Silk fibroin matrices for the controlled release of nerve growth factor (NGF)

Biomaterials

Volumn 28, Issue 30, 2007, Pages 4449-4460

  Uebersax, Lorenz ^a   Mattotti, Marta ^a   Papaloïzos, Michaël ^b   Merkle, Hans P ^a   Gander, Bruno ^a   Meinel, Lorenz ^a  

^a ETH ZURICH   (Switzerland)

^b Center for Hand Surgery and Therapy   (Switzerland)

Author keywords

Bioactivity; Nerve conduits; Nerve growth factor; PC12 cells; SEC; Silk fibroin

Indexed keywords

BIOACTIVITY; BIODEGRADATION; CELLS; DRUG PRODUCTS; METABOLISM;

NERVE CONDUITS; NERVE GROWTH FACTOR; SILK FIBROIN;

NEUROLOGY;

BIOMATERIAL; COLLAGEN TYPE 1; DNA; LAMININ; RECOMBINANT NERVE GROWTH FACTOR; SILK FIBROIN;

ANIMAL CELL; AQUEOUS SOLUTION; ARTICLE; BIOCOMPATIBILITY; BIODEGRADABILITY; CELL DIFFERENTIATION; CELL STRAIN; CONTROLLED DRUG RELEASE; CONTROLLED STUDY; DIFFERENTIAL SCANNING CALORIMETRY; DNA CONTENT; DRUG ACTIVITY; ENZYME LINKED IMMUNOSORBENT ASSAY; FILM; FOURIER TRANSFORMATION; FREEZE DRYING; GEL PERMEATION CHROMATOGRAPHY; INFRARED SPECTROSCOPY; NERVE CONDUIT; NERVE FIBER GROWTH; NERVE REGENERATION; NONHUMAN; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SCANNING ELECTRON MICROSCOPY;

ACETATES; ANIMALS; AREA UNDER CURVE; BIOCOMPATIBLE MATERIALS; BOMBYX; BUFFERS; CALORIMETRY, DIFFERENTIAL SCANNING; CATTLE; CELL DIFFERENTIATION; CELL PROLIFERATION; CHROMATOGRAPHY, GEL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COLLAGEN TYPE I; DELAYED-ACTION PREPARATIONS; ENZYME-LINKED IMMUNOSORBENT ASSAY; FIBROINS; HYDROGEN-ION CONCENTRATION; LAMININ; NERVE GROWTH FACTOR; NEURITES; PC12 CELLS; RATS; SILK; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; SUBSTRATE SPECIFICITY;

EID: 34547763721     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2007.06.034     Document Type: Article

References (63)

1. Belkas J.S., Shoichet M.S., and Midha R. Peripheral nerve regeneration through guidance tubes. Neurol Res 26 2 (2004) 151-160
2. Horch K. Guidance of regrowing sensory axons after cutaneous nerve lesions in the cat. J Neurophysiol 42 5 (1979) 1437-1449
3. Abernethy D.A., Thomas P.K., Rud A., and King R.H. Mutual attraction between emigrant cells from transected denervated nerve. J Anat 184 Part 2 (1994) 239-249
4. Lumsden A.G., and Davies A.M. Earliest sensory nerve fibres are guided to peripheral targets by attractants other than nerve growth factor. Nature 306 5945 (1984) 786-788
5. Kim D.H., Han K., Tiel R.L., Murovic J.A., and Kline D.G. Surgical outcomes of 654 ulnar nerve lesions. J Neurosurg 98 5 (2003) 993-1004
6. de Medinaceli L., Prayon M., and Merle M. Percentage of nerve injuries in which primary repair can be achieved by end-to-end approximation: review of 2181 nerve lesions. Microsurgery 14 4 (1993) 244-246
7. Miyamoto Y. Experimental study of results of nerve suture under tension vs. nerve grafting. Plast Reconstr Surg 64 4 (1979) 540-549
8. Battiston B., Geuna S., Ferrero M., and Tos P. Nerve repair by means of tubulization: literature review and personal clinical experience comparing biological and synthetic conduits for sensory nerve repair. Microsurgery 25 4 (2005) 258-267
9. Aebischer P., Guenard V., and Brace S. Peripheral nerve regeneration through blind-ended semipermeable guidance channels: effect of the molecular weight cutoff. J Neurosci 9 10 (1989) 3590-3595
10. Aebischer P., Guenard V., and Valentini R.F. The morphology of regenerating peripheral nerves is modulated by the surface microgeometry of polymeric guidance channels. Brain Res 531 1-2 (1990) 211-218
11. Guenard V., Valentini R.F., and Aebischer P. Influence of surface texture of polymeric sheets on peripheral nerve regeneration in a two-compartment guidance system. Biomaterials 12 2 (1991) 259-263
12. Danielsson P.A., Adolfsson L., and Dahlin L.B. Different effect on axonal outgrowth of application of non-absorbable or absorbable tubes around a nerve repair. Scand J Plast Reconstr Surg Hand Surg 35 4 (2001) 347-353
13. Bunting S., Di Silvio L., Deb S., and Hall S. Bioresorbable glass fibres facilitate peripheral nerve regeneration. J Hand Surg [Br] 30 3 (2005) 242-247
14. Gamez E., Ikezaki K., Fukui M., and Matsuda T. Photoconstructs of nerve guidance prosthesis using photoreactive gelatin as a scaffold. Cell Transplant 12 5 (2003) 481-490
15. Goraltchouk A., Freier T., and Shoichet M.S. Synthesis of degradable poly(l-lactide-co-ethylene glycol) porous tubes by liquid-liquid centrifugal casting for use as nerve guidance channels. Biomaterials 26 36 (2005) 7555-7563
16. Cai J., Peng X., Nelson K.D., Eberhart R., and Smith G.M. Synergistic improvements in cell and axonal migration across sciatic nerve lesion gaps using bioresorbable filaments and heregulin-beta1. J Biomed Mater Res A 69 2 (2004) 247-258
17. Dalton P.D., Flynn L., and Shoichet M.S. Manufacture of poly(2-hydroxyethyl methacrylate-co-methyl methacrylate) hydrogel tubes for use as nerve guidance channels. Biomaterials 23 18 (2002) 3843-3851
18. Ducic I., Maloney Jr. C.T., and Dellon A.L. Reconstruction of the spinal accessory nerve with autograft or neurotube? two case reports. J Reconstr Microsurg 21 1 (2005) 29-33 discussion 34
19. Navissano M., Malan F., Carnino R., and Battiston B. Neurotube for facial nerve repair. Microsurgery 25 4 (2005) 268-271
20. Hinckley D.K., Lyles C.A., and Mattox D.E. Repair of peripheral nerves of unequal diameters. Laryngoscope 101 11 (1991) 1150-1154
21. Chen H.H., and Liu H.M. The use of collagen polymer tube and fibrin clot in peripheral nerve repair. Proc Natl Sci Council Repub China B 18 2 (1994) 58-63
22. Itoh S., Takakuda K., Kawabata S., Aso Y., Kasai K., Itoh H., et al. Evaluation of cross-linking procedures of collagen tubes used in peripheral nerve repair. Biomaterials 23 23 (2002) 4475-4481
23. Collins R.L., Christiansen D., Zazanis G.A., and Silver F.H. Use of collagen film as a dural substitute: preliminary animal studies. J Biomed Mater Res 25 2 (1991) 267-276
24. Lundborg G., Dahlin L.B., Danielsen N., Gelberman R.H., Longo F.M., Powell H.C., et al. Nerve regeneration in silicone chambers: influence of gap length and of distal stump components. Exp Neurol 76 2 (1982) 361-375
25. Doolabh V.B., Hertl M.C., and Mackinnon S.E. The role of conduits in nerve repair: a review. Rev Neurosci 7 1 (1996) 47-84
26. Ebadi M., Bashir R.M., Heidrick M.L., Hamada F.M., Refaey H.E., Hamed A., et al. Neurotrophins and their receptors in nerve injury and repair. Neurochem Int 30 4-5 (1997) 347-374
27. Gundersen R.W., and Barrett J.N. Neuronal chemotaxis: chick dorsal-root axons turn toward high concentrations of nerve growth factor. Science 206 4422 (1979) 1079-1080
28. Hari A., Djohar B., Skutella T., and Montazeri S. Neurotrophins and extracellular matrix molecules modulate sensory axon outgrowth. Int J Dev Neurosci 22 2 (2004) 113-117
29. Hadlock T., Sundback C., Koka R., Hunter D., Cheney M., and Vacanti J. A novel, biodegradable polymer conduit delivers neurotrophins and promotes nerve regeneration. Laryngoscope 109 9 (1999) 1412-1416
30. Fine E.G., Decosterd I., Papaloizos M., Zurn A.D., and Aebischer P. GDNF and NGF released by synthetic guidance channels support sciatic nerve regeneration across a long gap. Eur J Neurosci 15 4 (2002) 589-601
31. Nguyen C.B., Szonyi E., Sadick M.D., Hotaling T.E., Mendoza-Ramirez J.L., and Escandon E. Stability and interactions of recombinant human nerve growth factor in different biological matrices: in vitro and in vivo studies. Drug Metab Dispos 28 5 (2000) 590-597
32. Lam X.M., Duenas E.T., and Cleland J.L. Encapsulation and stabilization of nerve growth factor into poly(lactic-co-glycolic) acid microspheres. J Pharm Sci 90 9 (2001) 1356-1365
33. Uebersax L., Hagenmuller H., Hofmann S., Gruenblatt E., Muller R., Vunjaknovakovic G., et al. Effect of Scaffold design on bone morphology in vitro. Tissue Eng 12 12 (2006) 3417-3429
34. Nazarov R., Jin H.J., and Kaplan D.L. Porous 3-D scaffolds from regenerated silk fibroin. Biomacromolecules 5 3 (2004) 718-726
35. Altman G.H., Diaz F., Jakuba C., Calabro T., Horan R.L., Chen J., et al. Silk-based biomaterials. Biomaterials 24 3 (2003) 401-416
36. Meinel L., Hofmann S., Karageorgiou V., Kirker-Head C., McCool J., Gronowicz G., et al. The inflammatory responses to silk films in vitro and in vivo. Biomaterials 26 2 (2005) 147-155
37. Panilaitis B., Altman G.H., Chen J., Jin H.J., Karageorgiou V., and Kaplan D.L. Macrophage responses to silk. Biomaterials 24 18 (2003) 3079-3085
38. Cunniff P.M., Fossey S.A., Auerbach M.A., Song J.W., Kaplan D.L., Adams W., et al. Mechanical and thermal properties of Dragline Silk from the spider Nephila cavipes. Polym Adv Technol 5 (1994) 401-410
39. Lange F. Künstliche Bänder aus Seide. Münch Med Wochenschr 54 17 (1907) 834-836
40. Lange F. Ueber die Sehnenplastik. Verh Dtsch Orthop 2 (1903) 10-12
41. Uebersax L., Fedele D.E., Schumacher C., Kaplan D.L., Merkle H.P., Boison D., et al. The support of adenosine release from adenosine kinase deficient ES cells by silk substrates. Biomaterials 27 26 (2006) 4599-4607
42. Hofmann S., Foo C.T., Rossetti F., Textor M., Vunjak-Novakovic G., Kaplan D.L., et al. Silk fibroin as an organic polymer for controlled drug delivery. J Control Release 111 1-2 (2006) 219-227
43. Greene L.A., and Tischler A.S. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci USA 73 7 (1976) 2424-2428
44. Doherty P., Mann D.A., and Walsh F.S. Cell-cell interactions modulate the responsiveness of PC12 cells to nerve growth factor. Development 101 3 (1987) 605-615
45. Foley J.D., Grunwald E.W., Nealey P.F., and Murphy C.J. Cooperative modulation of neuritogenesis by PC12 cells by topography and nerve growth factor. Biomaterials 26 17 (2005) 3639-3644
46. Sofia S., McCarthy M.B., Gronowicz G., and Kaplan D.L. Functionalized silk-based biomaterials for bone formation. J Biomed Mater Res 54 1 (2001) 139-148
47. Patist C.M., Mulder M.B., Gautier S.E., Maquet V., Jerome R., and Oudega M. Freeze-dried poly(d,l-lactic acid) macroporous guidance scaffolds impregnated with brain-derived neurotrophic factor in the transected adult rat thoracic spinal cord. Biomaterials 25 9 (2004) 1569-1582
48. Midha R., Munro C.A., Dalton P.D., Tator C.H., and Shoichet M.S. Growth factor enhancement of peripheral nerve regeneration through a novel synthetic hydrogel tube. J Neurosurg 99 3 (2003) 555-565
49. Piotrowicz A., and Shoichet M.S. Nerve guidance channels as drug delivery vehicles. Biomaterials 27 9 (2006) 2018-2027
50. Yang Y., De Laporte L., Rives C.B., Jang J.H., Lin W.C., Shull K.R., et al. Neurotrophin releasing single and multiple lumen nerve conduits. J Control Release 104 3 (2005) 433-446
51. Santin M., Motta A., Freddi G., and Cannas M. In vitro evaluation of the inflammatory potential of the silk fibroin. J Biomed Mater Res 46 3 (1999) 382-389
52. Meinel L., Karageorgiou V., Fajardo R., Snyder B., Shinde-Patil V., Zichner L., et al. Bone tissue engineering using human mesenchymal stem cells: effects of scaffold material and medium flow. Ann Biomed Eng 32 1 (2004) 112-122
53. Meinel L., Hofmann S., Karageorgiou V., Zichner L., Langer R., Kaplan D., et al. Engineering cartilage-like tissue using human mesenchymal stem cells and silk protein scaffolds. Biotechnol Bioeng 88 3 (2004) 379-391
54. Karageorgiou V., Meinel L., Hofmann S., Malhotra A., Volloch V., and Kaplan D. Bone morphogenetic protein-2 decorated silk fibroin films induce osteogenic differentiation of human bone marrow stromal cells. J Biomed Mater Res A 71 3 (2004) 528-537
55. Karageorgiou V., Tomkins M., Fajardo R., Meinel L., Snyder B., Wade K., et al. Porous silk fibroin 3-D scaffolds for delivery of bone morphogenetic protein-2 in vitro and in vivo. J Biomed Mater Res A 78 2 (2006) 324-334
56. Itoh S., Matsuda A., Kobayashi H., Ichinose S., Shinomiya K., and Tanaka J. Effects of a laminin peptide (YIGSR) immobilized on crab-tendon chitosan tubes on nerve regeneration. J Biomed Mater Res B Appl Biomater 73 2 (2005) 375-382
57. Hauw J.J., Novikoff A.B., Novikoff P.M., Boutry J.M., and Robineaux R. Culture of nervous tissue on collagen in Leighton tubes. Brain Res 37 2 (1972) 301-309
58. Dresner H.S., King T.A., Clark H.B., Juhn S.K., and Levine S.C. Peripheral facial nerve regeneration using collagen conduit entubulation in a cat model. Ann Otol Rhinol Laryngol 115 8 (2006) 631-642
59. Chen Z.L., and Strickland S. Laminin gamma1 is critical for Schwann cell differentiation, axon myelination, and regeneration in the peripheral nerve. J Cell Biol 163 4 (2003) 889-899
60. Matsumoto K., Ohnishi K., Kiyotani T., Sekine T., Ueda H., Nakamura T., et al. Peripheral nerve regeneration across an 80-mm gap bridged by a polyglycolic acid (PGA)-collagen tube filled with laminin-coated collagen fibers: a histological and electrophysiological evaluation of regenerated nerves. Brain Res 868 2 (2000) 315-328
61. Altman G.H., Horan R.L., Lu H.H., Moreau J., Martin I., Richmond J.C., et al. Silk matrix for tissue engineered anterior cruciate ligaments. Biomaterials 23 20 (2002) 4131-4141
62. Herrup K., and Shooter E.M. Properties of the beta nerve growth factor receptor of avian dorsal root ganglia. Proc Natl Acad Sci USA 70 12 (1973) 3884-3888
63. Cheng Q., Peng T.Z., Hu X.B., and Yang C.F. Charge-selective recognition at fibroin-modified electrodes for analytical application. Anal Bioanal Chem 382 1 (2005) 80-84