Initial evaluation of vascular ingrowth into superporous hydrogels.

There is a need for new materials and architectures for tissue engineering and regenerative medicine. Based upon our recent results developing novel scaffold architecture, we hypothesized that this new architecture would foster vascularization, a particular need for tissue engineering. We report on the potential of superporous hydrogel (SPH) scaffolds for in vivo cellular infiltration and vascularization.

Cervical cancer treatment with a locally insertable controlled release delivery system.

Local delivery of cancer chemotherapeutics enables sustained drug levels at the site of action thereby reducing systemic side effects. A novel insertable polymeric drug delivery system for cervical cancer treatment is presented. Cisplatin, the first line of therapy employed for cervical cancers, was incorporated in a poly(ethylene-co-vinyl acetate) (EVAc) device that is similar to those currently used for vaginal contraceptive delivery.

Osteoblast-like cell attachment to and calcification of novel phosphonate-containing polymeric substrates.

In an attempt to interact natural bone and bone cells with biomaterials and to begin to develop modular tissue engineering scaffolds, substrates containing phosphonate groups were identified to mimic mineral-protein and natural polymer-protein interactions. In this study, we investigated poly(vinyl phosphonic acid) copolymer integration with existing materials as a graft-copolymer surface modification. Phosphonate-containing copolymer-modified surfaces were created and shown to have varying phosphate content within different polymeric surfaces.

Cellular alignment by grafted adhesion peptide surface density gradients.

The extracellular matrix and extracellular matrix-associated proteins play a major role in growth and differentiation of tissues and organs. To date, few methods have been developed that allow researchers to examine the affect of surface density gradients of adhesion molecules in a controlled manner. Fibroblasts cultured on surfaces with a surface density gradient of RGD peptide aligned parallel to the gradient while fibroblasts on constant density RGD surfaces spread but did not align as has been shown in numerous earlier studies.