Ramanujan Saroja, Pluen Alain, McKee Trevor D, Brown Edward B, Boucher Yves, Jain Rakesh K
E. L. Steele Laboratory for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA.
Biophys J. 2002 Sep;83(3):1650-60. doi: 10.1016/S0006-3495(02)73933-7.
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.
通过光漂白后的荧光恢复来测量示踪分子在由0 - 4.5% w/v溶液制备的I型胶原凝胶中的扩散系数。当调整以考虑体内曲折度时,凝胶中的扩散系数与先前在四种具有等效胶原浓度的人肿瘤异种移植中的测量值相匹配。相比之下,当以与这些肿瘤中报道的浓度相当的浓度制备时,透明质酸溶液对扩散的阻碍程度较小。通过在静水压力下通过凝胶的流量确定的胶原渗透性,与将布林克曼有效介质模型应用于扩散数据所获得的预测值进行了比较。渗透性预测在低浓度下与实验结果匹配,但在高浓度下低估了测量值。凝胶中的渗透性测量与先前在肿瘤中的测量值不匹配。通过透射电子显微镜和光学显微镜对凝胶进行可视化显示,在较低浓度下有长胶原纤维网络,在高浓度下有较短的纤维。在胶原溶液预凝胶化过程中检测到可忽略不计的组装。然而,在预凝胶化和后凝胶化样品中扩散同样受到阻碍。这些凝胶和肿瘤中扩散与对流数据的比较表明,在肿瘤中胶原对扩散的阻碍可能比对流更大。这些发现对肿瘤中的药物递送和组织工程应用具有重要意义。