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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/22183

Title: Stem cell delivery with polymer hydrogel for treatment of intervertebral disc degeneration: from 3D culture to design of the delivery device for minimally invasive therapy
Authors: Kumar, Deepak
Lyness, Alexander M.
Gerges, Irini
Lenardi, Cristina
Forsyth, Nicholas R.
Liu, Yang
Keywords: Regenerative medicine
Cell encapsulation
Tissue engineering
Cell delivery
Device design
Issue Date: 2016
Publisher: Cognizant Communication Corporation
Citation: KUMAR, D. ...et al., 2016. Stem cell delivery with polymer hydrogel for treatment of intervertebral disc degeneration: from 3D culture to design of the delivery device for minimally invasive therapy. Cell Transplantation, 25 (12), pp. 2213-2220.
Abstract: Nucleus pulposus (NP) tissue damage can induce detrimental mechanical strain on the biomechanical performance of intervertebral disc (IVD) causing subsequent disc degeneration. A novel, photocurable, injectable, synthetic polymer hydrogel (pHEMA-co-APMA grafted with PAA) has already demonstrated success in encapsulating and differentiating human mesenchymal stem cells (hMSCs) towards an NP phenotype during hypoxic conditions. After demonstration of promising results in our previous work, in this study, we have further investigated the inclusion of mechanical stimulation and its impact on hMSC differentiation towards an NP phenotype through the characterization of matrix markers such as SOX-9, Aggrecan and Collagen II. Furthermore, investigations were undertaken in order to approximate delivery parameters for an injection delivery device, which could be used to transport hMSCs suspended in hydrogel into the IVD. hMSC laden hydrogel solutions were injected through various needle gauge sizes in order to deter its impact on postinjection cell viability and IVD tissue penetration. Interpretation of this data informed the design of a potential minimally invasive injection device, which could successfully inject hMSCs encapsulated in a UV curable polymer into NP, prior to photocrosslinking in situ.
Description: This is an Open Access Article. It is published by Cognizant Communication Corporation under the Creative Commons Attribution 3.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/3.0/
Sponsor: This study was supported by the EPSRC Centre of Innovative Manufacturing in Regenerative Medicine, Royal Society funding for International Joint Project and FP7 SkelGen.
Version: Published
DOI: 10.3727/096368916X692618
URI: https://dspace.lboro.ac.uk/2134/22183
Publisher Link: http://dx.doi.org/10.3727/096368916X692618
ISSN: 1555-3892
Appears in Collections:Published Articles (Mechanical, Electrical and Manufacturing Engineering)

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