Detailed Information on Publication Record
2017
Black Phosphorus Nanoparticles Potentiate the Anticancer Effect of Oxaliplatin in Ovarian Cancer Cell Line
FOJTŮ, Michaela, Xinyi CHIA, Zdeněk SOFER, Michal MASAŘÍK, Martin PUMERA et. al.Basic information
Original name
Black Phosphorus Nanoparticles Potentiate the Anticancer Effect of Oxaliplatin in Ovarian Cancer Cell Line
Authors
FOJTŮ, Michaela (203 Czech Republic, belonging to the institution), Xinyi CHIA (702 Singapore), Zdeněk SOFER (203 Czech Republic), Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution) and Martin PUMERA (702 Singapore)
Edition
Advanced Functional Materials, Wrinheim, Wiley-VCH Verlag, 2017, 1616-301X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10400 1.4 Chemical sciences
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 13.325
RIV identification code
RIV/00216224:14110/17:00095042
Organization unit
Faculty of Medicine
UT WoS
000412319400006
Keywords in English
black phosphorus; drug delivery; nanoparticles ovarian; cancer oxaliplatin
Tags
Tags
International impact, Reviewed
Změněno: 20/3/2018 17:41, Soňa Böhmová
Abstract
V originále
During the past few years, growing attention has been paid to black phosphorus (BP) and its unique optical, electrical, and catalytic properties. Furthermore, BP has proven to be biocompatible and biodegradable; qualities that present new opportunities for its utilization in the field of life sciences. However, despite all its suitable properties and applicability, its utilization in biomedicine is still in its infancy. This study reports on the synthesis of black phosphorus nanoparticles (BP NPs) and exploration of thier applicability in targeted drug delivery. BP NPs are loaded with platinum agents—cisplatin and oxaliplatin—and subjected to in vitro evaluation of targeted drug delivery. The BP NPs are not only able to load the investigated platinum derivatives on their surfaces, but also to transfer the therapeutic cargo to target specific tissue and to combine their effect with oxaliplatin, which leads to further potentiation of the anticancer effect.
Links
GA16-05961S, research and development project |
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MUNI/A/1355/2016, interní kód MU |
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ROZV/24/LF/2016, interní kód MU |
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