TY - JOUR
T1 - Nano-bio interaction between graphite oxide nanoparticles and human blood components
AU - Kim, Hyoung Mi
AU - Kim, Kyoung Min
AU - Lee, Kyunghong
AU - Kim, Yoon Suk
AU - Oh, Jae Min
PY - 2012/11
Y1 - 2012/11
N2 - We investigated the effect of graphite oxide (GO) nanoparticles, which are an emerging nanomaterial with potential applications as drug-delivery nanocarriers, on human blood cells and plasma proteins. Graphite oxides were successfully prepared by oxidizing graphite with potassium permanganate and sulfuric acid. Powder X-ray diffraction patterns, FTIR, and Raman spectra show that the oxidation of graphite worked well and yielded GO nanolayers. To evaluate the interaction of GO with human blood components, we studied its hemolytic effect and protein binding kinetics. The nanoparticles did not show any significant hemolytic effect during 30 min at a very high concentration of 10 mg/mL, showing high compatibility with human blood. The interaction between GO nanoparticles and human blood cells was visualized with optical microscopy. Some nanoparticles were found at the periphery of blood cells, however, significant damages or morphological changes of blood cells upon exposure to nanoparticles were not detected. When we treated GO nanoparticles with plasma proteins, such as human serum albumin, γ-immunoglobulin, and fibrinogen, they showed concentration-dependent binding behavior, and the binding constant is comparable with other biocompatible nanoparticles. The interaction between graphite oxide (GO) nanoparticles and blood components are demonstrated. The GO nanoparticles are biocompatible, that is, they behave inert with blood cells and plasma proteins.
AB - We investigated the effect of graphite oxide (GO) nanoparticles, which are an emerging nanomaterial with potential applications as drug-delivery nanocarriers, on human blood cells and plasma proteins. Graphite oxides were successfully prepared by oxidizing graphite with potassium permanganate and sulfuric acid. Powder X-ray diffraction patterns, FTIR, and Raman spectra show that the oxidation of graphite worked well and yielded GO nanolayers. To evaluate the interaction of GO with human blood components, we studied its hemolytic effect and protein binding kinetics. The nanoparticles did not show any significant hemolytic effect during 30 min at a very high concentration of 10 mg/mL, showing high compatibility with human blood. The interaction between GO nanoparticles and human blood cells was visualized with optical microscopy. Some nanoparticles were found at the periphery of blood cells, however, significant damages or morphological changes of blood cells upon exposure to nanoparticles were not detected. When we treated GO nanoparticles with plasma proteins, such as human serum albumin, γ-immunoglobulin, and fibrinogen, they showed concentration-dependent binding behavior, and the binding constant is comparable with other biocompatible nanoparticles. The interaction between graphite oxide (GO) nanoparticles and blood components are demonstrated. The GO nanoparticles are biocompatible, that is, they behave inert with blood cells and plasma proteins.
KW - Blood cells
KW - Fluorescence spectroscopy
KW - Graphite
KW - Hemolysis
KW - Nanoparticles
KW - Proteins
UR - http://www.scopus.com/inward/record.url?scp=84868590578&partnerID=8YFLogxK
U2 - 10.1002/ejic.201200587
DO - 10.1002/ejic.201200587
M3 - Article
AN - SCOPUS:84868590578
SN - 1434-1948
SP - 5343
EP - 5349
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 32
ER -