TY - JOUR
T1 - Preparation and biological evaluation of photoluminescent carbonaceous nanospheres
AU - Qian, Jun
AU - Chen, Jiantao
AU - Ruan, Shaobo
AU - Shen, Shun
AU - He, Qin
AU - Jiang, Xinguo
AU - Zhu, Jianhua
AU - Gao, Huile
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Carbon nanospheres (CNP) possess several unique properties that render CNP superior to traditional organic dyes and quantum dots in the biological application. However, the interaction of CNP with biological systems was far from well-known. In this study, a simple method using cocoon silk was used to synthesize photoluminescent CNP. The particle size of CNP was 100.6. nm with well dispersity. The excitation/emission wavelength was 340. nm and 442. nm. Cellular uptake demonstrated the uptake of CNP by A549 cells was a time-, concentration- and energy-dependent procedure. Endosome was involved in the uptake rather than mitochondria. Through several uptake inhibitors, it showed the uptake was energy-dependent and mainly mediated by clathrin-mediated endocytosis. In vivo, CNP were mainly distributed in heart and lung, while only a modest amount of CNP was distributed in spleen, liver and kidney. The distribution in tumor was relatively low, which made CNP a candidate for heart cell imaging. At as high as 2. mg/mL, CNP showed no obvious toxicity to cells. The hemolysis rate of CNP was also lower than 10%. These results suggested CNP was relatively safe in biological application.
AB - Carbon nanospheres (CNP) possess several unique properties that render CNP superior to traditional organic dyes and quantum dots in the biological application. However, the interaction of CNP with biological systems was far from well-known. In this study, a simple method using cocoon silk was used to synthesize photoluminescent CNP. The particle size of CNP was 100.6. nm with well dispersity. The excitation/emission wavelength was 340. nm and 442. nm. Cellular uptake demonstrated the uptake of CNP by A549 cells was a time-, concentration- and energy-dependent procedure. Endosome was involved in the uptake rather than mitochondria. Through several uptake inhibitors, it showed the uptake was energy-dependent and mainly mediated by clathrin-mediated endocytosis. In vivo, CNP were mainly distributed in heart and lung, while only a modest amount of CNP was distributed in spleen, liver and kidney. The distribution in tumor was relatively low, which made CNP a candidate for heart cell imaging. At as high as 2. mg/mL, CNP showed no obvious toxicity to cells. The hemolysis rate of CNP was also lower than 10%. These results suggested CNP was relatively safe in biological application.
KW - Carbon nanospheres
KW - Cell uptake mechanism
KW - Safety
KW - Tissue distribution
UR - http://www.scopus.com/inward/record.url?scp=84901999405&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2014.05.016
DO - 10.1016/j.jcis.2014.05.016
M3 - Article
C2 - 24935192
AN - SCOPUS:84901999405
SN - 0021-9797
VL - 429
SP - 77
EP - 82
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -