Laura Bray

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Queensland University of Technology
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Recent Grants

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Development of a translational bioengineered microenvironment model to advance pre-clinical acute myeloid leukaemia research

Open Date: 2020-06-01

Close Date:

Grant: Close

A Micro-Physiological System to Mimic Human Microbiome-Organ Interactions

Open Date: 2020-01-01

Close Date: 2022-12-31

Grant: Close

ARC Training Centre for Cell and Tissue Engineering Technologies

Open Date: 2019-01-01

Close Date: 2023-12-31

Grant: Close

Dissecting the molecular and cellular mechanisms of angiogenesis and bone metastasis in a bioengineered microenvironment model of prostate cancer.

Open Date: 2016-06-01

Close Date: 2017-05-01

Grant: Close

Development of 3D bioengineered microenvironment models for cancer research

Open Date: 2016-03-01

Close Date: 2017-02-01

Articles (12)

Extrusion-based bioprinting has gained widespread popularity in biofabrication due to its ability to assemble cells and biomaterials in precise patterns and form tissue-like constructs. To achieve this, bioinks must have rheological properties suitable for printing while maintaining cytocompatibility. However, many commonly used biomaterials do not meet the rheological requirements and therefore require modification for bioprinting applications. This study demonstrates the incorporation of Laponite-RD (LPN) into gelatin methacryloyl (GelMA) to produce highly customizable bioinks with desired rheological and mechanical properties for extrusion-based bioprinting. Bioink formulations were based on GelMA (5%–15% w/v) and LPN (0%–4% w/v), and a comprehensive rheological design was applied to evaluate key rheological properties necessary for extrusion-based bioprinting. The results showed that GelMA bioinks with LPN (1%–4% w/v) exhibited pronounced shear thinning and viscoelastic behavior, as well as improved thermal stability. Furthermore, a concentration window of 1%–2% (w/v) LPN to 5%–15% GelMA demonstrated enhanced rheological properties and printability required for extrusion-based bioprinting. Construct mechanical properties were highly tunable by varying polymer concentration and photocrosslinking parameters, with Young's moduli ranging from ∼0.2 to 75 kPa. Interestingly, at higher Laponite concentrations, GelMA cross-linking was inhibited, resulting in softer hydrogels. High viability of MCF-7 breast cancer cells was maintained in both free-swelling droplets and printed hydrogels, and metabolically active spheroids formed over 7 days of culture in all conditions. In summary, the addition of 1%–2% (w/v) LPN to gelatin-based bioinks significantly enhanced rheological properties and retained cell viability and proliferation, suggesting its suitability for extrusion-based bioprinting.

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2024

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2023

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2023

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2022

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2022

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2020

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2020

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2020

Collaborators (17)

Ben Newland

Cardiff University

UNITED KINGDOM
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Mark Adams

Queensland University of Technology

AUSTRALIA
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Erik Walter Thompson

Queensland University of Technology

AUSTRALIA
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Mikhail Tsurkan

Leibniz-Institut für Polymerforschung Dresden e.V.

GERMANY
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Amal Senevirathne

Queensland University of Technology

AUSTRALIA
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Akhilandeshwari Ravichandran

Queensland University of Technology

AUSTRALIA
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Flavia Medeiros Savi

Queensland University of Technology

AUSTRALIA
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Nicholas Harvey

King’s College London

UNITED KINGDOM
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Travis J. Klein

-

AUSTRALIA
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Marie-Luise Wille

Queensland University of Technology

AUSTRALIA
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Larisa Haupt

Queensland University of Technology

AUSTRALIA
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Gail Risbridger

Professor

MONASH UNIVERSITY

AUSTRALIA
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Mohammad Mirkhalaf

Queensland University of Technology

AUSTRALIA
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Onur Bas

Queensland University of Technology

AUSTRALIA
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Prasad KDV Yarlagadda

Queensland University of Technology

AUSTRALIA
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Julien Clegg

Demonstrator/Teaching assistant

Queensland University of Technology

AUSTRALIA
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Chiara Bastiancich

Assistant Professor (RTD-B)

Università degli Studi di Torino

ITALY
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