Combining Boolean method with delay times for determining behaviors of biological networks.

Boolean functions have been used to analyze the molecular networks of cells. For example, A --> B represents if A becomes active B will be activated. This method is effective for qualitatively analyzing networks but is not suitable for studies of kinetic behaviors of networks.

Degradability of polymers for implantable biomedical devices.

Many key components of implantable medical devices are made from polymeric materials. The functions of these materials include structural support, electrical insulation, protection of other materials from the environment of the body, and biocompatibility, as well as other things such as delivery of a therapeutic drug. In such roles, the stability and integrity of the polymer, over what can be a very long period of time, is very important.

Maximum conductivity of packed nanoparticles and their polymer composites.

Adding conductive fillers to nonconductive polymers is a common way to make soft conductive materials such as conductive adhesives. An important issue is how to achieve high volume conductivity with acceptable mechanical performance. Two questions pertaining to this issue were studied in this paper.

In vitro biostability evaluation of polyurethane composites in acidic, basic, oxidative, and neutral solutions.

New and improved properties can often be achieved by compounding two or more different but compatible materials. But, can failure possibility also be increased by such a compounding strategy? In this article, we compared the in vitro biostability of composites with that of the pure polymer. We tested three model composites in oxidative, acidic, basic, and neutral solutions.

Kinetics and time-temperature equivalence of polymer degradation.

We studied the hydrolysis kinetics of amorphous polylactide. It was found the hydrolysis rate had a slow-to-fast transition at a certain molecular weight (Mn). This transition was not correlated with the mass loss and water uptake of samples, nor the pH values of testing media.

Adjusting drug diffusivity using miscible polymer blends.

Tuning the release rates of drugs was accomplished with miscible polymer blends. Dexamethasone (DX) was formulated in a miscible polymer blend composed of two poly(ether urethane)s, one in which DX diffuses relatively quickly and the other in which DX diffuses relatively slowly. Matrices that provide drug diffusion coefficients from 7 x 10(-13) to 3 x 10(-19) cm2/s were obtained by adjusting the blend ratio.