Abstract: The present invention provides a device for wound treatment, comprising a chamber that includes an inner surface and defines a treatment space, the chamber being made of a flexible, impermeable material. The device further includes a plurality of structures configured to exert mechanical stress on a wound, the plurality of structures intruding from the inner surface of the chamber into the treatment space. The device further includes a tube having a first end connected to the chamber, the tube being in fluid communication with the treatment space so as to enable at least one selected from the group of applying negative pressure to the treatment space and applying a therapeutic modality.
Type:
Grant
Filed:
May 27, 2008
Date of Patent:
January 21, 2014
Assignee:
Applied Tissue Technologies, LLC
Inventors:
Elof Eriksson, W. Robert Allison, Christian Baker
Abstract: An apparatus is provided to enable the direct gene transfer of genetic material into a target cell site (“microseeding”), as a means of obtaining long term expression of native or non-native polypeptides in a host. The apparatus includes a matrix of microneedles that oscillate at a predetermined frequency and receive the genetic material from a delivery system that is integrated with the apparatus.
Type:
Grant
Filed:
February 25, 2003
Date of Patent:
September 9, 2008
Assignee:
Applied Tissue Technologies, LLC
Inventors:
Elof Eriksson, Christian Baker, W. Robert Allison, Tom Johnson, Anthony Downing, David Porait, Denis Labombard, John Navickas, Patrick Guiney
Abstract: Direct gene transfer of genetic material into an external or internal target cell site (“microseeding”), in optional combination with a wound treatment chamber, are particularly effective as a means of obtaining long term expression of native or non-native polypeptides in a host. A wide variety of proteins and materials can be expressed, either for secretion into the general blood and lymphatic system, or to alter the properties of the protein, for example, to not express proteins eliciting an immune response. The use of the optional wound chamber system for gene transfer to skin target sites also allows non-invasive assessment of the success of transfer by assaying for the presence of the expressed protein in wound fluid, in contrast to the prior art use of invasive techniques, such as biopsies, in order to achieve the same assessment of early expression.