SBIR-STTR Award

Development Of Individual Chambers For Alcohol Delivery
Award last edited on: 3/5/07

Sponsored Program
SBIR
Awarding Agency
NIH : NIAAA
Total Award Amount
$965,305
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Maury D Cole

Company Information

La Jolla Alcohol Research Inc

PO Box 13397
La Jolla, CA 92039
   (619) 306-3339
   customerservice@ljari.com
   www.ljari.com
Location: Single
Congr. District: 52
County: San Diego

Phase I

Contract Number: 1R43AA012018-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1998
Phase I Amount
$100,000
At present, investigators who want to expose laboratory rodents to alcohol can inject the drug, feed it through a chocolate-base diet, or deliver it in contained chambers in the form of vapors. Currently available alcohol chambers contain several cages which each house 3-6 rodents. The purpose of this Phase I feasibility study is to show that we can build smaller chambers in which laboratory rodents (primarily rats or mice) are exposed to alcohol vapors under tightly controlled conditions. The proposed chambers will house 1-4 rats or 3-6 mice, depending on weights. This prototype has two main advantages over presently available methods. First, each chamber can be individually controlled, which means that target blood alcohol levels (BALs) can be finely regulated. Second, the animals can be equipped with permanent intravenous or intracerebroventricular cannulae to samples biological fluids and/or inject treatments without manipulating the animals or opening the chambers. Over the past 8 months, we have built 6 such cages to demonstrate that most of the problems encountered should be solvable, provided we have the appropriate resources. These problems include the presence of condensation, the maintenance of environmentally safe chambers (i.e. from which no alcohol vapors, escape) despite the presence of portholes for the passage of the cannulae, and the adequacy of standard air sources commonly available in the laboratory to propel the alcohol vapors through the system. The objectives that need to be reached under Phase I are (1) to automate the system, which is presently cumbersome and labor-intensive, (2) to bring the problem of condensation to its final solution, (3) to ensure that the final parameters of air velocity do not lead to the release of ACTH and corticosterone, taken as indexes of stress, and (4) to demonstrate that the prototype can be extended to at least 12 chambers. Once the prototype is finalized, the investigator will be provided with a pre-assembled set of cages with all necessary components, and charts that will enable him/her to reach the target BALs on the basis of the animal's weight The long-term commercial objectives, however, are to build a system that can be used not only to deliver alcohol, but also toxic substances that need to be contained, su ch as nicotine, carcinogens, etc. We therefore believe that the prototype for which we want to demonstrate feasibility, will be attractive to a wide variety of researchers who need environmentally safe and easy to use devices to study the effects of these substances. Proposed Commercial Applications:On the basis of numerous conversations with colleagues, as well as our own experience in the field, we have no doubt that such a device would find a ready market and thus have excellent commercial potential. There are many investigators who expose rodents to alcohol, and all those who do not require voluntary drug intake will welcome an easy-to-use, reliable, flexible and affordable device to do so, which does not require extensive labor. In addition, this technology can be used to expose animals to reagents other than alcohol, that need to be contained such as nicotine, carcinogens, pollutants, potential irritants, etc. This provides a major advance in the field of toxicology.

Thesaurus Terms:
alcohol, biomedical equipment development, controlled environment chamber Rodentia, inhalation drug administrationNATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM

Phase II

Contract Number: 2R44AA012018-02A2
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2001
(last award dollars: 2003)
Phase II Amount
$865,305

The ability to expose experimental rodents to alcohol over periods of hours to days is crucial to research. At present, the methods used to do so include repeated injections, feeding the animals a liquid diet containing alcohol, or group-housing them in large chambers through which alcohol vapors are circulated. The disadvantages of these methods include the presence of a stressful procedure, an inadequate diet and/or the inability to access individual animals while they are in the vapor environment. Under Phase I, we developed a prototype that showed the feasibility of building individual rat cages through which we could circulate known amount of alcohol vapors. This system allowed us to develop charts which correlated blood alcohol levels (BALs) to pre-determined parameters of alcohol delivery. Phase II will expand the scientific ideas successfully explored under Phase I. As investigators use different rat strains, both males and females, and want to treat their animals for several days, we will develop charts for male and female (both virgin and pregnant) Sprague-Dawley, Wistar and Long-Evans rats. This is necessary because alcohol metabolism varies between strains and genders, and changes during pregnancy. Consequently we cannot assume that the charts developed under Phase I are applicable to other models. We will also modify the existing rat prototype so that the chambers can accommodate food holders and water bottles, as well as outlets for cannulae, while the integrity of the system is maintained during long-term housing. A stand holding syringes and/or the recording instruments will be built, that fits over the chambers. Finally, we found that mice housed in rat chambers had very heterogeneous BALs. Therefore an important aspect of our work will consist in building chambers for mice, a species that is increasingly used in alcohol research, but which will require a redesign of the system to accommodate their smaller size. Once this new design has been determined, we will develop charts correlating parameters of alcohol delivery to target BALs in mice of three commonly used strains, BALB/c, C57BL/6 and DBA/2. The finished rat and mouse products will represent a very significant improvement over presently available systems. It will be versatile, user-friendly and affordable. While originally designed for alcohol work, we anticipate that it will be easily modifiable for other volatile, non-corrosive substances, including those that are presently difficult to study because they are highly toxic.

Thesaurus Terms:
Rodentia, alcohol, biomedical equipment development, controlled environment chamber, inhalation drug administration animal care laboratory mouse, laboratory rat