In vitro hemocompatibility testing of medical devices
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
32698094
DOI
10.1016/j.thromres.2020.07.027
PII: S0049-3848(20)30318-2
Knihovny.cz E-zdroje
- Klíčová slova
- Coagulation, Hemocompatibility, Human blood, Leukocyte, Platelet,
- MeSH
- hemokoagulace * MeSH
- hemolýza MeSH
- lidé MeSH
- techniky in vitro MeSH
- testování materiálů MeSH
- trombocyty * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Hemocompatibility testing is essential for the safe use of medical devices that come into contact with blood. There are various evaluation methodologies. In vivo, ex vivo and in vitro systems can be used and different categories can be evaluated in different ways. This review deals with in vitro hemocompatibility testing mainly on the basis of ISO standard 10993-4 recommendations and possibly new research results. This is a summary of all tested categories, i.e. coagulation, hemolysis, hematology and activation of leukocytes and platelets and the complement system. The main principle of evaluation and the possibilities of testing using various methodologies are always described. In the next part, variants of the method of blood incubation with the tested medical device from the static system to the circulation are described. Circulation can be provided, for example, by means of the Chandler Loop or parallel-plate chambers.
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