Tuning tissue growth with scaffold degradation in enzyme-sensitive hydrogels: a mathematical model

被引:66
作者
Akalp, Umut [1 ]
Bryant, Stephanie J. [1 ]
Vernerey, Franck J. [1 ]
机构
[1] Univ Colorado, Dept Mech Engn, Dept Chem & Biol Engn, Program Mat Sci & Engn, Boulder, CO 80309 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PEG HYDROGELS; ARTICULAR-CARTILAGE; POROUS-MEDIA; SWOLLEN MEMBRANES; SOLUTE DIFFUSION; GEL PROPERTIES; STEM-CELLS; MATRIX; REGENERATION; TRANSPORT;
D O I
10.1039/c6sm00583g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Despite tremendous advances in the field of tissue engineering, a number of obstacles remain that hinder its successful translation to the clinic. One challenge that relates to the use of cells encapsulated in a hydrogel is identifying a hydrogel design that can provide an appropriate environment for cells to successfully synthesize and deposit new matrix molecules while providing a mechanical support that can resist physiological loads at the early stage of implementation. A solution to this problem has been to balance tissue growth and hydrogel degradation. However, identifying this balance is difficult due to the complexity of coupling diffusion, deposition, and degradation mechanisms. Very little is known about the complex behavior of these mechanisms, emphasizing the need for a rigorous mathematical approach that can assist and guide experimental advances. To address this issue, this paper discusses a model for interstitial growth based on mixture theory, that can capture the coupling between cell-mediated hydrogel degradation (i.e., hydrogels containing enzyme-sensitive crosslinks) and the transport of extracellular matrix (ECM) molecules released by encapsulated cells within a hydrogel. Taking cartilage tissue engineering as an example, the model investigates the role of enzymatic degradation on ECM diffusion and its impact on two important outcomes: the extent of ECM transport (and deposition) and the evolution of the hydrogel's mechanical integrity. Numerical results based on finite element analysis show that if properly tuned, enzymatic degradation yields the appearance of a highly localized degradation front propagating away from the cell, which can be immediately followed by a front of growing neotissue. We show that this situation is key to maintaining mechanical properties (e.g., stiffness) while allowing for deposition of new ECM molecules. Overall, our study suggests a hydrogel design that could enable successful tissue engineering (e.g., of cartilage, bone, etc.) where mechanical integrity is important.
引用
收藏
页码:7505 / 7520
页数:16
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