Protective biocompatability

A miniature, needle-type glucose sensor based on a tri-layer membrane configuration has been prepared and evaluated both in vitro and in vivo. The perfluorinated ionomer, Nafion, was used as a protective, biocompatible, outer coating, and poly(o-phenylenediamine) as an inner coating to reduce interference by small, electroactive compounds. Glucose oxidase immobilized in a bovine serum albumin matrix was sandwiched between these coatings. Heat curing of the assembled sensor at 120 C improved the stability of the Nafion layer and extended the sensor lifetime. 

Vitahium FHS ahoy is a cobalt—chromium—molybdenum ahoy having a high modulus of elasticity. This ahoy is also a preferred material. When combiaed with a properly designed stem, the properties of this ahoy provide protection for the cement mantle by decreasing proximal cement stress. This ahoy also exhibits high yields and tensile strength, is corrosion resistant, and biocompatible. Composites used ia orthopedics include carbon—carbon, carbon—epoxy, hydroxyapatite, ceramics, etc. 

Tessier, P. Y., Pichon, L., VUlechaise, P, Linez, P., Angleraud, B., MubumbUa, N., Fouquet, V, Straboni, A., Milhet, X., and Hildebrand, H. F., Carbon Nitride Thin Films as Protective Coatings for Biomaterials Synthesis, Mechanical and Biocompatibility Characterizations, Diamond Relat. Mater, Vol. 12,2003,pp. 1066-1069. 

After 7 days, the acute inflammatory response at the implantation site was evaluated. Bisphenol A resulted in a moderate level of irritation at the implantation site and was clearly the least biocompatible test substance. Tyrosine derivatives containing the benzyloxycar-bonyl group caused a slight inflammatory response, while all other tyrosine derivatives produced no abnormal tissue response at all. These observations indicate that tyrosine dipeptide derivatives, even if fully protected, are more biocompatible than BPA, a synthetic diphenol. ... 

In an attempt to identify more biocompatible diphenols for the design of degradable biomaterials, we studied derivatives of tyrosine dipeptide as potential monomers. After protection of the amino terminus and the carboxylic acid terminus, the reactivity of tyrosine dipeptide (Figure 1) could be expected to be similar to the reactivity of industrial diphenols. Thus, derivatives of tyrosine dipeptide could be suitable replacements for BPA in the synthesis of a variety of new polymers that had heretofore not been accessible as biomaterials due to the lack of diphenolic monomers with good biocompatibility. 

In an attempt to identify new, biocompatible diphenols for the synthesis of polyiminocarbonates and polycarbonates, we considered derivatives of tyrosine dipeptide as potential monomers. Our experimental rationale was based on the assumption that a diphenol derived from natural amino acids may be less toxic than many of the industrial diphenols. After protection of the amino and carboxylic acid groups, we expected the dipeptide to be chemically equivalent to conventional diphenols. In preliminary studies (14) this hypothesis was confirmed by the successful preparation of poly(Z-Tyr-Tyr-Et iminocarbonate) from the protected tyrosine dipeptide Z-Tyr-Tyr-Et (Figure 3). Unfortunately, poly (Z-Tyr-Tyr-Et iminocarbonate) was an insoluble, nonprocessible material for which no practical applications could be identified. This result illustrated the difficulty of balancing the requirement for biocompatibility with the need to obtain a material with suitable "engineering" properties. 

The interaction in an interface of device/tissue is limited by two factors. There is the corrosive environment, such as biological fluid, which contains salts and proteins among other cellular structures in which the sensor device must survive [47, 48], Second, there is the encapsulation material which may induce a toxic reaction due to poor biocompatibility and hemocompatibility [49, 50], It is crucial to use a biomaterial that can overcome both limiting factors to maintain the lifetime of the sensor device and protect the body [51, 52],... 

Although the titanium oxide layer at the surface of the nitinol is highly biocompatible and protects the underlying substrate from electrochemical corrosion, the titanium oxide layer itself is mechanically very brittle. Under mechanical stress, such as the shear of blood flow in the aorta or under the bending moments of aortic pulsations, the titanium oxide surface layer can fracture, exposing the underlying metal to corrosion. Not only is corrosion undesirable in terms of biocompatibility (i.e., leaching of nickel and its... 

Dehvering pharmaceutical agents to specific cells in the body is a difficult task involving complex interactions between many elements. Delivery systems have several fundamental requirements to achieve this task. The delivery vehicle must be ingesti-ble, implantable, or injectable to introduce the dmg into the body. The system must then protect the drug from the body s defense mechanisms in order to accumulate in selected cells. Once at the target, the delivery system should release the enclosed pharmaceutical agent with a controllable and predictable profile. Finally, the delivery vehicle should be biocompatible, nontoxic, and easily eliminated from the body. 

Richardson, S.C.W., Kolbe, H.V.J., Duncan, R. (1999). Potential of low molecular mass chitosan as a DNA delivery system biocompatibility, body distribution and ability to complex and protect DNA. Int J. Pharm., 178, 231-243. 

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