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User:Langleym/sandbox

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Langleym/sandbox
Names
IUPAC name
4-hydroxy-4H-furo[3,2-c]pyran-2(6H)-one
Other names
2-Hydroxy-3,7-dioxabicyclo[4.3.0]nona-5,9-dien-8-one
Clairformin
Claviform
Expansine
Clavacin
Clavatin
Expansin
Gigantin
Leucopin
Patuline
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
EC Number
  • 205-735-2
KEGG
UNII
  • InChI=1S/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2 checkY
    Key: ZRWPUFFVAOMMNM-UHFFFAOYSA-N checkY
  • InChI=1/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2
    Key: ZRWPUFFVAOMMNM-UHFFFAOYAU
  • O=C\1O/C2=C/COC(O)C2=C/1
Properties
C7H6O4
Molar mass 154.12 g/mol
Appearance Compact prisms
Density 1.52 g/ml
Melting point 110 °C (230 °F; 383 K)
Soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tracking categories (test):


Overview

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Patulin is a mycotoxin produced by a variety of molds, in particular, Aspergillus and Penicillium and Byssochlamys. Most commonly found in rotting apples, the amount of patulin in apple products is generally viewed as a measure of the quality of the apples used in production. Additionally, patulin has been found in other foods such as grains, fruits, and vegetables. While not considered a particularly potent toxin, a number of studies have shown patulin to be genotoxic; which has led to some to theorize that it may be a carcinogen, although animal studies have remained inconclusive.[2] Patulin has shown antimicrobial properties against some microorganisms. [3] Several countries have instituted patulin restrictions in apple products. The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice. [4] In the European Union, the limit is set to 50 micrograms per kilogram (µg/kg) in both apple juice and cider, and to half of that concentration, 25 µg/kg in solid apple products and 10 µg/kg in products for infants and young children. These limits came into force on 1 November 2003. [5]

Chemistry

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Patulin is a white powder soluble in low pH water and organic solvents. It is a polyketide lactone that is heat stable, so it is not destroyed by pasteurization or thermal denaturation. [6] However, stability following fermentation is lessened [7].Isoepoxydon dehydrogenase (IDH) is an important enzyme in the multi-step biosynthesis of patulin and its gene is present in other fungi which may potentially produce the toxin [8]. It is reactive with sulfur dioxide, so antioxidant and antimicrobial agents may be useful to destroy it [9]. Levels of nitrogen, manganese, and pH as well as abundance of necessary enzymes regulate the biosynthetic pathway of patulin [10].

Uses

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Patulin was originally used as an antibiotic against gram-positive and gram-negative bacteria, however after several toxicity reports it is no longer used for that purpose.[11] It was specifically trialed to be used against the common cold.[12] Patulin is used as a potassium uptake inhibitor in laboratory applications. [13]

Sources of Exposure

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Frequently, patulin is found in apples, and apple product such as juices, jams, and ciders. It has also been detected in other fruits including cherries, blueberries, plums, bananas, strawberries, and grapes [14]. Fungal growth leading to patulin production is most common on damaged fruits. [15] Patulin has also been detected in grains like barley, wheat, corn and their processed products as well as in shellfish. [16], [17] Dietary intake of patulin from apple juice has been estimated at between 0.03 to 0.26μg/kg bw/day in various age groups and populations. [18] Content of patulin in apple juice is estimated to be less than 10-15μg/L.[19] [20] A number of studies have looked into comparisons of organic vs conventional harvest of apples and levels of patulin contamination.[21],[22] For example, one study showed 0.9% of children drinking organic apple juice exceeded the tolerable daily intake (TDI) for patulin [23]. A recent article described detection of patulin in marine strains of Penicillium, indicating a potential risk in shellfish consumption [24].

Toxicity

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A subacute rodent NOAEL of 43μg/kg body weight as well as genotoxicity studies were primarily the cause for setting limits for patulin exposure, although a range of other types of toxicity also exist. [25]

Acute

Patulin is primarily toxic through affinity to sulfhydryl groups (SH) which results in inhibition of enzymes. Oral LD 50 in rodent models have ranged between 20-100mg/kg. [26] In poultry, the oral LD50 range was reported between 50-170mg/kg. [27] Other routes of exposure are more toxic, yet less likely to occur. Major acute toxicity findings include gastrointestinal problems, neurotoxicity (ie convulsions), pulmonary congestion and edema.[28]

Subacute

Studies in rats showed decreased weight, and gastric, intestinal, and renal function changes, while repetitive doses lead to neurotoxicity. Reproductive toxicity in males were also reported. [29] A NOAEL in rodents was observed at 43μg/kg bw. [30]

Genotoxicity

WHO concluded that patulin is genotoxic based on variable genotoxicity data, however it is considered a group 3 carcinogen by the International Agency for Research on Cancer (IARC) since data was inconclusive [31].

Reproduction studies

Patulin decreased sperm count and altered sperm morphology in the rat. [32] Also, it resulted in abortion of F1 litters in rats and mice after i.p. injection [33]. Embryotoxicity and teratogenicity were also reported in chick eggs [34].

Immunotoxicity

Patulin was found to be immunotoxic in a number of animal and even human studies. Reduced cytokine secretion, oxidative burst in macrophages, increased splenic T lymphocytes, and increased neutrophil numbers are a few endpoints noticed. [35]. However, dietary relevant exposure would not be likely to alter immune response [36].

Human health

Although there are only very few reported cases and epidemiological data, the FDA has set an action limit of 50ppb in cider due to its potential carcinogenicity and other reported adverse effects [37]. In humans, it was tested as an antibiotic intranasally for use against the common cold with few significant adverse effects, yet also had negligible or no beneficial effect [38].

Risk Management and Regulations

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Patulin exposure can be successfully managed by following good agricultural practices such as removing mold, washing, and not using rotten or damaged apples for baking, canning,or juice production. [39], [40].

US

The provisional tolerable daily intake (PTDI) for patulin was set at 0.43 µg/kg bw by the FDA [41] based on a NOAEL of 0.3mg/kg bw per week [42]. Monte Carlo analysis was done on apple juice to compare exposure and the PTDI. Without controls or an action limit, 90th percentile of consumers would not be above the PTDI. However, children 1-2yrs old would be 3x higher than the PDTI. Hence, an action limit of 50 µg/kg was set [43].


WHO

The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice.[44]


EU

The European Union (EU) has set a maximum limits of 50μg/kg pertaining to fruit juices and drinks, while solid apple products have a limit of 25μg/kg. For certain foods intended for infants, and even lower limit of 10μg/kg is observed.


To test for patulin contamination, a variety of methods and sample preparation methods have been employed including thin layer chromatography (TLC), gas chromatography (GC),high performance liquid chromatography (HPLC), capillary electrophoresis [45].

References

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  1. ^ Merck Index, 11th Edition, 7002
  2. ^ "Patulin: a Mycotoxin in Apples". Perishables Handling Quarterly (91): 5. August 1997
  3. ^ Merck Index, 11th Edition, 7002
  4. ^ "Foodborne hazards (World Health Organization". Retrieved 2007-01-22.
  5. ^ Patulin information leaf from Fermentek
  6. ^ http://www.sigmaaldrich.com/catalog/product/sigma/p1639?lang=en&region=US
  7. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  8. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  9. ^ Llewellyn, G.C.; McCay, J.A.; Brown, R.D.; Musgrove, D.L.; Butterworth, L.F.; Munson, A.E.; White, K.L., Jr. Immunological evaluation of the mycotoxin patulin in female B6C3F1 mice. Food Chem. Toxicol. 1998, 36, 1107–1111.
  10. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  11. ^ Medical Research Council. Clinical trial of patulin in the common cold. Lancet1944; ii: 373-5.
  12. ^ Medical Research Council. Clinical trial of patulin in the common cold. Lancet1944; ii: 373-5.
  13. ^ http://www.sigmaaldrich.com/catalog/product/sigma/p1639?lang=en&region=US
  14. ^ Llewellyn, G.C.; McCay, J.A.; Brown, R.D.; Musgrove, D.L.; Butterworth, L.F.; Munson, A.E.; White, K.L., Jr. Immunological evaluation of the mycotoxin patulin in female B6C3F1 mice. Food Chem. Toxicol. 1998, 36, 1107–1111.
  15. ^ http://www.orangepippin.com/resources/general/patulin
  16. ^ Llewellyn, G.C.; McCay, J.A.; Brown, R.D.; Musgrove, D.L.; Butterworth, L.F.; Munson, A.E.; White, K.L., Jr. Immunological evaluation of the mycotoxin patulin in female B6C3F1 mice. Food Chem. Toxicol. 1998, 36, 1107–1111.
  17. ^ Pouchous et all. Shellfish
  18. ^ Wouters, FA, and Speijers, GJA.. JECFA Monograph on Patulin . World Health Organization Food Additives Series 35( http://www.inchem.org/documents/jecfa/jecmono/v26je10.htm)
  19. ^ Wouters, FA, and Speijers, GJA.. JECFA Monograph on Patulin .
  20. ^ World Health Organization Food Additives Series 35( http://www.inchem.org/documents/jecfa/jecmono/v26je10.htm)
  21. ^ Pique, E., et al. Occurrence of patulin in organic and conventional apple juice. Risk Assesment. Recent Advances in Pharmacuetical Sciences, III, 2013: 131-144.
  22. ^ http://www.foodsafetynews.com/2013/04/recall-of-organic-juices-a-lesson-in-mycotoxins/#.Uk3Ld9LksnE
  23. ^ Beark et al 2007
  24. ^ Pouchous et all. Shellfish
  25. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  26. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  27. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  28. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  29. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  30. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm.
  31. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  32. ^ Selmanoglu, G. Evaluation of the reproductive toxicity of patulin in growing male rats. Food Chem. Toxicol. 2006, 44, 2019–2024.
  33. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  34. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  35. ^ Puel, O.; Galtier, P.; and Oswale, I.P. Biosynthesis and Toxicological Effects of Patulin. Toxins 2010.
  36. ^ Llewellyn, G.C.; McCay, J.A.; Brown, R.D.; Musgrove, D.L.; Butterworth, L.F.; Munson, A.E.; White, K.L., Jr. Immunological evaluation of the mycotoxin patulin in female B6C3F1 mice. Food Chem. Toxicol. 1998, 36, 1107–1111.
  37. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  38. ^ Medical Research Council. Clinical trial of patulin in the common cold. Lancet1944; ii: 373-5.
  39. ^ http://www.orangepippin.com/resources/general/patulin
  40. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  41. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  42. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  43. ^ http://www.fda.gov/food/foodborneillnesscontaminants/naturaltoxins/ucm212520.htm
  44. ^ "Foodborne hazards (World Health Organization". Retrieved 2007-01-22.
  45. ^ Variability and uncertainty assessment of patulin exposure for preschool children in Flanders


[edit]

a) http://www.foodsafetywatch.org/factsheets/patulin/

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