SBIR/STTR Research Award
Prostate Gamma Probe
Award amount
$113,465Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- MOSAIC IMAGING TECHNOLOGY
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
Mosaic plans to develop a novel transrectal gamma probe that will
detect and localize prostate carcinoma in and around the prostate. The
system has been optimized for detecting and localizing ProstaScint
uptake sites in and near the Prostate. The probe is a miniaturized,
collimated solid-state detector. The design is constrained by the
requirements that the probe be small enough for intra-rectal use and that
it operate effectively for the 247 keV emission of 111 In-labeled
ProstaScint. The Phase 1 program describes and will experimentally
evaluate two complementary collimation schemes for the probe. One is
a conventional, but low-sensitivity multi-hole collimator. The other is a
novel, high-sensitivity collimator. The Phase 1 plan consists of three
parts: 1) constructing the collimator evaluation platform (phantoms,
fixtures, acquisition hardware, processing software) required to carry
out the experiments, 2) carrying out a set of proof-of-principle
experiments designed to establish the feasibility of using one or both
collimator designs a miniaturized probe to intra-rectally detect and
localize prostate cancer, and 3) summarizing the results and
conclusions of Phase 1 and laying the foundation for the Phase 2
Clinical Prototype.
PROPOSED COMMERCIAL APPLICATIONS:
Mosaic's gamma probe would aid Urologists working with Nuc Med
Physician or Radiologist to verify prostate cancer and help direct
biopsies toward the cancer. The probe could detect and localize the
cancer within area of the prostate to be sampled rather than the current
practice of performing multi-needle sampling or additional biopsies. It
would be used after an elevated PSA has been confirmed but before
biopsy.
Technology keywords
Not reported