SBIR-STTR Award

Microfluidic Systems for Assisted Reproductive Technologies
Award last edited on: 4/28/2006

Sponsored Program
SBIR
Awarding Agency
USDA
Total Award Amount
$339,990
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Eric M Walters

Company Information

Vitae LLC (AKA: Micro Agri Systems)

812 East Dayton Street Suite 208
Madison, WI 53703
   (608) 222-1908
   dbeebe@vitaellc.com
   www.vitaellc.com
Location: Single
Congr. District: 02
County: Dane

Phase I

Contract Number: 99-33610-7535
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1999
Phase I Amount
$64,990
The growth of animal reproductive technologies including in vitro fertilization, transgenic animals and cloning has been dramatic in recent years. However, a parallel growth in physical tools to aid and further advance these techniques to practical use has not occurred. One specific problem that we have identified and will address in this proposal is the development of new technology for the study and facilitation of in vitro embryo culture. Embryo culture represents a critical step in many animal reproductive techniques such as genetic improvement, selective breeding and genome manipulation including marker-assisted selection embryo genotyping, embryo transfer, embryo manipulation, embryo cryopreservation, gene transfer and cloning. The potential impact of improved embryo culture efficiencies is clear. For example, embryo transfer involving cattle, sheep, goats, deer and swine is an approximately $20 billion/year industry worldwide. The focus of this proposal is a research and development effort aimed at understanding the key issues relevant to the development and use of a novel embryo culture system for increased yield.

Anticipated Results/Potential Commercial Applications of Research:
:We will develop methods for fabricating micro culture systems capable of retaining multiple embryos in uniquely identified locations while dynamically controlling the local fluid environment surrounding the embryo. Dynamic miniaturized culture systems have several potential advantages over traditional culture methods. The ability to monitor thousands of individual pre-implantation embryos and their secretions while controlling the buffer composition should lead to increased culture efficiencies. In addition, the proposed miniaturized systems will use smaller quantities of buffer and expensive additives leading to significant cost savings. We will work closely with expensive additives leading to significant cost savings. We will work closely with Infigen, Inc., a Division of American Breeders Service, to ensure commercial relevance.

Phase II

Contract Number: 2001-33610-11065
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2001
Phase II Amount
$275,000
The importance of reproduction in livestock production is tremendous. However, little progress has been made with regard to decreasing embryonic mortality. The instruments used for in vitro embryo production (IVP) have not changed dramatically over several decades. This research is aimed at development, testing and optimization of microfluidic devices and associated procedures for in vitromaturation (IVM), in vitro fertilization (IVF) and embryo culture (EC) of bovine embryos. The three specific aims of this proposal are: 1) to develop Polydimeythlsiloxane (PDMS-based) devices for dynamic IVP studies, 2) to study the effect of dynamic flow conditions on IVM, IVF and EC separately and in combination, and 3) to explore the use of microfluidic, tectonic-based microsystems for IVP. Currently, static culture is the standard practice for IVP of mammalian embryos. The dynamic systems that are being used currently use flow rates several orders of magnitude higher than the proposed system. The proposed system will allow precise control of fresh medium past the oocytes/embryos, and allow the composition of the medium to be gradually changed over a period of time. These microfluidic systems will provide embryos with dramatically improved microenvironments that more closely mimic in vitro conditions and lead to improved embryonic development. ANTICIPATED RESULTS & POTENTIAL COMMERCIAL APPLICATIONS OF RESEARCH The anticipated result from this proposal is that the microfluidic devices will enhance in vitro production of bovine embryos, as well as have a device that is commercially ready for beta testing in laboratories and species. Many assisted reproduce technologies such as cloning, cryopreservation, and intracytoplasmic sperm injection rely heavily on in vitro produced oocytes/embryos. This proposed microfluidic platform will greatly enhance the viability of oocytes/embryos exiting the in vitro production system as well as automation of many of the assisted reproductive technologies.