In vitro cytotoxicity evaluation of selected materials for
wound dressing application

a 2022

In vitro cytotoxicity evaluation of selected materials for wound dressing application

KAUEROVÁ, Tereza, Peter KOLLÁR a Pavel SUCHÝ

Základní údaje

Originální název

In vitro cytotoxicity evaluation of selected materials for wound dressing application

Název česky

In vitro hodnocení cytotoxicity vybraných krycích materiálu pro hojení ran

Autoři

KAUEROVÁ, Tereza (203 Česká republika, domácí), Peter KOLLÁR (203 Česká republika, domácí) a Pavel SUCHÝ (203 Česká republika, domácí)

Vydání

27th Interdisciplinary Toxicology Conference TOXCON 2022, 2022

Další údaje

Jazyk

angličtina

Typ výsledku

Konferenční abstrakt

Obor

30108 Toxicology

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Kód RIV

RIV/00216224:14160/22:00134443

Organizační jednotka

Farmaceutická fakulta

ISSN

Klíčová slova anglicky

medical devices; wound dressings; cytotoxicity

Štítky

rivok, ÚFTo

Změněno: 29. 5. 2023 13:52, JUDr. Sabina Krejčiříková

Anotace

V originále

Every medical device that is in contact with human body must be subjected to series of biological tests during the risk assessment process. Cytotoxicity testing belongs to the group of endpoints for biological evaluation of medical devices and its whole process is defined in ISO 10993-5 “Biological evaluation of medical devices – Part 5: Tests for in vitro cytotoxicity”. In a short time, it provides an initial information about toxicity, which serves as a good indicator of general toxic properties and thus it can reduce the number of in vivo models required for subsequent toxicity analyzes. There are different approaches to cytotoxicity testing, either direct contact toxicity evaluation or elution methods. In our study, we focused on the latter approach, namely on optimizing the preparation of the material extracts in accordance with recommendations from ISO 10993-12 “Biological evaluation of medical devices – Part 12: Sample preparation and reference materials”. Based on the specific properties of tested materials, we selected volume of solvent used per surface area of test samples. Material samples were extracted in appropriate cell culture medium supplemented with serum. The materials were extracted at 37 °C for 24 hours with continuous circulation of sterile material immersed in the extraction medium in sealed tubes. In addition, we further extended the analyzes to dose ranging cytotoxicity evaluation to determine the level at which cytotoxicity no longer occurs.

Návaznosti

TH04020540, projekt VaV

Název: Nová bioaktivní hemostatika a krytí ran na bázi kolagenu a celulózy

Investor: Technologická agentura ČR, Nová bioaktivní hemostatika a krytí ran na bázi kolagenu a celulózy

Citovat

KAUEROVÁ, Tereza, Peter KOLLÁR a Pavel SUCHÝ. In vitro cytotoxicity evaluation of selected materials for wound dressing application. In 27th Interdisciplinary Toxicology Conference TOXCON 2022. 2022. ISSN 0372-7025.

@proceedings{2235906,
   author = {Kauerová, Tereza and Kollár, Peter and Suchý, Pavel},
   booktitle = {27th Interdisciplinary Toxicology Conference TOXCON 2022},
   keywords = {medical devices; wound dressings; cytotoxicity},
   language = {eng},
   title = {In vitro cytotoxicity evaluation of selected materials for wound dressing application},
   url = {https://www.mmsl.cz/pdfs/mms/2022/88/39.pdf},
   year = {2022}
}

TY  - CONF
ID  - 2235906
AU  - Kauerová, Tereza - Kollár, Peter - Suchý, Pavel
PY  - 2022
TI  - In vitro cytotoxicity evaluation of selected materials for wound dressing application
KW  - medical devices
KW  - wound dressings
KW  - cytotoxicity
UR  - https://www.mmsl.cz/pdfs/mms/2022/88/39.pdf
N2  - Every medical device that is in contact with human body must be subjected to series of biological tests during the risk assessment process. Cytotoxicity testing belongs to the group of endpoints for biological evaluation of medical devices and its whole process is defined in ISO 10993-5 “Biological evaluation of medical devices – Part 5: Tests for in vitro cytotoxicity”. In a short time, it provides an initial information about toxicity, which serves as a good indicator of general toxic properties and thus it can reduce the number of in vivo models required for subsequent toxicity analyzes. There are different approaches to cytotoxicity testing, either direct contact toxicity evaluation or elution methods. In our study, we focused on the latter approach, namely on optimizing the preparation of the material extracts in accordance with recommendations from ISO 10993-12 “Biological evaluation of medical devices – Part 12: Sample preparation and reference materials”. Based on the specific properties of tested materials, we selected volume of solvent used per surface area of test samples. Material samples were extracted in appropriate cell culture medium supplemented with serum. The materials were extracted at 37 °C for 24 hours with continuous circulation of sterile material immersed in the extraction medium in sealed tubes. In addition, we further extended the analyzes to dose ranging cytotoxicity evaluation to determine the level at which cytotoxicity no longer occurs.
ER  -

KAUEROVÁ, Tereza, Peter KOLLÁR a Pavel SUCHÝ. In vitro cytotoxicity evaluation of selected materials for wound dressing application. In \textit{27th Interdisciplinary Toxicology Conference TOXCON 2022}. 2022. ISSN~0372-7025.

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