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Size dependent translocation and fetal accumulation of gold nanoparticles from maternal blood in the rat

Semmler-Behnke, Manuela, Lipka, Jens, Wenk, Alexander, Hirn, Stephanie, Schäffler, Martin, Tian, Furong, Schmid, Günter, Oberdörster, Günter, Kreyling, Wolfgang G·2014·Particle and Fibre Toxicology

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Figure 1 Schematics of potential NP transport including the uterine wall, the amniotic membrane enclosing the individual fetus and the placental barrier; potential NP transport pathways: (1) across the trophoblastic layers and through their transtrophoblastic channels within the placenta and (2) across the uterine wall and amniotic membrane. Hemotrichorial rat placentas are reported to have transtrophoblastic canaliculi of about 20¿25 nm diameter through the trophoblastic layers II and III connecting maternal and fetal blood across the placental barrier [29],[31]. There is convincing evidence that these channels are continuous [30],[33] and are also present in the human placenta. At gestation day 18?±?1 the yolk sac has considerably shrunk and is not shown in these schematics.
Figure 1 Schematics of potential NP transport including the uterine wall, the amniotic membrane enclosing the individual fetus and the placental barrier; potential NP transport pathways: (1) across the trophoblastic layers and through their transtrophoblastic channels within the placenta and (2) across the uterine wall and amniotic membrane. Hemotrichorial rat placentas are reported to have transtrophoblastic canaliculi of about 20¿25 nm diameter through the trophoblastic layers II and III connecting maternal and fetal blood across the placental barrier [29],[31]. There is convincing evidence that these channels are continuous [30],[33] and are also present in the human placenta. At gestation day 18?±?1 the yolk sac has considerably shrunk and is not shown in these schematics.CC BY · PubMed Central
Figure 2 Comparison of pregnant versus non-pregnant rats: comparison of 24-hour retained198AuNP fractions relative to the initially administered dose in either pregnant rats in their 3rdtrimester or non-pregnant controls: upper panel 1.4 nm AuNP; middle panel 18 nm AuNP; lower panel 80 nm AuNP. Note that fractions are 198Au radioactivity- and, hence, Au-mass based. Compartments are the (A) mononuclear phagocytic system (MPS consisting of liver, spleen, lungs), (B) the remaining carcass (remainder) including skeleton, soft tissues, skin and all other organs and (C) the uterus with or without the progeny. MPS and remainder samples were corrected for 198AuNP in the remaining blood. Note the uterus of the pregnant rats comprises of the uterine walls, the placentas and all amnions with fetuses. Data are given as fractions of the intravenously injected 198AuNP doses. (n?=?4; * p?<?0.05; ** p?<?0.01; *** p?<?0.001; **** p?<?=0.0001). Statistical analysis by one-way analysis of variance (ANOVA) followed by post hoc Sidak¿s multiple comparisons test.
Figure 2 Comparison of pregnant versus non-pregnant rats: comparison of 24-hour retained198AuNP fractions relative to the initially administered dose in either pregnant rats in their 3rdtrimester or non-pregnant controls: upper panel 1.4 nm AuNP; middle panel 18 nm AuNP; lower panel 80 nm AuNP. Note that fractions are 198Au radioactivity- and, hence, Au-mass based. Compartments are the (A) mononuclear phagocytic system (MPS consisting of liver, spleen, lungs), (B) the remaining carcass (remainder) including skeleton, soft tissues, skin and all other organs and (C) the uterus with or without the progeny. MPS and remainder samples were corrected for 198AuNP in the remaining blood. Note the uterus of the pregnant rats comprises of the uterine walls, the placentas and all amnions with fetuses. Data are given as fractions of the intravenously injected 198AuNP doses. (n?=?4; * p?<?0.05; ** p?<?0.01; *** p?<?0.001; **** p?<?=0.0001). Statistical analysis by one-way analysis of variance (ANOVA) followed by post hoc Sidak¿s multiple comparisons test.CC BY · PubMed Central
Figure 3 Twenty-four-hour fractional retention of198AuNP relative to the initially administered dose in blood, uterus and progeny of pregnant rats on day 18 ± 1 of gestation: fractions of198AuNP in blood and the various intra-uterine compartments: total blood, uterine wall, placentas + umbilical cords + amniotic membranes, total amniotic fluid and all fetuses. (nd = below detection limit of gamma-spectrometer; i.e. < 0.3 ng of 80 nm AuNP corresponding to <5 x 105 80 nm AuNP). Mean values ± SEM are given, n = 4 rats. Results of the statistical ANOVA analysis are given in Table 1.
Figure 3 Twenty-four-hour fractional retention of198AuNP relative to the initially administered dose in blood, uterus and progeny of pregnant rats on day 18 ± 1 of gestation: fractions of198AuNP in blood and the various intra-uterine compartments: total blood, uterine wall, placentas + umbilical cords + amniotic membranes, total amniotic fluid and all fetuses. (nd = below detection limit of gamma-spectrometer; i.e. < 0.3 ng of 80 nm AuNP corresponding to <5 x 105 80 nm AuNP). Mean values ± SEM are given, n = 4 rats. Results of the statistical ANOVA analysis are given in Table 1.CC BY · PubMed Central

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Research works printed but not linked: 60

  1. Oberdörster G, Oberdörster E, Oberdörster J: Nanotoxicology: An Emerging Discipline Evolving from Studies of Ultrafine Particles. Environ Health Perspect 2005, 113: 823–839. 10.1289/ehp.7339 · DOI · Paper page
  2. Mills NL, Amin N, Robinson SD, Anand A, Davies J, Patel D, de la Fuente JM, Cassee FR, Boon NA, Macnee W, Millar AM, Donaldson K, Newby DE: Do inhaled carbon nanoparticles translocate directly into the circulation in humans? Am J Respir Crit Care Med 2006, 173: 426–431. 10.1164/rccm.200506-865OC · DOI
  3. Kreyling WG, Semmler-Behnke M, Seitz J, Scymczak W, Wenk A, Mayer P, Takenaka S, Oberdorster G: Size dependence of the translocation of inhaled iridium and carbon nanoparticle aggregates from the lung of rats to the blood and secondary target organs. Inhal Toxicol 2009,21(Suppl 1):55–60. 10.1080/08958370902942517 · DOI
  4. Lipka J, Semmler-Behnke M, Sperling RA, Wenk A, Takenaka S, Schleh C, Kissel T, Parak WJ, Kreyling WG: Biodistribution of PEG-modified gold nanoparticles following intratracheal instillation and intravenous injection. Biomaterials 2010, 31: 6574–6581. 10.1016/j.biomaterials.2010.05.009 · DOI
  5. Schleh C, Semmler-Behnke M, Lipka J, Wenk A, Hirn S, Schaffler M, Schmid G, Simon U, Kreyling WG: Size and surface charge of gold nanoparticles determine absorption across intestinal barriers and accumulation in secondary target organs after oral administration. Nanotoxicology 2012, 6: 36–46. 10.3109/17435390.2011.552811 · DOI · Paper page
  6. Hirn S, Semmler-Behnke M, Schleh C, Wenk A, Lipka J, Schaffler M, Takenaka S, Moller W, Schmid G, Simon U, Kreyling WG: Particle size-dependent and surface charge-dependent biodistribution of gold nanoparticles after intravenous administration. Eur J Pharm Biopharm 2010, 77: 407–416. 10.1016/j.ejpb.2010.12.029 · DOI
  7. Wiebert P, Sanchez-Crespo A, Falk R, Philipson K, Lundin A, Larsson S, Moller W, Kreyling WG, Svartengren M: No significant translocation of inhaled 35-nm carbon particles to the circulation in humans. Inhal Toxicol 2006, 18: 741–747. 10.1080/08958370600748455 · DOI
  8. Wiebert P, Sanchez-Crespo A, Seitz J, Falk R, Philipson K, Kreyling WG, Moller W, Sommerer K, Larsson S, Svartengren M: Negligible clearance of ultrafine particles retained in healthy and affected human lungs. Eur Respir J 2006, 28: 286–290. 10.1183/09031936.06.00103805 · DOI
  9. Möller W, Felten K, Sommerer K, Scheuch G, Meyer G, Meyer P, Haussinger K, Kreyling WG: Deposition, retention, and translocation of ultrafine particles from the central airways and lung periphery. Am J Respir Crit Care Med 2008, 177: 426–432. 10.1164/rccm.200602-301OC · DOI
  10. Semmler-Behnke M, Kreyling WG, Lipka J, Fertsch S, Wenk A, Takenaka S, Schmid G, Brandau W: Biodistribution of 1.4- and 18-nm gold particles in rats. Small 2008, 4: 2108–2111. 10.1002/smll.200800922 · DOI
  11. Kreyling WG, Hirn S, Möller W, Schleh C, Wenk A, Celik G, Lipka J, Schäffler M, Haberl N, Johnston BD, Sperling R, Schmid G, Simon U, Parak WJ, Semmler-Behnke M: Air¿Blood Barrier Translocation of Tracheally Instilled Gold Nanoparticles Inversely Depends on Particle Size. ACS Nano 2013, 8: 222–223. 10.1021/nn403256v · DOI · Paper page
  12. Rinderknecht A, Prudhomme R, Poreda R, Gelein R, Corson N, Pidruczny A, Finkelstein J, Oberdörster G, Elder A: Biokinetics of AU nanoparticles relative to size surface coating and portal of entry. 47th Annual Society of Toxicology Meeting; Seattle, WA 2008.
  13. Schweitzer AD, Revskaya E, Chu P, Pazo V, Friedman M, Nosanchuk JD, Cahill S, Frases S, Casadevall A, Dadachova E: Melanin-Covered Nanoparticles for Protection of Bone Marrow During Radiation Therapy of Cancer. Int J Radiat Oncol Biol Phys 2010,78(5):1494–1502. 10.1016/j.ijrobp.2010.02.020 · DOI
  14. Fuchs R, Ellinger I: Endocytic and transcytotic processes in villous syncytiotrophoblast: role in nutrient transport to the human fetus. Traffic 2004, 5: 725–738. 10.1111/j.1600-0854.2004.00221.x · DOI
  15. Takeda K, Suzuki KI, Ishihara A, Kubo-Irie M, Fujimoto R, Tabata M, Oshio S, Nihei Y, Ihara T, Sugamata M: Nanoparticles Transferred from Pregnant Mice to Their Offspring Can Damage the Genital and Cranial Nerve Systems. J Health Sci 2009, 55: 95–102. 10.1248/jhs.55.95 · DOI · Paper page
  16. Sugamata M, Ihara T, Sugamata M, Takeda K: Maternal exposure to diesel exhaust leads to pathological similarity to autism in newborns. J Health Sci 2006, 52: 486–488. 10.1248/jhs.52.486 · DOI
  17. Sugamata M, Ihara T, Takano H, Oshio S, Takeda K: Maternal diesel exhaust exposure damages newborn murine brains. J Health Sci 2006, 52: 82–84. 10.1248/jhs.52.82 · DOI
  18. Ritz B, Wilhelm M, Hoggatt KJ, Ghosh JK: Ambient air pollution and preterm birth in the environment and pregnancy outcomes study at the University of California, Los Angeles. Am J Epidemiol 2007, 166: 1045–1052. 10.1093/aje/kwm181 · DOI
  19. Coggins CRE, Ayres PH, Mosberg AT, Sagartz JW, Hayes AW: Subchronic Inhalation Study in Rats Using Aged and Diluted Sidestream Smoke from a Reference Cigarette. Inhal Toxicol 1993, 5: 77–95. 10.3109/08958379309034495 · DOI
  20. Witschi H, Lundgaard SM, Rajini P, Hendrickx AG, Last JA: Effects of exposure to nicotine and to sidestream smoke on pregnancy outcome in rats. Toxicol Lett 1994, 71: 279–286. 10.1016/0378-4274(94)90114-7 · DOI
  21. Gospe SM Jr, Zhou SS, Pinkerton KE: Effects of environmental tobacco smoke exposure in utero and/or postnatally on brain development. Pediatr Res 1996, 39: 494–498. 10.1203/00006450-199603000-00018 · DOI
  22. Wick P, Malek A, Manser P, Meili D, Maeder-Althaus X, Diener L, Diener PA, Zisch A, Krug HF, von Mandach U: Barrier Capacity of Human Placenta for Nanosized Materials. Environ Health Perspect 2010, 118: 432–436. 10.1289/ehp.0901200 · DOI · Paper page
  23. Myllynen PK, Loughran MJ, Howard CV, Sormunen R, Walsh AA, Vahakangas KH: Kinetics of gold nanoparticles in the human placenta. Reprod Toxicol 2008, 26: 130–137. 10.1016/j.reprotox.2008.06.008 · DOI · Paper page
  24. Yamashita K, Yoshioka Y, Higashisaka K, Mimura K, Morishita Y, Nozaki M, Yoshida T, Ogura T, Nabeshi H, Nagano K, Abe Y, Kamada H, Monobe Y, Imazawa T, Aoshima H, Shishido K, Kawai Y, Mayumi T, Tsunoda S, Itoh N, Yoshikaw T, Yanagihara I, Saito S, Tsutsumi Y: Silica and titanium dioxide nanoparticles cause pregnancy complications in mice. Nat Nanotechnol 2011, 6: 321–328. 10.1038/nnano.2011.41 · DOI
  25. Keelan JA: Nanotoxicology: Nanoparticles versus the placenta. Nat Nanotechnol 2011, 6: 263–264. 10.1038/nnano.2011.65 · DOI
  26. Rattanapinyopituk K, Shimada A, Morita T, Sakurai M, Asano A, Hasegawa T, Inoue K, Takano H: Demonstration of the Clathrin- and Caveolin-Mediated Endocytosis at the Maternal-Fetal Barrier in Mouse Placenta after Intravenous Administration of Gold Nanoparticles. J Vet Med Sci 2013, 76: 377–387. 10.1292/jvms.13-0512 · DOI
  27. Ockleford CD, Whyte A: Differeniated regions of human placental cell surface associated with exchange of materials between maternal and foetal blood: coated vesicles. J Cell Sci 1977, 25: 293–312. · DOI
  28. Ockleford CD, Whyte A, Bowyer DE: Variation in the volume of coated vesicles isoalted from human placenta. Cell Biol Int Rep 1977, 1: 137–146. 10.1016/0309-1651(77)90034-0 · DOI
  29. Kertschanska S, Kosanke G, Kaufmann P: Pressure dependence of so-called transtrophoblastic channels during fetal perfusion of human placental villi. Microsc Res Tech 1997, 38: 52–62. 10.1002/(SICI)1097-0029(19970701/15)38:1/2<52::AID-JEMT7>3.0.CO;2-W · DOI
  30. Kertschanska S, Stulcova B, Kaufmann P, Stulc J: Distensible transtrophoblastic channels in the rat placenta. Placenta 2000, 21: 670–677. 10.1053/plac.2000.0558 · DOI
  31. Knipp GT, Audus KL, Soares MJ: Nutrient transport across the placenta. Adv Drug Deliv Rev 1999, 38: 41–58. 10.1016/S0169-409X(99)00005-8 · DOI
  32. Schmid G: The relevance of shape and size of Au55 clusters. Chem Soc Rev 2008, 37: 1909–1930. 10.1039/b713631p · DOI
  33. King BF: A cytological study of plasma membrane modifications, intercellular junctions, and endocytic activity of amniotic epithelium. Anat Rec 1978, 190: 113–125. 10.1002/ar.1091900110 · DOI
  34. Modena AB, Fieni S: Amniotic fluid dynamics. Acta Biomed 2004,75(Suppl 1):11–13.
  35. Saunders M: Transplacental transport of nanomaterials. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2009, 1: 671–684. 10.1002/wnan.53 · DOI
  36. Sadauskas E, Jacobsen NR, Danscher G, Stoltenberg M, Vogel U, Larsen A, Kreyling W, Wallin H: Biodistribution of gold nanoparticles in mouse lung following intratracheal instillation. Chem Central J 2009, 3: 16. 10.1186/1752-153X-3-16 · DOI
  37. Workshop IRSI: The relevance of the rat lung response to particle overload for human risk assessment: A workshop consensus report. Inhal Toxicol 2000, 12: 1–17.
  38. Conner SD, Schmid SL: Regulated portals of entry into the cell. Nature 2003, 422: 37–44. 10.1038/nature01451 · DOI
  39. Pan Y, Leifert A, Ruau D, Neuss S, Bornemann J, Schmid G, Brandau W, Simon U, Jahnen-Dechent W: Gold Nanoparticles of Diameter 1.4 nm Trigger Necrosis by Oxidative Stress and Mitochondrial Damage. Small 2009, 5: 2067–2076. 10.1002/smll.200900466 · DOI
  40. Lundqvist M, Stigler J, Elia G, Lynch I, Cedervall T, Dawson KA: Nanoparticle size and surface properties determine the protein corona with possible implications for biological impacts. Proc Natl Acad Sci U S A 2008, 105: 14265–14270. 10.1073/pnas.0805135105 · DOI · Paper page
  41. Lynch I, Dawson KA: Protein-nanoparticle interactions. Nano Today 2008, 3: 40–47. 10.1016/S1748-0132(08)70014-8 · DOI
  42. Schäffler M, Sousa F, Wenk A, Sitia L, Hirn S, Schleh C, Haberl N, Violatto M, Canovi M, Andreozzi P, Salmona M, Bigini P, Kreyling WG, Krol S: Blood protein coating of gold nanoparticles as potential tool for organ targeting. Biomaterials 2014, 35: 3455–3466. 10.1016/j.biomaterials.2013.12.100 · DOI
  43. Cheung CY, Brace RA: Amniotic fluid volume and composition in mouse pregnancy. J Soc Gynecol Investig 2005, 12: 558–562. 10.1016/j.jsgi.2005.08.008 · DOI
  44. Robertson P, Faber JJ, Brace RA, Louey S, Hohimer AR, Davis LE, Anderson DF: Responses of amniotic fluid volume and its four major flows to lung liquid diversion and amniotic infusion in the ovine fetus. Reprod Sci 2009, 16: 88–93. 10.1177/1933719108324888 · DOI
  45. Underwood MA, Gilbert WM, Sherman MP: Amniotic Fluid: Not Just Fetal Urine Anymore. J Perinatol 2005, 25: 341–348. 10.1038/sj.jp.7211290 · DOI
  46. Lutz HG: Clusters and Colloids. From Theory to Applications. VCH Verlagsgesellschaft, Weinheim/VCH Publishers, New York; 1995.
  47. Tominaga T, Tenma S, Watanabe H, Giebel U, Schmid G: Tracer Diffusion of a Ligand-Stabilized Two-Shell Gold Cluster. Chem Lett 1996, 25: 1033–1034. 10.1246/cl.1996.1033 · DOI
  48. Möller W, Gibson N, Geiser M, Pokhrel S, Wenk A, Takenaka S, Schmid O, Bulgheroni A, Simonelli F, Kozempel J, Holzwarth U, Wigge C, Eigeldinger-Berthou S, Mädler L, Kreyling W: Gold nanoparticle aerosols for rodent inhalation and translocation studies. J Nanoparticle Res 2013, 15: 1–13. 10.1007/s11051-013-1574-9 · DOI
  49. Semmler-Behnke M, Kreyling WG, Schulz H, Takenaka S, Butler JP, Henry FS, Tsuda A: Nanoparticle delivery in infant lungs. Proc Natl Acad Sci U S A 2012, 109: 5092–5097. 10.1073/pnas.1119339109 · DOI
  50. Hainfeld JF, O'Connor MJ, Dilmanian FA, Slatkin DN, Adams DJ, Smilowitz HM: Micro-CT enables microlocalisation and quantification of Her2-targeted gold nanoparticles within tumour regions. Br J Radiol 2011, 84: 526–533. 10.1259/bjr/42612922 · DOI
  51. Khlebtsov N, Dykman L: Biodistribution and toxicity of engineered gold nanoparticles: a review of in vitro and in vivo studies. Chem Soc Rev 2011, 40: 1647–1671. 10.1039/c0cs00018c · DOI
  52. Paciotti GF, Myer L, Weinreich D, Goia D, Pavel N, McLaughlin RE, Tamarkin L: Colloidal gold: a novel nanoparticle vector for tumor directed drug delivery. Drug Deliv 2004, 11: 169–183. 10.1080/10717540490433895 · DOI
  53. Kim Y, Lobatto ME, Kawahara T, Lee Chung B, Mieszawska AJ, Sanchez-Gaytan BL, Fay F, Senders ML, Calcagno C, Becraft J, Tun Saung M, Gordon R, Stroes ES, Ma M, Farokhzad OC, Fayad ZA, Mulder WJ, Langer R: Probing nanoparticle translocation across the permeable endothelium in experimental atherosclerosis. Proc Natl Acad Sci U S A 2014, 111: 1078–1083. 10.1073/pnas.1322725111 · DOI
  54. Mieszawska AJ, Kim Y, Gianella A, van Rooy I, Priem B, Labarre MP, Ozcan C, Cormode DP, Petrov A, Langer R, Farokhzad OC, Fayad ZA, Mulder WJ: Synthesis of polymer-lipid nanoparticles for image-guided delivery of dual modality therapy. Bioconjug Chem 2013, 24: 1429–1434. 10.1021/bc400166j · DOI
  55. McArdle HJ, Andersen HS, Jones H, Gambling L: Copper and Iron Transport Across the Placenta: Regulation and Interactions. J Neuroendocrinol 2008, 20: 427–431. 10.1111/j.1365-2826.2008.01658.x · DOI
  56. Turkevitch J, Stevenson PC, Hillier J: A study of the nucleation and growth processes in the synthesis of colloidal gold. Discuss Faraday Soc 1951, 11: 55–75. 10.1039/df9511100055 · DOI
  57. Schmid G, Lehnert A: The Complexation of Gold Colloids. Angew Chem Int Ed 1989, 28: 780–781. 10.1002/anie.198907801 · DOI
  58. Semmler M, Seitz J, Erbe F, Mayer P, Heyder J, Oberdorster G, Kreyling WG: Long-term clearance kinetics of inhaled ultrafine insoluble iridium particles from the rat lung, including transient translocation into secondary organs. Inhal Toxicol 2004, 16: 453–459. 10.1080/08958370490439650 · DOI · Paper page
  59. Semmler-Behnke M, Takenaka S, Fertsch S, Wenk A, Seitz J, Mayer P, Oberdorster G, Kreyling WG: Efficient elimination of inhaled nanoparticles from the alveolar region: evidence for interstitial uptake and subsequent reentrainment onto airways epithelium. Environ Health Perspect 2007, 115: 728–733. 10.1289/ehp.9685 · DOI · Paper page
  60. Kreyling WG, Semmler M, Erbe F, Mayer P, Takenaka S, Schulz H, Oberdörster G, Ziesenis A: Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low. J Toxicol Environ Health-Part A 2002, 65: 1513–1530. 10.1080/00984100290071649 · DOI · Paper page

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Metadata

Authors
Semmler-Behnke, M., Lipka, J., Wenk, A., Hirn, S., Schäffler, M., Tian, F., Schmid, G., Oberdörster, G., & Kreyling, W. G.
Venue
Particle and Fibre Toxicology
Published
2014-09-10
Volume
11
Issue
1
ISSN
1743-8977
Cited by
135
References
3
Language
en

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