Size-dependent long-term tissue response to biostable nanowires in the brain

Biomaterials

Volumn 42, Issue , 2015, Pages 172-183

  Gällentoft, Lina ^a   Pettersson, Lina M E ^a   Danielsen, Nils ^a   Schouenborg, Jens ^a   Prinz, Christelle N ^a,b   Linsmeier, Cecilia Eriksson ^a  

^a LUND UNIVERSITY   (Sweden)

^b LUND UNIVERSITY   (Sweden)

Author keywords

Biocompatibility; Brain; Inflammation; Nanoparticle

Indexed keywords

ASBESTOS; ASPECT RATIO; BIOCOMPATIBILITY; BRAIN; NANOPARTICLES; NANOWIRES; NEURAL NETWORKS; PATHOLOGY; TISSUE;

HIGH ASPECT RATIO; INFLAMMATION; INFLAMMATORY RESPONSE; NANO-STRUCTURED; NEURAL IMPLANTS; NEURAL INTERFACES; NEURONAL NETWORKS; TISSUE RESPONSE;

NEURONS;

NANOWIRE; BIOMATERIAL; SUSPENSION;

ABDOMEN; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOCOMPATIBILITY; BRAIN TISSUE; CONCENTRATION RESPONSE; CONTROLLED STUDY; ENCEPHALITIS; FEMALE; GLIA CELL; IMPLANT INFLAMMATION; INFANT; LUNG PARENCHYMA; MEDICAL DEVICE COMPLICATION; MOLECULAR STABILITY; NEUROLOGICAL IMPLANT; NONHUMAN; PARTICLE SIZE; RAT; TISSUE REACTION; ANIMAL; ASTROCYTE; BRAIN; CELL COUNT; CONFOCAL MICROSCOPY; DRUG EFFECTS; INFLAMMATION; MACROPHAGE; METABOLISM; MICROGLIA; NERVE CELL; PATHOLOGY; SPRAGUE DAWLEY RAT; SUSPENSION; TIME; ULTRASTRUCTURE;

RATTUS;

ANIMALS; ASTROCYTES; BIOCOMPATIBLE MATERIALS; BRAIN; CELL COUNT; FEMALE; INFLAMMATION; MACROPHAGES; MICROGLIA; MICROSCOPY, CONFOCAL; NANOWIRES; NEURONS; PARTICLE SIZE; RATS, SPRAGUE-DAWLEY; SUSPENSIONS; TIME FACTORS;

EID: 84919654275     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2014.11.051     Document Type: Article

References (40)

1. Awan N.R., Lozano A., Hamani C. Deep brain stimulation: current and future perspectives. Neurosurg Focus 2009, 27:E2.
2. Daly J.J., Wolpaw J.R. Brain-computer interfaces in neurological rehabilitation. Lancet Neurol 2008, 7:1032-1043.
3. Hochberg L.R., Serruya M.D., Friehs G.M., Mukand J.A., Saleh M., Caplan A.H., et al. Neuronal ensemble control of prosthetic devices by a human with tetraplegia. Nature 2006, 442:164-171.
4. Kipke D.R., Shain W., Buzsaki G., Fetz E., Henderson J.M., Hetke J.F., et al. Advanced neurotechnologies for chronic neural interfaces: new horizons and clinical opportunities. JNeurosci 2008, 28:11830-11838.
5. Biran R., Martin D.C., Tresco P.A. Neuronal cell loss accompanies the brain tissue response to chronically implanted silicon microelectrode arrays. Exp Neurol 2005, 195:115-126.
6. Marin C., Fernandez E. Biocompatibility of intracortical microelectrodes: current status and future prospects. Front Neuroeng 2010, 3:8.
7. Szarowski D.H., Andersen M.D., Retterer S., Spence A.J., Isaacson M., Craighead H.G., et al. Brain responses to micro-machined silicon devices. Brain Res 2003, 983:23-35.
8. Williams J.C., Hippensteel J.A., Dilgen J., Shain W., Kipke D.R. Complex impedance spectroscopy for monitoring tissue responses to inserted neural implants. JNeural Eng 2007, 4:410-423.
9. Biran R., Martin D.C., Tresco P.A. The brain tissue response to implanted silicon microelectrode arrays is increased when the device is tethered to the skull. JBiomed Mater Res A 2007, 82:169-178.
10. Gilletti A., Muthuswamy J. Brain micromotion around implants in the rodent somatosensory cortex. JNeural Eng 2006, 3:189-195.
11. Lind G., Eriksson Linsmeier C., Schouenborg J. The density differences between tissue and neural probes is a key factor for glial scarring. Sci Rep 2013, 3:2942.
12. Thelin J., Jorntell H., Psouni E., Garwicz M., Schouenborg J., Danielsen N., et al. Implant size and fixation mode strongly influence tissue reactions in the CNS. Plos One 2011, 6:e16267.
13. Cellot G., Cilia E., Cipollone S., Rancic V., Sucapane A., Giordani S., et al. Carbon nanotubes might improve neuronal performance by favouring electrical shortcuts. Nat Nanotechnol 2009, 4:126-133.
14. Keefer E.W., Botterman B.R., Romero M.I., Rossi A.F., Gross G.W. Carbon nanotube coating improves neuronal recordings. Nat Nanotechnol 2008, 3:434-439.
15. Hallstrom W., Martensson T., Prinz C., Gustavsson P., Montelius L., Samuelson L., et al. Gallium phosphide nanowires as a substrate for cultured neurons. Nano Lett 2007, 7:2960-2965.
16. Piret G., Perez M.-T., Prinz C.N. Neurite outgrowth and synaptophysin expression of postnatal CNS neurons on GaP nanowire arrays in long-term retinal cell culture. Biomaterials 2013, 34:875-887.
17. Prinz C., Hallstrom W., Martensson T., Samuelson L., Montelius L., Kanje M. Axonal guidance on patterned free-standing nanowire surfaces. Nanotechnology 2008, 19:345101.
18. Suyatin D.B., Wallman L., Thelin J., Prinz C.N., Jörntell H., Samuelson L., et al. Nanowire-based electrode for acute invivo neural recordings in the brain. PLoS One 2013, 8:e56673.
19. Donaldson K., Murphy F., Duffin R., Poland C. Asbestos, carbon nanotubes and the pleural mesothelium: a review of the hypothesis regarding the role of long fibre retention in the parietal pleura, inflammation and mesothelioma. Part Fibre Toxicol 2010, 7:5.
20. Poland C., Duffin R., Kinloch I., Maynard A., Wallace W., Seaton A., et al. Carbon nanotubes introduced into the abdominal cavity of mice show asbestos-like pathogenicity in a pilot study. Nat Nanotechnol 2008, 3:423-428.
21. Schinwald A., Murphy F.A., Prina-Mello A., Poland C.A., Byrne F., Movia D., et al. The threshold length for fiber-induced acute pleural inflammation: shedding light on the early events in asbestos-induced mesothelioma. Toxicol Sci 2012, 128:461-470.
22. Suyatin D.B., Hallstrom W., Samuelson L., Montelius L., Prinz C.N., Kanje M. Gallium phosphide nanowire arrays and their possible application in cellular force investigations. JVac Sci Technol B 2009, 27:3092-3094.
23. Hallstrom W., Lexholm M., Suyatin D.B., Hammarin G., Hessman D., Samuelson L., et al. Fifteen-piconewton force detection from neural growth cones using nanowire arrays. Nano Lett 2010, 10:782-787.
24. Mohammadi S., Esposito M., Cucu M., Ericson L.E., Thomsen P. Tissue response to hafnium. JMater Sci Mater Med 2001, 12:603-611.
25. Matsuno H., Yokoyama A., Watari F., Uo M., Kawasaki T. Biocompatibility and osteogenesis of refractory metal implants, titanium, hafnium, niobium, tantalum and rhenium. Biomaterials 2001, 22:1253-1262.
26. Maggiorella L., Barouch G., Devaux C., Pottier A., Deutsch E., Bourhis J., et al. Nanoscale radiotherapy with hafnium oxide nanoparticles. Future Oncol 2012, 8:1167-1181.
27. Loo Y.-L., Willett R.L., Baldwin K.W., Rogers J.A. Additive, nanoscale patterning of metal films with a stamp and a surface chemistry mediated transfer process: applications in plastic electronics. Appl Phys Lett 2002, 81:562-564.
28. Eriksson Linsmeier C., Prinz C.N., Pettersson L.M.E., Caroff P., Samuelson L., Schouenborg J., et al. Nanowire biocompatibility in the brain - looking for a needle in a 3D stack. Nano Lett 2009, 9:4184-4190.
29. Davis R.K., Stevenson G.T., Busch K.A. Tumor incidence in normal sprague-dawley female rats. Cancer Res 1956, 16:194-197.
30. Prejean J.D., Peckham J.C., Casey A.E., Griswold D.P., Weisburger E.K., Weisburger J.H. Spontaneous tumors in Sprague-Dawley rats and swiss mice. Cancer Res 1973, 33:2768-2773.
31. Nakazawa M., Tawaratani T., Uchimoto H., Kawaminami A., Ueda M., Ueda A., et al. Spontaneous neoplastic lesions in aged Sprague-Dawley rats. Exp Anim 2001, 50:99-103.
32. Thompson S.W., Huseby R.A., Fox M.A., Davis C.L., Hunt R.D. Spontaneous tumors in the Sprague-Dawley rat. JNatl Cancer Inst 1961, 27:1037-1057.
33. Schinwald A., Chernova T., Donaldson K. Use of silver nanowires to determine thresholds for fibre length-dependent pulmonary inflammation and inhibition of macrophage migration invitro. Part Fibre Toxicol 2012, 9:47.
34. Agarwal R., Singh V., Jurney P., Shi L., Sreenivasan S.V., Roy K. Mammalian cells preferentially internalize hydrogel nanodiscs over nanorods and use shape-specific uptake mechanisms. Proc Natl Acad Sci U S A 2013, 110:17247-17252.
35. Hanisch U.K. Microglia as a source and target of cytokines. Glia 2002, 40:140-155.
36. Streit W., Mrak R., Griffin W.S. Microglia and neuroinflammation: a pathological perspective. JNeuroinflammation 2004, 1:14.
37. Verkhratsky A., Butt A. General pathophysilogy of glia. Glial neurobiology: a textbook 2007, 153-165. John Wiley & Sons, Ltd, Chichester, UK. A. Verkhratsky, A. Butt (Eds.).
38. McKeever P.E., Balentine J.D. Macrophages migration through the brain parenchyma to the perivascular space following particle ingestion. Am J Pathol 1978, 93:153-164.
39. Weller R.O., Djuanda E., Yow H.Y., Carare R.O. Lymphatic drainage of the brain and the pathophysiology of neurological disease. Acta Neuropathol 2009, 117:1-14.
40. Kaminski M., Bechmann I., Pohland M., Kiwit J., Nitsch R., Glumm J. Migration of monocytes after intracerebral injection at entorhinal cortex lesion site. JLeukoc Biol 2012, 92:31-39.