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Volumn 26, Issue 36, 2005, Pages 7555-7563

Synthesis of degradable poly(l-lactide-co-ethylene glycol) porous tubes by liquid-liquid centrifugal casting for use as nerve guidance channels

Author keywords

Centrifugal casting; Nerve guidance channels; Poly(ethylene glycol); Poly(lactide); Polymer tubes

Indexed keywords

BIODEGRADATION; BIOSYNTHESIS; CARBOXYLIC ACIDS; HYDROGELS; MASS SPECTROMETRY; MORPHOLOGY; TISSUE CULTURE;

EID: 23944477624     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2005.05.026     Document Type: Article
Times cited : (30)

References (29)
  • 1
    • 0035424661 scopus 로고    scopus 로고
    • Peripheral nerve injury: A review and approach to tissue engineered constructs
    • G.R.D. Evans Peripheral nerve injury: a review and approach to tissue engineered constructs T Anat Rec 263 2001 396 404
    • (2001) T Anat Rec , vol.263 , pp. 396-404
    • Evans, G.R.D.1
  • 4
    • 0025041853 scopus 로고
    • Enhancement of peripheral nerve regeneration
    • B.R. Seckel Enhancement of peripheral nerve regeneration Muscle Nerve 14 1990 785
    • (1990) Muscle Nerve , vol.14 , pp. 785
    • Seckel, B.R.1
  • 5
    • 0021796098 scopus 로고
    • Increased rate of peripheral nerve regeneration using bioresorbable nerve guides and a laminin-containing gel
    • R. Madison, C. Da Silva, and P. Dikkes Increased rate of peripheral nerve regeneration using bioresorbable nerve guides and a laminin-containing gel Exp Neurol 88 1985 767
    • (1985) Exp Neurol , vol.88 , pp. 767
    • Madison, R.1    Da Silva, C.2    Dikkes, P.3
  • 6
    • 0036020557 scopus 로고    scopus 로고
    • Manufacture of poly(2-hydroxyethyl methacrylate-co-methylmethacrylate) hydrogel tubes for use as nerve guidance channels
    • P.D. Dalton, L. Flynn, and M.S. Shoichet Manufacture of poly(2-hydroxyethyl methacrylate-co-methylmethacrylate) hydrogel tubes for use as nerve guidance channels Biomaterials 23 2002 3843 3851
    • (2002) Biomaterials , vol.23 , pp. 3843-3851
    • Dalton, P.D.1    Flynn, L.2    Shoichet, M.S.3
  • 7
    • 9644262290 scopus 로고    scopus 로고
    • Long-term in vivo biomechanical properties and biocompatibility of poly(2-hydroxyethyl methacrylate-co-methyl methacrylate) nerve conduits
    • J.S. Belkas, C.A. Munro, M.S. Shoichet, M. Johnston, and R. Midha Long-term in vivo biomechanical properties and biocompatibility of poly(2-hydroxyethyl methacrylate-co-methyl methacrylate) nerve conduits Biomaterials 26 2005 1741 1749
    • (2005) Biomaterials , vol.26 , pp. 1741-1749
    • Belkas, J.S.1    Munro, C.A.2    Shoichet, M.S.3    Johnston, M.4    Midha, R.5
  • 8
    • 23944505762 scopus 로고    scopus 로고
    • Coil-reinforced hydrogel tubes promote nerve regeneration equivalent to that of nerve autografts
    • Y. Katayama, R. Montenegro, T. Freier, R. Midha, and M.S. Shoichet Coil-reinforced hydrogel tubes promote nerve regeneration equivalent to that of nerve autografts Biomaterials 2005 accepted
    • (2005) Biomaterials
    • Katayama, Y.1    Montenegro, R.2    Freier, T.3    Midha, R.4    Shoichet, M.S.5
  • 9
    • 0031042958 scopus 로고    scopus 로고
    • Bioartificial nerve grafts based on absorbable guiding filament structures-early observations
    • N. Terada, L.M. Bjursten, and D. Dohi Bioartificial nerve grafts based on absorbable guiding filament structures-early observations Scand J Plast Reconstr 1 1997
    • (1997) Scand J Plast Reconstr , vol.1
    • Terada, N.1    Bjursten, L.M.2    Dohi, D.3
  • 10
    • 33645384649 scopus 로고
    • Clinical nerve reconstruction with a bioabsorbable polyglycolic acid tube
    • A.L. Dellon, and S.E. Mackinnon Clinical nerve reconstruction with a bioabsorbable polyglycolic acid tube Plast Reconstr Surg 849 1988
    • (1988) Plast Reconstr Surg , vol.849
    • Dellon, A.L.1    MacKinnon, S.E.2
  • 11
    • 0031365852 scopus 로고    scopus 로고
    • Design of macroporous biodegradable polymer scaffolds for cell transplantation
    • V. Maquet, and R. Jerome Design of macroporous biodegradable polymer scaffolds for cell transplantation Mater Sci Forum 250 1997 15 42
    • (1997) Mater Sci Forum , vol.250 , pp. 15-42
    • Maquet, V.1    Jerome, R.2
  • 12
    • 33645402532 scopus 로고
    • S.W. Shalaby Carl Hanser Verlag Biomedical polymers Monich
    • S.W. Shalaby, and A. Johnson S.W. Shalaby Designed-to-degrade systems 1994 Carl Hanser Verlag Biomedical polymers Monich 1 34
    • (1994) Designed-to-degrade Systems , pp. 1-34
    • Shalaby, S.W.1    Johnson, A.2
  • 13
    • 0031272252 scopus 로고    scopus 로고
    • More about the polymerization of lactides in the presence of stannous octoate
    • G. Schwach, J. Coudane, R. Engel, and M. Vert More about the polymerization of lactides in the presence of stannous octoate J Polym Sci Polym Chem 35 1997 3431 3440
    • (1997) J Polym Sci Polym Chem , vol.35 , pp. 3431-3440
    • Schwach, G.1    Coudane, J.2    Engel, R.3    Vert, M.4
  • 14
    • 0031272235 scopus 로고    scopus 로고
    • Reversible kinetics and thermodynamics of the homopolymerization of l-lactide with 2-ethylhexanoic acid Tin(II) salt
    • D.R. Witzke, R. Narayan, and J.J. Kolstad Reversible kinetics and thermodynamics of the homopolymerization of l-lactide with 2-ethylhexanoic acid Tin(II) salt Macromolecules 30 1997 7075 7085
    • (1997) Macromolecules , vol.30 , pp. 7075-7085
    • Witzke, D.R.1    Narayan, R.2    Kolstad, J.J.3
  • 16
    • 33645411418 scopus 로고    scopus 로고
    • Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate, 1. Polymerization of η-caprolactone
    • A. Kowalski, A. Duda, and S. Penczek Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate, 1. Polymerization of η-caprolactone Macromol Rapid Commun 35 1998 723 750
    • (1998) Macromol Rapid Commun , vol.35 , pp. 723-750
    • Kowalski, A.1    Duda, A.2    Penczek, S.3
  • 17
    • 0034620357 scopus 로고    scopus 로고
    • 2-initiated polymerizations of lactide: A mechanistic study
    • 2-initiated polymerizations of lactide: a mechanistic study Macromolecules 33 2000 702 709
    • (2000) Macromolecules , vol.33 , pp. 702-709
    • Kowalski, A.1    Duda, A.2    Penczek, S.3
  • 19
    • 0034350436 scopus 로고    scopus 로고
    • Polymerizations of - Caprolactone and l,l-dilactide initiated with stannous octoate and stannous butoxide - A comparison
    • A. Duda, S. Penczek, and A. Kowalski Polymerizations of - caprolactone and l,l-dilactide initiated with stannous octoate and stannous butoxide - a comparison Macromol Symp 153 2000 41 53
    • (2000) Macromol Symp , vol.153 , pp. 41-53
    • Duda, A.1    Penczek, S.2    Kowalski, A.3
  • 20
    • 0035978454 scopus 로고    scopus 로고
    • Synthesis of polylactides in the presence of co-initiators with different numbers of hydroxyl groups
    • H. Korhonen, A. Helminen, and J.V. Suppala Synthesis of polylactides in the presence of co-initiators with different numbers of hydroxyl groups Polymer 42 2001 7541 7549
    • (2001) Polymer , vol.42 , pp. 7541-7549
    • Korhonen, H.1    Helminen, A.2    Suppala, J.V.3
  • 21
    • 0031556504 scopus 로고    scopus 로고
    • Synthesis of polymer network scaffolds from l-lactide and poly(ethylene glycol) and their interaction with cells
    • D.K. Han, and J.A. Hubbell Synthesis of polymer network scaffolds from l-lactide and poly(ethylene glycol) and their interaction with cells Macromolecules 30 1997 6077 6083
    • (1997) Macromolecules , vol.30 , pp. 6077-6083
    • Han, D.K.1    Hubbell, J.A.2
  • 22
    • 0034254594 scopus 로고    scopus 로고
    • Synthesis of acrylate functional telechelic poly(lactic acid) oligomer by transesterification
    • G. Coullerez, C. Lowe, P. Pechy, H.H. Kausch, and J. Hilborn Synthesis of acrylate functional telechelic poly(lactic acid) oligomer by transesterification J Mater Sci - Mater Med 11 2000 505 510
    • (2000) J Mater Sci - Mater Med , vol.11 , pp. 505-510
    • Coullerez, G.1    Lowe, C.2    Pechy, P.3    Kausch, H.H.4    Hilborn, J.5
  • 23
    • 0032118795 scopus 로고    scopus 로고
    • Ring opening polymerization of d,l-lactide in the presence of zinc metal and zinc lactate
    • G. Schwach, J. Coudane, R. Engel, and M. Vert Ring opening polymerization of d,l-lactide in the presence of zinc metal and zinc lactate Polym Int 46 1998 177 182
    • (1998) Polym Int , vol.46 , pp. 177-182
    • Schwach, G.1    Coudane, J.2    Engel, R.3    Vert, M.4
  • 24
    • 0012549301 scopus 로고    scopus 로고
    • G.H.I.M. Walenkamp Thieme Verlag Stuttgart
    • R. Wenz G.H.I.M. Walenkamp Biomaterials in surgery 1998 Thieme Verlag Stuttgart 132 135
    • (1998) Biomaterials in Surgery , pp. 132-135
    • Wenz, R.1
  • 25
    • 0036668163 scopus 로고    scopus 로고
    • Biodegradable polymer networks based on oligolactide macromers: Synthesis, properties and biomedical applications
    • M. Schnabelrauch, S. Vogt, Y. Larcher, and I. Wilke Biodegradable polymer networks based on oligolactide macromers: synthesis, properties and biomedical applications Biomol Eng 19 2002 295 298
    • (2002) Biomol Eng , vol.19 , pp. 295-298
    • Schnabelrauch, M.1    Vogt, S.2    Larcher, Y.3    Wilke, I.4
  • 27
    • 0036254733 scopus 로고    scopus 로고
    • In vitro and in vivo degradation studies for development of a biodegradable patch based on poly(3-hydroxybutyrate)
    • T. Freier, C. Kunze, C. Nischan, S. Kramer, K. Sternberg, M. Saß, U.T. Hopt, and K.P. Schmitz In vitro and in vivo degradation studies for development of a biodegradable patch based on poly(3-hydroxybutyrate) Biomaterials 23 2002 2649 2657
    • (2002) Biomaterials , vol.23 , pp. 2649-2657
    • Freier, T.1    Kunze, C.2    Nischan, C.3    Kramer, S.4    Sternberg, K.5    Saß, M.6    Hopt, U.T.7    Schmitz, K.P.8
  • 28
    • 0000724725 scopus 로고
    • Synthesis, characterization, and polymerization of glycidyl methacrylate derivatized dextran
    • W.N.E. Van Dijk-Wolthuis, O. Franssen, H. Talsma, and M.J. Van Steenbergen Synthesis, characterization, and polymerization of glycidyl methacrylate derivatized dextran Macromolecules 28 1995 6317 6322
    • (1995) Macromolecules , vol.28 , pp. 6317-6322
    • Van Dijk-Wolthuis, W.N.E.1    Franssen, O.2    Talsma, H.3    Van Steenbergen, M.J.4
  • 29
    • 0031338785 scopus 로고    scopus 로고
    • A new class of polymerizable dextrans with hydrolysable groups: Hydroxyethyl methacrylated dextran with and without oligolactate spacer
    • W.N.E. Van Dijk-Wolthuis, S.K.Y. Tsang, J.J. Kettenes-van den Bosch, and W.E. Hennink A new class of polymerizable dextrans with hydrolysable groups: hydroxyethyl methacrylated dextran with and without oligolactate spacer Polymer 38 1997 6235 6242
    • (1997) Polymer , vol.38 , pp. 6235-6242
    • Van Dijk-Wolthuis, W.N.E.1    Tsang, S.K.Y.2    Kettenes-Van Den Bosch, J.J.3    Hennink, W.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.