PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Tetrachloroeten : dokumentacja proponowanych dopuszczalnych wielkości narażenia zawodowego

Autorzy
Treść / Zawartość
Identyfikatory
Warianty tytułu
EN
Tetrachloroethene : documentation of proposed values of occupational exposure limits (OELs)
Języki publikacji
PL
Abstrakty
PL
Tetrachloroeten jest bezbarwną, lotną cieczą stosowaną jako rozpuszczalnik chlorowany w pralniach chemicznych, w przemyśle: metalowym, maszynowym i lotniczym, a także jako zmywacz farb i lakierów. Stanowi półprodukt do syntezy związków chemicznych. Znalazł zastosowanie jako medium w wymiennikach ciepła, w weterynarii oraz do dezynfekcji ziarna drogą odymiania. Wielkość produkcji tetrachloroetenu w Unii Europejskiej wynosi 100 000 ÷ 1 000 000 t/rok. Monografię wraz z propozycją normatywu higienicznego dla tetrachloroetenu opracowano ponownie ze względu na ustalenie nowej wartości dopuszczalnej w materiale biologicznym (BLV) w SCOEL, obejmującej pomiar stężenia tetrachloroetenu w powietrzu wydychanym oraz zmniejszenie wartości BLV we krwi, w porównaniu do dotychczas zalecanej przez Międzyresortową Komisję ds. NDS i NDN wartości dopuszczalnego stężenia tetrachloroetenu w materiale biologicznym (DSB). Zdaniem SCOEL, w przypadku substancji wchłaniających się przez skórę, do których należy tetrachloroeten, istnieje szczególna potrzeba monitorowania biologicznego narażenia pracowników w celu zapewnienia najwyższego możliwego poziomu ochrony. W Unii Europejskiej zaklasyfikowano tetrachloroeten do substancji rakotwórczych kategorii zagrożenia 2, z przypisanym zwrotem: podejrzewa się, że powoduje raka. Według opinii ekspertów Międzynarodowej Agencji Badań nad Rakiem (IARC 2014) istnieją ograniczone dowody rakotwórczego działania tetrachloroetenu na ludzi oraz wystarczające dowody działania rakotwórczego związku na zwierzęta doświadczalne (rak wątrobowokomórkowy, gruczolak wątrobowokomórkowy oraz białaczka limfatyczna). Zarówno u ludzi, jak i u zwierząt doświadczalnych skutki narażenia ostrego i przewlekłego na tetrachloroeten są związane przede wszystkim z: ośrodkowym układem nerwowym, wątrobą i nerkami. Zaburzenia ze strony ośrodkowego układu nerwowego manifestują się: bólami i zawrotami głowy, upośledzeniem lub zniesieniem koordynacji ruchowej, a także innymi zaburzeniami stwierdzanymi za pomocą testów neuropsychologicznych. Objawem toksyczności ostrej i inhalacyjnej jest także działanie drażniące tetrachloroetenu na oczy i błony śluzowe dróg oddechowych. Za działanie mutagenne tetrachloroetenu są odpowiedzialne głównie jego metabolity powstające w procesie sprzęgania z glutationem w wątrobie, a następnie aktywowane w nerkach przy udziale beta-liazy. Wyniki badań epidemiologicznych nie wskazują jednoznacznie na wpływ tetrachloroetenu na rozrodczość człowieka, czy działanie embriotoksyczne. Wprawdzie wpływ na rozrodczość, działanie embriotoksyczne i teratogenne tetrachloroetenu odnotowano w niektórych badaniach na zwierzętach doświadczalnych, ale narażanych na tę substancję w bardzo dużych stężeniach. W Polsce obowiązuje wartość najwyższego dopuszczalnego stężenia (NDS) tetrachloroetenu na poziomie 85 mg/m³ oraz wartość najwyższego dopuszczalnego stężenia chwilowego (NDSCh) na poziomie 170 mg/m³ . Jako dopuszczalne stężenie w materiale biologicznym (DSB) przyjęto stężenie tetrachloroetenu we krwi włośniczkowej na poziomie 1,2 mg/l, 15 ÷ 20 min po zakończeniu pracy, w 4. ÷ 5. dniu narażenia Skutkiem krytycznym działania tetrachloroeteu są zaburzenia w ośrodkowym układzie nerwowym. Wartość normatywu higienicznego ustalono na podstawie wartości LOAEL (najniższe stężenie wywołujące skutki szkodliwe) wynoszącej 680 mg/m³ , uzyskanej z badania na ochotnikach narażanych na tetrachloroeten, przez 1 h. U ochotników w badanym stężeniu odnotowano: bóle głowy, senność oraz niewielkie podrażnienie oczu. Zaproponowana wartość NDS tetrachloroetenu wynosi 85 mg/m³ , a wartość NDSCh – 170 mg/m³ . Zaproponowano jako wartość DSB tetrachloroetenu przyjąć stężenie we krwi włośniczkowej 0,3 mg/l pobranej przed ostatnią zmianą roboczą, w 5. dniu pracy. Zalecono oznakować tetrachloroeten notą „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
Tetrachloroethene is a colorless, volatile liquid used as a chlorinated solvent in chemical laundries, in metal, machine, aerospace and paint and varnish removers. It is an intermediate for the synthesis of chemical compounds. It has found use as a medium in heat exchangers, in veterinary medicine and for disinfection of grain by fumigation. The production volume of tetrachloroethene in the EU is 100,000–1,000,000 t / year. The monograph along with the proposed hygiene standard for tetrachloroethene was re-developed due to the setting of a new limit value in biological material (BLV) in SCOEL, including measurement of tetrachloroethene concentration in exhaled air and a decrease in BLV value in blood, compared to the one recommended by the Inter-Ministry Committee for OEL and OEL the value of permissible concentration of tetrachloroethene in biological material (DSB). According to SCOEL, for substances absorbed through the skin, including tetrachloroethene, there is a particular need to monitor workers' biological exposure to ensure the highest possible level of protection. According to the harmonized EU classification, tetrachloroethene is a category-2 carcinogen with risk phrase: Suspected of causing cancer. There is limited evidence of a carcinogenic effect of tetrachloroethene in humans and sufficient evidence of a carcinogenic effect in laboratory animals (hepatocellular carcinoma and hepatocellular adenoma and lymphocytic leukemia). In both humans and laboratory animals, the effects of acute and chronic exposure to tetrachloroethene are primarily associated with the central nervous system, liver and kidneys. Central nervous system disorders are manifested by headache, dizziness, impairment or abnormal coordination, and other disorders found with neuropsychological tests. Acute inhalation toxicity is also irritating to tetrachloroethene on the eyes and respiratory mucosa. The metabolites of tetrachloroethene are mainly responsible for its metabolites formed in the process of conjugation with glutathione in the liver and then activated in the kidneys with the participation of beta-lyase. The results of epidemiological studies do not clearly indicate the effect of tetrachloroethene on human reproduction or embryotoxic effects. Admittedly, effects on reproduction, embryotoxic and teratogenic effects of tetrachloroethene have been reported in some studies on laboratory animals, exposed to this substance in very high concentrations, though. In Poland, the maximum permissible concentration of tetrachloroethe at 85 mg/m³ and the maximum permissible instantaneous concentration at 170 mg / m³ are currently in force. The determined DSB value is 1.2 mg tetrachloroethene /L capillary blood in a sample taken 15–20 min after the end of work on the 4th and 5th day of exposure. The critical effect of tetrachloroete are disorders in the central nervous system. The value of the hygiene standard was derived based on the LOAEL value (lowest concentration causing harmful effects) of 680 mg /m³ , obtained from a study on volunteers exposed to tetrachloroethene for 1 h. In volunteers at the tested concentration headache and drowsiness and slight eye irritation were noted. The proposed MAC value for tetrachloroethene is 85 mg/m³ , and the MAC value is 170 mg/m³ . It was proposed to take a concentration of 0.3 mg/l capillary blood collected before the last work shift on the 5th day of work as the DSB value of tetrachloroethene. It was recommended to label tetrachloroethene with the notation "skin" (absorption of the substance through the skin may be as important as when inhaled). This article discusses the problems of occupational safety and health, which are covered by health sciences and environmental engineering.
Rocznik
Strony
105--148
Opis fizyczny
Bibliogr. 165 poz., rys., tab.
Twórcy
  • Instytut Medycyny Pracy im. prof. dr. med. Jerzego Nofera 91-348 Łódź ul. św. Teresy od Dzieciątka Jezus 8 POLAND
Bibliografia
  • 1. ACGIH (2018). American Conference of Industrial Hygienists. Guide to Occupational Exposure Values. Cincinnati, USA.
  • 2. ACGIH (2001). Tetrachloroethylene. [W:] Baza danych. Documentation of the TLVs. Cincinnati, USA, 2018.
  • 3. ACGIH (2009). Tetrachloroethylene. [W:] Baza danych. Documentation of the BEIs. Cincinnati, USA, 2018.
  • 4. Ahlborg G. Jr. (1990). Pregnancy outcome among women working in laundries and drycleaning shops using tetrachloroethylene. Am. J. Ind. Med. 17, 567–575.
  • 5. Altmann L., Neuhann H.F., Kramer U., Witten J., Jermann E. (1995). Neurobehavioral and neurophysiological outcome of chronic low-level tetrachloroethene exposure measured in neighbourhoods of dry cleaning shops. Environmental Research 69, 83-89.
  • 6. Anttila A., Pukkala E., Sallmén M., Hernberg S., Hemminki K. (1995). Cancer incidence among Finnish workers exposed to halogenated hydrocarbons. JOEM 37, 797–806.
  • 7. Aschengrau A., Ozonoff D., Paulu C., Coogan P., Vezina R., Heeren T., Zhang Y. (1993). Cancer risk and tetrachloroethylene-contaminated drinking water in Massachusetts. Arch. Environ. Health 48, 284–292.
  • 8. Bartsch H., Malaveille C., Barbin A., Planche G. (1978). Mutagenic and alkylating metabolites of halo-ethylenes, chlorobutadienes and dichlorobutanes produced by rodent or human liver tissues. Arch. Toxicol. 41, 249–277.
  • 9. Blair A., Stewart P.A., Tolbert P.E., Grauman D., Moran F.X., Vaught J., Rayner J. (1990). Cancer and other causes of death among a cohort of dry cleaners. Br. J. Ind. Med. 47, 162–168.
  • 10. Blair A., Petralia S.A., Stewart P.A. (2003). Extended mortality follow-up of a cohort of dry cleaners. Annals of Epidemiology 13, 50–56.
  • 11. Birner G., Rutkowska A., Dekant W. (1996). N-acetyl-S- (1,2,2-trichlorovinyl)-L-cysteine and 2,2,2-trichloroethanol: two novel metabolites of tetrachloroethene in humans after occupational exposure. Drug Metab. Dispos. 24, 41–48 [PMID:8825189].
  • 12. Bolanowska W., Gołacka J. (1972). Wchłanianie i wydalanie czterochloroetylenu u ludzi w warunkach eksperymentalnych. Med. Pracy 23, 109–119.
  • 13. Bond G.G., McLaren E.A., Sabel F.L., Bodner K.M., Lipps T.E., Cook R.R. (1990). Liver and biliary tract cancer among chemical workers. Am. J. Ind. Med. 18, 19–24.
  • 14. Bonnet P., Francin J.M., Gradiski D., Raoult G., Zissu D. (1980). Determination de la concentration léthale 50 des principaux hydrocarbures aliphatiques chlorés chez le rat. Ach. Mal. Prof. Med. Trav. Seew. Soc. 41, 317–321.
  • 15. Brodkin C.A., Daniell W., Checkoway H., Echeverria D., Johnson J., Wang K., Sohaey R., Green D., Redlich C., Gretch D. i in. (1995). Hepatic ultrasonic changes in workers exposed to perchloroethylene. Occupational and Environmental Medicine 52, 679–85.
  • 16. Buben J.A. i O’Flaherty E.J. (1985). Delineation of the role of metabolism in the hepatotoxicity of trichloroethylene and perchloroethylene: a dose-effect study. Toxicol. Appl. Pharmacol. 78, 105–122. DOI:10.1016/0041-008X(85)90310-2 PMID:2994252.
  • 17. Cai S.X., Huang M.Y., Chen Z. i in., (1991). Subjective symptom increase among dry-cleaning workers exposed to tetrachloroethylene vapor. Ind Health 29, 111–121. DOI:10.2486/ indhealth.29.111PMID:1765547.
  • 18. Calvert G.M., Ruder A.M., Petersen M.R. (2011). Mortality and end-stage renal disease incidence among dry cleaning workers. Occup. Environ. Med. 68, 709–716.
  • 19. Cavalleri A., Gobba F., Paltrinieri M. i in. (1994). Perchloroethylene exposure can induce colour vision loss. Neurosci Lett 179, 162–166. DOI:10.1016/0304-3940(94)90959-8 PMID:7845613.
  • 20. Chiu W.A. i Ginsberg G.L. (2011). Development and evaluation of a harmonized physiologically based pharmacokinetic (PBPK) model for perchloroethylene toxicokinetics in mice, rats, and humans. Toxicol Appl. Pharmacol. 253, 203–234. DOI:10.1016/j.taap.2011.03.020 PMID:214 6 6818.
  • 21. Chien Y.C. (1997). The influences of exposure pattern and duration on elimination kinetics and exposure assessment of tetrachloroethylene in humans[PhD t hesis]. New Brunswick, NJ: Rutgers University [cyt. za: IARC 2014].
  • 22. Chiu W.A., Micallef S., Monster A.C., Bois F.Y. (2007). Toxicokinetics of inhaled trichloroethylene and tetrachloroethylene in humans at 1 ppm: empirical results and comparisons with previous studies. Toxicol Sciences 95, 23–36. DOI:10.1093/ toxsci/kfl129 PMID:17032701.
  • 23. Chmielewski J., Tomaszewski R., Gołębiowski P., Kowalewski W., Kwiatkowski S.R., Szczekocki W., Winnicka A. (1976). Clinical observations of the occupational exposure to tetrachloroethylene. Bull. Inst. Marit. Trop. Med. Gdynia 27, 197–295.
  • 24. Coler H.R., Rossmiller H.R. (1953). Tetrachlorethylene exposure in a small industry. AMA Arch. Ind. Hyg. Occup. Med. 8, 227–233. PMID:13079324.
  • 25. Colleen H.A., Maronpot R.R., Pereira M.A., Foley J.F., Malarkey D.E., Anderson M.W. (1994). Ras proto-oncogene activation in dichloroacetic acid, trichloroethylene- and tetrachloro-ethylene-induced liver tumors in B6C3F1 mice. Carcinogenesis 15, 2255–2261.
  • 26. Daniel J.W. (1963). The metabolism of 36Cl-labelled trichloroethylene and tetrachloroethylene in the rat. Biochem. Pharmacol., 12, 795-802. PMID: 14071536.
  • 27. DECOS (2003). Tetrachloroethylene (PER). Evaluation of the effects on reproduction, recommendation for classification. The Hague: Health Council of the Netherlands, publication no. 2003/04OSH.
  • 28. DECOS (2004). Tetrachloroethylene (PER) – 2. Health-based occupational exposure limit for short-term exposure. The Hague: Health Council of the Netherlands, publication no. 2004/03OSH.
  • 29. Dekant W., Metzler M., Henschler D. (1986). Identification of S-1,2,2-trichlorovinyl-N-acetylcysteine as a urinary metabolite of tetrachloroethylene: bioactivation through glutathione conjugation as a possible explanation of its nephrocarcinogenicity. J. Biochem. Toxicol. 1, 57–72. DOI:10.1002/ jbt.2570010206 PMID: 3271876.
  • 30. DFG (2005). Deutsche Forschungsgemeinschaft Grenzwerte in biologischem Material Deckblatt zu Tetrachloroethylene. The MAK-Collection. Part II: BAT Value Documentations, Vol. 4. DFG, Deutsche Forschungsgemeinschaft Copyright, WILEY-VCH Verlag GmbH & Co. KGaA.
  • 31. DFG (2017). Deutsche Forschungsgemeinschaft MAK Value Documentation Tetrachloroethylene in German language. The MAK Collection for Occupational Health and Safety. Vol 2, No 2, 1–108.
  • 32. Doherty R.E. (2000). A history of the production and use of carbon tetrachloride, tetrachloroethylene, trichloroethylene and 1,1,1-trichloroethane in the United States, Part 1 Historical background: carbon tetrachloride and tetrachloroethylene. J. Environmental Forensics 1, 69–81. DOI:10.1006/ enfo.2000.0010.
  • 33. Droz P.O. i Guillemin M.P. (1986). Occupational exposure monitoring using breath analysis. J. Occup. Med. 28, 593.
  • 34. Dyrektywa Komisji (UE) 2017/164 z dnia 31 stycznia 2017 r. ustanawiająca czwarty wykaz wskaźnikowych dopuszczalnych wartości narażenia zawodowego zgodnie z dyrektywą Rady 98/24/WE oraz zmieniająca dyrektywy Komisji 91/322/ EWG, 2000/39/WE i 2009/161/UE.
  • 35. echa.europa.eu/pl/registration-dossier Europejska Agencja Chemikaliów.
  • 36. Echeverria D., White R.F., Sampaio C. (1995). A behavioral evaluation of PCE exposure in patients and dry cleaners. A possible relationship between clinical and preclinical effects. JOEM 37, 667–680.
  • 37. Elovaara E., Hemminki K., Vainio H. (1979). Effects of methylene chloride, trichloroethane, trichloroethylene, tetrachloroethylene and toluene on the development of chick embryos. Toxicology 12, 111–119.
  • 38. EPA (1985). Health Assessment Document for Tetrachloroethylene (Perchloroethylene). US Environmental Protection Agency, Washington DC 20460.
  • 39. EPA (2012). Environmental Protection Agency. Toxicological review of Tetrachloroethylene (Perchloroethylene) [CAS No. 127–18–4] in support of summary information on the Integrated Risk Information System (IRIS). EPA/635/R-08/011F. Washington, DC, USA.
  • 40. Essing H.G., Schäcke G., Schaller K.H., Valentin H. (1973). Occupational medicine studies on the dynamics of perchlorethylene in the organism. Med Welt 24, 242–244. PMID:473169 0 [publication in German].
  • 41. Essing H.G. (1975). Field study on the hepato- and nephrotoxicity of perchloroethylene after long-term occupational exposure. Schrift. Arbeitsmed., Sozialmed., Präventivmed. 59 [publication in German) < SASP**, 10.1-9, 11.1-4.
  • 42. Fernandez J., Guberan E., Caperos J. (1976). Experimental human exposures to tetrachloroethylene vapor and elimination in breath after inhalation. Am. Ind. Hyg. Assoc. J. 37, 143– 150. DOI:10.1080/0002889768507437. PMID:1266733.
  • 43. Ferroni C., Selis L., Mutti A., Folli D., Bergamaschi E., Franchini I. (1992). Neurobehavioral and neuroendocrine effects of occupational exposure to perchloroethylene. Neurotoxicology 13, 243–7.
  • 44. Franke W., Eggeling F. (1969). Clinico-statistical investigation of workers exposed to perchloroethylene in dry-cleaning establishments. Med. Welt 9, 453–460.
  • 45. Friberg L., Kylin B., Nystrom A. (1953). Toxicities of trichloroethylene and tetrachloroethylene in fujiwara s pyridine-alkali reaction. Acta Pharmacol. Toxicol. 9, 303–312.
  • 46. Frantz S.W., Watanabe P.G. (1983). Tetrachloroethylene: balance and tissue distribution in male Sprague-Dawley rats by drinking-water administration. Toxicol. Appl. Pharmacol. 69, 66–72. DOI:10.1016/0041-008X(83)90120-5PMID:6857689.
  • 47. Garnier R., Bédouin J., Pépin G., Gaillard Y. (1996). Coinoperated dry cleaning machines may be responsible for acute tetrachloroethylene poisoning: report of 26 cases including one death. J. Toxicol. Clin. Toxicol. 34, 191–197. DOI:10.3109/15563659609013769PMID:8618253.
  • 48. Gennari P., Naldi M., Motta R., Nucci M.C., Giacomini C., Violante F.S., Raffi G.B. (1992). gamma-Glutamyltransferase isoenzyme pattern in workers exposed to tetrachloroethylene. American Journal of Industrial Medicine 21, 661–671.
  • 49. GESTIS (2018). International limit values [dostęp: wrzesień 2018: http://limitvalue.ifa.dguv.de/WebForm_ueliste2.aspx].
  • 50. GIS (2018). Główny Inspektor Sanitarny. Dane według Stacji Sanitarno-Epidemiologicznej w Bydgoszczy.
  • 51. Goldsworthy T.L., Popp J.A. (1987). Chlorinated Hydrocarbon-Induced Peroxisomal Enzyme Activity in Relation to Species and Organ Carcinogenicity. Toxicol. Appl. Pharmacol. 88, 225–233.
  • 52. Gradiski D., Bonnet P., Rault G., Magadur J.L., Francin J.M. (1978). Toxicité aiguë comparée par inhalation des principaux solvants aliphatiques chlorés. Arch. Mal. Prof. Med. Trav. Secur. Soc. 39, 249–257.
  • 53. Green T., Odum J., Nash J.A., Foster J.R. (1990). Perchloroethylene-induced rat kidney tumors: an investigation of the mechanisms involved and their relevance to humans. Toxicol. Appl. Pharmacol. 103, 77–89.
  • 54. Guberan E., Fernandez J. (1974). Control of industrial exposure to tetrachloroethylene by measuring alveolar concentrations: theoretical approach using a mathematical model. Br. J. Ind. Med. 31, 159–167. PMID:4830767.
  • 55. Guglielmi G.L., Casini T., Bertelli A., Galmozzi E., Bertelli A.A. (1992). Effect of ethanol chronic use on hepatotoxicity in rats exposed to tetrachloroethylene. Int. J. Tissue React. 14, 281–5.
  • 56. Hake C.L., Stewart R.D. (1977). Human exposure to tetrachloroethylene inhalation and skin contact. Environ. Health Perspect. 21, 231–238.
  • 57. Hardin B.D., Bond G.P., Sikov M.R., Andrew F.D., Beliles R.P., Niemeier R.W. (1981). Testing of selected workplace chemicals for teratogenic potential. Scand. J. Work Environ. Health 7 (Suppl. 4), 66–75.
  • 58. Haynes W.M. (2012). CRC Handbook of Chemistry and Physics (Internet Version). Boca Raton, FL: CRC Press/Taylor and Francis, No. EPA/625/R-96/010b, 92nd Ed. [http://www.epa. gov/osw/hazard/test-methods/sw846/pdfs/8260b.pdf].
  • 59. Haworth S., Lawlor T., Mortelmans K., Speck W., Zeiger E. (1983). Salmonella mutagenicity test results for 250 chemicals. Environ. Mutag., Suppl. 1, 3–142.
  • 60. Heineman E.F., Cocco P., Gomez M.R., Dosemeci M., Stewart P.A., Hayes R.B., Hoar Zahm S., Thomas T.L., Blair A. (1994). Occupational exposure to chlorinated aliphatic hydro-carbons and risk of astrocytic brain cancer. Am. J. Ind. Med. 26, 155–169.
  • 61. Henschler D., Lehnert G. (Eds) (1994). Tetrachloroethene. [W:] Biological exposure values for occupational toxicants and carcinogens – Critical data evaluation for BAT and EKA values, Vol. 1, VCH, Weinheim, pp. 139–151.
  • 62. Honma T., Hasegawa H., Sato M., Sudo A. (1980). Changes of free amino acid content in rat brain after exposure to trichloroethylene and tetrachloroethylene. Industrial Health 18, 1–8.
  • 63. HSDB (2018). TOXNET profile from Hazardous Substances Data Base. Tetrachloroethylene [dostęp: wrzesień 2018; https://toxnet.nlm.nih.gov].
  • 64. IARC (1995). Dry cleaning, some chlorinated solvents and other industrial chemicals. IARC Monogr Eval Carcinog Risks Hum, 63: 1–551.PMID:9139130.
  • 65. IARC (2014). Tetrachloroethylene. Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 106, 219–350.
  • 66. Ikeda M., Otsuji H., Imamura T., Komoike Y. (1972). Urinary excretion of total trichloro-compounds, trichloroethanol, and trichloroacetic acid as a measure of exposure to trichloroethylene and tetrachloroethylene. Br. J. Ind. Med. 29, 328–333. PMID:5044605.
  • 67. Ikeda M., Koizumi A., Watanabe T., Endo A., Sato K. (1980). Cytogenetic and cytokinetic investigations of lymphocytes from workers occupationally exposed to tetrachloroethylene. Toxicol. Lett., 5, 251–256.
  • 68. Ikeda M., Imamura T. (1973). Biological half-life of trichloroethylene and tetrachloroethylene in human subjects. Int. Arch. Arbeitsmed., 31, 209–224.
  • 69. IPCS (1984). International Programme on Chemical Safety. Environmental Health Criteria 31. Tetrachloroethylene. World Health Organization, Geneva 15–18.
  • 70. Jakobson I., Wahlberg J.E., Holmberg B., Johansson G. (1982). Uptake via the blood and elimination of 10 organic solvents following epicutaneous exposure of anesthetized guinea pigs. Toxicol. Appl. Pharmacol. 63, 181–187. DOI:10.1016/0041- 008X(82)90039-4 PMID:7089968.
  • 71. Jalihal S.S., Barlow A.M. (1984). Leukaemia in dry cleaners (Letter to Editor). J.R. Soc. Health 104, 42.
  • 72. JISA (1993). Japan Industrial Safety Association. Carcinogenicity Study of Tetrachloroethylene by Inhalation in Rats and Mice. Hadano, Japan: Japan Industrial Safety Association.
  • 73. Karlsson J.E., Rosengren L.E., Kjellstrand P., Haglid K.G. (1987). Effects of low-dose inhalation of three chlorinated aliphatic organic solvents on deoxyribonucleic acid in gerbil brain. Scandinavian Journal of Work. Environment & Health 13, 453–458.
  • 74. Kjellstrand P., Holmquist B., Kanje M. i in. (1984). Perchloroethylene: effects on body and organ weights and plasma butyrylcholinesterase activity in mice. Acta pharmcologica et toxicological 54, 414–424.
  • 75. Kjellstrand P., Holmquist B., Jonsson I., Romare S., Mansson L. (1985). Effects of organic solvents on motor activity in mice. Toxicology, 35, 35–46.
  • 76. Klaassen C.D., Plaa G.L. (1966). Relative effects of various chlorinated hydrocarbons on liver and kidney function in mice. Toxicol. Appl. Pharmacol. 9, 139–151.
  • 77. Klaassen C.D., Plaa G.L. (1967). Relative effects of various chlorinated hydrocarbons on liver and kidney function in dogs. Toxicol. Appl. Pharmacol. 10, 119–131.
  • 78. Kylin B., Reichard H., Sümegi I., Yllner S. (1963). Hepatotoxicity of inhaled trichloroethylene, tetrachloroethylene and chloroform, single exposure. Acta Pharmacol. Toxicol. 20, 16–26.
  • 79. Kyrklund T., Alling C., Kjellstrand P., Haglid K.G. (1984). Chronic effects of perchloroethylene on the composition of lipid and acyl groups in cerebral cortex and hippocampus of the gerbil. Toxicol. Lett. 22, 343–349. DOI:10.1016/0378- 4274(84)90112-7 PMID:6485008.
  • 80. Kyrklund T., Kjellstrand P., Haglid K.G. (1987). Lipid composition and fatty acid pattern of the gerbil brain after exposure to perchloroethylene. Archives of Toxicology 60, 397–400.
  • 81. T., Kjellstrand P., Haglid K.G. (1988). Effects of exposure to Freon 11, 1,1,1-trichloroethane or perchloroethylene on the lipid and fatty-acid composition of rat cerebral cortex. Scandinavian Journal of Work. Environment & Health 14, 91–94.
  • 82. Kyrklund T., Kjellstrand P., Haglid K.G. (1990). Long-term exposure of rats to perchloroethylene, with and without a postexposure solvent-free recovery period: effects on brain lipids. Toxicology Letters 52, 279–85.
  • 83. Koizumi A., Kumai M., Ikeda M., (1982). In vivo suppression of 1,1,1-trichloroethane metabolism by coadministered tetrachloroethylene: an inhalation study. Bull. Environ. Contam. Toxicol. 29, 196–199.
  • 84. Köppel C., Arndt I., Arendt U., Koeppe P. (1985). Acute tetrachloroethylene poisoning–blood elimination kinetics during hyperventilation therapy. J. Toxicol. Clin. Toxicol. 23, 103– 115. DOI:10.3109/15563658508990621PMID:4057308.
  • 85. Kringstad K.P., Ljungquist P.O., de Sousa F., Stromberg L.M. (1981). Identification and mutagenic properties of some chlorinated aliphatic compounds in the spent liquor from kraft pulp chlorination. Environ. Sci. Technol. 15, 562–566.
  • 86. Lash L.H., Qian W., Putt D.A. i in, (1998). Glutathione conjugation of perchloroethylene in rats and mice in vitro: sex-, species-, and tissue-dependent differences. Toxicol. Appl. Pharmacol. 150, 49–57. DOI:10.1006/taap.1998.8402. PMID:9630452.
  • 87. Lash L.H., Parker J.C. (2001). Hepatic and renal toxicities associated with perchloroethylene. Pharmacol. Rev. 53, 177–208.
  • 88. Lauwerys R., Herbrand J., Buchet J.P., Bernard A., Gaussin J. (1983). Health surveillance of workers exposed to tetrachloroethylene in dry-cleaning shops. International Archives of Occupational and Environmental Health 52, 69–77.
  • 89. Levine B., Fierro M.F., Goza S.W., Valentour J.C. (1981). A tetrachloroethylene fatality. Journal Forensic Sciences 26, 206– 209. PMID:7205186.
  • 90. Ling S., Lindsay W.A. (1971). Perchloroethylene burns (letter). Br. Med. J. 3, 115.
  • 91. Lynge E., Thygesen L. (1990). Primary liver cancer among women in laundry and dry-cleaning work in Denmark. Scand. J. Work Environ. Health 16, 108–112.
  • 92. Lynge E., Andersen A.,Rylander L., Tinnerberg H.,Lindbohm M.L.,Pukkala E.,Romundstad P.,Jensen P.,Clausen L.B.,Johansen K. (2006). Cancer in persons working in dry cleaning in the Nordic countries. Environmental Health Perspectives 114(2), 213–9.
  • 93. Lukaszewski T. (1979). Acute tetrachloroethylene fatality. Clin. Toxicol. 15, 411–415.
  • 94. McKernan L.T., Ruder A.M., Petersen M.R., Hein M.J., Forrester C.L., Sanderson W.T., Ashley D.L. i Butler M.A. (2008). Biological exposure assessment to tetrachloroethylene for workers in the dry cleaning industry. Environmental Health 87, 12, 1–10 [https://doi.org/10.1186/1476-069X-7-12].
  • 95. Mackler L.C., Phelps D.K. (1966). JAMA 197, 662–663.
  • 96. Mallin K. (1990). Investigation of a bladder cancer cluster in Northwestern Illinois. Am. J. Epidemiol. 132, 96–106.
  • 97. Mazza A. (1972). Enzyme modifications following experimental tetrachloroethylene intoxication. Folia Med. (Naples), 55, 373–381.
  • 98. Monster A.C., Boersma G., Steenweg H. (1979). Kinetics of tetrachloroethylene in volunteers; influence of exposure concentration and work load. Int. Arch. Occup. Environ. Health. 42, 303–309. DOI:10.1007/BF00377784PMID:422271.
  • 99. Moslen M.T., Reynolds E.S., Szabo S. (1977). Enhancement of the metabolism and hepatotoxicity of trichloroethylene and perchloroethylene. Biochemical Pharmacology 26, 369–375.
  • 100. Müller C., Franke C., Wagner A. i in. (1989). Development of a rational monitoring strategy for workers exposed to tetrachloroethylene (publication in German). Z Gesamte Hyg, 35, 547–550. PMID:2555973.
  • 101. Mutti A., Alinovi R., Bergamaschi E., Biagini C., Cavazzini S., Franchini I., Lauwerys R., Bernard A.M., Roels H., Gelpi E., Rosello J., Ramis I., Price R.G., Taylor S.A., De Broe M., Nuyts G.D., Stolte H., Fels L.M., Herbort C. (1992). Nephropathies and exposure to per-chloroetylene in drycleaners. The Lancet 340, 189–193.
  • 102. Münzer M., Heder K. (1972). Results of the occupational medicinal and technical inspection of dry-cleaning establishments. Zbl. Arbeitsmed. 22, 133–138.
  • 103. NCI, National Cancer Institute (1977). Bioassay of Tetrachloroethylene for Possible Carcinogenicity (CAS No. 127- 18- 4), (NCI Tech. Rep. Ser. No. 13; NIH Publ. No. 77–813). Bethesda, MD, USA. US Department of Health, Education a nd Welfare.
  • 104. Nakatsuka H., Watanabe T., Takeuchi Y., Hisanaga N., Shibata E., Suzuki H., Huang Y., Chen Z., Qu Q.S., Ikeda M. (1992). Absence of blueyellow color vision loss among workes exposed to toluene or tetrachloroethylene, mostly at levels below occupational exposure limits. Int. Arch. Occup. Environ. Health 64, 113–117.
  • 105. NEG-DECOS (2003). Tetrachloroethylene (PER). The Nordic Expert Group for Criteria Documentation of Health Risks from Chemicals and The Dutch Expert Committee on Occupational Standards. Stockholm: National Institute for Working Life.
  • 106. Nelson B.K., Taylor B.J., Setzer J.V., Hornung R.W. (1979). Behavioral teratology of perchloroethylene in rats. J. Environ. Pathol. Toxicol. 3(1–2), 233–250.
  • 107. NIOSH (1976). Criteria for a Recommended Standard. Occupational Exposure to Tetrachloroethylene. U.S. Department of Health, Education, and Welfare.
  • 108. NTP, National Toxicology Program (1986). Toxicology and Carcinogenesis Studies of Tetrachloroethylene (Perchloroethylene), (CAS No. 127–18–4) in F344/N Rats and B6C3F1 Mice (Inhalation Studies). National Toxicology Program Tech. Rep. Ser. 311, 1–197. PMID:1274 8718.
  • 109. Odum J., Green T., Foster J.R., Hext P.M. (1988). The role of trichloroacetic acid and peroxisome proliferation in the differences in carcinogenicity of perchloroethylene in the mouse and rat. Toxicol. Appl. Pharmacol. 92, 103–112.
  • 110. Olsen G.W., Hearn S., Cook R.R., Currier M.F., Allen S. (1989). Mortality experience of a cohort of Louisiana chemical workes. J. Occup. Med. 31, 32–34.
  • 111. O’Neil M.J., Heckelman P.E., Roman C.B. (2006). The Merck Index. 14th Ed. Whitehouse Station, NJ, USA: Merck & Co. Monograph Number 09639.
  • 112. Palacek I. (1970). So-called chemical asthma. Arhiv Za Higijenu Rada I Toksikologiju 21, 161–166 (cyt. wg NEG-DECOS 2003).
  • 113. Patel R., Janakiraman N., Johnson R., Elman J.B. (1973). Pulmonary edema and coma from perchloroethylene. J. Am. Med. Assoc. 223, 1510.
  • 114. Pegg D.G., Zempel J.A., Braun W.H., Watanabe P.G. (1979). Disposition of tetrachloro(14C)ethylene following oral and inhalation exposure in rats. Toxicol. Appl. Pharmacol. 51, 465–474. DOI:10.1016/0041-008X(79)90371-5PMID:538758.
  • 115. Pezzagno G., Imbriani M., Ghittori S. (1988). Urinary concentration, environmental concentration, and respiratory uptake of some solvents. Effect of the work load. Am. Ind. Hyg. Assoc. 49, 546–552.
  • 116. Plaa G.L., Larson R.E.. (1965). Relative nephrotoxic properties of chlorinated methane, ethane and ethylene derivatives in mice. Toxicol. Appl. Pharmacol. 7, 37–44.
  • 117. Rampy L.W., Quast J.F., Leong B.K.J., Gehring P.J. (1985). Results of a Long-Term Inhalation Toxicity Study. Perchloroethylene in Rats. Toxicology Research Laboratory, Health and Environmental Research, The Dow Chemical Co., Midland, MI; cited in U.S. Environmental Protection Agency: Drinking Water Criteria Document for Tetrachloroethylene. NTIS Pub. No. PB-86-118-114. U.S. National Technical Information Service, Springfield, VA.
  • 118. Ratnoff W.D., Gress R.E. (1980). The familial occurence of polycythemia vera: report of a father and son, with consideration of the possible etiologic role of exposure to organic solvents, including tetrachloroethylene. Blood, 56, 233–236.
  • 119. Redmond S.F., Schappert K.R., (1987). Occupational dermatitis associated with garments. J. Occup. Med. 29(3), 243–4.
  • 120. Reichert D. (1983). Biological actions and interactions of tetrachloroethylene. Mutat. Res., 123, 411–429.
  • 121. Rosengren L.E., Kjellstrand P., Haglid K.G. (1986). Tetrachloroethylene: levels of DNA and S-100 in the gerbil CNS after chronic exposure. Neurobehavioural Toxicology and Teratology 8, 201–6.
  • 122. Rowe V.K., McCollister D.D., Spencer H.C., i in. (1952). Vapor Toxicity of Tetrachloroethylene for Laboratory Animals and Human Subjects. AMA Arch. Ind. Hyg. Occup. Med. 5, 566–579.
  • 123. Rozporządzenie Ministra Rodziny, Pracy i Polityki Społecznej z dnia 12 czerwca 2018 r. w sprawie najwyższych dopuszczalnych stężeń i natężeń czynników szkodliwych dla zdrowia w środowisku pracy. DzU z dnia 03.07.2018 r., poz. 1286 [Polish legal act].
  • 124. Rozporządzenie Parlamentu Europejskiego i Rady (WE) nr 1272/2008 z dnia 16.12.2008 r. w sprawie klasyfikacji, oznakowania i pakowania substancji i mieszanin, zmieniającego i uchylającego dyrektywy 67/648/EWG i 1999/45/ WE oraz zmieniającego rozporządzenie WE nr 1907/2006 ze zm. (Rozporządzenie Komisji (WE) nr 790/2009) [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]. Dz. Urz. UE z dnia 31.12.2008 (L 353).
  • 125. Ruder A.M., Ward E.M., Brown D.P. (1994). Cancer mortality in female and male dry-cleaning workes. J. Occup. Med. 36, 867–874.
  • 126. Savolainen H., Pfaffli P., Tengen M., Vainio H. (1977). Biochemical and behavioural effects of inhalation exposure to tetrachloroethylene and dichloromethane. Journal of Neuropathology and Experimental Neurology 36, 941–949.
  • 127. Schreiber J.S. (1997). Transport of organic chemicals to breast milk: Tetrachloroethene case study. Washington, DC, USA: Taylor and Francis. Schreiber J.S., Hudnell H.K., Geller A. Met i in. (2002). Apartment residents’ and day care workers’ exposures to tetrachloroethylene and deficits in visual contrast sensitivity. Environ Health Perspect 110, 655–664. DOI:10.1289/ ehp.02110655PMID:12117642.
  • 128. Schumann A.M., Quast J.F., Watanabe P.G. (1980). The pharmacokinetics and macromolecular interactions of perchloroethylene in mice and rats as related to oncogenicity. Toxicol. Appl. Pharmacol. 55, 207–219. DOI:10.1016/0041-008X- (80)90082-4PMID:74 23514.
  • 129. Schwetz B.A., Leong B.K.J., Gehring P.J. (1975). The effect of maternally inhaled trichloro- ethylene, perchloroethylene, methyl chloroform, and methylene chloride on embryonal and fetal development in mice and rats. Toxicol. Appl. Pharmacol. 32, 84–96.
  • 130. SCOEL/SUM/133 ( 2009). Recommendation of the Scientific Committee on Occupational Exposure Limits for Tetrachloroethylene (Perchloroethylene) Seeber A. (1989). Neurobehavioral toxicity of long-term exposure to tetrachloroethylene. Neurotoxicol. Teratol. 11, 579–583.
  • 131. Seidel H.J., Weber L., Barthel E. i in. (1992). Hematological toxicity of tetrachloroethylene in mice. Archives of toxicology 66, 228–230.
  • 132. Seldén A.I., Ahlborg G. Jr. (2011). Cancer morbidity in Swedish dry-cleaners and laundry workers: historically prospective cohort study. Int. Arch Occup. Environ. Health. 84, 435–443.
  • 133. Seiji K., Jin C., Watanabe T., Nakatsuka H., Ikeda M. (1990). Sister chromatid exchanges in peripherol lymphocytes of workers exposed to benzene, trichloroethylene, or tetra-chloroethylene, with reference to smoking habits. Int. Arch. Occup. Environ. Health 62, 171–176.
  • 134. Skender L.J., Karacić V., Prpić-Majić D. (1991). A comparative study of human levels of trichloroethylene and tetrachloroethylene after occupational exposure. Arch. Environ. Health 46, 174–178. doi:10.1080/00039896.1991.9 9374 4 6PMID:2039273.
  • 135. Smythe H.F. Jr., Weil C.S., West J.S., Carpenter C.P. (1969). An exploration of joint toxic action: twenty-seven industrial chemicals intubated in rats in all possible pairs. Toxicol. Appl. Pharmacol. 14, 340–347.
  • 136. Solet D., Robins T.G. (1991). Renal function in dry cleaning workers exposed to perchloroethylene. American Journal of Industrial Medicine 20, 601–614.
  • 137. Sparrow G.P. (1977). Connective tissue disorder similar to vinyl chloride disease in a patient exposed to perchloroethylene. Clin. Exp. Dermatol. 2, 17–22.
  • 138. Spirtas R., Stewart P.A., Lee J.S.. Marano D.E., Forbes C.D., Grauman D.J., Pettigrew H.M., Blair A., Hoover R.N., Cohen J.L. (1991). Retrospective cohort mortality study of workers at an aircraft maintenance facility. I. Epidemiological results. Br. J. Ind. Med. 48, 515–530.
  • 139. Stewart R.D., Arbor A., Gay H.H., Erley D.S., Hake C.L., Schaffer A.W. (1961). Human exposure to tetrachloroethylene vapor. Archives of Environmental Health 2, 516–522.
  • 140. Stewart R.D., Dodd H.C. (1964). Absorption of carbon tetrachloride, trichloethylene, tetrachloroethylene, methylene chloride, and 1,1,1-trichloroethane through human skin. Am. Ind. Hyg. Assoc. J. 25, 439–466.
  • 141. Stewart R.D., Baretta E.D., Dodd H.C., Torkelson T.R. (1970). Experimental human exposure to tetrachloroethylene. Arch. Environ. Health 20, 225–229. DOI:10.1080/00039896.1970.10 665579PMID:5411393.
  • 142. Stewart R.D. (1977). Effects of Perchloroethylene/Drug Interaction on Behavior and Neurological Function. DHEW (NIOSH) Pub. No. 77-191; NTIS Pub. No. PB-83-174-607. U.S. National Technical Information Service, Springfield, VA.
  • 143. Storm J.E., Mazor K.A., Aldous K.M. i in. (2011). Visual contrast sensitivity in children exposed to tetrachloroethylene [Erratum in: Arch. Environ. Occup. Health 66(4):250 Arch. Environ. Occup. Health 66, 166–177. DOI:10.1080/19338244 .2010.539638 PMID:21864105.
  • 144. Tada O. (1969). J. Sci. Labour. 45, 757–760.
  • 145. Taskinen H.K., Anttila A., Lindbohm M.L., Sallmén M., Hemminki K. (1989). Spontaneous abortions and congenital malformations among the wives of men occupationally exposed to organic solvents. Scand. J. Work Environ. Health 15, 345–352.
  • 146. Taskinen H.K. (1995). Nordic criteria for reproductive toxicity. JOEM 37, 970–973.
  • 147. Theiss J.C., Stoner G.D., Shimkin M.B., Weisburger E.K. (1977). Test for carcinogenicity of organic contaminants of United States drinking waters for pulmonary tumor in strain A mice. Cancer Res. 37, 2717–2720.
  • 148. Trevisan A., Maccà I., Rui F. i in. (2000). Kidney and liver biomakers in female dry-cleaning workers exposed to perchloroethylene. Biomarkers 5, 399–409. DOI:10.1080/135475000750052411.
  • 149. Tsuruta H. (1975). Percutaneous absorption of organic solvents: 1) comparative study of the in vivo percutaneous absorption of chlorinated solvents in mice Ind Health 13, 227– 236. DOI:10.2486/indhealth.13.227.
  • 150. TURI (2006). Perchloroethylene. [In:] Five Chemical Alternatives Assessment Study.Toxics Use Reduction Institute.
  • 151. Tuttle T.C., Wood G.D., Grether C.B. (1976). Behavioral and neurological evaluation of workers exposed to perchloroethylene. Columbia (Final report a contract HSM 9/73/35 Westinghouse Behavioral Services Centre) [cyt. za: Ikeda, Imamura 1973].
  • 152. Tuttle T.C., Wood G.D., Crether C.B., i in. (1977). A behavioural and neurological evaluation of dry cleaners exposed to perchloroethylene. US DHEW/NIOSH Report No. 77–214.
  • 153. Vamvakas S., Herkenhoff M., Dekant W., Henschler D. (1989). Mutagenicity of tetrachloro-ethylene in the Ames test - metabolic activation by conjugation with glutathione. J. Biochem. Toxicol. 4, 21–27.
  • 154. Van Duuren B.L., Goldschmidt B.M., Loewengart G. i in. (1979). Carcinogenicity of halogenated olefinic and aliphatic hydrocarbons in mice. Journal of the Natlional Cancer Institute 63, 1433–1439.
  • 155. Van Duuren B.L., Kline S.A., Seidman I. (1983). Chemical structure and carcinogenicity relationships of some chloroalkene oxides and their parent olefins. Cancer Res. 43, 159– 162. PMID: 6847764.
  • 156. Verplanke A.J., Leummens M.H., Herber R.F. (1999). Occupational exposure to tetrachloroethene and its effects on the kidneys. Journal of Occupational and Environmental Medicine 41, 11–16.
  • 157. Vlaanderen J., Straif K., Ruder A., Blair A., Hansen J., Lynge E., Charbotel B., Loomis D., Kauppinen T., Kyyronen P., Pukkala E., Weiderpass E., Guha N. (2014). Tetrachloroethylene exposure and bladder cancer risk: a metaanalysis of drycleaningworker studies. Environ Health Perspect 122, 661–666 [http:// dx.doi.org/10.1289/ehp.1307055].
  • 158. Völkel W., Friedewald M., Lederer E. i in. (1998). Biotransformation of perchloroethene: dose-dependent excretion of trichloroacetic acid, dichloroacetic acid, and N-acetyl-S- (trichlorovinyl)-L-cysteine in rats and humans after inhalation. Toxicol. Appl. Pharmacol. 153, 20–27. DOI:10.1006/ taap.1998.8548. PMID:9875296.
  • 159. Vyskocil A., Emminger S., Tejral .J, Fiala Z., Ettlerova E., Cermanova A. (1990). Study on kidney function in female workers exposed to perchlorethylene. Human and Experimental Toxicology 9, 377–80.
  • 160. Walles SAS (1986). Induction of single-strand breaks in DNA of mice by trichloroethylene and tetrachloroethylene. Toxicol. Lett. 31, 31–35. DOI:10.1016/0378-4 274(86)9 0191-8 PMID:3715914.
  • 161. Wang S., Karlsson J.E., Kyrklund T., Haglid K. (1993). Perchloroethylene-induced reduction in glial and neuronal cell marker proteins in rat brain. Pharmacol. Toxicol. 72, 273–278. DOI:10.1111/j.1600- 0773.1993.tb016 49. PMID:8372046.
  • 162. Weisburger E.K. (1977). Carcinogenicity studies on halogenated hydrocarbons. Environmental Health Perspectives 21, 7–16. DOI:10.1289/ehp.77217/ PMID:206428.
  • 163. Windham G.C., Shusterman D., Swan S.H., Fenster L., Eskenazi B. (1991). Exposure to organic solvents and adverse pregnancy outcome. Am. J. Ind. Med. 20, 421–459.
  • 164. Yllner S. (1961). Urinary metabolites of 14C-tetrachloethylene in mice. Nature 191:820.
  • 165. Zimmerli B., Guler H.P., Schlatter Ch. (1982). Accumulation and excretion of perchloroethylene in laying hens after oral administration. Mitt. Geb. Lebensm. Hyg. 73, 438454 [publication in German].
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-c37fce01-3197-4858-96da-563d4536e2eb
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.