CHEMICAL ENGINEERING METHODS IN ANALYSES OF 3D CANCER CELL CULTURES: HYDRODYNAMIC AND MASS TRANSPORT CONSIDERATIONS

A multidisciplinary approach based on experiments and mathematical modeling was used in biomimetic system development for three-dimensional (3D) cultures of cancer cells. Specifically, two cancer cell lines, human embryonic teratocarcinoma NT2/D1 and rat glioma C6, were immobilized in alginate microbeads and microfibers, respectively, and cultured under static and flow conditions in perfusion bioreactors. At the same time, chemical engineering methods were applied to explain the obtained results. The superficial medium velocity of 80 mu m s(-1) induced lower viability of NT2/D1 cells in superficial microbead zones, implying adverse effects of fluid shear stresses estimated as similar to 67 mPa. On the contrary, similar velocity (100 mu m s(-1)) enhanced the proliferation of C6 glioma cells within microfibers compared to static controls. An additional study of silver release from nanocomposite Ag/honey/alginate microfibers under perfusion indicated that the medium partially flows through the hydrogel (interstitial velocity of similar to 10 nm s(-1)). Thus, a diffusion-advection-reaction model described the mass transport to immobilized cells within microfibers. Substances with diffusion coefficients of similar to 10(-)(19)-10(-11) m(2) s(-)(1) are sufficiently supplied by diffusion only, while those with significantly lower diffusivities (similar to 10(-1)(9) m(2) s(-1)) require additional convective transport. The present study demonstrates the selection and contribution of chemical engineering methods in tumor model system development.

Automated summary

A multidisciplinary approach was utilized in this study to develop a biomimetic system for 3D cultures of cancer cells. Cancer cell lines were immobilized in alginate microbeads and microfibers and cultured under different conditions. Chemical engineering methods were used to explain the results obtained. The study showed that fluid shear stresses affected the viability of cancer cells, and different velocities had different effects on the proliferation of glioma cells. Moreover, the mass transport within the microfibers was described using a diffusion-advection-reaction model.