A spinal cord surrogate with nanoscale porosity for in vitro simulations of restorative neurosurgical techniques

被引:21
作者
Gillies, GT
Wilhelm, TD
Humphrey, JAC
Fillmore, HL
Holloway, KL
Broaddus, WC
机构
[1] Univ Virginia, Dept Mech & Aerosp Engn, Charlottesville, VA 22904 USA
[2] Virginia Commonwealth Univ, Div Neurosurg, Richmond, VA 23298 USA
关键词
D O I
10.1088/0957-4484/13/5/308
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of strategies for the regrowth of axons through a section of damaged spinal cord could benefit from the availability of an in vitro model in which the potential clinical utility of candidate techniques could be assessed preliminarily. We have designed a spinal cord surrogate for this purpose; it uses 0.6% agarose gel as the parenchymal component and has a fibrous-like longitudinal structure. At this concentration, the pore size distribution of the homogeneous gel ranges from less than 10 nm to more than 1000 nm while the average pore size ranges from 100 to 300 nm. The average pore size is larger than that of the extracellular space in the tissues of the central nervous system, which is of the order of 20 urn. However, the addition of fibres to the surrogate gel model significantly modifies its longitudinal permeability, as assessed by monitoring the distribution of marker dye material during direct infusion into the surrogate. This makes the model useful for evaluating infusion-based techniques that will ultimately be employed for the delivery of growth factors and other agents to the growing axonal processes in injured spinal cord. The role foreseen for this type of surrogate in investigations of the nanomechanics of restorative neurosurgical procedures is discussed. (Some figures in this article are in colour only in the electronic version).
引用
收藏
页码:587 / 591
页数:5
相关论文
共 26 条
[1]  
Aymard P, 2001, BIOPOLYMERS, V59, P131, DOI 10.1002/1097-0282(200109)59:3<131::AID-BIP1013>3.0.CO
[2]  
2-8
[3]   HYDROGEL-BASED 3-DIMENSIONAL MATRIX FOR NEURAL CELLS [J].
BELLAMKONDA, R ;
RANIERI, JP ;
BOUCHE, N ;
AEBISCHER, P .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (05) :663-671
[4]   Cellular engineering: Molecular repair of membranes to rescue cells of the damaged nervous system [J].
Borgens, RB .
NEUROSURGERY, 2001, 49 (02) :370-378
[5]   Distribution and stability of antisense phosphorothioate oligonucleotides in rodent brain following direct intraparenchymal controlled-rate infusion [J].
Broaddus, WC ;
Prabhu, SS ;
Gillies, GT ;
Neal, J ;
Conrad, WS ;
Chen, ZJ ;
Fillmore, H ;
Young, HF .
JOURNAL OF NEUROSURGERY, 1998, 88 (04) :734-742
[6]  
Broaddus WC, 2001, NEUROIMAG CLIN N AM, V11, P727
[7]   Bridging areas of injury in the spinal cord [J].
Bunge, MB .
NEUROSCIENTIST, 2001, 7 (04) :325-339
[8]  
Chada S, 1997, J CELL SCI, V110, P1179
[9]   Intraparenchymal drug delivery via positive-pressure infusion: Experimental and modeling studies of poroelasticity in brain phantom gels [J].
Chen, ZJ ;
Broaddus, WC ;
Viswanathan, RR ;
Raghavan, R ;
Gillies, GT .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2002, 49 (02) :85-96
[10]   Scaling analysis of the concentration dependence on elasticity of agarose gel [J].
Fujii, T ;
Yano, T ;
Kumagai, H ;
Miyawaki, O .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2000, 64 (08) :1618-1622