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Yuan-Yun Lin , Ling Chao*, Kevin C.-W. Wu*
Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan
Discussions 	
Objective 	
Acknowledgements 	
Characterization	
SEM of MCNs
E-mail :lingchao@ntu.edu.tw and kevinwu@ntu.edu.tw
Synthesis of A Novel Phospholipid Layer/Mesoporous Carbon Nanoparticles (MCNs)
Core/Shell Structure as An Anticancer Drug Nanovehicle
for Efficient Drug Loading
Synthesis of a Novel Phospholipid Layer/MCNs	
Experimental 	
Doxorubicin
Hydrophobic Drug Loading
Lipid coating
MCNs
Vial DOPC@CCl4
Remove organic solvent
under N2
Mix well
Add solution
Drug Loading Testing
centrifugation
Optical MicroscopeFluorescence Photometer
Analysis
TEM of MCNs
50 nm
BET of MCNs
Relative Pressure (p/p0)
VolumeAbsorbed(cm3g-1)
Pore Diameter (nm)VP
0
50
100
150
200
250
300
350
0 0.2 0.4 0.6 0.8 1 1.2
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0.45
0.5
0 50 100 150 200
Drug Loading
0
20
40
60
80
100
Loading(%)
Results	
Because of their high surface area and the hydrophobicity,
mesoporous carbon nanoparticles (MCN) were successfully
synthesized and utilized as a potential drug nanocarrier. In
addition, a phospholipid layer was applied as a gate-keeper to
control the load/release behavior of drugs. The MCN/
phospholipid core/shell structure here provides a new
alternative for next-generation bio-medical applications.
The research was supported by the National Taiwan University.
Synthesis of a Novel Phospholipid Layer/Mesoporous Carbon Nanoparticles for Intracellular Drug Delivery.	
MCNs 
Drug loading Lipids mixing
!
Cell Culture
(a)
 (b)
drug

100 nm
5 µm
MCN+doxo.:
16.23 µmole/ doxo./g MCN
MCN+doxo.+lipid:
8.76 µmole/ doxo./g MCN
MCN+doxo. MCN+doxo.+lipid
Texas Red @DHPE
MCN
fluorescence

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YUAN-YUN LIN_ISOMRM

  • 1. Yuan-Yun Lin , Ling Chao*, Kevin C.-W. Wu* Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan Discussions Objective Acknowledgements Characterization SEM of MCNs E-mail :lingchao@ntu.edu.tw and kevinwu@ntu.edu.tw Synthesis of A Novel Phospholipid Layer/Mesoporous Carbon Nanoparticles (MCNs) Core/Shell Structure as An Anticancer Drug Nanovehicle for Efficient Drug Loading Synthesis of a Novel Phospholipid Layer/MCNs Experimental Doxorubicin Hydrophobic Drug Loading Lipid coating MCNs Vial DOPC@CCl4 Remove organic solvent under N2 Mix well Add solution Drug Loading Testing centrifugation Optical MicroscopeFluorescence Photometer Analysis TEM of MCNs 50 nm BET of MCNs Relative Pressure (p/p0) VolumeAbsorbed(cm3g-1) Pore Diameter (nm)VP 0 50 100 150 200 250 300 350 0 0.2 0.4 0.6 0.8 1 1.2 0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4 0.45 0.5 0 50 100 150 200 Drug Loading 0 20 40 60 80 100 Loading(%) Results Because of their high surface area and the hydrophobicity, mesoporous carbon nanoparticles (MCN) were successfully synthesized and utilized as a potential drug nanocarrier. In addition, a phospholipid layer was applied as a gate-keeper to control the load/release behavior of drugs. The MCN/ phospholipid core/shell structure here provides a new alternative for next-generation bio-medical applications. The research was supported by the National Taiwan University. Synthesis of a Novel Phospholipid Layer/Mesoporous Carbon Nanoparticles for Intracellular Drug Delivery. MCNs Drug loading Lipids mixing ! Cell Culture (a) (b) drug 100 nm 5 µm MCN+doxo.: 16.23 µmole/ doxo./g MCN MCN+doxo.+lipid: 8.76 µmole/ doxo./g MCN MCN+doxo. MCN+doxo.+lipid Texas Red @DHPE MCN fluorescence