Biomedical Engineering Reference
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d n 4 y 3 n g | 8
Figure 7.11
(A) The chemical structure of mPEG 45 -b-PCL 80 -b-PPEEA 10 and schematic
illustration of micellar nanoparticle formation and the loading of paclitaxel
and siRNA. (B) Confocal laser scanning microscope (CLSM) image of the
intracellular distribution of Rho-paclitaxel micelleplex FAM-siRNA in MDA-MB-
435s cells after incubation for 2 h (6306). The scale bar is 10 mm. Paclitaxel
and siRNA were labeled with rhodamine (red) and fluorescein (green),
respectively. Cell nuclei were stained with 49,6-diamidino-2-phenylindole
(DAPI; blue). (C) Inhibition of MDA-MB-435s xenograft tumor growth by
paclitaxel micelleplex siPlk1 in comparison with various formulations (n 5 6).
(D) Dose-response study of paclitaxel delivered by paclitaxel micelleplex siNonsense
on the inhibition of MDA-MB-435s xenograft tumor growth (n 5 6).
Paclitaxel doses were 10- to 1000-fold higher (106 to 10006) compared
to those used in the paclitaxel micelleplex siPlk1 . (Adapted from Sun et al. 123
with permission from the American Chemical Society.)
 
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