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Depto. de Atención a la Salud, Universidad Autónoma Metropolitana‐Xochimilco,
México.
Laboratorio de Nanotecnología, Instituto Nacional de Neurología “MVS”, México.
C
Cancer d fi i i
definition
12
10
4
2
0
1922
1950
1980
1990
1998
1999
2001
Fuente: http://www.dgepi.salud.gob.mx/
Cancer Treatment
Conventional
C ti l forms
f off drug
d
administration generally
relyy on p pills,, eye
y drops, p,
ointments and intravenous
solutions. But in the last
few years we have
witnessed an explosion in
research aimed at creating
new drug delivery systems.
Local Drug delivery
Local application or direct tumor injection of
p
chemotherapeutic g has been p
drugs p
proposed as a
method by which local drug concentrations can be
maximized in the immediate tumor environment
while systemic exposure and non‐target organ
toxicity is minimized
9 Low
L
concentrations
9 toxic side
effects
Platinum based drugs
Platinum‐based drugs
The interest in platinum‐based antitumor drugs has its origin
in the 1960’s.
Platinating agents have been extensively used as treatment in
several types of cancer. A property common to many
chemical carcinogens is that they are DNA reactive.
y Conventional platinum-based drugs are DNA reactive
Pt-DNA adducts
Platinum complexes are now
among the most widely used
drugs for the treatment of
cancer.
The search for improved
platinum drugs continues with
the
h goalsl off reducing
d i the h toxic
i
side effects and broadening the
spectrum of activity to
tumours resistant
to cisplatin.
Nanoparticles of biodegradable polymers may provide a
solution for the problems in chemotherapy
• sustained, controlled and targeted delivery;
i.e. personalized chemotherapy;
•delivery
d l off therapeutic
h agents across
physiological drug barriers;
•chemotherapy at home
Nanotechnology
Laboratory
UAM-INNN
Our designed materials
Our designed materials
Pt/TiO2 and Pt/SiO2 nanoparticles, with:
• High surface area
•Surface acidity (Lewis acidity)
• Well dispersed Pt (1%) over TiO2 or SiO2 nanoparticles surface
•Stabilized Pt(II) species
•High surface hydroxilation degree
2
Pt-SiO2-Piridina
% Tranmittance
1
B
C
D
E
0
1700 1650 1600 1550 1500 1450 1400
-1
Wavenumber (cm )
Nanostructured biocatalysts for GBM treatment
In vivo tests
C6 cells inoculated in motor cortex and
treated by means of an implant formed by
the biocatalyst.
C6 cells inoculated intraperitoneally and
treated by means of an injection of
y j
suspended nanopaticles.
H‐E micrographs
g p of (a) tumor treated
( ) with Pt/SiO
/ 2‐Pt(NH
( 3)4Cl2 2 ,,
(b) 20X y (c) TUNEL technique.
a b c
Particles
Control Platinum complex
Titania Titania-Platinum 60
Tumoral weight reduction
50 24 6%
24.6%
20
10
0
CONTROL Pt TiO2 TiO2-Pt
*p=0.03 when compared with control