Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells. / Jaworski, Sławomir; Biniecka, Paulina; Bugajska, Zaneta; Duniluk, Karolina; Dyjak, Slawomir ; Strojny, Barbara; Kutwin, Marta; Wierzbicki, Mateusz; Grodzik, Marta; Chwalibog, André.

I: International Journal of Nanomedicine, Bind 2017, Nr. 12, 2017, s. 3839-3849.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jaworski, S, Biniecka, P, Bugajska, Z, Duniluk, K, Dyjak, S, Strojny, B, Kutwin, M, Wierzbicki, M, Grodzik, M & Chwalibog, A 2017, 'Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells', International Journal of Nanomedicine, bind 2017, nr. 12, s. 3839-3849. https://doi.org/10.2147/IJN.S135932

APA

Jaworski, S., Biniecka, P., Bugajska, Z., Duniluk, K., Dyjak, S., Strojny, B., Kutwin, M., Wierzbicki, M., Grodzik, M., & Chwalibog, A. (2017). Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells. International Journal of Nanomedicine, 2017(12), 3839-3849. https://doi.org/10.2147/IJN.S135932

Vancouver

Jaworski S, Biniecka P, Bugajska Z, Duniluk K, Dyjak S, Strojny B o.a. Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells. International Journal of Nanomedicine. 2017;2017(12):3839-3849. https://doi.org/10.2147/IJN.S135932

Author

Jaworski, Sławomir ; Biniecka, Paulina ; Bugajska, Zaneta ; Duniluk, Karolina ; Dyjak, Slawomir ; Strojny, Barbara ; Kutwin, Marta ; Wierzbicki, Mateusz ; Grodzik, Marta ; Chwalibog, André. / Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells. I: International Journal of Nanomedicine. 2017 ; Bind 2017, Nr. 12. s. 3839-3849.

Bibtex

@article{afdc2003f6ef47bebffe4f560af9cb30,
title = "Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells",
abstract = "A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m2/g, well-developed porosity, and high electrical conductivity. These unique properties and ability to transfer charge create a possibility of employing HNC as a moderator of tumor cell growth. As the charge of HNC may interfere with cell membranes by adhesion and by bonding with cell receptors, it may block the supply of nutrients. The interactions of HNC with the U87 cells can also lead to the excessive generation of reactive oxygen species (ROS) and activate apoptotic mechanisms in cancer cells. The investigation was performed using U87 human glioblastoma and PCS-201–010 normal fibroblast cell lines, where cell morphology and ultrastructure, viability, ROS production, type of cell death, mitochondrial transmembrane potential, and the expression of genes engaged in apoptosis pathways are studied. The results demonstrate that cytotoxicity of HNC particles increases with concentration from 5 to 100 µg/mL by activation of apoptosis through the mitochondrial pathway, without inducing necrosis. Our research indicates the potential applicability of HNC in cancer therapy.",
author = "S{\l}awomir Jaworski and Paulina Biniecka and Zaneta Bugajska and Karolina Duniluk and Slawomir Dyjak and Barbara Strojny and Marta Kutwin and Mateusz Wierzbicki and Marta Grodzik and Andr{\'e} Chwalibog",
year = "2017",
doi = "10.2147/IJN.S135932",
language = "English",
volume = "2017",
pages = "3839--3849",
journal = "International Journal of Nanomedicine",
issn = "1176-9114",
publisher = "Dove Press Ltd",
number = "12",

}

RIS

TY - JOUR

T1 - Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human gliblastoma grade IV cells

AU - Jaworski, Sławomir

AU - Biniecka, Paulina

AU - Bugajska, Zaneta

AU - Duniluk, Karolina

AU - Dyjak, Slawomir

AU - Strojny, Barbara

AU - Kutwin, Marta

AU - Wierzbicki, Mateusz

AU - Grodzik, Marta

AU - Chwalibog, André

PY - 2017

Y1 - 2017

N2 - A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m2/g, well-developed porosity, and high electrical conductivity. These unique properties and ability to transfer charge create a possibility of employing HNC as a moderator of tumor cell growth. As the charge of HNC may interfere with cell membranes by adhesion and by bonding with cell receptors, it may block the supply of nutrients. The interactions of HNC with the U87 cells can also lead to the excessive generation of reactive oxygen species (ROS) and activate apoptotic mechanisms in cancer cells. The investigation was performed using U87 human glioblastoma and PCS-201–010 normal fibroblast cell lines, where cell morphology and ultrastructure, viability, ROS production, type of cell death, mitochondrial transmembrane potential, and the expression of genes engaged in apoptosis pathways are studied. The results demonstrate that cytotoxicity of HNC particles increases with concentration from 5 to 100 µg/mL by activation of apoptosis through the mitochondrial pathway, without inducing necrosis. Our research indicates the potential applicability of HNC in cancer therapy.

AB - A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m2/g, well-developed porosity, and high electrical conductivity. These unique properties and ability to transfer charge create a possibility of employing HNC as a moderator of tumor cell growth. As the charge of HNC may interfere with cell membranes by adhesion and by bonding with cell receptors, it may block the supply of nutrients. The interactions of HNC with the U87 cells can also lead to the excessive generation of reactive oxygen species (ROS) and activate apoptotic mechanisms in cancer cells. The investigation was performed using U87 human glioblastoma and PCS-201–010 normal fibroblast cell lines, where cell morphology and ultrastructure, viability, ROS production, type of cell death, mitochondrial transmembrane potential, and the expression of genes engaged in apoptosis pathways are studied. The results demonstrate that cytotoxicity of HNC particles increases with concentration from 5 to 100 µg/mL by activation of apoptosis through the mitochondrial pathway, without inducing necrosis. Our research indicates the potential applicability of HNC in cancer therapy.

U2 - 10.2147/IJN.S135932

DO - 10.2147/IJN.S135932

M3 - Journal article

C2 - 28572728

VL - 2017

SP - 3839

EP - 3849

JO - International Journal of Nanomedicine

JF - International Journal of Nanomedicine

SN - 1176-9114

IS - 12

ER -

ID: 178852840