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Abstracts Book - IMRC 2018

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• SB6-P107<br />

FABRICATION AND STUDY OF CURCUMIN LOADED<br />

NANOPARTICLES BASED ON PCL FOR SCA7 TREATMENT<br />

María Luisa Del Prado Audelo 1,2 , María Cristina Piña Barba 3 , Jonathan Javier Magaña Aguirre 4 ,<br />

Gerardo Leyva Gómez 5 , David Quintanar Gerrero 1<br />

1 Facultad de Estudios Superiores Cuautitlán, UNAM., Ingeniería y Tecnología, Mexico. 2 Facultad<br />

de Química, UNAM, Pharmacy, Mexico. 3 Instituto de Investigaciones en Materiales, Metálicos y<br />

Cerámicos, Mexico. 4 Instituto Nacional de Rehabilitacion, Genética y genómica, Mexico.<br />

5 Facultad de Química, UNAM, Farmacia, Mexico.<br />

The spinocerebellar ataxias (SCAs) are a large and diverse group of autosomaldominant,<br />

progressive neurodegenerative diseases. They share the clinical<br />

feature of progressive ataxia, reflecting degeneration of the cerebellum and,<br />

often, other connected regions of the nervous system (plyglutamine spino). The<br />

most common SCAs are caused by expansion of a CAG nucleotide repeat that<br />

encodes polyglutamine (polyQ) in the relevant disease proteins.<br />

Spinocerebellar ataxia type 7 (SCA7) is unique among CAG / polyglutamine<br />

(polyQ) repeat diseases due to dramatic intergenerational instability in repeat<br />

length and an associated cone-rod dystrophy retinal degeneration phenotype.<br />

SCA7 is caused by a polyQ expansion in the protein ataxin-7.<br />

Emerging insights into the mechanisms underlying polyQ SCAs suggest that<br />

these diseases may be treated through at least two principal therapeutic routes.<br />

The first is to pharmacologically modulate the perturbed cerebellar circuitry, as<br />

a symptomatic or possibly disease-modifying therapy. The second is to reduce<br />

levels of toxic disease-gene products.<br />

However, the therapeutic effects of drugs are very limited, but often causing<br />

systemic side effects, because almost all large molecule drugs and more than<br />

98% small molecule candidate drugs are unable to reach the brain tissue due to<br />

their poor permeability across the Blood-brain Barrier.<br />

One promising solution is the employment of polymeric nanoparticles (NPs)<br />

such as ε-polycaprolactone (PCL) NPs as drug carrier. The main of this work is<br />

the elaboration and physicochemical characterization of PCL NPs loaded with<br />

curcumin, wich is a fascinating molecule that has a wide use in medicine for<br />

diseases such as cancer and Alzheimer, to explore the potential of application<br />

as a terapeutic treatment for SCA7.

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