbrough R.D. (1980). Acute dimethylnitrosamine poisoning outbreak. J. Forensic Sci. 25, 874–882 [cyt. za: Toxicological Profile 1989].
  • 36. Crampton R.F. (1980). Carcinogenic dose-related response to nitrosamines. Oncology 37(4), 251–254 [cyt. za: DECOS 1999; MAK 1987].
  • 37. Czygan P., Greim H., Garro A.J., Hutter F., Schaffner F., Popper M., Rosenthal D., Cooper D.Y. (1973). Microsomal metabolism of dimethylnitrosamine and the cytochrome P-450 dependency of its activation to a mutagen. Cancer Res. 33, 2983–2986.
  • 38. CzynRak (2018). Czynniki rakotwórcze – informacje z centralnego rejestru danych o narażeniu na substancje, mieszaniny, czynniki lub procesy technologiczne o działaniu rakotwórczym lub mutagennym. Łódź, Instytut Medycyny Pracy.
  • 39. Dahl A.R. (1985). Mmutagenicity of some dialkylnitrosamines, cyclic nitrosamines and N,N-diethanol-nitrosamine in Salmonella typhimurium with rat and rabbit nasal, lung and liver S9 homogenates. Mutat. Res. 158(3), 141–147 [cyt. za: CCRIS 2010].
  • 40. Daugherty J.P., Clapp N.K. (1976). Studies on nitrosamine metabolism: I. Subcellular distribution of radioactivity in tumor- -susceptible tissues of RFM mice following administration of 14C-dimethyl-nitrosamine. Life Sci. 19, 265–271 [cyt. za: Toxicological Profile 1989].
  • 41. de Vocht F. (2005). Improved exposure and assessment in the rubber manufacturing industry. [In:] F. De Vocht, R. Vermeulan, I. Burstyn, U. Bergendorf, T. Sorahan, W. Sobala, M. Heise, H. Kromhout, namens het EU-EXASRUB consorcium. Utrecht Institute foe Risk Assessment Sciences. NvvA Symposium [cyt. za: van Bruggen i in. 2007].
  • 42. DECOS (1999). N-Nitrosodimethylamine (N-NITROZODIMETYLOAMINA) – Health based calculated occupational cancer risk values. Dutch Expert Committee on Occupational Standards, a committee of the Health Council of the Netherlands to the Minister and State Secretary of Social Affairs and Employment. No. 1999/12OSH, The Hague, 20 December 1999.
  • 43. den Engelse L., Bentvelzen P.A.J., Emmelot P (1969/70). Studies on lung tumours. I. Metylation of deoxyribonucleotic acid and tumour formation following administration of dimethylnitrosamine to mice. Chem.-Biol. Interact. 1, 394–406 [cyt. za: IARC 1978].
  • 44. den Engelse L., Hollander C.F., Misdorp W (1974). A sex-dependent difference in the type of tumours induced by dimethylnitrosamine in the livers of C3Hf mice. Eur. J. Cancer 19, 129–135 [cyt. za: IARC 1978].
  • 45. Diaz Gomez M.I., Swann P.F., Magee P.N. (1977). The absorption and metabolism in rats of small oral doses of dimethylnitrosamine. Biochem. J. 164, 497–500.
  • 46. Druckey H., Preussman R., Ivankovic S., Schmahl D. (1967). Organotrope Carcinogene Wirkungen bei 65 verschidenen N-nitrosoverbindungen an BD-Ratten. [Organotropic carcinogenic effects of 65 various N-nitroso-compounds on BD rats]. Z. Krebsforsch. 69(2), 103–201 [cyt. za: DECOS 1999; ECETOC 1990; IARC 1978; Klein i in. 1991; Toxicolological Profile 1989].
  • 47. Dunkel V.C., Zeiger E., Brusick D., Mccoy E., Mcgregor D., Mortelmans K., Rosenkranz H.S., Simmon V.F. (1984). Reproducibility of microbial mutagenicity assays: I. tests with Salmonella typhimurium and Escherichia coli using a standardized protocol. Environ. Mol. Mutagen. 6 (Suppl. 2), 1–254 [cyt. za: CCRIS 2010].
  • 48. ECETOC (1990). Human exposure to N-nitrosamines, their effects and a risk assessment for N- nitroso-diethanolamine in personal care products. Technical Raport No 41. Belgium, Brussels.
  • 49. Eisenbrand G., Jazowski C., Preussmann (1975). Gas chromatographic determination of N-nitrosamino acid by trimetylsilylation and single-ion mass fragmentography. J. Chromatogr. 115, 602–606 [cyt. za: KZŚ 1986].
  • 50. EPA IRIS (2017). N-nitrosodimethylamine. CASRN 62-75- 9. Integrated Risk Information System. U.S. Environmental Protection Agency. National Center for Environmental Assessment [dostęp: maj 2017; https://cfpub.epa.gov/ncea/Iris/ Iris_documents/documents/subst/0045_summary.pdf].
  • 51. Epstein S.S., Arnold E., Andrea J., Bass W., Bishop Y. (1972). Detection of dominant lethal mutations in the mouse. Toxicol. Appl. Pharmacol. 23, 288–325 [cyt. za: ECETOC 1990; IARC 1978].
  • 52. Espinosa-Aguirre J.J., Rubio J., Cassani M., Nosti R., Caballero S., Gonzalez I., Martinez G. (1996). Induction of microsomal enzymes in liver of rats treated with cyclohexanol. Mutat. Res. 368(2), 103–107 [cyt. za: CCRIS 2010].
  • 53. Fajen J.M. (1982). Summary report on N-nitrosamines in the factory environment. IARC Sci. Publ. No. 41, 223–229.
  • 54. Farber E. (1980). Toxicological significance of liver hypertrophy produced by inducers of drug-metabolizing enzymes. CIBA Foundation Symposium, Environmental chemicals, enzyme function and human disease. Amsterdam, Excerpta Medica [cyt. za: Jabłoński 2001].
  • 55. Fine D.H. (1978). An assessment of human exposure to N-nitroso compounds. IARC Sci. Publ. No. 19, 267–274.
  • 56. Fine D.H. (1980). Exposure assessment to preformed environmental N-nitroso compounds from the point of view of our own studies. Oncology 37(4), 199–202 (streszczenie).
  • 57. Fine D.H., Reisch J., Rounbehler D.P. (1980). Nitrosamines in new automobiles. IARC Sci. Publ. No. 31, 541–551.
  • 58. Fiume L., Campadelli-Fiume G., Magee P.N., Holsman J. (1970). Cellular injury and carcinogenesis. Inhibition of metabolism od dimethylnitrosamine by aminoacetonitrile. Biochem. J. 120, 601–605.
  • 59. Fong Y.Y., Chan W.C. (1973a). Dimethylnitrosamine in Chinese marine salt fish. Food Cosmet. Toxicol. 11, 841–845 [cyt. za: KZŚ 1986].
  • 60. Fong Y.Y., Chan W.C. (1973b). Bacterial production of dimethylnitrosamine in salted fish. Nature 243, 421–422 [cyt. za: KZŚ 1986].
  • 61. Frei J.V. (1970). Toxicity, tissue changes, and tumor induction in inbred Swiss mice by methylnitrosamine and amide compounds. Cancer Res. 30, 11–17.
  • 62. Freund H.A. (1937). Clinical manifestations and studies in parenchymatous hepatitis. Ann. Int. Med. 10, 1144–1155 [cyt. za: Toxicological Profile 1989].
  • 63. Fujii K., Sato H. (1970). Response of adult mastomys to subcutaneous injection of N-nitrosodimethylamine. Gann 61, 425–434 [cyt. za: IARC 1978].
  • 64. Fussgaenger R.P., Ditschuneit H. (1980). Lethal exitus of a patient with N-nitrosodimethylamine poisoning 2.5 years following the first ingestion and signs of intoxication. Oncology 37, 273–277 [cyt. za: Toxicological Profile 1989].
  • 65. George J. (2006). Mineral metabolism in dimethylnitrosamine-induced hepatic fibrosis. Clin. Biochem. 39, 984-991.
  • 66. George J., Chandrakasan G. (2000). Biochemical abnormalities during the progression of hepatic fibrosis induced by dimethylnitrosamine. Clin. Biochem. 33(7), 563–570.
  • 67. George J., Rao K.R., Stern R., Chandrakasan G. (2001). Dimethylnitrosamine-induced liver injury in rats: the early deposition of collagen. Toxicology 156, 129–138.
  • 68. GESTIS (2012). International limit values for chemical agents Occupational Exposure Limits (OELs) [http://www.dguv.de/ ifa/en/gestis/limit_values/index.jsp]; Guide to Occupational Exposure Values 2012 [http://limitvalue.ifa.dguv.de/].
  • 69. Gichner T., Velemisky J. (1986). Organic solvents inhibit the mutagenicity of promutagens dimethylnitrosamine and methylbutylnitrosamine in higer plant Arabidopsis thaliana. Mutagenesis 1, 107–109 [cyt. za: Jabłoński 2001].
  • 70. Guttenplan J.B. (1989). An important role for cytosol in the microsomal metabolism of N-nitrosodimethylamine to a mutagen: evidence for two different mutagenic metabolites. Cancer Lett. 47(1-2), 63–67 [cyt. za: CCRIS 2010].
  • 71. Guttenplan J.B. (1993). Effects of cytosol on mutagenesis induced by N-nitrosodimethylamine, N-nitroso-methylurea and alpha-acetoxy-N- nitrosodimethylamine in different strains of Salmonella: evidence for different ultimate mutagens from N-nitrosodimethylmine. Carcinogenesis 14(5), 1013–1019 [cyt. za: CCRIS 2010].
  • 72. Haas H., Mohr U., Küger F.W. (1973). Comparative studies with different doses of N-nitrosomorpholine, N-nitrosopiperidine, N-nitrosomethylurea and dimethylnitrosamine in Syrian golden hamsters. J. Nat. Cancer Inst. 51, 1295–1301 [cyt. za: IARC 1978; MAK 1987].
  • 73. Hadjiolov D., Markow D. (1973). Fine structure of heamangioendothelial sarcomas in the rat liver induced with N-nitrosodimethylamine. Arch. Geschwulstforsch. 42, 120–126 [cyt. za: ECETOC 1990; IARC 1978].
  • 74. Haggerty H.G., Holsapple M.P. (1990). Role of metabolism in dimethylnitrosamine-induced immunosuppression: a review. Toxicology 63(1), 1–23.
  • 75. Hamilton A., Hardy H.L. (1974). Industrial toxicology. 3rd ed. Publ. Science Group, Inc. Acron, MA, 311 [cyt. za: Toxicological Profile 1989].
  • 76. Hamilton C.M., Dabbs J.E., Cunningham G.D., Vernett L.A., Mirsalis J.C., Snyder R.R. (1997). Evaluation of positive controls for the in vitro unscheduled DNA synthesis assay using hepatocytes from induced (Aroclor 1254) and uninduced male cynomolgus monkey. Environ. Mol. Mutagen. 30(3), 354–358 [cyt. za: CCRIS 2010].
  • 77. Hard G.C., Butler W.M. (1970). Toxicity of dimethylnitrosamine for the rat testis. J. Path. 102, 201–207.
  • 78. Heath D.F. (1962). The decomposition and toxicity of dialkylnitrosamines in rats. Biochem. J. 85, 72–91.
  • 79. Heath D.F., Magee P.N. (1962). Toxic properties of dialylnitrosamines and some related compounds. Br. J. Ind. Med. 19, 276–282.
  • 80. Herrold K.M. (1967). Histogenesis of malignant liver tumors induced by dimethylnitrosamine. An experimental study in Syrian hamsters. J. Nat. Cancer Inst. 39(6), 1099–1111 [cyt. za: HSDB 2017; IARC 1978].
  • 81. Hoch-Ligeti C., Argus M.F., Arcos J.C. (1968). Combined carcinogenic effects of dimethylnitrosamine and 3-methylcholanthrene in the rat. J. Nat. Cancer Inst. 40, 535–549 [cyt. za: IARC 1978].
  • 82. Holsapple M.P., Bick P.H., Duke S.S. (1985). Effects of N-nitrosodimethylamine on cell-mediated immunity. J. Leukoc. Biol. 37(4), 367–381 [cyt. za: Toxicological Profile 1989].
  • 83. Holsapple M.P., Tucker A.N., McNermey P.J., White K.L. (1984). Effects of N-nitrosodimethylamine on humoral immunity. J. Pharmacol. Exper. Ther. 229(2), 493–500.
  • 84. Homburger F., Handler A.M., Soto E., Hsuch S.S., Van Dongen C.G., Russfield A.B. (1976). Adenocarcinoma of the glandular stomach following 3-methylcholanthrene, N-nitrosodiethylamine feeding in carcinogen-susceptible inbred Syrian hamsters. J. Nat. Cancer Inst. 57, 141–144 [cyt. za: IARC 1978].
  • 85. HSDB (2017). Hazardous Substances Data Bank – komputerowa baza danych. N-nitrosodimethylamine. National Library of Medicine. Bethseda, Maryland [dostęp: 25.07.2017].
  • 86. IARC (1978). Monographs on the evaluation on the carcinogenic risk of chemicals to humans. Some N-nitroso compounds 17, 125–175.
  • 87. IARC (2015). List of classifications (Klasyfikacja czynników rakotwórczych) .
  • 88. IARC (1981). Monographs on the Evaluation on the Carcinogenic Risk of Chemicals to Humans, Wood, Leather and some associated industries 25.
  • 89. IFA (2017). GESTIS International Limit Values. Institut für Arbeitsschutz der Deutschen Gesetzlichen Unfallversicherung. GESTIS International Limit Value [pdf]. [http://limitvalue.ifa.dguv.de/WebForm_ueliste.aspx; dostęp: maj 2017].
  • 90. Ii J., Cardesa A. Patil K., Althoff J., Pour P. (1976). Comparative studies of neoplastic response to a single dose of nitroso compounds. Z. Krebsforsch. 86, 165–170 [cyt. za: IARC 1978; MAK 1987].
  • 91. Ito N. (1973). Experimental studies on tumours of the urinary system of rats induced by chemical carcinogens. Acta Path. Jap. 23, 87-105 [cyt. za: IARC 1978].
  • 92. Jabłoński J. (2001). N-Nitrozodimetyloamina – znaczenie toksykologiczne [N-Nitrosodimethylamine--toxicologic significance]. Post. Hig. Med. Dośw. [Advances in Hygiene and Experimental Medicine] 55(2), 319–337.
  • 93. Jabłoński J., Moniuszko-Jakoniuk J., Sieńko D. (1995). Nitrozoaminy [Nitrosamines]. Med. Pr. 46(1), 67–74.
  • 94. Jacobson K.H., Wheelwright M.J., Clem J.H., Shannon R.N. (1955). Studies on the toxicology of N-nitroso-dimethylamine vapor. Arch. Ind. Health 12, 612–622 [cyt. za: ECETOC 1990]
  • 95. Johansson E.B., Tjälve H. (1978). The distribution of 14C-dimethylnitrosamine in mice. Autoradiographic studies in mice with inhibited and noninhibited dimethylnitrosamine metabolism and a comparison with the distribution of 14C-formaldehyde. Toxicol. Appl. Pharmacol. 45, 565–575 [cyt. za: Toxicological Profile 1989]. Jönsson L.S., Lindh C.H., Bergendorf U., Axmon A., Littorin M., Jönsson B.A.G. (2009). N-Nitrosamines in the southern Swedish rubber industries – exposure, health effects, and immunologic markers. Scand. J. Work. Environ. Health 35(3), 203–211.
  • 96. Kawanishi T., Ohno Y., Takahashi A., Takanaka A., Kasuya Y., Omori Y. (1984). Nature of N-nitroso-dimethylamine demethylase in hepatic microsomes of rats. Arch. Toxicol. 56, 7–11 [cyt. za: Jabłoński 2001].
  • 97. Keefer L.K., Anjo T., Heur Y.H. (1987). Potential for metabolic deactivation of carcinogenetic N-nitroso-dimethyalmine in vivo. IARC Sci. Publ. No. 84, 113–116 [cyt. za: Toxicological Profile 1989].
  • 98. Keefer L.K., Lijinsky W., Garcia H. (1973). Deuterium isotope effect on the carcinogenicity of dimethylnitrosamine in rat liver. J. Nat. Cancer Inst. 51(1), 299–302 [cyt. za: DECOS 1999; MAK 1987].
  • 99. Kim K.R., Lee S.J., Seo J.K., Shon M.Y., Sung N.J. (2002). The formation of N-nitrosamine in soy sauce, soybean paste and beer under simulated gastric digestion. J. Korean Soc. Food Sci. Nutr. 31, 378–383 [cyt. za: Park i in. 2015].
  • 100. Kim S.H., Park K.Y., Suh M.J. (1991). Mutagenicity of N-nitrosodimethylamine in Salmonella/microsome assay and the effect of Vitamin C on the formation of N-nitrosodimethylamine. Han’guk Yongyang Siklyong Hakhoechi 20(3), 260–265 [cyt. za: CCRIS 2010].
  • 101. Klein R.G., Janowsky I., Pool-Zobel B.L., Schmezer P., Hermann R., Amelung F, Spiegelhalder B., Zeller W.J. (1991). Effects of long term inhalation of N-nitrosodimethylamine in rats. IARC Sci. Publ. No. 105, 322–328.
  • 102. Klein R.G., Janowsky I., Schmezer P., Hermann R., Spiegelhalder B., Zeller W.J. Pool B.L. (1989). Effect of long-term inhalation of N-nitroso-dimethylamine (NDMA) and SO2/NOx in rats. Exp. Pathol. 37, 273–280.
  • 103. Klein R.G., Schmezer P. (1984). Quantitative measurement of the exhalation rate of volatile N-nitrosamine in inhalation experiments with anesthetized Sprague-Dawley rats. IARC Sci. Publ. No. 57, 513–517 [cyt. za: Toxicological Profile 1989].
  • 104. Koehl W., Eisenbrands G. (1999). N-Nitroso compounds [In:] H. Marquardt, S.G. Schäfer, R. McClellan, F. Welsch. Toxicology. Chapter 31. San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, Academic Press, 743–754.
  • 105. Koppang N., Rimeslatten H. (1976). Toxic and carcinogenic effects of nitrosodimethylamine in mink. IARC Sci. Publ. No. 14, 443–452 [cyt. za: Toxicological Profile 1989].
  • 106. Kowalewski K., Todd E.F. (1971). Carcinoma of the gallblader induced in hamsters by insertion of cholesterol pellets and feeding dimethylnitrosamine. Proc. Soc. Exp. Biol. 136, 482–486 [cyt. za: IARC 1978].
  • 107. Kuwahara A., Otsuka H., Nagamatsu A. (1972). Induction of hemanogiomatous lesions with dimethylnitrosamine: influence of route of administration and strain of mice. Gann 499–502 [cyt. za: IARC 1978; Public Health Goal… 2006].
  • 108. Kyrtopoulos S.A., Anderson L.M., Chhabra S.K., Souliotis V.L., Pletsa V., Valavanis C., Georgiadis P. (1997). DNA adducts and the mechanism of carcinogenesis and cytotoxicity of methylating agents of environmental and clinical significance. Cancer Detect. Prev. 21, 391–405 [cyt. za: Jabłoński 2001].
  • 109. KZŚ, Kryteria Zdrowotne Środowiska (1986). Azotany, azotyny i związki nitrozowe. Warszawa, PZWL.
  • 110. Le Page R.N., Christie G.S. (1969a). Induction of liver tumours in the rabbit by feeding dimethyl-nitrosamine. Brit. J. Cancer 23, 125–131.
  • 111. Le Page R.N., Christie G.S.M. (1969b). Induction of liver tumours in the guinea pig by feeding dimethylnitrosamine. Pathology 1, 49–56 [cyt. za: IARC 1978].
  • 112. Lechevrel M., Wild C.P. (1997). Absence of a differential induction of cytochrome p-450 2E1 by different alcoholic beverages in rats: implications for the etiology of human oesophageal cancer. Arch. Toxicol. 71, 690–695 [cyt. za: Jabłoński 2001].
  • 113. Lee E.S., Shin M.O., Yoon S., Moon J.O. (2010). Resveratrol inhibits dimethylnitrosamine-induced hepatic fibrosis in rats. Arch. Pharm. Res. 33(6), 925–932.
  • 114. Lee V.M., Cameron R.G., Archer M.C. (1998). Zonal location of compensatory hepatocyte proliferation following chemically induced hepatotoxicity in rats and humans. Toxicol. Pathol. 26, 621–627.
  • 115. Lewis R.J. (2004). Sax’s dangerous properties of industrial materials. 11th ed. Vol. 3. Willey Interscience, A John Wiley & Sons, Inc. Publication, 2709–2710.
  • 116. Lijinsky W. (1987). Structure-activity relations in carcinogenesis by N-nitroso compounds. Cancer Metastis Rev. 6, 301–356 [cyt. za: ECETOC 1990].
  • 117. Lijinsky W. (1992). Chemistry and biology of N-nitroso compounds. UK, Cambridge, Cambridge University Press, [cyt za: Clapp i in. 2012].
  • 118. Lijinsky W. (1999). N-Nitroso compounds in the diet. Mutat. Res. 443, 129–138.
  • 119. Lijinsky W., Kovatch R.M., Riggs C.W. (1987). Carcinogenesis by nitrosodialkylamines and azoxyalkanes given by gavage to rats and hamsters. Cancer Res. 47, 3968–3972.
  • 120. Lijinsky W., Reuber M.D. (1981). Comparative carcinogenesis by some aliphatic nitrosamines in Fischer rats. Cancer Lett. 14, 297–302 [cyt. za: ECETOC 1990; Public Health Goal… 2006].
  • 121. Lijinsky W., Reuber M.D. (1984). Carcinogenesis in rats by nitrosodimetyloamine and other nitrosomethylalkylamines at low doses. Cancer Lett. 22(1), 83-88 [cyt. za: ECETOC 1990; Public Health Goal… 2006].
  • 122. Lilly L.J., Bahner B., Magee P.N. (1975). Chromosome aberrations induced in rat lymphocytes by N-nitroso compounds as a possible basis for carcinogen screening. Nature 258, 611– 612 [cyt. za: IARC 1978].
  • 123. Liu Y.X., Guttenplan J.B. (1992). Mutational specificities of N-nitrosamines in a host-mediated assay: comparison with direct-acting N-nitroso compounds in vitro and an approach to deducing the nature of ultimate mutagens in vivo. Mol. Carcinog. 6(4), 232–237 [cyt. za: CCRIS 2010].
  • 124. Lorr N.A., Miller K.W., Chung H.R., Yang C.S. (1984). Potentiation of the hepatotoxicity of N-nitroso-dimethylamine by fasting, diabetes, acetone, and isopropanol. Toxicol. Appl. Pharmacol. 73(3), 423-431 [cyt. za: Toxicological Profile 1989].
  • 125. Lotlikar P.D., Baldy W.J., Dwyer E.N. (1975). Dimethylnitrosamine demethylation by reconstituted liver microsomal cytochrome P-450 enzyme system. Biochem. J. 152, 705–708 [cyt. za: Toxicological Profile 1989].
  • 126. Loveday K.S., Lugo M.H., Resnick M.A., Anderson B.E., Zeiger E. (1989). Chromosome aberration and sister chromatid exchange tests in chinese hamster ovary cells in vitro: II. Results with 20 chemicals. Environ. Mol. Mutagen. 13(1), 60–94 [cyt. za: CCRIS 2010].
  • 127. Ma F., Zhang Z., Jiang J., Hu J. (2015). Chromium(VI) potentiates the DNA adducts (O6 -methylguanine) formation of N-nitrosodimethylamine in rat: implication on carcinogenic risk. Chemisphere 139, 256–259.
  • 128. Maduagwu E.N., Bassir O. (1980). A comparative assessment of toxic effects of dimethylnitrosamine, six different species. Toxicol. Appl. Pharmacol. 53, 211–219.
  • 129. Magee P.N. (1956). Toxic liver injury. The metabolism of dimethylnitrosamine. Biochem. J. 64, 676–682.
  • 130. Magee P.N., Farber E. (1962). Toxic liver injury and carcinogenesis. Methylation of rat-liver nucleic acids by dimethylnitrosamine in vivo. Biochem. J. 83, 114–124.
  • 131. Magee P.N., Hultin T. (1962). Toxic liver injury cad carcinogenesis. Methylation of protein of rat-liver slices by dimethylnitrosamine in vitro. Biochem. J. 83, 106–114.
  • 132. Magge P.N., Barnes J.M. (1956). The production of malignant primary hepatic tumours in the rat by feeding dimethylnitrosamine. Br. J. Cancer 10, 114–122.
  • 133. MAK (1987). N-Nitrosamines. Classification/MAK value. DFG Deutsche Forschungsgemeinschaft, Occupational Toxicants, Critical data evaluation of MAK values and classification of carcinogens, Vol. 1. VCH Verlagsgesellschaft mbH, Weinheim, Federal Republic of German, 1991. N-Nitrosamines MAK Value Documentation.
  • 134. MAK (2016). List of MAK and Bat values 2016. Permanent Senate Commission for the investigation of health hazard of chemical compounds in the work area. Report 52. https:// onlinelibrary.willey.com/doi/10.1002/9783527805983.ch2/pdf [list of substances, pdf], [dostęp: maj 2017].
  • 135. Maling H.M., Stripp B., Sipes I.G., Highman B., Saul W., Williams M.A.. (1975). Enhanced hepatotoxicity of carbon tetrachloride, thioacetamide, and dimethylnitrosamine by preatment of rats with ethanol and some comparisons with potentiation by isopropanol. Toxicol. Appl. Pharmacol. 33(2), 291–308 [cyt. za: Toxicological Profile 1989].
  • 136. Matsushima T., Hayashi M., Matsuoka A., Ishidate M., Miura K.F., Shimizu H., Suzuki Y., Morimoto K.,. Ogura, Mure K., Koshi K., Sofuni T. (1999). Validation of the in vitro micronucleus test in a chinese hamster lung cell line (CHL/IU). Mutagenesis 14(6), 569–580 [cyt. za: CCRIS 2010].
  • 137. McCracken, M.D., Bottoms G..D, Carlton W.W. (1973). Tumorigenesis of dimethylnitrosamine in the Pekin duck (Abstract No. 23). Toxicol. Appl. Pharmacol. 25, 447–448 [cyt. za: IARC 1978].
  • 138. McLean A.E.M., Magge P.N. (1970). Increased renal carcinogenesis by dimethylnitrosamine in protein deficient rats. Br. J. Exp. Path. 51, 587–590 [cyt. za: IARC 1978].
  • 139. McLean E., Bras G., McLean A.E.M. (1965). Vonous occlusions in the liver following dimethylnitrosamine. Br. J. Exp. Pathol. 46(3), 36–37.
  • 140. Mirvish S.S. (1995). Role of N-nitroso compounds (NOC) and N-nitrosation in etiology of gastric, esophageal, nasopharyngeal and bladder cancer and contribution to cancer of known exposure to NOC. Cancer Lett. 93, 17–48.
  • 141. Mitch W.A., Sharp J.O., Trussell R.R., Valentine R.L., Alvarez- -Cohen L., Sedlak D.L. (2003). N-Nitroso-dimethylamine as a drinking water contaminant: a review. Environ. Eng. Sci. 20(5), 389-404 [cyt. za: Public Health Goal… 2006].
  • 142. Mitchell A.D., Casciano D.A., Meltz M.L., Robinson D.E., San R.H.C., Williams G.M., von Halle E.S. (1983). Unscheduled DNA synthesis tests: a report of the U.S. Environmental Protection Agency Gene-Tox Program. Mutat. Res. 123, 363–410 [cyt. za: CCRIS 2010].
  • 143. Miyazaki K., Lu M.D., Nakayama F. (1990). Unscheduled DNA synthesis after treatment with 20-methyl-cholanthrene and N-nitrosodimethylamine in primary culture of human gallbladder epithelial cells. Mutat. Res. 235(2), 81–84 [cyt. za: CCRIS 2010].
  • 144. Mohr U., Haas H., Hlfrich J. (1974). The carcinogenic effects of dimethylnitrosamine and nitrosomethyl urea in European hamsters (Cricetus cricetus L.). Brit. J. Cancer 29, 359-364. [cyt. za: IARC 1989].
  • 145. Moiseev G.E., Benemansky V.D. (1975). [The carcinogenic activity of low concentrations of nitrosodimethylamine in inhalation]. Vopr. Onkol. 21(6), 107–109 [cyt. za: DECOS 1999; ECETOC 1990; IARC 1978; Klein i in. 1991; MAK 1987; Toxicolological Profile 1989].
  • 146. Monorca S., Feretti D., Zanardini A., Moretti M., Villarini M., Spiegelhalder B., Zerbini I., Gelatti U., Lebbolo E. (2001). Monitoring airborne genotoxicants in the rubber industry using genotoxicity tests and chemical analyses. Mutat. Res. 490(2), 159–169.
  • 147. Montesano R., Mohr U., Magee P.N., Hilfrich H., Haas H. (1974). Additive effect in the induction of kidney tumours in rats treated with dimethylnitrosamine and ethylmethanesulphonate. Br. J. Cancer 29, 50–58.
  • 148. Mori Y., Imura K., Hirano K. (1993). N-Benzylimidazole a potent inducer of rat liver enzymes involved in mutagenic activation of various carcinogens. Mutat. Res. 302(2), 129–133 [cyt. za: CCRIS 2010].
  • 149. Mostafa M.H., El-Bassiouni E.A., El-Sewedy S.M., Tawfic T., El-Sebae A.H. (1983). Influence of pretreatment with various insecticides on the N-demethylation of dimethylnitrosamine. Environ. Res. 32(1), 57–61 [cyt. za: HSDB 2017].
  • 150. Movelle T., Bouchikhi B., Debry G. (1991). The occurrence of volatile N-nitrosamines in French foodstuffs. Food Chem. 42, 321–338 [cyt. za: Park i in. 2015].
  • 151. Murphy G.P., Mirand E.A., Johnson G.S., Schmidt J.D., Scott W.W. (1966). Renal tumors induced by a single dose of dimethylnitrosamine: morphologic, functional, enzymatic, and hormonal characterization. Incest. Urol. 4, 39–56 [cyt. za IARC 1978].
  • 152. Mwanza T., Miyamoto T., Okumura M., Kadosawa T., Fujinaga T. (1997). Ultrasonography, biochemical and hematological profiles In liver disease caused by intravenous administration of dimethylnitrosamine in dogs. Jpn. J. Vet. Res. 45(3), 153–161.
  • 153. Natarajan A.T., Tates A.D., Van Buul P.P.W., Meijers M., De Vogel N. (1976). Cytogenetic effects of mutagens/carcinogens after activation in a microsomal system in vitro. I. Induction of chromosome aberration and sister chromatide exchanges by diethylnitrosamine (DEN) and dimethylnitrosamine (DMN) in CHO cells in the presence of rat-liver microsomes. Mutat. Res. 37, 83–90 [cyt. za: IARC 1978].
  • 154. Ng W.L., Fong L.Y.Y., Newborne P.M. (1984). Forestomach aquamous papillomas in the rat: effect of dietary zinc deficiency on induction. Cancer Lett. 22, 329–332 [cyt. za: Toxicological Profile 1989].
  • 155. Noronha R.F.X., Goodall C.M. (1972). Nasal tumours in starved rats injected once with dimethylnitrosamine. N. Z. Med. J. 75, 374–375 [cyt. za: IARC 1978].
  • 156. Noronha R.F.X., Goodall C.M. (1976). Enhancement of hepatic and renal tumorigenesis in thyroidectomized NZR/ Gd rats treated with dimethylnitrosamine. J. Surg. Oncol. 8, 539–550 [cyt. za: IARC 1978].
  • 157. Nowak A., Libudzisz Z. (2008). Kancerogeny w przewodzie pokarmowym człowieka. Żywność. Nauka. Technologia. Jakość 4(59), 9–25.
  • 158. Oury B., Limasset J. Protois J. (1997). Assessment of exposure to carcinogenic N-nitrosamines in the rubber industry. Int. Arch. Occup. Environ. Health 70(4), 261–271.
  • 159. Paolini M., Sapigni E., Hrelia P., Scotti M., Morotti M., Cantelli-Forti G. (1991). Wide spectrum detection of precarcinogens in short-term bioassays by simultaneous superinduction of multiple forms of cytochrome P450 isoenzymes. Carcinogenesis 12(5), 759–766 [cyt. za: CCRIS 2010].
  • 160. Park J., Seo J., Lee J. Kwon H. (2015). Distribution of seven N-nitrosamines in food. Toxicol. Res. 31(3), 279–288.
  • 161. Pedal I., Besserer K., Goerttler K., Heymar B., Mittmeyer H.J., Oehmichen M., Schmahl D. (1982). Fatal nitrosamine poisoning. Arch. Toxicol. 50(2), 101–112 [cyt. za: Jabłoński 2001].
  • 162. Pegg A.E. (1980). Metabolism of N-nitrosodimethylamine. IARC Publ. Sci. No 27, 3–22.
  • 163. Peto R., Gray R., Brantom P., Grasso P. (1991). Dose and time relationships for tumor induction in the liver and esophagus of 4080 inbred rats by chronic ingestion of N-nitrozodiethylamine or N-nitrosodimethylamine. Cancer Res. 51, 6452–6469.
  • 164. Phillips J.C., Lake B.G., Heading C.E., Gangolli S.D., Lloyd A.G. (1975). Studies on the metabolism of dimethylnitrosamine in the rat. I. Effect of dose, route of administration and sex. Food Cosmet. Toxicol. 13(2), 203–209 [cyt. za: Toxicological Profile 1989].
  • 165. Phillipson C.E., Ioannides C. (1984). A comparative study of the bioactivation of nitrosamines to mutagens by various animal species including man. Carcinogenesis 5(8), 1091–1094 [cyt. za: CCRIS 2010].
  • 166. Pound A.W., Lawson T.A., Horn L. (1973). Increased carcinogenic action of dimethylnitrosamine after prior administration of carbon tetrachloride. Br. J. Cancer 27, 451–459.
  • 167. Propping P., Röhrborn G., Buselmaier W. (1972). Comparative investigations on the chemical induction of point mutations and dominant lethal mutations in mice. Mol. Gen. Genet. 117, 197–209 [cyt. za: IARC 1978].
  • 168. Public Health Goal for N-nitrosodimethylamine in drinking water (2006). Raport przygotowany przez Pesticide and Environmental Branch Office of Environmental Health Hazard Assessment California Environmental Protection Agency [https://oehha.ca.gov/media/dowloads/water/chemicals/ phg/122206N-Nitrozodimetyloaminaphg_0.pdf].
  • 169. Raabe O.G. (1986). Inhalation uptake of selected chemical vapors at trace levels. Report to California State Air Resources Board, Sacramento. NTIS PB86-209863 [cyt. za: Toxicological Profile 1989].
  • 170. Ragga-Tabu C., Sleight D. (1992). Sequential study in rats of nasal and hepatic lesions induced by N-nitrosodimethylamine and N-nitrosopyrrolidine. Fundam. Appl. Toxicol. 19, 147–156.
  • 171. Reh B., Fajen J. (1996). Worker exposures to nitrosamines in a rubber vehicle sealing plant. Am. Ind. Hyg. Assoc. J. 57(10), 918–923 [cyt. za: van Bruggen i in. 2007].
  • 172. Reznik G. (1975). The carcinogenic effect of dimethylnitrosamine on the Chinese hamster (Cricetulus griseus). Cancer Lett. 1, 25–28 [cyt. za: IARC 1978].
  • 173. Reznik G., Mohr U., Kmoch M. (1976). Carcinogenic effects of different nitroso-compounds in Chines hamster. I. Dimethylnitrosamine and N-diethylnitrosamie. Br. J. Cancer 33, 411–418.
  • 174. Rogaczewska T., Wróblewska-Jakubowska J.K. (1996). Narażenie zawodowe na N-nitrozoaminy w przemysle opon samochodowych [Occupational exposure to N-nitrosamine in the production of automobile tires]. Med. Pr. 47(6), 569– 575 [cyt. za: van Bruggen i in. 2007].
  • 175. Roszczenko A., Jabłoński J., Moniuszko-Jakoniuk J. (1996). Wpływ N-nitrozodimetyloaminy na aktywność wybranych enzymów w surowicy krwi szczura. Med. Pr. 47(1), 49–53.
  • 176. Rozporządzenie Parlamentu Europejskiego i Rady (WE) nr 1272/2008 z dnia 16.12.2008 r. w sprawie klasyfikacji, oznakowania i pakowania substancji i mieszanin, zmieniające i uchylające dyrektywy 67/648/EWG i 1999/45/WE oraz zmieniające rozporządzenie WE nr 1907/2006 (tzw. rozporządzenie CLP). Dz. Urz. UE L 353 z dnia 31.12.2008 r. ze zm. [Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/ EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006].
  • 177. RTECS, Registry of Toxic Effects of Chemical Substances (2017). N-Nitrosodimethylamine. National Institutes for Occupational Safety and Health, Cincinnati, Ohio.
  • 178. Rumruen K., Pool B.L. (1984). Metabolic activation capabilities of S9 and hepatocytes from uninduced rats to convert carcinogenic N-nitrosamines to mutagens. Mutat. Res. 140(2-3), 147–153 [cyt. za: CCRIS 2010].
  • 179. Sawada S., Asakura S., Daimon H., Furihata C. (1995). Comparison of autoradiography, liquid scintillation counting and immunoenzymatic staining of 5-bromo-2’-deoxyuridine for measurement of unscheduled DNA synthesis and replicative DNA synthesis in rat liver. Mutat. Res. 344(3,4), 109–116 [cyt. za: CCRIS 2010].
  • 180. Selden J.R., Dolbeare F., Clair J.H., Miller J.E., McGettigan K., Dijohn J.A., Dysart G.R., Deluca J.G. (1994). Validation of a flow cytometric in vitro DNA repair (UDS) assay in rat hepatocytes. Mutat. Res. 315(2), 147–167 [cyt. za: CCRIS 2010].
  • 181. Sen N.P. (1972). The evidence for the presence of dimethylnitrosamine in mest products. Food Cosmet. Toxicol. 10, 219–223 [cyt. za: KZŚ 1986].
  • 182. Skaare J.U., Nafstad I. (1978). Interaction of vitamin E and selenium with the hepatotoxic agent dimethylnitrosamine. Acta Pharmacol. Toxicol. 43(2), 119–128 [cyt. za: Toxicological Profile 1989].
  • 183. Smetanin E.E. (1971). [On transplacental blastomogenic effect of dimethylnitrosamine and nitrosomethylurea]. Vopr. Onkol. 17, 75–81 [cyt. za: IARC 1978; Public Health Goal… 2006], [publication in Russian].
  • 184. Souliotis V.L., Henneman J.R., Reed C.D., Chhabra S.K., Diwan B.A., Anderson L.M., Kyrtopoulos S.A. (2002). DNA adducts and liver DNA replication in rats during chronic exposure to N-nitrosodimethylamine (NDMA) and their relationships to the dose-dependence of NDMA hepatocarcinogenesis. Mutat. Res. 500, 75–87.
  • 185. Souliotis V.L., van Delft J.H., Steenwinkel M.J., Baan R.A., Kyrtopoulos S.A. (1998). DNA adducts, mutant frequencies and mutation spectra in lambda lacZ transgenic mice treated with N-nitrosodimethylamine. Carcinogenesis 19, 731–739 [cyt. za: Jabłoński 2001].
  • 186. Spiegelhalder B. (1983). Carcinogens in the workroom air in the rubber industry. Scand. J. Work. Environ. Health 9 (Suppl. 2), 15–25.
  • 187. Spiegelhalder B., Eisenbrand G., Preussmenn R. (1982). Urinary excretion of N-nitrosamines in rats and human. IARC Sci. Publ. No. 41, 443–449.
  • 188. Spiegelhalder B., Preussman R. (1982). Nitrosamines and rubber. IARC, Sci. Publ. 41, 231–243.
  • 189. Stenback F., Ferrero A., Montesano R., Shubik P. (1973). Synergistic effect of ferric oxide on dimethylnitrosamine carcinogenesis in the Syrian golden hamster. Z. Krebsforsch. Klin. Onkol. Cancer Res. Clin. Oncol. 79(1), 31–38.
  • 190. Suzuki H., Ikeda N., Kobayashi K., Terashima Y., Shimada Y., Suzuki T., Hagiwara T., Hatakeyama S., Nagaoka K., Yoshida J., Saito Y., Tanaka J., Hayashi M. (2005). Evaluation of liver and peripheral blood micronucleus assays with 9 chemicals using young rats. Mutat. Res. 583(2), 133–145 [cyt. za: CCRIS 2010].
  • 191. Swann P.F., Magee P.N. (1968). Nitrosamine – induced carcinogenesis. The alkylation of nucleic acids of the rat by N-methyl-N-nitrosourea, dimethylnitrosamine, dimethyl sulphate and methyl methanesulphonate. Biochem. J. 110, 39–47.
  • 192. Szymczyk I., Starzyński Z., Szymczak W. (1996). N-Nitrozodimetyloamina. Wytyczne Szacowania Ryzyka Zdrowotnego dla Czynników Rakotwórczych. Zeszyt 2. Łódź, IMP [publication in Polish].
  • 193. Tates A.D., Neuteboom I., de Vogel N., den Engelse L. (1983). The induction of chromosomal damage in rat hepatocytes and lymphocytes. I. Time-dependent changes of the clastogenic effects of diethylnitrosamine, dimethylnitrosamine and ethyl methanesulfonate. Mutat. Res. 107(1), 131–151 [cyt. za: HSDB 2017].
  • 194. Terracini B., Magee P.N., Barnes J.M. (1967). Hepatic pathology in rats on low dietary levels of dimethylnitrosamine. Brit. J. Cancer 21, 559–565.
  • 195. Terracini B., Palestro G., Giglirdi R., Montesano R. (1966). Carcinogenicity of dimethylnitrosamine in Swiss mice. Brit. J. Cancer 20, 871–876.
  • 196. Terracini B., Testa M.C., Carbral J.R., Day N. (1973). The effecys of long-term feeding of DDT to BALB’c mice. Int. J. Cancer 11(3), 747–764 [cyt. za: Public Health Goal… 2006]
  • 197. The Merck Index – An encyclopedia of chemicals, drugs, and biologicals (2001). [ed.] M.J. O’Neil. 13th ed. Whitehouse Station, NJ, Merck and Co., Inc., 1189.
  • 198. Tinwell H., Lefevre P.A., Ashby J. (1994). Mutation studies with dimethylnitrosamine in young and old lac I transgenic mice. Mutat. Res. 307(2), 501–508 [cyt. za: CCRIS 2010].
  • 199. Tomatis L., Cefis F. (1967). The effects of multiple and single administration of dimethyl-nitrosamine to hamsters. Tumori 53, 447–462 [cyt. za: HSDB 2017; IARC 1978].
  • 200. Toth B., Magee P.N., Shubik P.H. (1964). Carcinogenesis study with dimethylnitrosamine administered orally to adult and subacutaneously to newborn BALB/c mice. Cancer Res. 24, 1712–1721.
  • 201. Toth B., Shubik P. (1967). Carcinogenic in AKR mice injected at birth with benzo(a)pyrene and dimethylnitrosamine. Cancer Res. 27, 43–51.
  • 202. Toxicological Profile (1989). Toxicological profile for N-nitrosodimethylamine. Agency for Toxic Substances and Disease Registry (ATSDR). U.S. Public Health Service in collaboration with U.S. Environmental Protection Agency (EPA). December 1989.
  • 203. TRGS 910 (2014). The Technical Rules for Hazardous Substances (TRGS). Annex 1: Substance-specific values for carcinogenic substances classified as category 1A or 1B according t CLP Regulation or TRGS 905. Table 1: List of substance- -specific acceptable and tolerable concentrations [dostęp: 03.10.2017; www.baua.de].
  • 204. Tricker A.R., Preussmann R. (1991). Carcinogenic N-nitrosamines in the diet: occurence, formation, mechanism and carcinogenic potential. Mut. Res. 259, 277–289 (cyt. za: Nowak, Libudzisz 2008).
  • 205. US EPA (1980). Ambient water quality criteria doc: Nitrosamines, p.C-32. EPA-440/5-80-064 (cyt. za: HSDB 2017).
  • 206. Valentin-Severin I., Thybaud V., Le Bon A.M., Lhuguenot J.C., Chagnon M.C. (2004). The autoradiographic test for unscheduled DNA synthesis: a sensitive assay for the detection of DNA repair in the HEPG2 cell line. Mutat. Res. 559(1-2), 211–217 [cyt. za: CCRIS 2010].
  • 207. van Bruggen M., van Putten E.M., Janssen P.C.J.M. (2007). Nitrosamines released from rubber crumb. RIVM report 60930002/2007 [www.rivm.nl/Onderwerpen/R/ Rubbergranulaat/Eerder_onderzoek_rubbergranulaat/ RIVM_609300002_2007_ven_Bruggen.org].
  • 208. Vendemiale G., Grattagliano I., Caruso M.L., Serviddio G. (2001). Increased oxidative stress in dimethylnitrosamine-induced liver fibrosis in the rat: effect of N-acetylcysteine and interferon-α. Toxicol. Appl. Pharmacol. 175, 130–139.
  • 209. Vesselinovitch S.D. (1969). The sex dependent difference in the development of liver tumours in mice administered dimethylnitrosamine. Cancer Res. 29(5), 1024–1027.
  • 210. Wade G.G., Mandel R., Ryser H.J.-P. (1987). Marked synergism of dimethylnitrosamine carcinogenesis in rats exposed to calcium. Cancer Res. 47, 6606–6613.
  • 211. Watanabe S., Kamiguchi Y. (2001). Chromosome analysis of human spermatozoa following in vitro exposure to cyclophosphamide, benzo(a)pyrene and N-nitrosodimethylamine in the presence of rat liver S9. Mutat. Res. 491, 57–63.
  • 212. Encyclopedia of Toxicology (1998). [ed.] P.O. Wexler. N- -Nitrosodimethylamine. Vol. 2, F-P, Academic Press. San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, 429–430.
  • 213. Wróblewska-Jakubowska K., Brzeźnicki S., Rogaczewska T. (1990). Ocena narażenia zawodowego na związki toksyczne w wybranym zakładzie produkcji opon samochodowych. Sprawozdanie z realizacji tematu CPBR 11.11.62 [dane niepublikowane], [cyt. za: Szymczyk i in. 1996], [upublished data in Polish].
  • 214. Yamane Y., Sakai K., Umeda T., Murata N., Ishizeki S., Ogihara I., Takahashi A., Iwasaki I., Ide G. (1984). Suppressive effect of cupric acetate on DNA alkylation, DNA synthesis and tumorigenesis in the liver of dimethylnitrosamine-treated rats. Gann 75(12), 1062–1069 [cyt. za: Toxicological Profile 1989].
  • 215. Yamazaki H., Inui Y., Yun C.H., Guengerich F.P., Shinada T. (1992). Cytochrome p-450 2E1 and 2A6 enzymes as major catalysis for metabolic activation of N-nitrosodialkylamines and tobacco-related nitrosamines in human liver microsomes. Carcinogenesis 13, 1789–1794 [cyt. za: Jabłoński 2001].
  • 216. Yoo J.H., Ning S.M., Patten C.J. Yang C.S. (1987). Metabolism and activation of N-nitrosodimethylamine by hamster and rat microsomes: comparative study with weanling and adult animals. Cancer Res. 47, 922–998 [cyt. za: Jabłoński 2001].
  • 217. Yoo J.-S.H., Guengerich F.P., Yang C.S. (1988). Metabolism of N-nitrosodialkylamines by human liver microsomes. Cancer Res. 88, 1499–1505 [cyt. za: Toxicological Profile 1989].
  • 218. Zak F.G., Holzer J.H., Singer E.J., Popper H. (1959). Renal and pulmonary tumors in rats fed dimethylnitrosamine. Cancer Res. 20, 96–99.
  • 219. Zielenska M., Guttenplan J.B. (1987). Effects of UV repair, error-prone repair and critical site of mutation on mutagenesis induced by N-nitrosamines. Mutat. Res. 180(1), 11–20 [cyt. za: CCRIS 2010].
Uwagi
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2019).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-69aa3554-0458-46a7-b3ac-a50c02f804e0
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.