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The effect of weak inertia in rotating high-aspect-ratio vessel bioreactors

Published online by Cambridge University Press:  27 November 2017

Mohit P. Dalwadi*
Affiliation:
Synthetic Biology Research Centre, University of Nottingham, Nottingham NG7 2RD, UK
S. Jonathan Chapman
Affiliation:
Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK
James M. Oliver
Affiliation:
Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK
Sarah L. Waters
Affiliation:
Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK
*
†Email address for correspondence: mohit.dalwadi@nottingham.ac.uk

Abstract

One method to grow artificial body tissue is to place a porous scaffold seeded with cells, known as a tissue construct, into a rotating bioreactor filled with a nutrient-rich fluid. The flow within the bioreactor is affected by the movement of the construct relative to the bioreactor which, in turn, is affected by the hydrodynamical and gravitational forces the construct experiences. The construct motion is thus coupled to the flow within the bioreactor. Over the time scale of a few hours, the construct appears to move in a periodic orbit but, over tens of hours, the construct drifts from periodicity. In the biological literature, this effect is often attributed to the change in density of the construct that occurs via tissue growth. In this paper, we show that weak inertia can cause the construct to drift from its periodic orbit over the same time scale as tissue growth. We consider the coupled flow and construct motion problem within a rotating high-aspect-ratio vessel bioreactor. Using an asymptotic analysis, we investigate the case where the Reynolds number is large but the geometry of the bioreactor yields a small reduced Reynolds number, resulting in a weak inertial effect. In particular, to accurately couple the bioreactor and porous flow regions, we extend the nested boundary layer analysis of Dalwadi et al. (J. Fluid Mech., vol. 798, 2016, pp. 88–139) to include moving walls and the thin region between the porous construct and the bioreactor wall. This allows us to derive a closed system of nonlinear ordinary differential equations for the construct trajectory, from which we show that neglecting inertia results in periodic orbits; we solve the inertia-free problem analytically, calculating the periodic orbits in terms of the system parameters. Using a multiple-scale analysis, we then systematically derive a simpler system of nonlinear ordinary differential equations that describe the long-time drift of the construct due to the effect of weak inertia. We investigate the bifurcations of the construct trajectory behaviour, and the limit cycles that appear when the construct is less dense than the surrounding fluid and the rotation rate is large enough. Thus, we are able to predict when the tissue construct will drift towards a stable limit cycle within the bioreactor and when it will drift out until it hits the bioreactor edge.

Information

Type
JFM Papers
Copyright
© 2017 Cambridge University Press 
Figure 0

Figure 1.A schematic of the HARV bioreactor set-up in (a) plan view (b) side view. The double-headed arrows denote the forcing in the system, corresponding to gravity (shown in a,b) and rotation of the bioreactor (shown in a). The single-headed arrows denote the movement of the tissue construct, which must be determined as part of the solution.

Figure 1

Figure 2.A schematic of the dimensional HARV bioreactor set-up in (a) plan view and (b) side view.

Figure 2

Table 1.Typical dimensional (left) and dimensionless (right) parameter values. The absolute upper bound of $1/12\approx 8.3\times 10^{-2}$ for $K$ can be obtained by considering unobstructed Poiseuille flow through a channel. Data for the HARV operating conditions and construct dimensions are taken from Wolf, Sams & Schwarz (1992), Freed & Vunjak-Novakovic (1997), Ingram et al. (1997), Schwarz & Anderson (1998), Yu et al. (2004), Cummings et al. (2009). Data for construct permeability are taken from Šimáček & Advani (1996), Sucosky et al. (2004), Nabovati, Llewellin & Sousa (2009). We use the standard acceleration due to gravity, and the density and viscosity values of water at room temperature for $\unicode[STIX]{x1D70C}$ and $\unicode[STIX]{x1D707}$, respectively. Although the dimensionless groupings can vary significantly in magnitude across the range of rotating bioreactors, we are interested in the HARV bioreactor where $\unicode[STIX]{x1D716}$ and $\unicode[STIX]{x1D716}_{1}$ are small (Cummings et al.2009).

Figure 3

Figure 3.The domains of the reduced system and the bipolar transformation defined in (3.8). (a) $(X,Y)$ coordinates and (b) $(\unicode[STIX]{x1D6FC},\unicode[STIX]{x1D6FD})$ coordinates.

Figure 4

Figure 4.The function $\unicode[STIX]{x1D6FE}_{1}(R)$ for various values of $K$, using $b=0.2$. The functions stop at $R=1-b$, which corresponds to where the tissue construct hits the bioreactor edge. The dashed lines are the small $R$ asymptotic solutions, and the dotted lines are the small $1-b-R$ solutions, both given in (4.7).

Figure 5

Figure 5.The three different periodic motion regimes at leading order, shown in the bioreactor domain, when $\overline{R}=0.25$. The black cross denotes the position of the construct centre in the steady regime, when $r(0)=0$, the blue line denotes a trajectory of the construct centre in the settling regime, when $r(0)=0.1<|\overline{R}|$, and the yellow line denotes a trajectory of the construct centre in the orbital regime, when $r(0)=0.45>|\overline{R}|$. The red dotted line denotes the boundary between orbital and settling motion; the periodic trajectory of the construct centre encloses the bioreactor centre for the former, but not for the latter. The dashed black line denotes the positions of the construct centre for which the construct hits the bioreactor edge, using $b=0.2$.

Figure 6

Figure 6.The parameter constraints to keep the construct from hitting the bioreactor edge. The white regions denote valid values and the grey regions denote invalid values. (a) $(\bar{\unicode[STIX]{x1D70C}},\overline{B})$ space: the white region is defined by $\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|<1-b$. (b) $(\bar{\unicode[STIX]{x1D70C}},r_{0})$ space: the white region is defined by $r_{0}+\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|<1-b$. The dotted red lines at $r_{0}=\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|$ define the boundaries between orbital and settling motion regimes, and the dashed blue line at $r_{0}=0$ denotes the steady regime.

Figure 7

Figure 7.Stability and bifurcation diagrams showing the possible long-time behaviours for the toy problem. In the unshaded region, the construct is in one of two general motion behaviours separated by the dotted blue lines, as discussed in the main text. In the shaded regions, the construct hits the bioreactor edge during the first attempted orbit, and our model breaks down. (a) The long-time construct behaviour in $(\bar{\unicode[STIX]{x1D70C}},\overline{B})$ parameter space. The shaded regions have boundaries defined by $\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|=1-b$. (b) A bifurcation diagram of $r_{0}$ against $\bar{\unicode[STIX]{x1D70C}}$, for fixed $\overline{B}\in ((1-b)/2,1-b)$. Over the long time, $r_{0}$ will vary in the direction of the arrows. The solid black line represents a stable limit cycle and the dashed black line an unstable spiral. The constraints and short-time motion regimes are the same as those in figure 6. That is, the orbital and settling motion regimes are above and below the dotted red line, respectively, which is obscured by the stable limit cycle for behaviour Ia, and the shaded regions have boundaries defined by $r_{0}+\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|=1-b$.

Figure 8

Figure 8.A schematic of the three possible motion regimes for the toy problem. In Regime Ia, the construct always tends to a stable limit cycle on the boundary between settling and orbital motion. In Regime Ib, the construct always tends to a stable limit cycle in orbital motion. In Regime II, the construct always spirals out until it hits the bioreactor edge. The crosses denote an unstable steady point and the blue solid lines denote a stable limit cycle.

Figure 9

Figure 9.(a) The function ${\mathcal{I}}$, defined in (4.46), and its component parts. We see that ${\mathcal{I}}$, and hence the contribution to the long-time drift, has a marked change in behaviour at the boundary between these two regions. (b) The value of $\text{d}r_{0}/\text{d}T$, defined in (4.46), using ${\mathcal{I}}$ from (a), and $\bar{\unicode[STIX]{x1D70C}}=1.01,1.1,1.2,1.3,1.4,1.5$. Additionally, the boundary between the settling and orbital regimes is denoted by a black dotted line, with settling on the left and orbital motion on the right. For each subfigure, we use parameter values $\overline{R}=0.2$, $b=0.2$, and $K=0.05$.

Figure 10

Figure 10.Stability and bifurcation diagrams showing the three possible long-time behaviours (separated by the dotted blue lines) for the full problem, as discussed in the main text. (a) The long-time construct behaviour in $(\bar{\unicode[STIX]{x1D70C}},\overline{B})$ parameter space. (b) A bifurcation diagram of $r_{0}$ against $\bar{\unicode[STIX]{x1D70C}}$, for $\overline{B}=0.1$. Over the long time scale, $r_{0}$ will vary in the direction of the arrows. The solid black line represents a stable limit cycle, the dashed black line represents an unstable spiral, and the dash-dotted line represents an unstable limit cycle. The orbital and settling motion regimes are above and below the dotted red line, respectively. The shaded region has boundary defined by $r_{0}+\overline{B}|1-\bar{\unicode[STIX]{x1D70C}}|=1-b$ and represents the construct trajectory hitting the bioreactor edge on the first orbit. We use $b=0.2$ and $K=0.05$.

Figure 11

Figure 11.A schematic of the three possible motion regimes for the full problem. In Regime Ib, the construct always tends to a stable limit cycle in orbital motion. In Regime II, the construct always spirals out until it hits the bioreactor edge. In Regime III, there exists both a stable and an unstable limit cycle, so the construct will either tend to the stable limit cycle or spiral out until it hits the bioreactor edge, depending on its initial position. The crosses denote an unstable steady point, the blue solid lines denote a stable limit cycle and the dash-dotted red lines denote an unstable limit cycle.

Figure 12

Figure 12.Comparison of numerical and asymptotic results for $b=0.2$ and $K=0.05$ in the asymptotic limit of $\overline{B}\rightarrow 0$. (a) The solid grey line is ${\mathcal{I}}$, obtained by resolving the solvability condition (4.46) using quadrature. The dashed black line in the asymptotic result (4.49) for ${\mathcal{I}}$ for small $R_{0}$. (b) A stability diagram, showing the three possible behaviours of the construct for varying $\bar{\unicode[STIX]{x1D70C}}$. The boundaries between behaviours are denoted with dotted blue lines, and the line $\bar{\unicode[STIX]{x1D70C}}=\bar{\unicode[STIX]{x1D70C}}^{\ast }$ (${\approx}0.606$ for the parameter values used in this figure), is obtained using the asymptotic result (4.50) for small $R_{0}$. The solid black line represents a stable spiral, the dashed black line represents an unstable spiral, and the dash-dotted line represents an unstable limit cycle. Over the long time scale, $R_{0}$ will vary as discussed in the main text, and the arrows denote the direction of change in $R_{0}$.

Figure 13

Figure 13.A schematic of the general boundary layer structure in the flow problem when $Re=O(1)$. The flow is from left to right. The relative size of each boundary layer has been exaggerated for illustrative purposes.

Figure 14

Figure 14.The extended boundary layer structure within the initial boundary layers for the flow problem when $1\ll Re\ll \unicode[STIX]{x1D716}^{-1}$ for (a) inflow and (b) outflow. The flow is from left to right. The relative size of each boundary layer has been exaggerated for illustrative purposes.

Figure 15

Figure 15.The function $\tilde{\unicode[STIX]{x1D6FD}}({\mathcal{A}})$, defined in (A 15). For ${\mathcal{A}}<0$, we find that $\tilde{\unicode[STIX]{x1D6FD}}({\mathcal{A}})$ is not unique. We denote the stable (lower) solution with a solid line and the unstable (upper) solution with a dashed line, and mark the point where these solution curves meet with an asterisk. Moreover, we note that there is no solution for ${\mathcal{A}}<-{\mathcal{A}}^{\ast }$, where ${\mathcal{A}}^{\ast }\approx 0.3541$.

Figure 16

Figure 16.The three functions $\unicode[STIX]{x1D6F1}$, $\unicode[STIX]{x1D6EC}_{a}$, and $\unicode[STIX]{x1D6EC}_{b}$, defined in (A 16a), (A 17b), and (A 17c), respectively. These functions are used to evaluate the coupling conditions (defined in (A 16b) and (A 17a)) between the moving outer regions of the tissue construct and the bulk bioreactor flow. The coupling conditions have been reduced to functions of a single parameter, ${\mathcal{A}}$, defined in (A 12). The solid lines are calculated from the definitions (A 16a), (A 17b), and (A 17c), and the dashed lines represent the extrapolation we discuss in the main text.