SBIR-STTR Award

Physiological testing for Hexavalent Chrome exposure in the human body
Award last edited on: 9/9/2013

Sponsored Program
SBIR
Awarding Agency
DOD : AF
Total Award Amount
$150,000
Award Phase
1
Solicitation Topic Code
AF121-220
Principal Investigator
Benjamin P Warner

Company Information

Caldera Pharmaceuticals Inc (AKA: XRPro Sciences Inc ~Icagen, Inc)

4222 Emperor Boulevard Suite 350
Durham, NC 27703
   (919) 941-5206
   info@cpsci.com
   www.cpsci.com,www.xrpro.com
Location: Single
Congr. District: 04
County: Durham

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2012
Phase I Amount
$150,000
Caldera Pharmaceuticals proposes to develop physiologic biomarkers requested by the US Air Force to quantify workplace exposure to hexavalent chrome (Cr+6). Exposure to Cr+6 is dangerous and unwanted, because it is a primary carcinogen (class 1 International Agency for Research on Cancer / IARC) and a known lung cancer carcinogen. Chromium (Cr) exists in several valence states, the most prevalent states are hexavalent Cr (Cr+6, which is associated with industrial exposure and toxicity) and trivalent Cr (Cr+3, which is stable and a biologically active form). Cr+3 is an essential nutrient for humans and shortages may cause heart conditions and metabolic disruptions or diabetes; it is classified as IARC Group 3. Although a limited amount of Cr+3 is necessary, large amounts may be hazardous. Cr supplements are taken readily and are available as trivalent Cr in chloride (CrCl3) or picolinate (CrPic) salt forms, but associated health effects are unknown. If ingested in large amounts, both Cr+3 and +6 can cause gastrointestinal problems and ulcers, or kidney and liver damage. There are no physiologic biomarkers for exposure to Cr+6, especially those that differentiate between various Cr species in vivo. Caldera XRpro(R) Technology will be used to screen for Cr-selective biomarker aptamers.

Keywords:
Chromium, Inhalation, Metal, Toxicity, Biomarker

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
----
Phase II Amount
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