In this paper, we derive an effective macroscale description suitable to describe the growth of biological tissue within a porous tissue-engineering scaffold. As in our recent work (Holden textit{et al.} A multiphase multiscale model for nutrient limited tissue growth, The ANZIAM Journal, 2018, doi:10.1017/S1446181118000044) the underlying tissue dynamics is described as a multiphase mixture, thereby naturally accommodating features such as interstitial growth and active cell motion. Via a linearisation of the underlying multiphase model (whose nonlinearity poses significant challenge for such analyses), we obtain, by means of multiple-scales homogenisation, a simplified macroscale model that nevertheless retains explicit dependence on both the microscale scaffold structure and the tissue dynamics. The model we obtain comprises Darcy flow, and differential equations for the volume fraction of cells within the scaffold and the concentration of nutrient, required for growth. These are coupled to underlying Stokes-type cell problems that provide permeability tensors to parameterise the macroscale description. In Holden textit{et al.}, the cell problems retain macroscale dependence, posing significant computational challenges; here, we obtain a decoupled system whereby the quasi-steady cell-problems may be solved separately from the macroscale description, thereby greatly reducing the complexity associated with fully-coupled multiscale descriptions. Moreover, we indicate how the formulation is influenced by a set of alternative microscale boundary conditions.S
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