MIRF research output · UBC

Research at MIRF.

We use quantitative preclinical PET, SPECT and CT to study how radiotracers, antibodies, nanoparticles and lipid-based drug carriers behave inside living systems — supporting theranostics, drug delivery, nanomedicine and translational pharmacology research at UBC and beyond.

63peer-reviewed papers
10+research areas
17+collaborating groups

What we can study.

The areas below represent some of our most common research applications, but they are far from exhaustive. MIRF specializes in quantitative molecular imaging, combining multi-isotope SPECT, PET and CT with biodistribution, pharmacokinetic, and therapy-efficacy studies to generate robust in vivo data. Because every scan produces quantitative measurements rather than simply anatomical images, we can investigate a wide range of questions related to drug delivery, target engagement, therapeutic response, and biological function in living systems.

Theranostics & Dosimetry

Development and evaluation of imaging-guided radionuclide therapies, including quantitative imaging, dosimetry calculations, and characterization of matched diagnostic–therapeutic isotope pairs.

Therapy Efficacy & Biodistribution

Assessment of therapeutic response through longitudinal imaging, survival studies, and quantitative whole-body biodistribution, enabling treatment effects to be monitored over time within the same animal model.

Radiolabeled Nanomedicine

In vivo tracking of gold, lipid, polymeric, and other nanoparticle-based platforms to characterize biodistribution, clearance pathways, target accumulation, and therapeutic delivery.

Drug Delivery & Pharmacokinetics

Quantitative evaluation of small molecules, biologics, antibodies, peptides, and inhaled therapeutics, supporting preclinical drug-development and translational research programs.

Imaging Methods & Multi-Tracer Studies

Development of advanced imaging methodologies, including dual-isotope and multi-tracer protocols, quantitative reconstruction, calibration strategies, phantom validation, and image-analysis workflows.

First to image — and quantify — new isotopes

Through a longstanding collaboration with TRIUMF, MIRF plays a leading role in evaluating the in vivo imaging potential of newly available radioisotopes. Many of these non-conventional radionuclides exhibit complex decay characteristics—including multiple gamma emissions and in-growing daughter products—that challenge accurate detection and quantification. MIRF develops and validates the required imaging protocols, including energy-window optimization, calibration, reconstruction, quantitative analysis, and dosimetry, to establish their feasibility for preclinical research. Recent achievements include the first preclinical imaging of 165Er and the first in vivo quantitative imaging studies of 226Ac and 197g/mHg. See the publications →

Beyond these applications

These examples represent only a subset of the studies supported by MIRF. Our quantitative imaging platform can be adapted to address diverse biological and therapeutic questions across oncology, immunology, neuroscience, cardiology, infectious disease, and drug development. If a molecule, cell, nanoparticle, or therapeutic agent can be labelled, there is a strong possibility it can be tracked, quantified, and studied in vivo.

Watch a tracer move through the body.

Static images reveal where a tracer accumulates; dynamic imaging reveals how it moves through the body over time. This SPECT/CT time-course follows the biodistribution of a radiotracer after oral administration, providing a quantitative 4D view of tracer uptake, distribution, and clearance—one of the key advantages of preclinical molecular imaging.

Watch a radiotracer move through the digestive system over time, revealing its transit, distribution, and eventual elimination. Use the controls to replay or navigate through the sequence.

What preclinical imaging makes possible.

Six flagship studies highlighting the range of MIRF-supported research, including nanomedicine, pulmonary delivery, dual-tracer imaging, targeted alpha therapy, and image-based dosimetry. In each case, quantitative PET/SPECT/CT imaging was central to providing the critical measurement for deriving the biological and therapeutic insights. Each card links to the corresponding publication.

In vivo biodistribution imaging of lipid nanoparticles from the Cullis-lab mRNA-delivery study. 2025 · Nanomedicine
111InSPECT/CTNanomedicine

Lipid nanoparticles that reach beyond the liver

A new liposomal lipid-nanoparticle design delivers mRNA to tissues beyond the liver. We radiolabelled the particles with 111In and followed them by quantitative SPECT/CT, revealing a roughly 15-fold longer circulation and broader organ uptake than conventional LNPs — cross-validated against ex vivo gamma counting.

Collaborators: Prof. P. Cullis (Life Sciences); Profs. Miffy Cheng and U. Häfeli (UBC Pharm Sci).
Read the paper
Side-by-side SPECT/CT images of the matched terbium-155 (imaging) and terbium-161 (therapy) crown-TATE pair in tumour-bearing mice. 2023 · Theranostic imaging
155Tb161TbSPECT/CTTheranostics

Matched terbium isotopes: image, then treat

Crown-TATE labelled with matched terbium isotopes — 155Tb to image, 161Tb to treat. Longitudinal SPECT/CT showed rapid, receptor-specific tumour uptake and that the diagnostic and therapeutic isotopes behave identically, so the scan reliably predicts where the therapy will act.

Collaborators: H. Yang, PhD (TRIUMF); Prof. F. Bénard (BC Cancer).
Read the paper
Imaging and biodistribution figure from the 225Ac-crown-TATE targeted alpha-therapy study (MIRF). 2024 · Targeted α-therapy
225Acα-therapyDosimetry

Alpha-emitting 225Ac-crown-TATE for neuroendocrine tumours

The same tumour-targeting molecule armed with the alpha-emitter 225Ac. Ex vivo biodistribution and MIRD dosimetry showed the highest absorbed dose went to the tumour, with significantly longer survival in treated mice. The imaging arm comes from its diagnostic partner (the 155Tb pair) — an imaging-guided path to therapy.

Collaborators: H. Yang, PhD (TRIUMF); Prof. F. Bénard (BC Cancer).
Read the paper
Award-winning SPECT/CT image showing where 111In-labelled nanoparticles deposit in the mouse lungs across different pulmonary administration routes. 2020 · Inhaled delivery Image of the Year 2020
111InSPECT/CTDrug delivery

Which way into the lung? Imaging settles it

Comparing how inhaled drugs reach the lung is notoriously hard to quantify by conventional analytical methods. By 111In-labelling the nanoparticles and mapping them with quantitative SPECT/CT, we ranked three routes in vivo: intratracheal instillation placed ~95% of the dose in the lungs and spraying ~88%, while intranasal delivery reached only ~29% — the rest ending up in the stomach. The resulting image was a co-winner of the 2020 MILabs Image of the Year Award.

Collaborators: Prof. U. Häfeli (UBC Pharm Sci); M. Yang (Wuya College of Innovation, Shenyang Pharmaceutical University & Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen).
Read the paper
2018 · Methods
111In67GaDual-tracer SPECTPharmacokinetics

Two tracers, one scan

We developed and validated simultaneous dual-isotope (111In + 67Ga) SPECT/CT, tracking two radiopharmaceuticals in the same animal at once — perfectly co-registered in space and time, with quantification errors under 20%. In a proof-of-concept, two co-injected agents’ pharmacokinetics were measured independently in a single mouse.

Collaborators: Profs. U. Häfeli (UBC Pharm Sci) and Vesna Sossi (UBC, Physics and Astronomy).
Read the paper
Quantitative 188Re SPECT/CT dosimetry image from the radioembolization study (MIRF). 2019 · Dosimetry
188ReSPECT/CTRadioembolization

Radioembolization with built-in dosimetry

Biodegradable 188Re-labelled microspheres for liver-tumour radioembolization. Because 188Re also emits a gamma photon, quantitative SPECT/CT mapped where the spheres lodged and how long they stayed — producing absorbed-dose maps showing the tumour received three-to-six times the dose of healthy liver. The therapy reports its own dose.

Collaborators: Prof. U. Häfeli.
Read the paper

63 peer-reviewed papers from MIRF and collaborators.

From 197Hg SPECT to 177Lu nanoparticle theranostics, our publications span 2014–2026 across radiochemistry, drug delivery, theranostics and methods development. The full filterable list is one click away.

Browse all publications
2025 Liposomal lipid nanoparticles for extrahepatic delivery of mRNA
Cheng MHY, Rodríguez-Rodríguez C, et al. · Nature Communications
2025 Quantitative dual-isotope SPECT/CT of the mercury-197m/g theranostic pair
Randhawa P, Rodríguez-Rodríguez C, et al. · EJNMMI Radiopharm. Chem.
2024 226Ac as a theranostic agent: imaging, dosimetry & therapy
Koniar H, Rodríguez-Rodríguez C, et al. · J. Nucl. Med.

Build your imaging skills.

Separate from our research program, MIRF also runs hands-on training in preclinical PET/SPECT and imaging data analysis — open to graduate students, postdocs and visiting researchers.

  UBC · MIRF

Preclinical imaging, taught by the people who do it every day.

Two workshop tracks — an introductory course covering preclinical imaging, the imaging modalities, and the principles of PET, SPECT and CT; and a hands-on imaging data analysis workshop on visualization, quantification and reporting.

  • Introduction to Preclinical Imaging
  • Imaging Data Analysis Workshop
See training & workshops

Have a molecule, a compound, or a question? Bring it to MIRF.

We collaborate with academic labs, biotech, radiopharma and translational research groups across Canada and internationally. Whether you need a single experiment or a multi-year project, we'll talk through the right approach.