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Biocompatibility materials/devices

The ability of these peptidomimetic collagen-structures to adopt triple helices portends the development of highly stable biocompatible materials with collagenlike properties. For instance, it has been found that surface-immobilized (Gly-Pro-Meu)io-Gly-Pro-NH2 in its triple-helix conformation stimulated attachment and growth of epithelial cells and fibroblasts in vitro [77]. As a result, one can easily foresee future implementations of biostable collagen mimics such as these, in tissue engineering and for the fabrication of biomedical devices. [Pg.24]

Combat medicine poses special problems. Chemical science and technology can aid in the rapid detection and treatment of injuries from chemical and biological weapons and other new weapons such as lasers. We need to develop blood substitutes with a long shelf life, and improved biocompatible materials for dealing with wounds. For the Navy, there are special needs such as analytical systems that can sample the seawater to detect and identify other vessels. We need good ways to detect mines, both at sea and on land. Land mines present a continued threat to civilians after hostilities have ended, and chemical techniques are needed to detect these explosive devices. [Pg.174]

Polyelectrolytes have been widely investigated as components of biocompatible materials. Biomaterials come into contact with blood when used as components in invasive instruments, implant devices, extracorporeal devices in contact with blood flow, implanted parts of hard structural elements, implanted parts of organs, implanted soft tissue substitutes and drug delivery devices. Approaches to the development of blood compatible materials include surface modification to give blood compatibility, polyelectrolyte-based systems which adsorb and/or release heparin as well as polyelectrolytes which mimic the biological activity of heparin. [Pg.39]

Biocompatible materials consisting of poly(ester-amides), (I), were prepared by DesNoyer et al. (2) and used in cardiovascular medical devices. [Pg.419]

These intermediates were then amidated with selected aminobenzene sulfonic acids. Materials produced in this process were used as biocompatible materials and in drug delivery devices. [Pg.481]

All in all, it is obvious that dextran will gain increasing importance as a carrier material in pharmaceutical applications, as a basis for bioactive derivatives and as a nanostructured device. Dextran and modified dex-trans should always be considered as a biocompatible material with a high structure-forming potential. [Pg.280]

Applications of these layers as supports for sensor devices and biocompatible materials as well as for adhesion promotion have illustrated the ability of polymer surface chemistry. [Pg.71]

Business Communications Company, Inc. (BCC). 25 Van Zant St., Norwalk, CT 06855, U.S.A. Phone +1 203-853-4266, Fax +1 203-853-0348. E-mail editor buscom.com. URL http // www.buscom.com. Provides industry research and technical market analysis in many industries, including advanced materials, biotechnology/life sciences, nanotechnology, and plastics/polymers. All reports are available online. Recent report titles include Biocompatible Materials for the Human Body, Patient Monitoring Devices, Biomedical Applications of Nanoscale Devices, and Advanced Drug Delivery Systems New Development, New Technologies. [Pg.287]

Overall, much effort has been made to develop biocompatible organic materials, which allows for the ultimate integration between the electronic device and biological system. The possibility of fabricating memory devices on biodegradable substrates, such as, rice paper and chitosan is also demonstrated. Biocompatible and flexible resistive switching memory devices are made on the basis of Ag-doped chitosan as the natural solid polymer electrolyte layer on the transparent and bendable substrate. Decomposable devices, where chitosan layer serves as the substrate while Mg as the electrode, have been also achieved (Hosseini and Lee, 2015). A comparison of the biocompatible material-based resistive switching memory devices is made in Table 3.2. [Pg.95]

Table 3.2 Comparison of Biocompatible Material-Based Resistive Random Access Memory Devices... Table 3.2 Comparison of Biocompatible Material-Based Resistive Random Access Memory Devices...
Irimia-Vladu, M., 2014. Green electronics biodegradable and biocompatible materials and devices for sustainable future. Chem. Soc. Rev. 43, 588-610. [Pg.100]

Although FDA does not have specific guidance for biocompatibility testing of polymers, the hitemational Standard ISO-10993 is recommended by the FDA for biological evaluation of biomedical devices. ISO-10993 entails 20 detailed standards to evaluate the biocompatibihty of a material device prior to clinical testing. These tests include both in vitro and in vivo assays as well as physicochemical characterization... [Pg.341]

EMM can also be effectively utihzed for fabrication of several of microfeatures for a wide range of microengineering applications such as fuel processing, aerospace, heat transfer, microfluidics, and biomedical applications. These microdevices have to often withstand high stresses at elevated temperatures during their service in different applications such as microcombustors, electrochemical reactions required at elevated temperatures in microreactors, and also in microthermal devices. For biomedical applications, microcomponents are to be made of biocompatible materials and... [Pg.198]

The hydrophilicity conferred by the presence of alkoxy groups in the polymeric pendant chains results in an enhancement of the solubility of these polymers (Kim et al. 2003). Thus, the inherent hydrophobicity of mcl-PHAs could be strongly modified by the introduction of hydrophilic moieties into the side chain, increasing their applicability as biocompatible materials for a wide range of biomedical devices. [Pg.148]

Artificial kidney designs will likely continue to experience incremental improvements in the materials and hemodynamic areas. New developments in biocompatible materials, superior transport methods for toxin removal, and improved patient management techniques will allow further maturation of hemodialysis and hemofiltration therapy. For example, considerable benefits could be realized from selective toxin removal without concomitant elimination of beneficial proteins. It has been suggested that future devices might utilize the absorption removal pathway with affinity methods as a primary technique to eliminate specific uremic toxins (Klinkmann and Vienken, 1995). [Pg.512]


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See also in sourсe #XX -- [ Pg.380 ]




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