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Dr Richard Lobb
Dr

Richard Lobb

Email: 

Overview

Background

I lead the extracellular vesicle (EV) Diagnostics and Therapeutics research theme within the Centre for Personalised Nanomedicine at the Australian Institute for Bioengineering and Nanotechnology (AIBN), University of Queensland. My research aims to transform EVs into precision tools for detecting, monitoring, and treating complex diseases of the brain and body by integrating EV biology, immunology, bioengineering, and nanotechnology.

My group is developing advanced analytical platforms for single-vesicle profiling in blood and other biofluids, enabling tissue-specific EV diagnostics that trace their cellular origin and act as a “molecular GPS” for disease activity throughout the body. In parallel, my program focuses on bioengineering organotropic EVs with targeted delivery capabilities to cross biological barriers and treat neurological disorders and cancer.

Through this work, I aim to advance next-generation EV technologies that provide real-time molecular insights into disease progression and enable new therapeutic strategies for brain cancer, metastatic CNS disease, traumatic brain injury, dementia, chronic traumatic encephalopathy (CTE), and motor neuron disease.

Availability

Dr Richard Lobb is:
Available for supervision

Qualifications

  • Doctor of Philosophy, The University of Queensland

Research interests

  • Extracellular Vesicles

    Clinical interest in extracellular vesicles (EVs) has grown rapidly as accumulating evidence highlights their central role in intercellular communication and systemic regulation. Small EVs, or exosomes, are nanoscale lipid bilayer vesicles (30–150 nm) constitutively secreted by virtually all cell types. They carry a diverse molecular cargo of proteins, lipids, and nucleic acids, including mRNA, miRNA, lncRNA, and both nuclear and mitochondrial DNA, reflecting the physiological state of their cell of origin. Consequently, EVs have emerged as versatile biomarkers and mediators of disease processes, offering new opportunities for diagnostics, prognostics, and therapeutic intervention across oncology, neurodegenerative and traumatic brain disorders, cardiovascular disease, and immune dysregulation. Importantly, tissue-derived EVs are readily detectable in a range of biofluids such as blood, urine, saliva, and cerebrospinal fluid, supporting their utility in minimally invasive “liquid biopsy” approaches for precision health.

  • Therapeutics

    The ability of small EVs to transfer biomolecules between cells highlights their potential in modulating intercellular communication for therapeutic purposes. Small EVs possess natural traits that facilitate effective drug delivery, including their ability to traverse biological barriers and be administered via various routes, offering flexibility in treatment strategies. These inherent advantages can be exploited with precise bioengineering of EV membrane proteins for targeted distribution to specific organs and cell types, improving therapeutic outcomes while minimizing unintended effects. As a result, EVs as an advanced bionanoparticle therapeutic may represent next-generation drug delivery resulting in safer and more effective therapies

Works

Search Professor Richard Lobb’s works on UQ eSpace

33 works between 2014 and 2025

21 - 33 of 33 works

2018

Journal Article

Breast cancer-derived exosomes alter macrophage polarization via gp130/STAT3 signaling

Ham, Sunyoung, Lima, Luize G., Chai, Edna Pei Zhi, Muller, Alexandra, Lobb, Richard J., Krumeich, Sophie, Wen, Shu Wen, Wiegmans, Adrian P. and Moeller, Andreas (2018). Breast cancer-derived exosomes alter macrophage polarization via gp130/STAT3 signaling. Frontiers in Immunology, 9 (MAY) 871, 871. doi: 10.3389/fimmu.2018.00871

Breast cancer-derived exosomes alter macrophage polarization via gp130/STAT3 signaling

2018

Other Outputs

Exosomes in the disease progression of non-small cell lung cancer (NSCLC) patients. Exosomes as biomarkers in NSCLC

Lobb, Richard John (2018). Exosomes in the disease progression of non-small cell lung cancer (NSCLC) patients. Exosomes as biomarkers in NSCLC. PhD Thesis, School of Medicine, The University of Queensland. doi: 10.14264/uql.2018.236

Exosomes in the disease progression of non-small cell lung cancer (NSCLC) patients. Exosomes as biomarkers in NSCLC

2017

Journal Article

Oncogenic transformation of lung cells results in distinct exosome protein profile similar to the cell of origin

Lobb, Richard J., Hastie, Marcus L., Norris, Emma L., van Amerongen, Rosa, Gorman, Jeffrey J. and Möller, Andreas (2017). Oncogenic transformation of lung cells results in distinct exosome protein profile similar to the cell of origin. Proteomics, 17 (23-24) 1600432, 1-10. doi: 10.1002/pmic.201600432

Oncogenic transformation of lung cells results in distinct exosome protein profile similar to the cell of origin

2017

Journal Article

Exosomes derived from mesenchymal non-small cell lung cancer cells promote chemoresistance

Lobb, Richard J., van Amerongen, Rosa, Wiegmans, Adrian, Ham, Sunyoung, Larsen, Jill E. and Moller, Andreas (2017). Exosomes derived from mesenchymal non-small cell lung cancer cells promote chemoresistance. International Journal of Cancer, 141 (3), 614-620. doi: 10.1002/ijc.30752

Exosomes derived from mesenchymal non-small cell lung cancer cells promote chemoresistance

2017

Journal Article

An electrochemical method for the detection of disease-apecific exosomes

Yadav, Sharda, Boriachek, Kseniia, Islam, Md Nazmul, Lobb, Richard, Moller, Andreas, Hill, Michelle M., Hossain, Md Shahriar Al, Nguyen, Nam-Trung and Shiddiky, Muhammad J. A. (2017). An electrochemical method for the detection of disease-apecific exosomes. ChemElectroChem, 4 (4), 967-971. doi: 10.1002/celc.201600391

An electrochemical method for the detection of disease-apecific exosomes

2017

Journal Article

Unique molecular profile of exosomes derived from primary human proximal tubular epithelial cells under diseased conditions

Wang, Xiangju, Wilkinson, Ray, Kildey, Katrina, Potriquet, Jeremy, Mulvenna, Jason, Lobb, Richard J., Moller, Andreas, Cloonan, Nicole, Mukhopadhyay, Pamela, Kassianos, Andrew J. and Healy, Helen (2017). Unique molecular profile of exosomes derived from primary human proximal tubular epithelial cells under diseased conditions. Journal of Extracellular Vesicles, 6 (1) 1314073, 1314073-1314073. doi: 10.1080/20013078.2017.1314073

Unique molecular profile of exosomes derived from primary human proximal tubular epithelial cells under diseased conditions

2017

Journal Article

Exosomes: key mediators of metastasis and pre-metastatic niche formation

Lobb, Richard J., Lima, Luize G. and Moller, Andreas (2017). Exosomes: key mediators of metastasis and pre-metastatic niche formation. Seminars in Cell and Developmental Biology, 67, 3-10. doi: 10.1016/j.semcdb.2017.01.004

Exosomes: key mediators of metastasis and pre-metastatic niche formation

2017

Book Chapter

Size exclusion chromatography: a simple and reliable method for exosome purification

Lobb, Richard and Moller, Andreas (2017). Size exclusion chromatography: a simple and reliable method for exosome purification. Extracellular vesicles: methods and protocols. (pp. 105-110) edited by Winston Patrick Kuo and Shidong Jia. New York, NY, United States: Humana Press. doi: 10.1007/978-1-4939-7253-1_9

Size exclusion chromatography: a simple and reliable method for exosome purification

2016

Journal Article

The biodistribution and immune suppressive effects of breast cancer-derived exosomes

Wen, Shu Wen, Sceneay, Jaclyn, Lima, Luize Goncalves, Wong, Christina S. F., Becker, Melanie, Krumeich, Sophie, Lobb, Richard J., Castillo, Vanessa, Wong, Ke Ni, Ellis, Sarah, Parker, Belinda S. and Moller, Andreas (2016). The biodistribution and immune suppressive effects of breast cancer-derived exosomes. Cancer Research, 76 (23), 6816-6827. doi: 10.1158/0008-5472.CAN-16-0868

The biodistribution and immune suppressive effects of breast cancer-derived exosomes

2016

Journal Article

Radiotherapy for non-small cell lung cancer induces DNA damage response in both irradiated and out-of-field normal tissues

Siva, Shankar, Lobachevsky, Pavel, MacManus, Michael P., Kron, Tomas, Möller, Andreas, Lobb, Richard J., Ventura, Jessica, Best, Nickala, Smith, Jai, Ball, David and Martin, Olga A. (2016). Radiotherapy for non-small cell lung cancer induces DNA damage response in both irradiated and out-of-field normal tissues. Clinical Cancer Research, 22 (19), 4817-4826. doi: 10.1158/1078-0432.CCR-16-0138

Radiotherapy for non-small cell lung cancer induces DNA damage response in both irradiated and out-of-field normal tissues

2015

Conference Publication

Purification and Analysis of Exosomes Derived From Primary Human Proximal Epithelial Cells (Ptec)

Wang, X., Kassianos, A. J., Potriquet, J., Lobb, R., Wilkinson, R. and Healy, H. (2015). Purification and Analysis of Exosomes Derived From Primary Human Proximal Epithelial Cells (Ptec). 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, Australia, 7-9 September 2015. HOBOKEN: WILEY-BLACKWELL.

Purification and Analysis of Exosomes Derived From Primary Human Proximal Epithelial Cells (Ptec)

2015

Journal Article

Optimized exosome isolation protocol for cell culture supernatant and human plasma

Lobb, Richard J., Becker, Melanie, Wen, Shu Wen, Wong, Christina S. F., Wiegmans, Adrian P., Leimgruber, Antione and Moller, Andreas (2015). Optimized exosome isolation protocol for cell culture supernatant and human plasma. Journal of Extracellular Vesicles, 4 (1) 27031, 27031. doi: 10.3402/jev.v4.27031

Optimized exosome isolation protocol for cell culture supernatant and human plasma

2014

Journal Article

Exosomes in cancer metastasis: Novel targets for diagnosis and therapy?

Wen, Shu Wen, Lobb, Richard and Moller, Andreas (2014). Exosomes in cancer metastasis: Novel targets for diagnosis and therapy?. Cancer Forum, 38 (2), 116-120.

Exosomes in cancer metastasis: Novel targets for diagnosis and therapy?

Funding

Current funding

  • 2025 - 2029
    Across the blood-brain barrier: digital profiling of circulating brain-derived extracellular vesicles to monitor primary brain cancer and brain metastases
    NHMRC Investigator Grants
    Open grant
  • 2022 - 2025
    nanoIMPAC: Monitoring immune toxicities and tumour immune evasion in lung cancer
    Cancer Australia
    Open grant

Past funding

  • 2024
    Liquid Biopsy array platform to monitor GBM Progression (The Mark Hughes Foundation grant administered by The University of Newcastle)
    University of Newcastle
    Open grant
  • 2021 - 2024
    Can the brain's immune cell be used to track treatment response in high-grade glioma? (University of Newcastle led Mark Huges Foundation Brain Cancer Innovation Project Grant)
    University of Newcastle
    Open grant
  • 2019 - 2022
    Engineering therapeutic cells for pan-cancer diagnosis and eradication
    CSIRO Synthetic Biology Fellowship
    Open grant

Supervision

Availability

Dr Richard Lobb is:
Available for supervision

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Available projects

  • A New Window into the Brain: Profiling Extracellular Vesicles for Neuro-Oncology

    Establish a liquid biopsy approach for brain cancer by mapping the molecular phenotype of blood-derived EVs from brain-resident cells. This project leverages tissue-specific EV markers and multiplexed nanotechnologies to enable minimally invasive monitoring of glioblastoma, brain metastases, and neuroinflammation.

  • Advanced Bionanoparticle Engineering for Therapeutics

    Develop next-generation extracellular vesicle (EV) engineering strategies for targeted therapeutic delivery. This project focuses on the design and functionalisation of EVs and synthetic mimetics, integrating bio-orthogonal chemistry, surface display technologies, and therapeutic cargo loading to optimise delivery to tumours and inflamed tissues.

  • Unravelling EV-Mediated Intercellular Communication in Health and Disease

    Investigate the functional roles of EVs in modulating recipient cell behaviour. This project combines controlled EV isolation with advanced in vitro/ in vivo models to dissect how EV cargo influences signalling pathways, immune responses, and cellular plasticity in the context of cancer and injury.

  • Multiplexed Nanotechnology for EV Analysis and Diagnostics

    Design and apply cutting-edge nanostructures—including nanopillar arrays and barcoded nanoparticles—for high-sensitivity EV capture and molecular profiling. This platform supports multi-marker EV analysis in clinical biospecimens, with applications in early detection, disease monitoring, and precision medicine.

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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