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no signii cant cytotoxicity to NIH 3T3 i broblast cells was observed, which  is  prom-
ising   for  their  potential  use  in  drug-delivery systems and tissue engineering
applications  [237] .
15.9.4
Bioimaging
h e CNCs having reactive functional groups on their surface and their high surface area
of 150 m 2 /g [37, 238] could be considered as a new generation of bioimaging probes
or drug nanocarriers. Dong and Roman have developed a simple method (a three-
step reaction) to attach l uorescent FITC molecules covalently to the surface of CNCs
for l uorescence bioassay and bioimaging application for  studying  the interaction of
CNCs with cells and in-vivo biodistribution of CNCs [239] . h e scheme and images
of aqueous suspension of CNCs and FITC-labeled CNCs are shown in Figure 15.17.
h e results showed insignii cant CNCs-FITC uptake by human brain microvascular
endothelial (HBMECs).
In this advancement, Mahmoud et al. investigated the ef ect of surface charge of
l uorescent-labeled CNCs as chemically synthesized CNCs-l uorescein isothiocyanate
(CNCs-FITC) and CNCs-rhodamine B isothiocyanate (CNCs-RBITC)) on cellular
O
O
H 2 N
O
( a )
HO
Cl
NH 4 OH
OH
O
O
Cellulose Nanocrystal
Cellulose Nanocrystal
Cellulose Nanocrystal
O
O
OH
O
O
OH
HOOC
HOOC
S
HN
C
NH
HO
N=C=S
O
Cellulose Nanocrystal
Figure 15.17 (a) Scheme of covalent attachment of l uorescent FITC molecules to the surface of CNCs;
(b) digital images of aqueous suspensions of (A) CNCs (0.8 wt%) and (B) FITC-labeled CNCs (0.5 wt%)
[239] .
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