A porous, self-sustaining body useful as a scaffold for bone grafting is provided. The scaffold comprises a carbonaceous matrix comprising a continuous phase having a surface and defining a plurality of open spaces throughout the matrix. The internal and external surfaces of the matrix are coated with a layer or film selected from the group consisting of osteogenic materials, therapeutic agents, and combinations thereof. The porous body comprises organic materials and is substantially free of metals. Methods of making and using the porous self-sustaining body are also provided, along with kits for facilitating the same.
An intervertebral implant for placement in the intervertebral space between two adjacent vertebral bodies is provided. The implant comprises a hollow cage and a porous core received within the cage. The cage comprises a superior surface configured to contact a first vertebral body, an inferior surface configured to contact a second vertebral body, and an outer wall extending between the superior surface and inferior surface. The outer wall comprises an exterior surface defining the outer perimeter of the implant, and an interior surface defining an inner (hollow) space or void. The porous core is received within the inner space or void, and preferably fills the void. The core comprises a carbonaceous matrix comprising a continuous phase having a surface and defining a plurality of open spaces throughout said matrix. Suitable carbonaceous matrices are selected from the group consisting of carbon foam, graphite foam, and combinations thereof. Methods of making and using the same, along with kits to facilitate such use are also provided.
Composite Magnetic Nanoparticle Drug Delivery System
A composite magnetic nanoparticle drug delivery system provides targeted controlled release chemotherapies for cancerous tumors and inflammatory diseases. The magnetic nanoparticle includes a biocompatible and biodegradable polymer, a magnetic nanoparticle, the biological targeting agent human serum albumin, and a therapeutic pharmaceutical composition. The composite nanoparticles are prepared by oil-in-oil emulsion/solvent evaporation and high shear mixing. An externally applied magnetic field draws the magnetic nanoparticles to affected areas. The biological targeting agent draws the nanoparticles into the affected tissues. Polymer degradation provides controlled time release delivery of the pharmaceutical agent.
Kardiotonos
Chief Science Officer
Center of Innovation For Biomaterials In Orthopaedic Research Jun 2008 - Jun 2015
Chief Scientific Officer
Orthopaedic Research Institute Dec 2007 - Jun 2015
Director
Wichita State University Dec 2007 - Jun 2015
Research Professor of Orthopaedic Surgery
Wichita State University Dec 2007 - Jun 2015
Professor of Biology
Education:
Guy’s Hospital Medical School, London, Uk 1977 - 1980
Doctorates, Doctor of Philosophy, Immunology, Medicine, Philosophy
Queen Elizabeth College, University of London, Uk 1973 - 1976
Bachelors, Microbiology
Skills:
Biomaterials Immunology Animal Models Drug Development Consulting Biocompatibility Immunopathology Orthopaedics Biological Response Modifiers Rheumatoid Arthritis Wear Debris Pharmaceutics