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Canadian Nanomedicine Expertise Database

As part of its legacy, the NanoMedicines Innovation Network (NMIN) developed this online database of Canadian nanomedicine researchers and the areas of expertise represented within their labs. The database is intended as a tool to facilitate collaboration among nanomedicine researchers and labs—within and beyond the NMIN Network, now and in the future.

The database can be searched by keyword in any or all fields.

If you are an established Canadian professional with expertise related to nanomedicine research and/or innovation, please take ~5 minutes to complete this brief survey and be included in this database.

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AllInstitutionResearcherNanodelivery typeTargeting approachApplicationDisease modelProtocolsInstrumentationAuxilliary expertise

Researcher: Mohsen Akbari

Institution: University of Victoria

Nanodelivery type

  • Polymer-based

Targeting approach

  • Physical targeting: pH sensitive; Temperature sensitive; Light sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Cancer (In vitro, Organoid, Primary cells)
  • Other: wound healing (In vitro, Organoid, In vivo: Mouse and pig models)

Protocols: Microfluidics

University of Victoria

Mohsen Akbari

Polymer-based

Physical targeting

pH sensitive

Temperature sensitive

Light sensitive

Drug delivery

Soluble molecules

Insoluble molecules

Cancer

Other     Wound healing

In vitro

Organoid

In vivo

Mouse and pig models

In vitro

Organoid

Primary cells

Microfluidics

Researcher: Russ Algar

Institution: University of British Columbia

Nanodelivery type

  • Polymer-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Aptamer

Application

  • Nano-imaging: Diagnostics; Fluorescent imaging
  • Other: Biosensors, Assays, Molecular Diagnostics

Disease model(s)

  • Cancer (In vitro)
  • Heart failure (In vitro)

Protocols: Microfluidics; Other (3D printing, device development, nanoparticle surface chemistry and bioconjugation; suite of steady-state and time-resolved optical spectroscopies; nanoparticle tracking analysis; single-molecule/particle fluorescence imaging)

University of British Columbia

Russ Algar

Polymer-based
Inorganic

Active targeting: Antibody or antibody fragments, Peptide, Aptamer

Nano-imaging:

Diagnostics

Fluorescent imaging

Other:

Biosensors, Assays, Molecular Diagnostics

Cancer In vitro

Heart failure In vitro

Microfluidics

Other:

3D printing, device development, nanoparticle surface chemistry and bioconjugation

Suite of steady-state and time-resolved optical spectroscopies, nanoparticle tracking analysis, single-molecule/particle fluorescence imaging

Researcher: Theresa M Allen

Institution: University of Alberta / University of British Columbia (UBC)

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Small molecule
  • Physical targeting: pH sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: mRNA/samRNA; ASO
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)

Protocols: Safety/pharmacology

University of Alberta / University of British Columbia (UBC)

Theresa M Allen

Lipid-based

Polymer-based

Active targeting: Antibody or antibody fragments; Peptide; Small molecule

Physical targeting: pH sensitive

Drug delivery: Soluble molecules; Insoluble molecules

Gene delivery: mRNA/samRNA; ASO

Peptide/protein delivery

Cancer (In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)

Safety/pharmacology

Researcher: Ildiko Badea

Institution: University of Saskatchewan

Nanodelivery type

  • Lipid-based
  • Inorganic

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Drug delivery
  • Gene delivery: DNA, siRNA
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo xenograft model, In vivo orthotopic model)

Instrumentation: Synchrotron techniques

Auxiliary expertise: Other: Human research ethics

University of Saskatchewan

Ildiko Badea

Lipid-based Inorganic

Physical targeting: pH sensitive

Drug delivery
Gene delivery: DNA, siRNA
Peptide/protein delivery

Cancer (In vitro, Organoid, In vivo xenograft model, In vivo orthotopic model)

Synchrotron techniques

Other: Human research ethics

Researcher: Marcel Bally

Institution: BC Cancer Research Centre; University of British Columbia

Nanodelivery type

  • Lipid-based
  • Other: peptide/protein

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo PDX model, In vivo syngeneic model, In vivo metastatic model, Primary cells, Human)
  • Infectious diseases: viral infections – BioSafety Level 2, BioSafety Level 3, In vitro (cells), In vivo (rodent)
  • Other: neurodegenerative diseases (In vitro, Organoid, In vivo: Alzheimer’s mice, lung injury models)

Protocols: Safety/pharmacology (Pre-GLP toxicity, GLP testing); Microfluidics; Pre-GMP & GMP manufacturing

Instrumentation: Everything needed for formulation characterization except cryo EM

Auxiliary expertise: Non-nano delivery systems; Regulatory science

BC Cancer Research Centre; University of British Columbia

Marcel Bally

Lipid-based

Other

peptide/protein

Active targeting

Antibody or antibody fragments

Peptide

Drug delivery

Soluble molecules

Insoluble molecules

Cancer

Infectious diseases

Viral infections

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo PDX model

In vivo syngeneic model

In vivo metastatic model

Primary cells

Human

BioSafety Level 2

BioSafety Level 3

In vitro (cells)

In vivo (rodent)

Safety/pharmacology

Microfluidics

Pre-GMP & GMP manufacturing

Pre-GLP toxicity

GLP testing

Everything needed for formulation characterization except cryo EM

Regulatory science

Non-nano delivery systems

Researcher: Louis-Philippe Bernier

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Gene delivery: mRNA/samRNA

Disease model(s)

  • Other: Neurological diseases; in vivo (rodent models)

Protocols: Safety/pharmacology (Pre-GLP toxicity)

University of British Columbia

Louis-Philippe Bernier

lipid-based

physical

pH sensitive

gene delivery

mRNA/samRNA

Neurological diseases
in vivo
rodent models

Safety/pharmacology

Pre-GLP toxicity

Researcher: Nicolas Bertrand

Institution: Laval University

Nanodelivery type

  • Polymer-based
  • Lipid-based

Targeting approach

  • Active targeting

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, Primary cells)
  • Other: Chronic kidney disease (In vivo: rat/mouse)

Protocols: Safety/pharmacology (Pre-GLP toxicity)

Laval University

Nicolas Bertrand

Lipid-based

Polymer-based

Active targeting

Drug delivery

Soluble molecules

Insoluble molecules

Cancer

Other

Chronic kidney disease

In vivo

Rats and mice

In vitro

In vivo xenograft model

Primary cells

Safety/pharmacology

Pre-GLP toxicity

Researcher: Anna Blakney

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Physical targeting: pH sensitive; Other (charge)

Application

  • Drug delivery: Soluble molecules
  • Gene delivery: mRNA/samRNA
  • Nano-imaging: Fluorescent imaging

Disease model(s)

  • Cancer (In vitro; In vivo xenograft model)
  • Infectious diseases: Viral infections; Bacterial infections; BioSafety Level 2; In vitro (cells); In vivo (rodent)

Protocols: Safety/pharmacology; Microfluidics

University of British Columbia

Anna Blakney

Lipid-based

Polymer-based

Physical targeting

pH sensitive

Other: charge

Drug delivery

Soluble molecules

Gene delivery

mRNA/samRNA

Nano-imaging

Fluorescent imaging

Cancer

In vitro

In vivo xenograft model

Infectious diseases

Viral infections

Bacterial infections

BioSafety Level 2

In vitro (cells)

In vivo (rodent)

Safety/pharmacology

Microfluidics

Researcher: Davide Brambilla

Institution: Université de Montréal

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Active targeting: Peptide; Aptamer

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, mRNA/samRNA

Disease model(s)

  • Rare diseases (In vitro; In vivo: Rodents)
  • Other: inflammatory diseases (In vitro; In vivo: Rodents)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics

Auxiliary expertise: Non-nano delivery systems; Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

Université de Montréal2

Davide Brambilla

Lipid-based

Polymer-based

Active targeting

Peptide

Aptamer

Drug delivery

Gene delivery

Soluble molecules

Insoluble molecules

DNA

mRNA/samRNA

Rare diseases

Other

Inflammatory diseases

In vitro

In vivo

Rodents

Safety/pharmacology

Microfluidics

Pre-GLP toxicity

Non-nano delivery systems

Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

Researcher: Warren Chan

Institution: University of Toronto

Nanodelivery type

  • LIpid-based
  • Polymer-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide
  • Physical targeting: Other (looking at the mechanism of targeting)

Application

  • Drug delivery: Soluble molecules
  • Gene delivery: siRNA, mRNA/samRNA

Disease model(s)

  • Cancer (In vivo xenograft model, In vivo orthotopic model, In vivo PDX model, In vivo syngeneic model, In vivo metastatic model)

Auxiliary expertise: We are mostly working on the mechanism of targeted delivery, rather than attempting to target for therapeutic purposes.

University of Toronto

Warren Chan

Lipid-based
Polymer-based
Inorganic

Active targeting
Physical targeting
Other

Antibody or antibody fragments
Peptide

Drug delivery
Gene delivery

Soluble molecules

siRNA
mRNA/samRNA

Cancer

We are mostly working on the mechanism of targeted delivery, rather than attempting to target for therapeutic purposes.

Researcher: Devika Chithrani

Institution: University of Victoria

Nanodelivery type

  • Lipid-based-based
  • Inorganic

Targeting approach

  • Active targeting: Peptide

Application

  • Other: Use of nanoparticles for improving radiosensitsation

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo syngeneic model)

Protocols: Safety/pharmacology: Pre-GLP toxicity

Instrumentation: A magnetic lens system to separate co-cultured cells

University of Victoria

Devika Chithrani

Lipid-based

Inorganic

Active targeting

Peptide

Other

Use of nanoparticles for improving radiosensitsation

Cancer

In vitro

In vivo xenograft model

In vivo syngeneic model

Safety/pharmacology

Pre-GLP toxicity

A magnetic lens system to separate co-cultured cells

Researcher: Marco Ciufolini

Institution: University of British Columbia (UBC); NanoVation Therapeutics

Nanodelivery type

  • Lipid-based

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Gene delivery: DNA; siRNA; mRNA/samRNA

Disease model(s)

  • Cancer
  • Rare diseases
  • Infectious diseases: Viral infections

Protocols: Other: synthetic organic chemistry

University of British Columbia; NanoVation Therapeutics

Marco Ciufolini

Lipid-based

Physical targeting

pH sensitive

Gene delivery DNA siRNA mRNA/samRNA

Cancer Rare diseases Infectious diseases Viral infections

Other synthetic organic chemistry

Researcher: Michael Doschak

Institution: University of Alberta

Nanodelivery type

  • Other: Metal oxide nanoparticle contrast agents

Targeting approach

  • Active targeting: Small molecule

Application

  • Drug delivery: Soluble molecules
  • Peptide/protein delivery
  • Nano-imaging: Theranostics; Fluorescent imaging; Other (Micro-CT and Micro-MRI)

Disease model(s)

  • Cancer (In vitro, In vivo metastatic model)
  • Arthritis (In vivo: post-traumatic OA models after ACL-transection and/or medial meniscectomy)
  • Other: osteoporosis (In vitro, In vivo: mouse, rat, rabbit)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Other (bone dynamic labels; Quantitative image analysis for bone volume and bone mineral density)

Instrumentation: in-vivo micro-CT; Bone electron probe microanalysis (EPMA)

Auxiliary expertise: Non-nano delivery systems; Regulatory science

University of Alberta

Michael Doschak

Other

Metal oxide nanoparticle contrast agents

Active targeting

Small molecule

Drug delivery

Peptide/protein delivery

Nano-imaging

Soluble molecules

Theranostics

Fluorescent imaging

Other

Micro-CT and Micro-MRI

Cancer

Arthritis

Other

Osteoporosis

In vitro

In vivo

mouse, rat, rabbit

In vitro

In vivo metastatic model

In vivo

post-traumatic OA models after ACL-transection and/or medial meniscectomy

Safety/pharmacology

Other

Pre-GLP toxicity bone dynamic labels; Quantitative image analysis for bone volume and bone mineral density

in-vivo micro-CT; Bone electron probe microanalysis (EPMA)

Regulatory science

Non-nano delivery systems

Researcher: Richard Epand

Institution: McMaster University

Nanodelivery type

  • LIpid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments

Application

  • Drug delivery: Insoluble molecules

Disease model(s)

  • Cancer (In vitro)
  • Rare diseases (In vitro)

Protocols: Safety/pharmacology

Instrumentation: Circular dichroism

Auxiliary expertise: Regulatory science

McMaster University

Richard Epand

Lipid-based

Active targeting

Antibody or antibody fragments

Drug delivery

Insoluble molecules

Cancer

Rare diseases

In vitro

In vitro

Safety/pharmacology

Circular dichroism

Regulatory science

Researcher: Joel Finbloom

Institution: University of British Columbia

Nanodelivery type

  • Polymer-based
  • Other: Peptide self-assembly

Targeting approach

  • Physical targeting: pH sensitive; Other (Enzyme activation; Dynamic bioconjugation)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Infectious diseases: Bacterial infections – BioSafety Level 2, In vitro (cells), In vivo (rodent)
  • Other: GI disorders (IBD) (In vitro, Organoid, In vivo: Colitis mouse model)

Auxiliary expertise: Non-nano delivery systems; Other: Bioconjugation chemistry

University of British Columbia

Joel Finbloom

Polymer-based

Other

Peptide self-assembly

Physical targeting

Other

pH sensitive

Enzyme activation. Dynamic bioconjugation

Drug delivery

Soluble molecules

Insoluble molecules

Infectious diseases

Other

Bacterial infections

GI disorders (IBD)

In vitro

Organoid

In vivo

Colitis mouse model

BioSafety Level 2

In vitro (cells)

In vivo (rodent)

Non-nano delivery systems

Other

Bioconjugation chemistry

Researcher: Marianna Foldvari

Institution: University of Waterloo

Nanodelivery type

  • Lipid-based
  • Other: surfactant and carbon nanomaterials

Targeting approach

  • Other: Peptides

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, mRNA/samRNA
  • Peptide/protein delivery

Disease model(s)

  • Other: neurodegenerative diseases – In vitro, In vivo: retinal diseases (glaucoma), skin diseases (scleroderma/morphoea)

Protocols: Pre-GMP & GMP manufacturing

Auxiliary expertise: Non-nano delivery systems

University of Waterloo

Marianna Foldvari

Lipid-based

Other

surfactant and carbon nanomaterials

Other

peptides

Drug delivery

Gene delivery

Peptide/protein delivery

Soluble molecules

Insoluble molecules

DNA

mRNA/samRNA

Other

neurodegenerative diseases

In vitro

In vivo”  retinal diseases (glaucoma), skin diseases (scleroderma/morphoea)

Pre-GMP & GMP manufacturing

Non-nano delivery systems

Researcher: Marc-André Fortin

Institution: Laval University

Nanodelivery type

  • Inorganic
  • Other: hydrogels, nanoparticle-eluting hydrogels

Targeting approach

  • Active targeting: Antibody or antibody fragments; Small molecule

Application

  • Nano-imaging: Diagnostics; Theranostics; PET; Other (MRI contrast agents, radiosensitization compounds for radio-oncology)
  • Other: MRI-visible inks for bioprinting and tissue engineering applications; radiosensitization compunds for radiooncology

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo xenograft model, In vivo orthotopic model)
  • Diabetes (Organoid)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Other: Relaxometry of MRI contrast agents, PET-operated Franz diffusion cells (for measuring diffusion coefficients of NPs across membranes)

Instrumentation: Relaxometric analysis of MRI contrast agents, PET biodistribution, 3D printing infrastructure (including bioprinting)

Auxiliary expertise: Non-nano delivery systems

Laval University

Marc-André Fortin

Inorganic

Other

hydrogels, nanoparticle-eluting hydrogels

Active targeting

Antibody or antibody fragments

Small molecule

Nano-imaging

Other

Diagnostics

Theranostics

PET

Other

MRI-visible inks for bioprinting and tissue engineering applications; radiosensitization compunds for radiooncology

MRI contrast agents, radiosensitization compounds for radio-oncology

Cancer

Diabetes

In vitro

Organoid

In vivo xenograft model

In vivo orthotopic model

Organoid

Safety/pharmacology

Other

Pre-GLP toxicity

Relaxometry of MRI contrast agents, PET-operated Franz diffusion cells (for measuring diffusion coefficients of NPs across membranes)

Relaxometric analysis of MRI contrast agents, PET biodistribution, 3D printing infrastructure (including bioprinting)

Non-nano delivery systems

Researcher: Marc A Gauthier

Institution: Institut National de la Recherche Scientifique

Nanodelivery type

  • Polymer-based

Targeting approach

  • Active Targeting: Antibody or antibody fragments; Peptide; Aptamer
  • Physical Targeting: pH sensitive; Temperature sensitive; Other (ROS; Enzymes; Thiol-Disulfide; etc.)

Application

  • Drug delivery: Soluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, Primary cells)
  • Other: several diseases (In vitro, In vivo)

Auxiliary expertise: Non-nano delivery systems

Institut National de la Recherche Scientifique

Marc A Gauthier

Polymer-based

Active Targeting: Antibody or antibody fragments; Peptide; Aptamer
Physical Targeting: pH sensitive; Temperature sensitive; Other (ROS; Enzymes; Thiol-Disulfide; etc.)

Drug delivery: Soluble molecules
Peptide/protein delivery

Cancer (In vitro, In vivo xenograft model, Primary cells)

Other: several diseases (In vitro, In vivo)

Non-nano delivery systems

Researcher: Azita Haddadi

Institution: University of Saskatchewan

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide
  • Physical targeting: temperature sensitive, light sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, Primary cells)
  • Heart failure (In vitro)
  • Infectious diseases: Viral infections – BioSafety Level 2; In vitro (cells), In vivo (rodent), In vivo (larger animals)

Auxiliary expertise: Non-nano delivery systems

University of Saskatchewan

Azita Haddadi

Lipid-based
Polymer-based

Active targeting: Antibody or antibody fragments; Peptide

Physical targeting: temperature sensitive, light sensitive

Drug delivery: Soluble molecules; Insoluble molecules

Peptide/protein delivery

Cancer (In vitro, In vivo xenograft model, Primary cells)

Heart failure (In vitro)

Infectious diseases: Viral infections – BioSafety Level 2; In vitro (cells), In vivo (rodent), In vivo (larger animals)

Non-nano delivery systems

Researcher: Andrew Halayko

Institution: University of Manitoba

Nanodelivery type

  • Lipid-based

Application

  • Drug delivery: Soluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Diabetes (In vitro, In vivo: mouse/rat)
  • Infectious diseases: Viral infections (In vitro, In vivo, Biosafety level 3)
  • Other: Inflammatory lung disease – asthma, COPD (In vitro, In vivo: mouse)

Instrumentation: Pulmonary function assessing small animals, as well as optical in vivo imaging

Auxiliary expertise: Other: We offer animal and cell models in which to test nano-vectors

University of Manitoba

Andrew Halayko

Lipid-based

Drug delivery

Peptide/protein delivery

Soluble molecules

Diabetes

Infectious diseases

Other

Viral infections

Inflammatory lung disease – asthma, COPD

In vitro

In vivo

Mouse

In vivo

Mouse / rat

In vitro

In vivo

Biosafety level 3

Pulmonary function assessing small animals, as well as optical in vivo imaging

We offer animal and cell models in which to test nano- vectors

Researcher: Robert Hancock

Institution: University of British Columbia

Nanodelivery type

  • LIpid-based
  • Polymer-based

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Drug delivery: Soluble molecules

Disease model(s)

  • Infectious diseases: Bacterial infections; BioSafety Level 2; In vitro (cells); In vitro (organoids); In vivo (rodent)
  • Other: Inflammation (Organoid; In vivo: skin abscess model; mouse sinusitis model)
University of British Columbia

Robert Hancock

Lipid-based

Polymer-based

Physical targeting

pH sensitive

Drug delivery

Soluble molecules

Infectious diseases

Other

Bacterial infections

Inflammation

Organoid

In vivo

Skin Abscess model; Mouse Sinusitis model

BioSafety Level 2

In vitro (cells)

In vitro (organoids)

In vivo (rodent)

Researcher: Ken Harder

Institution: University of British Columbia (UBC)

Nanodelivery type

  • Lipid-based

Targeting approach

  • Other: 5 or 6 component LNPs for immune cell specific targeting

Application

  • Gene delivery: mRNA/samRNA

Disease model(s)

  • Cancer (In vitro, In vivo syngeneic model, In vivo metastatic model)
  • Other: Alzheimer’s, obesity and atherosclerosis (In vitro, In vivo; mouse models)

Protocols: Other: CyTOF and CITE-seq protein and transcriptomic analysis of LNP targeting

Instrumentation: CyTOF

Auxiliary expertise: Non-nano delivery systems

University of British Columbia (UBC)

Ken Harder

Lipid-based

Other: 5 or 6 component LNPs for immune cell specific targeting

Gene delivery: mRNA/samRNA

Cancer (In vitro, In vivo syngeneic model, In vivo metastatic model)

Other: Alzheimer’s, obesity and atherosclerosis (In vitro, In vivo; mouse models)

Other: CyTOF and CITE-seq protein and transcriptomic analysis of LNP targeting

CyTOF

Non-nano delivery systems

Researcher: Emmanuel Ho

Institution: University of Waterloo

Nanodelivery type

  • Lipid-based
  • Polymer-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Small molecule
  • Physical targeting: pH sensitive; temperature sensitive; light sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro; In vivo xenograft model; In vivo orthotopic model; In vivo metastatic model)
  • Diabetes (In vitro)
  • Rare diseases (In vitro)
  • Infectious diseases: Viral infections; Bacterial infections; BioSafety Level 2; In vitro (cells); In vivo (rodent)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics

Instrumentation: 3D printing, mechanical testing, hot-melt injection molding, microfluidics, microwave sensors

Auxiliary expertise: Non-nano delivery systems

University of Waterloo

Emmanuel Ho

Lipid-based

Polymer-based

Inorganic

Active targeting (e.g., antibody modification of nanomedicine)

Physical targeting (e.g., use of pH sensitive nanomedicine)

Antibody or antibody fragments

Peptide

Small molecule

pH sensitive

Temperature sensitive

Light sensitive

Drug delivery

Gene delivery

Peptide/protein delivery

Soluble molecules

Insoluble molecules

DNA

siRNA

mRNA/samRNA

Cancer

Rare diseases

Diabetes

Infectious diseases

Viral infections

Bacterial infections

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo metastatic model

In vitro

In vitro

BioSafety Level 2

In vitro (cells)

In vivo (rodent)

Safety/pharmacology

Microfluidics

Pre-GLP toxicity

3D printing, Mechanical testing, hot-melt injection molding, microfluidics, microwave sensors

Non-nano delivery systems

Researcher: Umar Iqbal

Institution: National Research Council of Canada

Nanodelivery type

  • Lipid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide
  • Physical targeting: Other (novel lipids and new lipid chemistry)

Application

  • Gene delivery: mRNA/samRNA; ASO

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model, Human)
  • Rare diseases (Human)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics

National Research Council of Canada

Umar Iqbal

Lipid-based

Active targeting: Antibody or antibody fragments; Peptide

Physical targeting: Other (novel lipids and new lipid chemistry)

Gene delivery: mRNA/samRNA; ASO

Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model, Human)

Rare diseases (Human)

Safety/pharmacology (Pre-GLP toxicity); Microfluidics

Researcher: Jonathan Irish

Institution: Princess Margaret Research Institute

Nanodelivery type

  • Lipid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Small molecule

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Nano-imaging: Diagnostics; Theranostics; Fluorescent imaging; PET; SPECT

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo PDX model, In vivo syngeneic model, In vivo metastatic model, Primary cells, Human)

Protocols: Safety/pharmacology (Pre-GLP toxicity, GLP testing); Pre-GMP & GMP manufacturing

Auxiliary expertise: Non-nano delivery systems

Princess Margaret Research Institute

Jonathan Irish

Lipid-based

Active targeting

Antibody or antibody fragments

Small molecule

Drug delivery

Soluble molecules

Insoluble molecules

Nano-imaging

Diagnostics

Theranostics

Fluorescent imaging

PET

SPECT

Cancer

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo PDX model

In vivo syngeneic model

In vivo metastatic model

Primary cells

Human

Safety/pharmacology

Pre-GMP & GMP manufacturing

Pre-GLP toxicity

GLP testing

Non-nano delivery systems

Researcher: Yimei Jia

Institution: National Research Council Canada

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Small molcule
  • Physical targeting: pH sensitive; temperature sensitive
  • Other

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA, ASO
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo syngeneic model, Primary cells)
  • Arthritis (In vitro)
  • Diabetes (In vitro)
  • Infectious diseases: Viral infections; Bacterial infections; BioSafety Level 2; In vitro (cells); In vitro (organoids); In vivo (rodent)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Pre-GMP & GMP manufacturing; Microfluidics

Instrumentation: nanoassemblr ignite

national research council canada

yimei jia

Lipid-based

Polymer-based

Active targeting

Physical targeting

Other

Antibody or antibody fragments

Peptide

pH sensitive

Temperature sensitive

Drug delivery

Gene delivery

Peptide/protein delivery

Soluble molecules

Insoluble molecules

DNA

siRNA

mRNA/samRNA

ASO

Cancer

Arthritis

Diabetes

Infectious diseases

Viral infections

Bacterial infections

In vitro

Organoid

In vivo syngeneic model

Primary cells

In vitro

In vitro

BioSafety Level 2

In vitro (cells)

In vitro (organoids)

In vivo (rodent)

Safety/pharmacology

Microfluidics

Pre-GMP & GMP manufacturing

Pre-GLP toxicity

nanoassemblr ignite

Researcher: Jessica Kalra

Institution: University of British Columbia (UBC)

Nanodelivery type

  • Lipid-based

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Cancer (In vitro, Organoid)
  • Other: Neurological and inflammatory disease (In vitro, Organoid)

Protocols: Microfluidics

Auxiliary expertise: Other: In vivo modelling and imaging

University of British Columbia (UBC)

Jessica Kalra

Lipid-based

Drug delivery: Soluble molecules; Insoluble molecules

Cancer (In vitro, Organoid)

Other: Neurological and inflammatory disease (In vitro, Organoid)

Microfluidics

Other: In vivo modelling and imaging

Researcher: Christian Kastrup

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based
  • Inorganic

Targeting approach

  • Active targeting
  • Physical targeting
  • Other: Lipid and Glyco

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA, ASO

Disease model(s)

  • Cancer (In vivo metastatic model)
  • Rare diseases (In vivo: rodents and large animals; Human)
  • Infectious diseases – bacterial infections: BioSafety Level 2, In vivo (rodent)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics; Pre-GMP & GMP manufacturing

University of British Columbia

Christian Kastrup

Lipid-based
Inorganic

Active targeting
Physical targeting
Other

Lipid and Glyco
Drug delivery
Gene delivery
Soluble molecules
Insoluble molecules
DNA
siRNA
mRNA/samRNA
ASO

Cancer
Rare diseases
Infectious diseases

Bacterial infections
In vivo metastatic model
In vivo
Human
Rodents and Large Animals
BioSafety Level 2
In vivo (rodent)

Safety/pharmacology
Microfluidics
Pre-GMP & GMP manufacturing

Pre-GLP toxicity

Researcher: Marianna Kulka

Institution: Quantum and Nanotechnologies Research Center, University of Alberta

Nanodelivery type

  • Lipid-based
  • Polymer-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments; Aptamer
  • Physical targeting: pH sensitive

Application

  • Drug delivery: Soluble molecules, insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA

Disease model(s)

  • Other: Inflammation (In vitro; human)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics

Quantum and Nanotechnologies Research Center, University of Alberta

Marianna Kulka

Lipid-based Polymer-based Inorganic

Active targeting Physical targeting Antibody or antibody fragments Aptamer pH sensitive

Drug delivery Gene delivery Soluble molecules Insoluble molecules DNA siRNA mRNA/samRNA

Other inflammation In vitro Human

Safety/pharmacology Microfluidics Pre-GLP toxicity

Researcher: Hagar Labouta

Institution: University of Toronto

Nanodelivery type

  • Lipid-based
  • Polymer-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Small molecule
  • Physical targeting: pH sensitive; Temperature sensitive; Light sensitive

Application

  • Drug delivery
  • Gene delivery: siRNA, mRNA/samRNA

Disease model(s)

  • Cancer (In vitro, Organoid)
  • Rare diseases (In vitro, Organoid)
  • Other: Pregnancy-associated diseases (In vitro, Organoid)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics; Other: Organ-on-a-chip

Instrumentation: dynamic flow platform for applying shear stress

University of Toronto

Hagar Labouta

Lipid-based

Polymer-based

Inorganic

Active targeting

Physical targeting

Antibody or antibody fragments

Peptide

Small molecule

pH sensitive

Temperature sensitive

Light sensitive

Drug delivery

Gene delivery

siRNA

mRNA/samRNA

Cancer

Rare diseases

Other

Pregnancy-associated diseases

In vitro

Organoid

Safety/pharmacology

Microfluidics

Other

Pre-GLP toxicity

Organ-on-a-chip

dynamic flow platform for applying shear stress

Researcher: Afsaneh Lavasanifar

Institution: University of Alberta

Nanodelivery type

  • Polymer-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide

Application

  • Drug delivery: Insoluble molecules

Disease model(s)

  • Cancer (In vitro; In vivo xenograft model; In vivo orthotopic model; In vivo metastatic model)

Protocols: Other: Measurement of mucosal permeation and retention of drug delivery systems

Instrumentation: Dynamic Mucosal Retention/Permeation tester

Auxiliary expertise: Non-nano delivery systems

University of Alberta

Afsaneh Lavasanifar

Polymer-based

Active targeting

Antibody or antibody fragments

Peptide

Drug delivery

Insoluble molecules

Cancer

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo metastatic model

Other

Measurement of mucosal permeation and retention of drug delivery systems

Dynamic Mucosal Retention/Permeation tester

Non-nano delivery systems

Researcher: Sabrina Leslie

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based

Targeting approach

  • Physical targeting: pH sensitive; temperature sensitive

Application

  • Drug delivery: Insoluble molecules
  • Peptide/protein delivery
  • Nano-imaging: Fluorescent imaging

Disease model(s)

  • Cancer (In vitro)
  • Rare diseases (In vitro)

Protocols: Microfluidics; Other (Single-molecule and single-particle microscopy)

Instrumentation: Convex Lens-induced Confinement (CLiC)

Auxiliary expertise: Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

University of British Columbia

Sabrina Leslie

Lipid-based

Physical targeting

pH sensitive

Temperature sensitive

Drug delivery

Peptide/protein delivery

Nano-imaging

Insoluble molecules

Fluorescent imaging

Cancer

Rare diseases

In vitro

In vitro

Microfluidics

Other

Single-molecule and single-particle microscopy

Convex Lens-induced Confinement (CLiC)

Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

Researcher: Alex Leung

Institution: Evonik Canada

Nanodelivery type

  • Lipid-based

Application

  • Drug delivery
  • Gene delivery: siRNA, mRNA/samRNA

Protocols: Microfluidics; Pre-GMP & GMP manufacturing

Evonik Canada

Alex Leung

Lipid-based

Drug delivery Gene delivery siRNA mRNA/samRNA

Microfluidics Pre-GMP & GMP manufacturing

Researcher: Sherry Leung

Institution: Precision NanoSystems

Nanodelivery type

  • Lipid-based

Application

  • Gene delivery

Protocols: Microfluidics

Precision NanoSystems

Sherry Leung

Lipid-based

Gene therapy

Microfluidics

Researcher: Bowen Li

Institution: University of Toronto

Nanodelivery type

  • Lipid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Small molecule
  • Other targeting: Chemistry based targeting (e.g. ,affects protein corona formation by adjusting surface charge)

Application

  • Gene delivery: mRNA/samRNA

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo metastatic model)
  • Rare diseases (In vitro; In vivo: cystic fibrosis)
  • Infectious diseases – Viral infections: BioSafety Level 2; In vitro (cells); In vitro (organoids); In vivo (rodent)
University of Toronto

Bowen Li

Lipid-based

Active targeting

Other

Antibody or antibody fragments

Small molecule

Chemistry based targeting (e.g. affects protein corona formation by adjusting surface charge)

Gene delivery

mRNA/samRNA

Cancer

Rare diseases

Infectious diseases Viral infections

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo metastatic model

In vitro

In vivo   Cystic fibrosis

BioSafety Level 2

In vitro (cells)

In vitro (organoids)

In vivo (rodent)

Researcher: Shyh-Dar Li

Institution: University of British Columbia (UBC)

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Other: EPR effect, protein corona

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA, ASO
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)
  • Rare diseases (In vivo: cancer, genetic diseases)
  • Diabetes (In vivo: STZ induced)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Microfluidics

University of British Columbia (UBC)

Shyh-Dar Li

Lipid-based
Polymer-based

Other: EPR effect, protein corona

Drug delivery: Soluble molecules; Insoluble molecules
Gene delivery: DNA, siRNA, mRNA/samRNA, ASO
Peptide/protein delivery

Cancer (In vitro, Organoid, In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)
Rare diseases (In vivo: cancer, genetic diseases)
Diabetes (In vivo: STZ induced)

Safety/pharmacology (Pre-GLP toxicity)
Microfluidics

Researcher: Raimar Loebenberg

Institution: University of Alberta

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Physical targeting: Other (lymphatic)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro)
  • Infectious diseases: bacterial infections – BioSafety Level 2; In vitro (cells)

Protocols: Pre-GMP & GMP manufacturing

Instrumentation: clean room

Auxiliary expertise: Regulatory science

University of Alberta

Raimar Loebenberg

Lipid-based

Polymer-based

Physical targeting

Other

lymphatic

Drug delivery

Peptide/protein delivery

Soluble molecules, Insoluble molecules

Cancer

Infectious diseases

Bacterial infections

In vitro

BioSafety Level 2

In vitro (cells)

Pre-GMP & GMP manufacturing

clean room

Regulatory science

Researcher: Simon Matoori

Institution: Université de Montréal

Nanodelivery type

  • Lipid-based
  • Polymer-based

Disease model(s)

  • Diabetes (In vivo: db/db mice, STZ mice)

Auxiliary expertise: Non-nano delivery systems

Université de Montréal

Simon Matoori

Lipid-based

Polymer-based

Diabetes

In vivo   db/db mice, STZ mice

Non-nano delivery systems

Researcher: Naomi Matsuura

Institution: University of Toronto

Nanodelivery type

  • Lipid-based

Targeting approach

  • Other: Image-guided targeting (focusing energy from outside the patient for local uptake of therapeutics)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Nano-imaging: Diagnostics; Theranostics; Fluorescent imaging; PET; Other (ultrasound, CT)

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo syngeneic model)

Protocols: Microfluidics; Other: Ultrasound-guided focused ultrasound (FUS) delivery

Instrumentation: FUS, Ultrasound, Raman microscope, bioprinter

University of Toronto

Naomi Matsuura

Lipid-based

Other

Image-guided targeting (focusing energy from outside the patient for local uptake of therapeutics)

Drug delivery

Nano-imaging

Soluble molecules

Insoluble molecules

Diagnostics

Theranostics

Fluorescent imaging

PET

Other

ultrasound, CT

Cancer

In vitro

In vivo xenograft model

In vivo orthotopic model

In vivo syngeneic model

Microfluidics

Other

Ultrasound-guided focused ultrasound (FUS) delivery

FUS, Ultrasound, Raman microscope, bioprinter

Researcher: Michel Meunier

Institution: Polytechnique Montreal

Nanodelivery type

  • Lipid-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments
  • Physical targeting: Light sensitive

Application

  • Drug delivery: Soluble molecules
  • Gene delivery: siRNA, mRNA/samRNA

Disease model(s)

  • Cancer (In vitro)
  • Other: ophthalmology (In vitro)
Polytechnique Montreal

Michel Meunier

Lipid-based

Inorganic

Active targeting: Antibody or antibody fragments

Physical targeting: Light sensitive

Drug delivery: Soluble molecules

Gene delivery: siRNA, mRNA/samRNA

Cancer (In vitro)

Other: ophthalmology (In vitro)

Researcher: Robert Molday

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments
  • Physical targeting: pH sensitive

Application

  • Gene delivery: DNA, mRNA/samRNA
  • Peptide/protein delivery

Disease model(s)

  • Rare diseases (In vitro, Organoid, In vivo, mouse)
University of British Columbia

Robert Molday

Lipid-based

Active targeting Antibody or antibody fragments

Physical targeting

pH sensitive

Gene delivery

Peptide/protein delivery

DNA

mRNA/samRNA

Rare diseases

In vitro

Organoid

In vivo

mouse

Researcher: Ignace Moya

Institution: Krembil Institute

Nanodelivery type

  • Polymer-based

Targeting approach

  • Active targeting: Peptide

Application

  • Drug delivery: Soluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)
  • Other: stroke & COVID (In vitro, Human)

Protocols: Safety/pharmacology (GLP testing); Pre-GMP & GMP manufacturing

Instrumentation: HPLC (analytical and semiprep), peptide synthesizer, lyophilizer

Krembil Institute

Ignace Moya

Polymer-based

Active targeting

Peptide

Drug delivery

Peptide/protein delivery

Soluble molecules

Other                    stroke, and COVID

In vitro

Human

Safety/pharmacology

Pre-GMP & GMP manufacturing

GLP testing

HPLC (analytical and semiprep), peptide synthesizer, lyophilizer

Researcher: Clement Mugabe

Institution: Evonik

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Other: Passive targeting

Application

  • Drug Delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA, ASO
  • Peptide/protein delivery

Disease model(s)

  • Other: We work with many partners who have access to many disease models (In vitro)

Protocols: Pre-GMP & GMP manufacturing

Unique instrumentation: PAT to monitor downstream purification process for LNP formulations

Auxiliary expertise: Other: Evonik Vancouver Laboratories is a global CDMO for lipid nanoparticle and liposome-based formulations. We provide end-to-end services for lipid nanoparticle formulations including formulation and process development, scale up and clinical manufacturing of lipid based drug products. We offer a highly purified plant-derived cholesterol (PhytoChol) in GMP grade. We can also develop and manufacture custom-made lipids and polymers to support your clinical development.

Evonik

Clement Mugabe

Lipid-based Polymer-based

Other
Passive targeting

Drug delivery Gene delivery Peptide/protein delivery Soluble molecules Insoluble molecules DNA siRNA mRNA/samRNA ASO

Other We work with many partners who have access to many disease models In vitro

Pre-GMP & GMP manufacturing

PAT to monitor downstream purification process for LNP formulations

Other Evonik Vancouver Laboratories is a global CDMO for lipid nanoparticle and liposome-based formulations. We provide end-to-end services for lipid nanoparticle formulations including formulation and process development, scale up and clinical manufacturing of lipid based drug products. We offer a highly purified plant-derived cholesterol (PhytoChol) in GMP grade. We can also develop and manufacture custom-made lipids and polymers to support your clinical development.

Researcher: Keith Pardee

Institution: University of Toronto

Nanodelivery type

  • Polymer-based
  • Lipid-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Aptamer

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: mRNA/samRNA
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro)
  • Infectious diseases: viral infections – BioSafety Level 2, In vitro (cells)

Protocols: Microfluidics

Instrumentation: focus on molecular interactions with nanomaterials (bioconjugation)

Auxiliary expertise: Non-nano delivery systems

University of Toronto

Keith Pardee

Lipid-based

Polymer-based

Active targeting

Antibody or antibody fragments

Peptide

Aptamer

Gene delivery

Peptide/protein delivery

mRNA/samRNA

Cancer

Infectious diseases

Viral infections

In vitro

BioSafety Level 2

In vitro (cells)

Microfluidics

focus on molecular interactions with nanomaterials (bioconjugation)

Non-nano delivery systems

Researcher: Arghya Paul

Institution: University of Western Ontario

Nanodelivery type

  • Lipid-based
  • Polymer-based
  • Inorganic

Application

  • Drug delivery: Soluble molecules, Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA

Disease model(s)

  • Cancer: In vitro, Organoid, In vivo xenograft model
  • Diabetes: In vitro, In vivo
  • Other: Liver Disease

Protocols: Microfluidics

University of Western Ontario

Arghya Paul

Lipid-based
Polymer-based
Inorganic

Drug delivery
Gene delivery

Soluble molecules
Insoluble molecules

DNA
siRNA
mRNA/samRNA

Cancer
Diabetes
Other liver disease

In vitro
Organoid
In vivo xenograft model

 

Microfluidics

Researcher: Raymond Reilly

Institution: University of Toronto

Nanodelivery type

  • Inorganic

Targeting approach

  • Other: Local intratumoural infusion or implantation of gold nanoparticles

Application

  • Other: Radioisotope delivery

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo PDX model, In vivo syngeneic model, Human)

Protocols: Safety/pharmacology (Pre-GLP toxicity); Pre-GMP & GMP manufacturing

Instrumentation: Radioisotope measurement and small animal imaging systems (SPECT and PET)

Auxiliary expertise: Regulatory science

University of Toronto

Raymond Reilly

Inorganic

Other: Local intratumoural infusion or implantation of gold nanoparticles

Other: Radioisotope delivery

Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, In vivo PDX model
In vivo syngeneic model, Human)

Safety/pharmacology (Pre-GLP toxicity); Pre-GMP & GMP manufacturing

Radioisotope measurement and small animal imaging systems (SPECT and PET)

Regulatory science

Researcher: Colin Ross

Institution: University of British Columbia

Nanodelivery type

  • Polymer-based
  • Lipid-based
  • Other: AAV

Targeting approach

  • Active targeting

Application

  • Gene delivery: DNA, mRNA/samRNA

Disease model(s)

  • rare diseases (In vitro, In vivo)

Protocols: Safety/pharmacology

University of British Columbia

Colin Ross

Lipid-based

Polymer-based

Other

AAV

Active targeting

Gene delivery

DNA

mRNA/samRNA

Rare diseases

In vitro

In vivo

Safety/pharmacology

Researcher: Manish Sadarangani

Institution: University of British Columbia (UBC)

Nanodelivery type

  • Other: bacterial outer membrane vesicles

Targeting approach

  • Active targeting: Antibody or antibody fragments

Application

  • Other: vaccine delivery

Disease model(s)

  • Infectious diseases (Bacterial infections; In vitro [cells], In vivo [rodent]; BioSafety Level 2)

Auxiliary expertise: Regulatory science

University of British Columbia (UBC)

Manish Sadarangani

Other: bacterial outer membrane vesicles

Active targeting: Antibody or antibody fragments

Other: vaccine delivery

Infectious diseases (Bacterial infections; In vitro [cells], In vivo [rodent]; BioSafety Level 2)

Regulatory science

Researcher: Michael Serpe

Institution: University of Alberta

Nanodelivery type

  • Polymer-based

Targeting approach

  • Physical targeting: pH sensitive; Temperature sensitive; Light sensitive; Other (electric field, mechanical force)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules

Disease model(s)

  • Cancer (Human)
  • Other: General novel delivery system development (Human)

Protocols: Other: Codelivery of multiple molecules to a system, nanogel/hydrogel composites for fine tuning of drug delivery rate

Instrumentation: Multiangle, multi wavelength imaging ellipsometer, quartz crystal microbalance, contact angle goniometer, surface plasmon resonance

Auxiliary expertise: Non-nano delivery systems

University of Alberta

Michael Serpe

Polymer-based

Physical targeting

pH sensitive

Temperature sensitive

Light sensitive

Other

electric field, mechanical force

Drug delivery

Soluble molecules

Insoluble molecules

Cancer

Other

General novel delivery system development

Human

Human

Other

Codelivery of multiple molecules to a system, nanogel/hydrogel composites for fine tuning of drug delivery rate

Multiangle, multi wavelength imaging ellipsometer, quartz crystal microbalance, contact angle goniometer, surface plasmon resonance

Non-nano delivery systems

Researcher: Elizabeth Simpson

Institution: University of British Columbia

Nanodelivery type

  • Lipid-based

Application

  • Gene delivery: DNA

Disease model(s)

  • Rare diseases: Aniridia (a form of congenital blindness) (In vivo)
University of British Columbia

Elizabeth Simpson

Gene delivery

DNA

Rare diseases

In vivo

Aniridia a congenital blindness

Researcher: Ruby Sullan

Institution: University of Toronto Scarborough

Nanodelivery type

  • Polymer-based

Targeting approach

  • Active targeting: Peptide

Application

  • Drug delivery: Soluble molecules

Disease model(s)

  • Infectious diseases – Bacterial infections: BioSafety Level 2; In vitro (cells)

Instrumentation: Atomic force microscope (AFM)

University of Toronto Scarborough

Ruby Sullan

Polymer-based

Active targeting

Peptide

Drug delivery
Soluble molecules

Infectious diseases

Bacterial infections

BioSafety Level 2

In vitro (cells)

Atomic force microscope (AFM)

Researcher: Aneesh Thakur

Institution: Vaccine and Infectious Disease Organization, University of Saskatchewan

Nanodelivery type

  • Polymer-based
  • Lipid-based

Targeting approach

  • Other

Application

  • Gene delivery: mRNA/samRNA
  • Nano-imaging: Fluorescent imaging/li>

Disease model(s)

  • Infectious diseases: Viral infections, Bacterial infections – BioSafety Level 2, BioSafety Level 3, In vitro (cells), In vivo (rodent), In vivo (larger animals)

Protocols: Microfluidics; Other: Immune responses

University of Saskatchewan (Vaccine and Infectious Disease Organization)

Aneesh Thakur

Lipid-based

Polymer-based

Other

Gene delivery mRNA/samRNA

Nano-imaging     Fluorescent imaging

Infectious diseases           Viral infections

Bacterial infections

BioSafety Level 2

BioSafety Level 3

In vitro (cells)

In vivo (rodent)

In vivo (larger animals)

Microfluidics

Other

Immune responses

Researcher: Gilbert Walker

Institution: University of Toronto

Nanodelivery type

  • Lipid-based
  • Polymer-based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Small molecule
  • Physical targeting: pH sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: siRNA, ASO
  • Nano-imaging: Diagnostics

Disease model(s)

  • Cancer (In vitro)
  • Infectious diseases (Viral infections; Bacterial infections; BioSafety Level 2; In vitro [cells], In vivo [rodent])

Protocols: Microfluidics

Instrumentation: high resolution mechanical and IR imaging

University of Toronto

Gilbert Walker

Lipid-based
Polymer-based

Active targeting: Antibody or antibody fragments; Small molecule
Physical targeting: pH sensitive

Drug delivery: Soluble molecules; Insoluble molecules
Gene delivery: siRNA, ASO
Nano-imaging: Diagnostics

Cancer (In vitro)
Infectious diseases (Viral infections; Bacterial infections; BioSafety Level 2; In vitro [cells], In vivo [rodent])

Microfluidics

high resolution mechanical and IR imaging

Researcher: Ellen Wasan

Institution: University of Saskatchewan

Nanodelivery type

  • Polymer-based
  • Lipid-based

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Infectious diseases: Viral infections, Bacterial infections

Protocols: Microfluidics

Instrumentation: access to Canadian Light Source Synchrotron, Malvern Nanosizer

Auxiliary expertise: Non-nano delivery systems

University of Saskatchewan

Ellen Wasan

Lipid-based

Polymer-based

Physical targeting

pH sensitive

Drug delivery

Peptide/protein delivery

Soluble molecules

Insoluble molecules

Infectious diseases

Viral infections

Bacterial infections

Microfluidics

access to Canadian Light Source Synchrotron, Malvern Nanosizer

Non-nano delivery systems

Researcher: Kishor Wasan

Institution: University of British Columbia

Nanodelivery type

  • LIpid-based
  • Other: Lipid and Lipoprotein Metabolism as it is related to Drug Delivery

Targeting approach

  • Active targeting: Peptide; Small molecule
  • Physical targeting: Other (Lipoprotein Drug Delivery)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Peptide/protein delivery

Disease model(s)

  • Cancer (In vitro, In vivo xenograft model, In vivo orthotopic model, Human)
  • Infectious diseases: Viral infections, Bacterial infections: BioSafety Level 2, In vitro (cells), In vitro (organoids), In vivo (rodent)
  • Other: Neglected Tropical Diseases- parasitic diseases and fungal diseases (In vivo: Antifungal models, In vitro)

Protocols: Safety/pharmacology (Pre-GLP toxicity)

Auxiliary expertise: Non-nano delivery systems; Other: Pharmacokinetics and ADME

University of British Columbia

Kishor Wasan

Lipid-based

Other

Lipid and Lipoprotein Metabolism as it is related to Drug Delivery

Active targeting (e.g., antibody modification of nanomedicine)

Other

Small molecule

Lipoprotein Drug Delivery

Drug delivery

Soluble molecules

Insoluble molecules

Cancer

Infectious diseases

Other

Viral infections

Bacterial infections

Neglected Tropical Diseases- parasitic diseases and fungal diseases

In vitro

In vivo

Antifungal models.

In vitro

In vivo xenograft model

In vivo orthotopic model

Human

BioSafety Level 2

In vitro (cells)

In vitro (organoids)

In vivo (rodent)

Safety/pharmacology

Pre-GLP toxicity

Non-nano delivery systems

Other

Pharmacokinetics and ADME

Researcher: David Wishart

Institution: University of Alberta

Nanodelivery type

  • Lipid-based
  • Inorganic

Targeting approach

  • Active targeting: Antibody or antibody fragments

Application

  • Peptide/protein delivery
  • Other: assays

Disease model(s)

  • Cancer (human)
  • Infectious diseases: Viral infections, Bacterial infections – BioSafety Level 2, In vitro (cells), In vivo (larger animals)

Protocols: Microfluidics

Unique instrumentation: LC-MS, GC-MS, ICP-MS, NMR

Auxiliary expertise: Regulatory science; Marketing expertise; Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

University of Alberta

David Wishart

Lipid-based
Inorganic

Active targeting
Antibody or antibody fragments

Peptide/protein delivery
Other: assays

Cancer Infectious diseases Viral infections Bacterial infections Human BioSafety Level 2 In vitro (cells) In vivo (larger animals)

Microfluidics

LC-MS, GC-MS, ICP-MS, NMR

Regulatory science Marketing expertise Health Technology Assessment (HTA)/early Health technology Assessment (eHTA)

Researcher: Xiao Yu (Shirley) Wu

Institution: University of Toronto

Nanodelivery type

  • Polymer-based
  • Other: Polymer-lipid hybrid, polymer-lipid-inorganic based

Targeting approach

  • Active targeting: Antibody or antibody fragments; Peptide; Small molecule
  • Physical targeting: pH sensitive; Other (oxidative stress, disease state biomarkers)

Application

  • Drug delivery: Soluble molecules; Insoluble molecules
  • Gene delivery: DNA, siRNA, mRNA/samRNA, ASO
  • Peptide/protein delivery
  • Nano-imaging: Diagnostics; Theranostics; Fluorescent imaging; Other (MRI)

Disease model(s)

  • Cancer (In vitro, Organoid, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)
  • Diabetes (In vitro, In vivo: diabetic rats/mice)
  • Other: neurodegenerative diseases (In vitro, Organoid, In vivo: Alzheimer’s mice, lung injury models)

Protocols: Safety/pharmacology

Auxiliary expertise: Non-nano delivery systems

University of Toronto

Xiao Yu (Shirley) Wu

Polymer-based
Other: Polymer-lipid hybrid, polymer-lipid-inorganic based

Active targeting: Antibody or antibody fragments; Peptide; Small molecule
Physical targeting: pH sensitive; Other (oxidative stress, disease state biomarkers)

Drug delivery: Soluble molecules; Insoluble molecules
Gene delivery: DNA, siRNA, mRNA/samRNA, ASO<
Peptide/protein delivery
Nano-imaging: Diagnostics; Theranostics; Fluorescent imaging; Other (MRI)

Cancer (In vitro, Organoid, In vivo orthotopic model, In vivo syngeneic model, In vivo metastatic model)
Diabetes (In vitro, In vivo: diabetic rats/mice)
Other: neurodegenerative diseases (In vitro, Organoid, In vivo: Alzheimer’s mice, lung injury models)

Safety/pharmacology

Non-nano delivery systems

Researcher: Shan Zou

Institution: National Research Council Canada

Nanodelivery type

  • Lipid-based
  • Other: Graphane oxide and boron nitride nanotubes

Targeting approach

  • Physical targeting: pH sensitive

Application

  • Gene delivery: DNA, siRNA

Disease model(s)

  • Cancer (In vitro, Organoid)

Protocols: Safety/pharmacology (Pre-GLP toxicity)

Instrumentation: CARS

National Research Council Canada

Shan Zou

Lipid-based

Other

Graphane oxide and boron nitride nanotubes

Physical targeting

pH sensitive

Gene delivery

DNA

siRNA

Cancer

In vitro

Organoid

Safety/pharmacology       Pre-GLP toxicity

CARS