Oral exposure to polystyrene nanoparticles affects iron absorption

Nature Nanotechnology

Volumn 7, Issue 4, 2012, Pages 264-271

  Mahler, Gretchen J ^a   Esch, Mandy B ^b   Tako, Elad ^c   Southard, Teresa L ^d   Archer, Shivaun D ^b   Glahn, Raymond P ^c   Shuler, Michael L ^b  

^a BINGHAMTON UNIVERSITY   (United States)

^b Cornell University   (United States)

^c U S DEPARTMENT OF AGRICULTURE   (United States)

^d Department of Obstetrics Gynecology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALS; CYTOLOGY; IRON; POLYSTYRENES;

CHRONIC EXPOSURE; ENGINEERED NANOPARTICLES; IN-VITRO MODELS; INTESTINAL CELLS; INTESTINAL EPITHELIUM; IRON ABSORPTIONS; IRON TRANSPORT; POLYSTYRENE NANOPARTICLES;

NANOPARTICLES;

IRON; NANOPARTICLE; POLYSTYRENE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; INTESTINE EPITHELIUM; INTESTINE LOOP; IRON ABSORPTION; IRON TRANSPORT; LONG TERM EXPOSURE; NONHUMAN; PRIORITY JOURNAL;

EID: 84859610801     PISSN: 17483387     EISSN: 17483395     Source Type: Journal    
DOI: 10.1038/nnano.2012.3     Document Type: Article

References (47)

1. Sagalowicz, L. & Leser, M. E. Delivery systems for liquid food products. Curr. Opin. Colloid Interface Sci. 15, 61-72 (2010).
2. Yoav, D. L. Milk proteins as vehicles for bioactives. Curr. Opin. Colloid Interface Sci. 15, 73-83 (2010).
3. Edgar, A. Bioavailability of nanoparticles in nutrient and nutraceutical delivery. Curr. Opin. Colloid Interface Sci. 14, 3-15 (2009).
4. Sozer, N. & Kokini, J. L. Nanotechnology and its applications in the food sector. Trends Biotechnol. 27, 82-89 (2009).
5. Chaudhry, Q. et al. Applications and implications of nanotechnologies for the food sector. Food Addit. Contam. A 25, 241-258 (2008).
6. Singh, R. & Lillard, J. W. Jr. Nanoparticle-based targeted drug delivery. Exp. Mol. Pathol. 86, 215-223 (2009).
7. Stone, V. & Kinloch, I. Nanotoxicology: Characterization, Dosing and Health Effects (CRC, 2007).
8. Lomer, M. C. E., Thompson, R. P. H. & Powell, J. J. Fine and ultrafine particles of the diet: influence on the mucosal immune response and association with Crohn's disease. Proc. Nutr. Soc. 61, 123-130 (2002).
9. Kerneis, S., Bogdanova, A., Kraehenbuhl, J. P. & Pringault, E. Conversion by Peyer's patch lymphocytes of human enterocytes into M cells that transport bacteria. Science 277, 949-952 (1997).
10. Lomer, M. C. E., Harvey, R. S. J., Evans, S. M., Thompson, R. P. H. & Powell, J. J. Efficacy and tolerability of a low microparticle diet in a double blind, randomized, pilot study in Crohn's disease. Eur. J. Gastroenterol. Hepatol. 13, 101-106 (2001).
11. Lomer, M. C. E. et al. Intake of dietary iron is low in patients with Crohn's disease: a case-control study. Br. J. Nutr. 91, 141-148 (2004).
12. Lee, H. J. Protein drug oral delivery: the recent progress. Arch. Pharm. Res. 25, 572-584 (2002).
13. Des Rieux, A., Fievez, V., Garinot, M., Schneider, Y. J. & Preat, V. Nanoparticles as potential oral delivery systems of proteins and vaccines: a mechanistic approach. J. Control. Rel. 116, 1-27 (2006).
14. Galindo-Rodriguez, S. A., Allemann, E., Fessi, H. & Doelker, E. Polymeric nanoparticles for oral delivery of drugs and vaccines: a critical evaluation of in vivo studies. Crit. Rev. Ther. Drug. Carrier Syst. 22, 419-463 (2005).
15. Ma, Y., Yeh, M., Yeh, K-Y. & Glass, J. Iron imports. V. Transport of iron through the intestinal epithelium. Am. J. Physiol. Gastr. L. 290, G417-G422 (2006).
16. DeSesso, J. M. & Jacobson, C. F. Anatomical and physiological parameters affecting gastrointestinal absorption in humans and rats. Food. Chem. Toxicol. 39, 209-228 (2001).
17. Muir, A. & Hopfer, U. Regional specificity of iron uptake by small intestinal brush-border membranes from normal and iron-deficient mice. Am. J. Physiol. Gastr. L. 248, G376-G379 (1985).
18. Kararli, T. T. Comparison of the gastrointestinal anatomy, physiology, and biochemistry of humans and commonly used laboratory animals. Biopharm. Drug. Dispos. 16, 351-380 (1995).
19. Sharp, D. G. & Beard, J.W. Size and density of polystyrene particles measured by ultracentrifugation. J. Biol. Chem. 185, 247-253 (1950).
20. Whittow, G. C. Sturkie's Avian Physiology (Academic, 2000).
21. +-D-glucose cotransporter in jejunum of domestic chicken. Am. J. Physiol. Gastr. L. 282, G559-G564 (2002).
22. Dahlke, F., Ribeiro, A. M. L., Kessler, A. M., Lima, A. R. & Maiorka, A. Effects of corn particle size and physical form of the diet on the gastrointestinal structures of broiler chickens. Rev. Bras. Cienc. Avic. 5, 61-67 (2003).
23. Ojano-Dirain, C. P. et al. Determination of mitochondrial function and site-specific defects in electron transport in duodenal mitochondria in broilers with low and high feed efficiency. Poultry Sci. 83, 1394-1403 (2004).
24. Miles, R. D., Butcher, G. D., Henry, P. R. & Littell, R. C. Effect of antibiotic growth promoters on broiler performance, intestinal growth parameters, and quantitative morphology. Poultry Sci. 85, 476-485 (2006).
25. Klasing, K. C. Avian gastrointestinal anatomy and physiology. Semin. Avian Exot. Pet 8, 42-50 (1999).
26. Hidalgo, I. J., Raub, T. J. & Borchardt, R. T. Characterization of the human-colon carcinoma cell-line (Caco-2) as a model system for intestinal epithelial permeability. Gastroenterology 96, 736-749 (1989).
27. Lesuffleur, T., Barbat, A., Dussaulx, E. & Zweibaum, A. Growth adaptation to methotrexate of HT-29 human colon-carcinoma cells is associated with their ability to differentiate into columnar absorptive and mucus-secreting cells. Cancer Res. 50, 6334-6343 (1990).
28. Mahler, G. J., Shuler, M. L. & Glahn, R. P. Characterization of Caco-2 and HT29-MTX cocultures in an in vitro digestion/cell culture model used to predict iron bioavailability. J. Nutr. Biochem. 20, 494-502 (2009).
29. Schulte, R. et al. Translocation of Yersinia enterocolitica across reconstituted intestinal epithelial monolayers is triggered by Yersinia invasin binding to β1 integrins apically expressed on M-like cells. Cell Microbiol. 2, 173-185 (2000).
30. Giannasca, P. J., Giannasca, K. T., Leichtner, A. M. & Neutra, M. R. Human intestinal M cells display the sialyl Lewis A antigen. Infect. Immun. 67, 946-953 (1999).
31. Owen, R. L. & Ermak, T. H. Structural specializations for antigen uptake and processing in the digestive-tract. Springer Semin. Immun. 12, 139-152 (1990).
32. Narai, A., Arai, S. & Shimizu, M. Rapid decrease in transepithelial electrical resistance of human intestinal Caco-2 cell monolayers by cytotoxic membrane perturbents. Toxicol. In Vitro 11, 347-351 (1997).
33. Ranaldi, G., Marigliano, I., Vespignani, I., Perozzi, G. & Sambuy, Y. The effect of chitosan and other polycations on tight junction permeability in the human intestinal Caco-2 cell line. J. Nutr. Biochem. 13, 157-167 (2002).
34. Menard, S., Cerf-Bensussan, N. & Heyman, M. Multiple facets of intestinal permeability and epithelial handling of dietary antigens. Mucosal Immunol. 3, 247-259 (2010).
35. Söderholm, J. D. et al. Increased epithelial uptake of protein antigens in the ileum of Crohn's disease mediated by tumour necrosis factor a. Gut 53, 1817-1824 (2004).
36. Tako, E., Rutzke, M. A. & Glahn, R. P. Using the domestic chicken (Gallus gallus) as an in vivo model for iron bioavailability. Poultry Sci. 89, 514-521 (2010).
37. Tako, E. & Glahn, R. P. White beans provide more bioavailable iron than red beans: Studies in poultry (Gallus gallus) and an in vitro digestion/Caco-2 model. Int. J. Vitam. Nutr. Res. 80, 416-429 (2010).
38. Passaniti, A. & Roth, T. F. Purification of chicken liver ferritin by two novel methods and structural comparison with horse spleen ferritin. Biochem. J. 258, 413-419 (1989).
39. Mete, A. et al. Partial purification and characterization of ferritin from the liver and intestinal mucosa of chickens, turtledoves and mynahs. Avian Pathol. 34, 430-434 (2005).
40. Tako, E., Ferket, P. R. & Uni, Z. Changes in chicken intestinal zinc exporter mRNA expression and small intestinal functionality following intra-amniotic zinc-methionine administration. J. Nutr. Biochem. 16, 339-346 (2005).
41. Smirnov, A., Tako, E., Ferket, P. R. & Uni, Z. Mucin gene expression and mucin content in the chicken intestinal goblet cells are affected by in ovo feeding of carbohydrates. Poultry Sci. 85, 669-673 (2006).
42. Caspary, W. F. Physiology and pathophysiology of intestinal absorption. Am. J. Clin. Nutr. 55, 299S-308S (1992).
43. Pluske, J. R. et al. Maintenance of villus height and crypt depth, and enhancement of disaccharide digestion and monosaccharide absorption, in piglets fed on cows' whole milk after weaning. Br. J. Nutr. 76, 409-422 (1996).
44. Tarachai, P. & Yamauchi, K. Effects of luminal nutrient absorption, intraluminal physical stimulation, and intravenous parenteral alimentation on the recovery responses of duodenal villus morphology following feed withdrawal in chickens. Poultry Sci. 79, 1578-1585 (2000).
45. Basu, T. K. & Donaldson, D. Intestinal absorption in health and disease: micronutrients. Best Pract. Res. Clin. Gastroenterol. 17, 957-979 (2003).
46. Hilty, F. M. et al. Iron from nanocompounds containing iron and zinc is highly bioavailable in rats without tissue accumulation. Nature Nanotech. 5, 374-380 (2010).
47. NRC. Nutrient Requirements of Poultry 9th edn (National Academy Press, 1994).