Controlled nerve growth factor release from multi-ply alginate/chitosan-based nerve conduits

被引:54
作者
Pfister, Lukas A. [1 ]
Alther, Eva [1 ]
Papaloizos, Michael L. [2 ]
Merkle, Hans P. [1 ]
Gander, Bruno [1 ]
机构
[1] ETH, Inst Pharmaceut Sci, CH-8093 Zurich, Switzerland
[2] Ctr Hand Surg & Therapy, Geneva, Switzerland
关键词
NGF; release kinetics; nerve conduit; nerve regeneration;
D O I
10.1016/j.ejpb.2008.01.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The delivery kinetics of growth factors has been suggested to play an important role in the regeneration of peripheral nerves following axotomy. In this context, we designed a nerve conduit (NC) with adjustable release kinetics of nerve growth factor (NGF). A multi-ply system was designed where NC consisting of a polyelectrolyte alginate/chitosan complex was coated with layers of poly(lactide-co-glycolide) (PLGA) to control the release of embedded NGF. Prior to assessing the in vitro NGF release from NC, various release test media, with and without stabilizers for NGF, were evaluated to ensure adequate quantification of NGF by ELISA. Citrate (pH 5.0) and acetate (pH 5.5) buffered saline solutions containing 0.05% Tween 20 yielded the most reliable results for ELISA active NGF. The in vitro release experiments revealed that the best results in terms of reproducibility and release control were achieved when the NGF was embedded between two PLGA layers and the ends of the NC tightly sealed by the PLGA coatings. The release kinetics could be efficiently adjusted by accommodating NGF at different radial locations within the NC. A sustained release of bioactive NGF in the low nanogram per day range was obtained for at least 15 days. In conclusion, the developed multi-ply NGF loaded NC is considered a suitable candidate for future implantation studies to gain insight into the relationship between local growth factor availability and nerve regeneration. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:563 / 572
页数:10
相关论文
共 29 条
  • [1] Apfel SC, 1999, BRAIN PATHOL, V9, P393
  • [2] ARCHIBALD SJ, 1995, J NEUROSCI, V15, P4109
  • [3] ARMSTRONG NA, 1990, UNDERSTANDING EXPT D
  • [4] Nerve repair by means of tubulization: Literature review and personal clinical experience comparing biological and synthetic conduits for sensory nerve repair
    Battiston, B
    Geuna, S
    Ferrero, M
    Tos, P
    [J]. MICROSURGERY, 2005, 25 (04) : 258 - 267
  • [5] Peripheral nerve regeneration through guidance tubes
    Belkas, JS
    Shoichett, MS
    Midha, R
    [J]. NEUROLOGICAL RESEARCH, 2004, 26 (02) : 151 - 160
  • [6] Peripheral nerve regeneration: An opinion on channels, scaffolds and anisotropy
    Bellamkonda, RV
    [J]. BIOMATERIALS, 2006, 27 (19) : 3515 - 3518
  • [7] de Young LR, 1999, PROTEIN SCI, V8, P2513
  • [8] RhNGF slow unfolding is not due to proline isomerization: Possibility of a cystine knot loop-threading mechanism
    DeYoung, LR
    Burton, LE
    Liu, J
    Powell, MF
    Schmelzer, CH
    Skelton, NJ
    [J]. PROTEIN SCIENCE, 1996, 5 (08) : 1554 - 1566
  • [9] Formulation development and primary degradation pathways for recombinant human nerve growth factor
    Eng, M
    Ling, V
    Briggs, JA
    Souza, K
    CanovaDavis, E
    Powell, MF
    DeYoung, LR
    [J]. ANALYTICAL CHEMISTRY, 1997, 69 (20) : 4184 - 4190
  • [10] GDNF and NGF released by synthetic guidance channels support sciatic nerve regeneration across a long gap
    Fine, EG
    Decosterd, I
    Papaloïzos, M
    Zurn, AD
    Aebischer, P
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 15 (04) : 589 - 601