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Cancer: Catalytic Tessy López Universidad Autónoma Metropolitana National Institute of Neurology and Neurosurgery [email protected]

Nanotechnology 2008

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Cancer: Catalytic

Tessy LópezUniversidad Autónoma Metropolitana

National Institute of Neurology andNeurosurgery

[email protected]

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What is cancer?

Is a term used for diseases in which abnormal cells dividewithout control and are able to invade other tissues. Cancer cells can spread to other parts of the body through the blood

and lymphatic systems (metastasize).

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ClassificaThis classification describes

the type of tissue in which thecancer cells begin to develop.

Adenocarcinoma - originates intissue

• Glioma – glial tissue

• Carcinoma– epithelial tissue

• Leukemia– blood cells

• Lymphoma– lymphatic tissue

• Myeloma– bone marrow

• –

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Most cancers are named for

the organ or type of cell inwhich they begin.

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Glioblastoma Multiforme(GBM) are 35% brain cancer,

according to the OMSstatistics. Those are theprimary and more frequenttumors of the Central

Nervous System (CNS).

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NANOMEDICINE AND

Nanotechnology hasbeen applied in all

therapeutic areas of medicine.

The most extensiveinvestigations are in

cancer.

Nanoparticles can

deliver chemotherapydrugs directly to tumorcells and then give off asignal after the cells are

destroyed. Drugs

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The treatment of Central NervousSystem (CNS) is difficult due to theBlood Brain Barrier (BBB) cross.

Only low molecular weightmolecules, liposolubles, and anypeptidic compounds cross the BBB.

 

Passive diffusion or specific

MECHANISM

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Local application or direct tumor injection of cytotoxic drugs has been proposed as a

technique to use 100% .

Systemic exposure and non-target organ

toxicity is minimized 

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Gliadel: Drug delivery systemof carmustine in CNS to GBM

PRODUCT IN THE MARQUET

Only release thechemotherapy

during 10 days.

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We have an alternative drug deliveryWe have an alternative drug delivery

System. This deliver during six monthsSystem. This deliver during six months

thetheFollowing drugs: Carmustine andFollowing drugs: Carmustine andRelease from TiO2 Release from SiO2

Tumor with C6

cancer cells Sol-gel device with drug

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Catalytic Nanomedicineis a new wa to treat

We made a catalytic processin the nucleotides of the

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BIO-CATALYST UAM-INNN

1. Cis Pt/SBA-15

2. Pt(acac)2/SiO2

3. Pt(acac)2/TiO2

4. H2PtCl6/SiO2

5. H2PtCl

6/TiO

26. Temozolomida/TiO2

7. (NH2)4Cl2Pt/ SiO2

8. Doxorubicina/SiO2

9. Metotrexato/SiO2

10.Cis-diamindicloro-Platino (II)B

11.Cis-diamindicloro-Platino (II)A

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CHARACTERIZ

Pt/SiO2

640m2/g

Particle size of theSupport = 30 nmParticle size of thePlatinum = 3-5 nm

Brönsted andLewis acid sites

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Pt/TiOC6 cellular model wasused to form

a tumor of 5 cm of diameter.

n = 70

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Control Platinum complex

Titania Titania-Platinum

Control Platinum complex

Titania Titania-Platinum

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0

10

20

30

40

50

60

CONTROL Pt TiO2 TiO2-Pt

   T  u  m  o  r  a   l  w  e   i  g

   t   h   (  g  r   )

*

*p=0.03 when compared with control

Tumoral weight reduction

24.6%

43.4%55.7%

Average tumor size of C6 glioma in rats after treatment

0

10

20

30

40

50

60

CONTROL Pt TiO2 TiO2-Pt

   T  u  m  o  r  a   l  w  e   i  g

   t   h   (  g  r   )

*

*p=0.03 when compared with control

Tumoral weight reduction

24.6%

43.4%55.7%

Average tumor size of C6 glioma in rats after treatment

96%

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Particl

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• A significant growth inhibitionwas observed in animal treated

with Platinum-titania .• The existence of stronger

electron-acceptor centers (Ti4+ 

and Ti3+

ions) that can coordinatewith basic molecules placed atDNA and promoted the apoptosismechanism.

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t=0 t= 3 t=5 t=10

Degradation of DNA studies withour different

Nanoparticles: control release

7

t=72

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