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Driving innovations in manufacturing: Open Access research from DMEM

Strathprints makes available Open Access scholarly outputs by Strathclyde's Department of Design, Manufacture & Engineering Management (DMEM).

Centred on the vision of 'Delivering Total Engineering', DMEM is a centre for excellence in the processes, systems and technologies needed to support and enable engineering from concept to remanufacture. From user-centred design to sustainable design, from manufacturing operations to remanufacturing, from advanced materials research to systems engineering.

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Low level laser therapy and tissue engineered skin substitutes: effect on the proliferation rate of 3T3 mouse fibroblast cells

Ho, Gideon and Henderson, Catherine J. and Barbenel, Joseph C. and Grant, M.H. (2004) Low level laser therapy and tissue engineered skin substitutes: effect on the proliferation rate of 3T3 mouse fibroblast cells. Proceedings of SPIE: The International Society for Optical Engineering, 5610 (124).

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Abstract

With the rapid development of tissue engineering and gene therapy, collagen-based biomaterials are frequently used as cell transplant devices; an example is tissue-engineered skin substitutes. In this study of low level laser therapy (LLLT) we determined the influence of the irradiation and treatment parameters on the proliferation rate of 3T3 mouse fibroblast cells cultured on collagen-glycosaminoglycan (GAG) lattices and Petri dishes for up to 4 and 7 days respectively. Helium-Neon (He-Ne) laser at 1 - 4 J/cm2 was used to irradiate the cells. Using 5-carboxyfluorescein diacetate (CFDA) fluorescence, studies on the proliferation rate of irradiated cells before and after cell attachment, and on different treatment days were conducted. The viability of cells on collagen-GAG lattices were assessed using the MTT assay. It was found that in terms of cell proliferation, the cells irradiated at different fluences and treatment modes (at 3 J/cm2) showed no statistically significant difference from the control cells. Control cells on collagen-GAG lattices were found to be more viable than the irradiated cells. It was concluded that with existing experimental conditions, LLLT was found to have no statistically significant effect on the post-cell attachment proliferation and viability of 3T3 mouse fibroblast cells.