Biocompatibility of Polyaniline
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28610%2F10%3A63509216" target="_blank" >RIV/70883521:28610/10:63509216 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/70883521:28110/11:43867108 RIV/70883521:28610/11:43867108
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Biocompatibility of Polyaniline
Popis výsledku v původním jazyce
The term biocompatibility refers generally to the compatibility of material with the body tissues. Due to the fact that almost any foreign material triggers a defence, biological testing of materials which are in the contact with body is extremely important. Though PANi is the polymer of wide application, data on its biocompatibility are not plentiful. Polyaniline was studied mainly in-vivo in terms of implantability and post-implant evaluation of the changes both in the polymer and in the tissue surrounding implant the second group of test methods is focused on assessment of proliferation and/or differentiation of cells on PANi surfaces. Current study is focused on biocompatibility of PANi Samples in terms of cytotoxicity, irritation and delayed-typehypersensitivity of powder samples (according to EN ISO 10993-5 and EN ISO 10993-10). The combination of the above methods is primary intended for medical devices coming in contact with intact skin, mucosal membrane and breached or compro
Název v anglickém jazyce
Biocompatibility of Polyaniline
Popis výsledku anglicky
The term biocompatibility refers generally to the compatibility of material with the body tissues. Due to the fact that almost any foreign material triggers a defence, biological testing of materials which are in the contact with body is extremely important. Though PANi is the polymer of wide application, data on its biocompatibility are not plentiful. Polyaniline was studied mainly in-vivo in terms of implantability and post-implant evaluation of the changes both in the polymer and in the tissue surrounding implant the second group of test methods is focused on assessment of proliferation and/or differentiation of cells on PANi surfaces. Current study is focused on biocompatibility of PANi Samples in terms of cytotoxicity, irritation and delayed-typehypersensitivity of powder samples (according to EN ISO 10993-5 and EN ISO 10993-10). The combination of the above methods is primary intended for medical devices coming in contact with intact skin, mucosal membrane and breached or compro
Klasifikace
Druh
O - Ostatní výsledky
CEP obor
CD - Makromolekulární chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GA202%2F09%2F1626" target="_blank" >GA202/09/1626: Inteligentní kapaliny a komposity s řízenou strukturou</a><br>
Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2011
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů