Diffusion and convection in collagen gels: Implications for transport in the tumor interstitium

被引:421
作者
Ramanujan, S
Pluen, A
McKee, TD
Brown, EB
Boucher, Y
Jain, RK
机构
[1] Massachusetts Gen Hosp, Dept Radiat Oncol, EL Steele Lab Tumor Biol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
[3] MIT, Biol Engn Div, Cambridge, MA 02139 USA
关键词
D O I
10.1016/S0006-3495(02)73933-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Diffusion coefficients of tracer molecules in collagen type I gels prepared from 0-4.5% w/v solutions were measured by fluorescence recovery after photobleaching. When adjusted to account for in vivo tortuosity, diffusion coefficients in gels matched previous measurements in four human tumor xenografts with equivalent collagen concentrations. In contrast, hyaluronan solutions hindered diffusion to a lesser extent when prepared at concentrations equivalent to those reported in these tumors. Collagen permeability, determined from flow through gels under hydrostatic pressure, was compared with predictions obtained from application of the Brinkman effective medium model to diffusion data. Permeability predictions matched experimental results at low concentrations, but underestimated measured values at high concentrations. Permeability measurements in gels did not match previous measurements in tumors. Visualization of gels by transmission electron microscopy and light microscopy revealed networks of long collagen fibers at lower concentrations along with shorter fibers at high concentrations. Negligible assembly was detected in collagen solutions pregelation. However, diffusion was similarly hindered in pre and postgelation samples. Comparison of diffusion and convection data in these gels and tumors suggests that collagen may obstruct diffusion more than convection in tumors. These findings have significant implications for drug delivery in tumors and for tissue engineering applications.
引用
收藏
页码:1650 / 1660
页数:11
相关论文
共 42 条
[1]  
Alberts B., 1994, MOL BIOL CELL, P971
[2]   Direct in vivo measurement of targeted binding in a human tumor xenograft [J].
Berk, DA ;
Yuan, F ;
Leunig, M ;
Jain, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1785-1790
[3]  
BERK DA, 1993, BIOPHYS J, V65, P2428, DOI 10.1016/S0006-3495(93)81326-2
[4]   EFFECT OF CYTOSKELETAL GEOMETRY ON INTRACELLULAR DIFFUSION [J].
BLUM, JJ ;
LAWLER, G ;
REED, M ;
SHIN, I .
BIOPHYSICAL JOURNAL, 1989, 56 (05) :995-1005
[5]   Intratumoral infusion of fluid: estimation of hydraulic conductivity and implications for the delivery of therapeutic agents [J].
Boucher, Y ;
Brekken, C ;
Netti, PA ;
Baxter, LT ;
Jain, RK .
BRITISH JOURNAL OF CANCER, 1998, 78 (11) :1442-1448
[6]  
Brightman AO, 2000, BIOPOLYMERS, V54, P222
[7]  
Carman P. C., 1937, T I CHEM ENG-LOND, V15, P150, DOI [10.1016/S0263-8762(97)80003-2, DOI 10.1016/S0263-8762(97)80003-2]
[8]   Effect of vascular endothelial growth factor on cultured endothelial cell monolayer transport properties [J].
Chang, YS ;
Munn, LL ;
Hillsley, MV ;
Dull, RO ;
Yuan, J ;
Lakshminarayanan, S ;
Gardner, TW ;
Jain, RK ;
Tarbell, JM .
MICROVASCULAR RESEARCH, 2000, 59 (02) :265-277
[9]   Changes in brain cell shape create residual extracellular space volume and explain tortuosity behavior during osmotic challenge [J].
Chen, KC ;
Nicholson, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8306-8311
[10]  
CHENG PC, 1990, HDB BIOL CONFOCAL MI, P170