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Printable Handouts
Navigable Slide Index
- Introduction
- Designing small animal imaging facilities
- What do you plan to image?
- Imaging methods
- What species to use
- Regulatory oversight
- Infectious and carcinogenic agents
- Immunocompromised imaging (1)
- What level of service?
- Who will do the work?
- UCLA imaging experiments: two roles
- Animal handling training
- Systems and personnel requirements
- Planning the flow of the workspace
- New Crump Imaging Center
- PET-CT space
- Vivarium
- Support equipment
- Computer network configuration
- Database and image management
- Web-based scheduling and image retrieval
- Archiving and data retrieval
- Operational considerations
- Preclinical molecular imaging
- Why use animals?
- What is being imaged?
- Experimental design issues
- Glucose effects on FDG (1)
- Glucose effects on FDG (2)
- Probe uptake: anesthesia effects
- Isoflurane effects on FDG uptake
- Conventional anesthesia configuration
- Anesthesia support
- Anesthesia induction boxes
- Immunocompromised imaging (2)
- Staging mice
- Temperature control
- Brown fat uptake
- Temperature effects in tumor bearing mice
- Heating options
- Intraperitoneal injections
- Tail vein injections
- Dynamic imaging prep
- Blood sampling options
- Tail blood sampling: tail 'poke'
- Example images
- Biodistribution and radiation dosimetry
- Oncology imaging
- D2 receptor ligand imaging using microPET
- Perfusion and metabolism microPET images
- microPET: oncology - PET-only
- microPET: oncology - dual modality imaging
- Dynamic imaging of FHBG
- Fast temporal imaging: first past transit
- Imaging cancer using PET-reporter gene & FHBG
- Functional and morphological imaging
- Adenovirus validation in lymph node metastasis
- Optical imaging: bioluminescence/fluorescence
- Fluorescent growth factor on implanted scaffold
- Bone formation assessed using microCT
- Getting it right
- References and acknowledgements
Topics Covered
- Designing small animal imaging facilities
- Imaging methods
- Regulatory oversight
- Infectious and carcinogenic agents
- UCLA imaging experiments
- Animal handling training
- Systems and personnel requirements
- Planning the flow of the workspace
- Database and image management
- Archiving and data retrieval
- Operational considerations
- Preclinical molecular imaging: why use animals?
- Experimental design issues
- Anaesthesia
- Heating options
- Blood sampling
- Case studies
- Optical imaging
- Getting it right
Talk Citation
Stout, D. (2010, April 1). Pre-clinical imaging centers: design, animal handling and examples [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/ZOMX7789.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. David Stout has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Methods
Transcript
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0:00
Hello. My name is David Stout.
I'm the Director of the Preclinical Imaging Technology Center here at the UCLA Crump Institute for Molecular Imaging.
Today I'm going to go over some preclinical imaging design center ideas about designing center's, animal handling,
and examples of different types of molecular imaging modalities.
0:21
A wide range of imaging technologies have been developed within the past few years that are now capable of imaging small animals such as mice and rats.
The ability to image these smaller species has led to a rapid shift from using pigs, dogs or primates or any of the larger species.
It's advantageous to use these smaller animals because they're more cost effective and they're not endangered.
The sensitivity and the capabilities of these systems have greatly improved since earlier versions,
and now we're seeing a move towards multimodality imaging systems such as the PET-CT combination or perhaps an PET-MR,
or coupling of optical imaging systems with X-ray technology.
1:03
When designing an imaging center, the first place to start is to think about what is it that you plan to image.
Are you interested in simply doing cells or in vitro samples?
Would you like to be imaging in mice or perhaps rats?
Or is there a good scientific reason why you need to be in a larger species such as canines or primates?
Will you be working with biohazardous materials or infectious agents,
or as common in many places now doing oncology research,
will you be using immune compromised animals such as scid and nude mice?
Will there be a need for a mixture of species or a mixture of different types of bio hazards?
Once you have an idea about the types of things that you want to support in your imaging center,
then you can think about what are the best technologies that you would want to use to image the information that you're trying to obtain.
Is this going to be a PET scan facility?
Are you interested in using SPECT or bioluminescence or ultrasound or MR?
Each of these systems have unique different requirements,
both for housing the systems and how the systems are used.
For example, in MR, you need to be concerned about electromagnetic shielding.
Whereas, in PET and SPECT, you're using radioactivity in an open area.
CT will generate radioactivity, but in general CT systems are self-shielded.
Each of the imaging modalities have their own pros and cons as to where their strengths and where their weaknesses lie.